Dissertations / Theses on the topic 'Ganoderma diseases of plants'
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1
Roberts, Lyndal, and lyndalroberts@gmail com. "Australian Ganoderma : identification, growth & antibacterial properties." Swinburne University of Technology. Environment and Biotechnology Centre, 2004. http://adt.lib.swin.edu.au./public/adt-VSWT20060109.114954.
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Ganoderma species are one of the most widely researched fungi because of their
reported potent bioactive properties. Although there is much information related to
American, European and Asian isolates, little research has been conducted on
Australian Ganoderma isolates. Ganoderma may only be imported into Australia under
strict quarantine conditions, therefore, the isolation of a native strain that possesses
bioactivity may be industrially and commercially significant. Three Australian species
of this wood-decomposing fungus were isolated in northern Queensland. In this study,
they have been identified as three separate species. Further, they have been studied to
determine their optimal growth conditions in liquid culture and assessed for their
antibacterial properties.
Phylogeny inferred from the Internal Transcribed Spacer Regions (ITS) from the DNA
sequences resolved the three Australian Ganoderma species into separate clades. Two
isolates were identified to be isolates of Ganoderma cupreum (H1) and Ganoderma
weberianum (H2). The third isolate could only be identified to the genus level,
Ganoderma species, due to the lack of informative data that could be used for
comparison.
The effects of short term and long term storage on the viability of the fungi were
investigated on agar plates, agar slants and balsa wood at varying temperatures ranging
from 10 to 45�C. The most appropriate storage conditions were determined to be �80�C
on balsa wood chips for periods of up to 2 years without subculture, and on agar slants
at 4�C for up to a maximum of eight weeks. Light was observed to be detrimental to the
survival of Ganoderma H1 and Ganoderma H2 during storage. Growth trials using
potato dextrose agar plates determined the optimal temperature and pH for mycelial
growth to be 30�C and a pH of 6, for all isolates. Subsequent growth trials in liquid
media found that glucose, as the carbohydrate source, supported the greatest mycelial
growth of Ganoderma H1 and Ganoderma H2 and that galactose and fructose supported
the greatest growth of Ganoderma H3.
Abstract
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Aqueous (hot water) and organic (hexane (HEX), dichloromethane (DCM), ethyl
acetate (EtOAc), methanol (MeOH)) extracts from the liquid cultivated mycelium were
assessed for their antibacterial activity using disc diffusion assays. Extracts from the
mycelium of Ganoderma H1 exhibited activity against a greater number of Gram
positive bacteria than those from Ganoderma H2 and H3. Subsequent studies on the
DCM and EtOAc extracts from Ganoderma H1 determined the MIC and MBC against a
number of Gram positive bacteria, including Bacillus cereus, B. subtilis, Enterococcus
faecalis, Streptococcus pyogenes, Staphylococcus aureus, S. epidermidis and Listeria
monocytogenes, as well as Clostridium species, including Clostridium perfringens, C.
sporogenes and C. difficile, and some methicillin resistant Staphylococcus aureus
(MRSA) strains. Time course growth assays confirmed that the DCM and EtOAc
extracts predominantly exhibited bactericidal activity. Finally, the active compounds
were determined to be terpenoid in structure with some phenolic groups attached.
2
Miller, Robert Neil Gerard. "The characterization of Ganoderma populations in oil palm cropping systems." Thesis, University of Reading, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283672.
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Olsen, Mary W. "Diseases of Urban Plants in Arizona." College of Agriculture and Life Sciences, University of Arizona (Tucson, AZ), 1999. http://hdl.handle.net/10150/144807.
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26 pp.Geographically, Arizona can be divided roughly into four areas, southwest, central, southeast, and northern. These regions correspond with four climatic zones, allowing a large and diverse number of plants to be grown for landscaping purposes. But, interestingly, in this desert environment many of the parasitic diseases in landscape plants are caused by a limited number of plant pathogens. This publication discusses some of those diseases that are sufficiently important to the urban plants in all areas Arizona.
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Roberts, S. J. "Bacterial diseases of woody ornamental plants." Thesis, University of Leeds, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.375533.
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Mazumder, Anisha. "Analysis of extracts from higher plants to treat diseases." Thesis, University of Ulster, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588594.
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Herbal medicine is now globally accepted as an authenticated alternative system of therapy in the form of pharmaceuticals, functional foods, and nutraceuticals; a trend recognized and supported by the World Health Organization (WHO). For decades herbal drugs have shown to be promising for a number of diseases and their use has been supported by physicians and patients for their improved therapeutic benefits as they have less adverse effects when compared with many modern medicines. In this thesis, it was decided to explore the therapeutic potential of n- hexane, DCM and methanol crude extracts from the Nigella sativa plant obtained by using novel Soxhlet extraction. The studies have been conducted on the antibacterial activity of these crude extracts of Nigella sativa and also demonstrated the in vitro antitumour potential of the above crude extracts of the plant. The results indicated that hexane extract of Nigella sativa seeds showed the most potent antibacterial and antitumour activity. The research also aimed at designing novel drug delivery systems for herbal constituent. Lipid emulsion (Intralipid) as a drug carrier was selected to carry the hexane extract obtained from one Soxhlet cycle extraction from the Nigella sativa seeds and determined its antitumour effects. This herbal formulation was investigated using both in vitro and in vivo target systems. Both, in vitro and in vivo findings showed that the Intralipid could carry the active ingredient(s) of the hexane extract across the filtered membrane and the drug carrier (IL) showed the minimal toxicity. Furthermore, the possibility of using ultrasound to enhance the cytotoxicity of the herbal drug formulation was explored using both in vivo and in vitro target system. The results suggested that ultrasound enhanced the therapeutic potential of the antitumour herbal drug in both the systems.
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Sutherland, Margery Louise. "Recognition of host plants by vascular pathogens." Thesis, University of Reading, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.303155.
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Rodriguez, Juan Jose. "Movement and Accumulation of Candidatus Liberibacter Solanacearum in Potato Plants." Diss., North Dakota State University, 2012. https://hdl.handle.net/10365/26726.
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A new disease affecting potatoes was first detected in Mexico in 1993. Affected plants had aerial symptoms similar to those caused by potato purple top and psyllid yellows, but tubers had internal brown discoloration when sliced and dark stripes and streaks when processed to produce potato chips. The disease has been found in many potato production areas in Guatemala, Mexico, Honduras, New Zealand and the United States. The disease, termed Zebra Chip (ZC), has been associated with the presence of heavy infestations of the potato-tomato psyllid (Bactericera cockerelli). In 2009, a research group in New Zealand discovered that a new disease in tomato and pepper plants was caused by Candidatus Liberibacter solanacearum (Lso) and subsequently this same bacterium was associated with ZC in potato samples from Texas. The objectives of this study were: to assess the accumulation of Lso in various potato organs, to determine the effect of plant age on detection of Lso, symptom development and plant death, and (iii) to determine the effect of phosphorous acid on the development of ZC. Results from these studies showed significant differences in Lso populations between above and below ground tissues of the potato plant, with Lso populations in stolons and tubers being three to four times higher than those of leaf tissue and over seventy times greater than in stems. Time for detection of Lso by PCR in potato leaves of different ages at the time of inoculation ranged from 21 to 26 days after inoculation, symptoms development took 23 to 36 days. Plant death, took 24 to 47 days in plants of different age groups at the time of inoculation. In plants 15 weeks old at the time of inoculation, Lso was detected after 14 days in one plant out of 18; in plants 16 weeks old at the time of inoculation, Lso was detected after seven days in two plants out of 18. Phosphorous acid applications had no effect on the populations of Lso in potato tubers, onset of symptoms or plant death. All tubers showed ZC symptoms, making them unacceptable for the market.North Dakota State University. Department of Plant Pathology
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Knowles, Cindy-Lee. "Synergistic effects of mixtures of the kresoxim-methyl fungicide and medicinal plants extracts in vitro and in vivo against Botrytis Cinerea." Thesis, University of the Western Cape, 2005. http://etd.uwc.ac.za/index.php?module=etd&.
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The fungus Botrytis cinerea is an opportunistic pathogen on a wide variety of crops, causing disease known as grey mould through infections via wounds or dead plant parts. Synthetic fungicides for controlling this disease are fast becoming ineffective due to the development of resistance. This, coupled with consumers world wide becomng increasingly conscious of potential environment and health problems associated with the build up of toxic chemicals, (particularly in food products), have resulted in pressure to reduce the use of chemical pesticide volumes as well as its residues. An emerging alternative to random synthesis is the study and exploitation of naturally occurring products with fungicidal properties. There have been reports on the uses of synthetic fungicides for the control of plant pathogenic fungi. When utilized in two-way mixtures, such fungicides may maintain or enhance the level of control of a pathogen at reduced rates for both components utilized in combinations, or alone at normal rates. For this study it was hypothesize that the addition of plant extracts may enhance the antifungal efficacy of the synthetic strobilurin fungicide, kresoxim-methyl against Botrytis cinerea.
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Saqib, Muhammad. "Studies on new plant phytoplasma and viruses infections and molecular dissection of virus resistance using Medicago truncatula." Saqib, Muhammad (2008) Studies on new plant phytoplasma and viruses infections and molecular dissection of virus resistance using Medicago truncatula. PhD thesis, Murdoch University, 2008. http://researchrepository.murdoch.edu.au/288/.
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The work presented in this thesis is in two areas - study of novel pathogens resulting from new encounters between crop and native species and 'mining' for plant virus resistance genes in the model legume Medicago truncatula.
The history of agriculture in Western Australia (WA) is less than 150 years old. All major broadacre and horticultural crops grown in WA have been introduced from overseas. These introduced horticultural and field crops potentially carry pathogens which may be transferred to infect native vegetation. Conversely, cultivated plants are vulnerable to infection by pathogens present in indigenous plants. This potential for new disease encounters is compounded by expansion of agriculture to crop new land and by predicted climate changes. These changes may provide selective advantage to a particular pest or disease, enabling infection to increase and so increase crop losses or damage native species. Global trade in agricultural produce also increases the potential for introduction of exotic pathogens. The focus of the first part of the research was to look for new pathogens of crops and native plants in WA.
A series of field trips to study diseases in horticultural crops and native vegetation were made in the agricultural regions of Carnarvon, Broome, Kununurra, Perth and the surrounding metropolitan area. Although the initial focus was on virus diseases, the work expanded to study phytoplasma-associated diseases, because of their widespread occurrence and clear symptoms.
In the agricultural region around Kununurra the potyvirus Bean common mosaic virus (BCMV) was found infecting Phaseolus vulgaris crops. Sequencing of isolates collected provided the first reliable molecular confirmation of the presence of BCMV in Australia.
In joint work with K. Bayliss three commercial Paulownia tree plantations near Perth were found exhibiting symptoms of Witches'-Broom disease. The Paulownia trees were found to be associated with 'Candidatus Phytoplasma australiense' 16SrXII group. Chickpeas in the Kununurra region were found with symptoms of stunting, little leaf and proliferating branches and tested positive for phytoplasma. Sequencing confirmed the presence of a phytoplasma with high similarity to the 16SrII group 'Ca Phytoplasma aurantifolia' (peanut witches broom group). This is the first molecular evidence for a phytoplasma-associated disease in chickpea. Red clover (Trifolium pratense), several other pasture legumes and paddy melon (Cucumis myriocarpus) with symptoms of diminished leaf size, pallor, rugosity, leaf deformation, shoot proliferation and stunting were observed amongst pasture plots in south-western Australia. All species with these symptoms were positive for a phytoplasma resembling 'Ca Phytoplasma australiense, 16SrXII group. This association was confirmed for red clover and paddy melon by subsequent nested PCR and sequence analysis. This is the first time that 'Ca. Phytoplasma australiense, 16SrXII group, has been reported infecting these hosts in southern WA. Snakebean (Vigna unguiculata var. sesquipedalis) and tomato (Lycopersicon esculentum) plants with phytoplasma-like symptoms were found in the horticultural region at Broome. The symptoms on snakebean were typical of phytoplasma disease. Sequence analysis identified that the agent associated with the symptoms as a strain of sweet potato little leaf strain V4 (SPLL-V4) phytoplasma (16SrXII group, strain of 'Ca Phytoplasma australiense'). SPLL phytoplasma has not been reported in snakebean or tomato in this isolated agricultural region. In a survey in the Gascoyne region phytoplasma-like symptoms were found in tomato, eggplant and papaya. Previously in this region plants had been found to be associated with peanut witches broom phytoplasma 16SrII group 'Ca Phytoplasma aurantifolia'. Phytoplasma-like symptoms which included bunchy growth, witches' broom and 'little leaf' were observed in Allocasuarina fraseriana (Western Sheoak, Casuarina) and Acacia saligna (Acacia, Orange Wattle) trees in Kings Park and Botanic Garden Perth WA. Phytoplasma-associated disease was confirmed for the first time in native Australian casuarina and acacia trees in WA. Based on the identification of these phytoplasma associated diseases in WA, phytoplasma-associated diseases can be divided into two zones, because phytoplasma 16SrII group was found mostly in the north west of WA and the 16SrXII group in the south west of WA. This work has added to knowledge of the extent and distribution of phytoplasma disease in WA: it is concluded that crop-associated phytoplasma disease originated from native vegetation.
The aim of the second part of the research was to screen and map a virus resistance gene in the model legume M. truncatula to better understand host/pathogen interactions of legume-infecting viruses. Natural resistance genes found in M. truncatula could then be used to locate similar genes in grain legumes (e.g. chickpea and lupins) for practical applications. M. truncatula is a model legume which has a relatively small genome. International consortia have been established to develop genomic resources for M. truncatula. The M. truncatula core collection (from SARDI, South Australia) totalling 230 accessions was screened for resistance/susceptibility to four legume-infecting viruses: Alfalfa mosaic virus (AMV), Cucumber mosaic virus (CMV), Bean yellow mosaic virus (BYMV) and Subterranean clover mottle virus (SCMoV). Five plants from each of the 230 phenotypically distinct members of the M. truncatula core collection were challenged with one isolate of each virus using infectious sap together with five uninoculated control plants for each accession. The symptoms that developed were recorded and virus presence was confirmed by ELISA for inoculated and systemic leaves. Accessions that were potentially resistant were retested to check for escapes. The result from this screen was that 5 accessions were potentially resistant to AMV, 56 to BYMV, 21 to CMV and 42 to SCMoV. The remaining accessions were susceptible to all four viruses with symptoms which ranged from no apparent symptoms (symptomless systemic infection) to highly susceptible and plant death. In continuing work with DAFWA (Dr R. Jones) accessions potentially resistant to AMV, BYMV and CMV are being challenged with additional isolates to check for the presence of genes providing broader resistance.
The Sobemovirus SCMoV was chosen for further study because it is the most widespread viral pathogen of subterranean clover pastures in Australia. It is also a high titre, mechanically transmitted virus which gave the least escapes on infection. SCMoV has a linear, single-stranded positive-sense RNA genome of 4.25 Kb. Making use of natural resistance is an effective means to reduce pasture losses caused by SCMoV. From the screen of the core collection of M. truncatula, amongst the lines resistant to SCMoV a single dominant hypersensitive resistance was detected in line DZA-315. To accelerate mapping of the SCMoV resistance gene, an F8 RIL population of a cross between the resistant line (DZA-315) and a susceptible line (Jemalong-J6, A-17) was sourced and obtained from INRA Toulouse. A total of 166 RILs were phenotyped for resistance and susceptibility to SCMoV. Resistant and susceptible lines showed parental phenotypic symptoms with 84 being susceptible and 82 being resistant. This indicated the presence of a single resistance (R) gene. This phenotypic data was combined with genotypic data (76 polymorphic molecular markers) already available for this RIL population to provide a framework map. Mapmaker and Mapmanager mapping programs were used to locate the position of the resistance gene. This framework map indicated a position for the resistance gene on the long arm of chromosome 6.
Additional polymorphic SSR markers flanking the R gene locus on chromosome 6 were used to map the position of the R gene more closely. These SSR markers were developed from a parental cross of M. truncatula line A17 and A20 at UC Davis and from a parental cross between line A17 and DZA 315 developed at INRA Toulouse. Ten new polymorphic SSR markers were identified and located on the long arm of chromosome 6 after analysis of the F8 RIL population. When combined with the other phenotypic and genotypic data a more accurate map position for the SCMoV R gene was obtained. The results indicate that the R gene to SCMoV is located on the long arm of M. truncatula chromosome 6 between position 35 to 38 centimorgans (cM). The closest marker to the SCMoV R gene is marker mtic153 which is about 2.3 cM away. From existing maps of M. truncatula most of the R genes located in this region are of the TIR-NBS-LRR type and occur in R gene clusters. A series of BACs that span the region of interest have been identified in which SCMoV R gene should be present.
M. truncatula has been used as a model legume to study a number of symbiotic (e.g. rhizobium) and pathogenic interactions (e.g. fungal and nematode), but this is the only example of its use to study legume-virus interactions. The results obtained indicate the potential of using M. truncatula as a model to study resistance response to other legume viruses and provide a firm basis for identifying the hypersensitive R gene that confers resistance to SCMoV.
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Cole, Anthony Blaine Thomas. "Investigations into the hypersensitive response of Nicotiana species to virus infections /." free to MU campus, to others for purchase, 2001. http://wwwlib.umi.com/cr/mo/fullcit?p3012960.
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Yu, Weichang. "CAMV gene VI protein : a virulence factor and the host responses in Arabidopsis /." free to MU campus, to others for purchase, 2002. http://wwwlib.umi.com/cr/mo/fullcit?p3075411.
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Denman, Sandra. "Botryosphaeria diseases of proteaceae." Thesis, Stellenbosch : Stellenbosch University, 2002. http://hdl.handle.net/10019.1/52721.
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Dissertation (PhD (Agric))--University of Stellenbosch, 2002.ENGLISH ABSTRACT: Fungi belonging to the genus Botryosphaeria are heterotrophic micromycetes that can be pathogens on woody plants. They cause serious, and in some cases devastating losses to crops through leaf necrosis, stem cankers and plant death. The Proteaceae cut-flower industry in South Africa accounts for 70% of the national cut-flower enterprise. Botryosphaeria diseases are a major impediment to production and trade of Proteaceae and there is an urgent need to investigate the etiology, epidemiology and control of these diseases. Losses of one of the most important proteas, P. magnifica, amount to 50% or more, locally. The main aims of this study were therefore to establish the etiology and aspects of epidemiology of Botryosphaeria stem cankers on P. magnifica and other Proteaceae, and to investigate methods of disease control. Although there is a vast body of information pertaining to this fungus, which was reviewed in Chapter 1, there is relatively little information available on Botryosphaeria on Proteaceae. The taxonomy of Botryosphaeria requires thorough review, and molecular techniques need to be employed to resolve species identities. In Chapter 2, it was found that Phyllachora proteae, a leaf pathogen of proteas, produced a Fusicoccum anamorph, which is described as F. proteae. A sphaeropsis-like synanamorph was associated with F. proteae and a new combination for P. proteae is proposed in Botryosphaeria, as B. proteae. The taxonomy of Botryosphaeria is in disarray at both the generic and the specific level. In Chapter 3 the taxonomic history of Botryosphaeria is reviewed, and the genus circumscribed and distinguished from other morphologically similar genera. Although several anamorph genera have been linked to Botryosphaeria, based on morphological observations and phylogenetic analysis of lTS rDNA sequence data, two anamorph genera are now recognised, those with pigmented conidia (Diplodia), and those with hyaline conidia (Fusicoccum). Botryosphaeria proteae should thus be excluded from Botryosphaeria. Several pathogenic Botryosphaeria spp. have an endophytic phase within their hosts. They are therefore imported unwittingly into other countries where they may pose a risk to agriculture and indigenous vegetation. The current global distribution of Botryosphaeria spp. associated with Proteaceae is clarified and a key to these taxa associated with Proteaceae is provided in Chapter 4. Five Botryosphaeria spp. are associated with cut-flower Proteaceae worldwide viz. B. lute a, B. obtusa, B. protearum, B. proteae and B. rib is. B. protearum is described as a new species. A thorough understanding of disease epidemiology is essential to effect a reduction of losses. In Chapter 5, I show that on P. magnifica, lesions caused by Botryosphaeria protearum, which lead to the formation of stem cankers, are initiated in the mid-rib vein or margin of leaves. Koch's postulates were satisfied and it was found that the number of lesions that developed from artificial inoculations correlated with starch levels present in leaves at the time of inoculation. In Chapter 6 it is shown that B. protearum exists as an endophyte in leaves of P. magnifica in naturally occurring as well as cultivated plants. In natural stands of proteas stem cankers are rare, but in cultivated plantations the incidence is high. Nutritional analyses indicate that higher levels of nitrogen occur in leaves of cultivated plants in spring, which could enhance disease development. High levels of sodium in the leaves of wild plants may restrict disease development. The severe economic losses caused by B. protearum make the search for improved methods of disease control essential. Fungicide applications form an important component of an integrated approach to disease management. In Chapter 7, in vitro tests demonstrate that tebuconazole, benomyl, prochloraz me, iprodione and fenarimol reduce the mycelial growth of B. protearum effectively. In the field there was a 25-85% reduction in the occurrence of stem cankers by applying fungicides or sanitation pruning. The best control was achieved by using benomyl, bitertanol, fenarimol, iprodione, prochloraz manganese chloride alternated with mancozeb and tebuconazole prophylactically. If sanitation pruning is combined with regular applications of fungicides, disease can be combated.
AFRIKAANSE OPSOMMING: Mikrofungi wat tot die genus Botryosphaeria behoort, is heterotrofiese organismes, wat patogenies op houtagtige plante kan wees. Hulle veroorsaak ernstige, en in sommige gevalle, verwoestende verliese, deur blaarnekrose, stamkankers en plantafsterwing. Die Proteaceae snyblom-industrie in Suid-Afrika maak 70% van die nasionale snyblomindustrie uit. Botryosphaeria siektes is 'n belangrike struikelblok in die produksie en handeldryf van Proteaceae, en daar is 'n ernstige behoefte om die etiologie, epidemiologie en beheer van siektes te ondersoek. Verliese van een van die belangrikste proteas, P. magnifica, beloop plaaslik 50% of meer. Die hoof doelstellings van hierdie studie was dus om die etiologie en epidemiologie van Botryosphaeria stamkankers op P. magnifica en ander Proteaceae vas te stel en metodes van siektebeheer te ondersoek. Hoewel daar 'n wye hoeveelheid inligting rakende die swam bestaan, wat in Hoofstuk I hersien is, is daar relatief min inligting oor Botryosphaeria op Proteaceae beskikbaar. Die taksonomie van Botryosphaeria benodig deeglike hersiening, en molekulêre tegnieke word benodig om spesie-identiteite op te klaar. In Hoofstuk 2 is gevind dat Phyllachora proteae, 'n blaarpatogeen van proteas, 'n Fusicoccum anamorf produseer, wat as F. proteae beskryf word. 'n Sphaeropsis-agtige synanamorf is met F. proteae geassosieer en 'n nuwe kombinasie vir P. proteae is as B. proteae in Botryosphaeria voorgestel. Die taksonomie van Botryosphaeria is, beide op die genus- as die spesievlak, in wanorde. In Hoofstuk 3 word die taksonomiese geskiedenis van Botryosphaeria hersien, en die genus word omskryf en van ander morfologies soortgelyke genera onderskei. Hoewel verskeie anamorf genera al met Botryosphaeria op grond van morfologiese waarnemings en filogenetiese analise van ITS rDNA volgorde data verbind is, word twee anamorf genera nou herken, dié met gepigmenteerde konidia (Diplodia), en dié met deurskynende konidia (Fusicoccum). Botryosphaeria proteae moet dus van Botryosphaeria uitgesluit word. Verskeie patogeniese Botryosphaeria spp. het 'n endofitiese fase in hul lewenssiklus. Hulle word dus onwetend in ander lande ingevoer waar hulle 'n gevaar vir landbou en inheemse plantegroei kan inhou. Die huidige wêreldverspreiding van Botryosphaeria spp. wat met Proteaceae geassosieer word is opgeklaar, en in Hoofstuk 4 word 'n sleutel tot die taksa wat met Proteaceae geassosieer word verskaf. Vyf Botryosphaeria spp. word met snyblom Proteaceae wêreldwyd geassosieer, naamlik B. lutea, B. protearum, B. proteae, B. ribis en B. obtusa. B. protearum word as 'n nuwe spesie beskryf. 'n Deeglike kennis van siekte-epidemiologie is noodsaaklik ten einde verliese te verminder. In Hoofstuk 5 dui ek aan dat letsels wat lei tot stamkankers, veroorsaak deur Botryosphaeria protearum op P. magnifica, in die hoofnerf of rant van blare ontstaan. Koch se postulate is uitgevoer en daar is vasgestel dat die aantal letsels wat vanuit kunsmatige inokulasies ontwikkel het korreleer met die styselvlakke teenwoordig in die blare ten tye van die inokulasie. In Hoofstuk 6 word getoon dat B. protearum as 'n endofiet in die blare van P. magnifica. In natuurlike standplase van proteas is stamkankers skaars, maar in verboude plantasies is die voorkoms hoog. Voedingsanalises dui aan dat hoër vlakke van stikstof in die blare van verboude plante in die lente voorkom, wat siekte-ontwikkeling moontlik kan bevorder. Hoë vlakke van natrium in die blare van natuurlike plante mag siekteontwikkeling beperk. Die ernstige ekonomiese verliese wat deur B. protearum veroorsaak word, maak die soektog na verbeterde metodes van siektebeheer noodsaaklik. Fungisiedtoedienings maak 'n belangrike deel uit van 'n geïntegreerde benadering tot siektebeheer. In Hoofstuk 7 dui in vitro toetse aan dat tebuconazole, benomyl, prochloraz me, iprodione en fenarimol die miseliumgroei van B. protearum effektief verminder. 'n Vermindering van 25-85% is aangetoon in die voorkoms van stamkankers in die veld, deur die toediening van fungisiedes en sanitasiesnoei. Die beste beheer is verkry deur die voorkomende toediening van benomyl, bitertanol, fenarimol, iprodione en prochloraz manganese chloride, afgewissel met mancozeb en tebuconazole, op plante in die veld. Indien sanitasiesnoei met gereelde toedienings van fungisiedes gekombineer word, kan die siekte bekamp word.
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Pakela, Yolisa Patronella. "Interaction between Colletotrichum dematium and cowpea." Thesis, Pretoria: [s.n.], 2003. http://upetd.up.ac.za/thesis/available/etd-09022005-102127/.
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Waters, Ormonde Dominick Creagh. "Metabolism and infection in the Stagonospora nodorum-wheat pathosystem /." Murdoch University Digital Theses Program, 2008. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20090409.123159.
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Arthur, Fareed Kow Nanse. "Defense responses to fungal challenge in alfalfa (medicago sativa L.) plants and tissue cultures." Thesis, University of Nottingham, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.385239.
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McGovern, Kristen B. "Evaluation of Potential Organic Controls of Mummy Berry Disease Affecting Lowbush Blueberry in Maine." Fogler Library, University of Maine, 2007. http://www.library.umaine.edu/theses/pdf/McGovernKB2007.pdf.
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Király, Lóránt. "Interactions between cauliflower mosaic virus isolates and nicotiana species that determine systemic necrosis /." free to MU campus, to others for purchase, 1997. http://wwwlib.umi.com/cr/mo/fullcit?p9841160.
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羅美珍. "雲芝現代藥學及其抗腫瘤作用文獻研究." HKBU Institutional Repository, 2008. http://repository.hkbu.edu.hk/etd_ra/966.
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Jeffries, Alex Craig. "The study at the molecular level of the New Zealand isolate of Lucerne transient streak sobemovirus and its satellite RNA." Title page, contents and summary only, 1993. http://web4.library.adelaide.edu.au/theses/09PH/09phj47.pdf.
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Mamba, Phiwokuhle Bongisile. "Bioactivity of selected medicinal plants used for the treatment of sexually transmitted diseases." Diss., University of Pretoria, 2017. http://hdl.handle.net/2263/60834.
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Background: Sexually transmitted diseases (STD's) have a major impact on sexual and reproductive health worldwide. Each year, the World Health Organization (WHO) estimates 448 million new cases of curable STD's are diagnosed. The emergence of drug resistance in STD related microorganisms and potential side effects demand the discovery of newer drugs. The exploration of newer anti-microbial substances from natural sources may serve as promising alternatives. In this study, twelve medicinal plant species used traditionally in the treatment of STD's are investigated in this regard.
Methods: Ethanol plant extracts and three flavonoids were evaluated for their antimicrobial properties against one fungi and three bacteria, through the micro-dilution assay. To determine the anti-inflammatory activities of the extracts and compounds, the inhibitory effect was measured on the pro-inflammatory enzyme lipoxygenase, 15-LOX. Extracts were further evaluated for their inhibitory effect on the supercoiling activity of bacterial DNA gyrase by using the DNA gyrase kit. The extracts and compounds were lastly investigated for their anti-HIV activities against recombinant HIV-1 enzyme using non-radioactive HIV-RT colorimetric assay.
Results: Acacia karroo and Rhoicissus tridentata extracts showed good antimicrobial activity with MIC values ranging between 0.4 and 3.1 mg/ml. Extracts of Jasminum fluminense, Solanum tomentosum and flavonoid 2 and 3 had good anti-inflammatory activity with IC50 less than the positive control quercetin (IC50 = 48.86 ug/ml). Extracts of Diospyros mespiliformis, Peltophorum africanum, Rhoicissus tridentata and flavonoids 1 and 2 showed the best inhibitory activity against the bacterial DNA gyrase. A. karroo and flavonoid 3 exhibited moderate HIV RT inhibition activity of 66.8 and 63.7 % respectively. R. tridentata and Terminalia sericea had the best RT inhibition activity (75.7 and 100 %) compared to the positive control doxorubicin (96.5%) at 100 ug/ml concentration.
Conclusion: The observed activities may lead to new multi-target drugs against sexually transmitted diseases.Dissertation (MSc)--University of Pretoria, 2017.
Plant Science
MSc
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Liu, X. Q. (Xingquan). "Differentiation of garlic viruses." Thesis, McGill University, 1985. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=63286.
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Kimani, Esther Wairimu. "Serological detection of Didymella lycopersici (Kleb.)." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/29190.
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Polyclonal antisera produced against spores, soluble protein and the whole mycelium fractions of Didymella lycopersici reacted with the homologous and heterologous antigens. The most sensitive antiserum was that raised against the whole mycelium, the soluble protein and the spore, in decreasing order of sensitivity. Using the antiserum raised against the whole mycelium it was possible to detect D. lycopersici on diseased plants and infested seeds. Cross reactivity was observed between the antisera produced to D. lycopersici and D. applanata, D. bryoniae and other tomato fungal pathogens including Fusarium spp. and B. cinerea. ELISA was most sensitive and reliable compared to double immunodiffusion, and latex tests. No reactions were obtained using the latex agglutination procedure and no antiserum detected spores in double diffusion tests.
Protein profiles on SDS-PAGE revealed that the total number of protein bands decreased with increased age of cultures of D. lycopersici incubated in liquid media. Western blots probed with the antiserum raised against the whole mycelium showed that protein bands from extracts of both D. lycopersici and D. applanata were antigenic.Land and Food Systems, Faculty of
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MacDonald, Stuart Gerald. "Two viruses associated with blueberry scorch disease." Thesis, University of British Columbia, 1989. http://hdl.handle.net/2429/29421.
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Blueberry bushes with scorch symptoms were found during a survey of blueberry fields in British Columbia, Washington, and Oregon. Some of these bushes were infected with blueberry scorch virus (BBScV) while others contained a second virus which was sap transmissible to Nicotiana clevelandii, N. benthamiana, and N. tabacum cv. 'Havana 425' . This virus was purified from N. clevelandii and had isometric particles of approximately 30 nm in diameter, a coat protein subunit of 27,500 daltons and a tripartite genome. I was unable to transfer the virus from either infected N. clevelandii or infected blueberry to healthy N. clevelandii with Myzus persicae or Fimbriaphis fimbriata. Serological tests of this blueberry virus with antisera against members of the ilar-, cucumo-, bromo-, or nepovirus groups failed to indicate any relationship. In a subsequent survey using enzyme-linked immunosorbent assay, this isometric virus was found in blueberry plants from northern Washington state to central Oregon but has not yet been found in B.C.
Of the established members of the carlavirus group examined, BBScV is most closely related to potato virus S (PVS) and less closely related to carnation latent virus (CLV) and potato virus M (PVM). The difference in host range between BBScV and PVS would indicate that the BBScV is not a strain of PVS but is a separate virus that is related to PVS. Therefore, BBScV should be renamed blueberry scorch carlavirus (BBSCV).
BBSCV was also compared to a carlavirus isolated from blueberry in the Sheep Pen Hill blueberry growing area of New Jersey (referred to as SPHV). These viruses were compared serologically and by use of nucleic acid hybridizations. BBSCV and SPHV were found to be closely related and were concluded to be strains of the same virus. SPHV should be named the New Jersey strain of BBSCV.Land and Food Systems, Faculty of
Graduate
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Bonfiglioli, Roderick. "Studies on the ultrastructural localisation of viroids and other plant pathogens." Title page, contents and summary only, 1997. http://web4.library.adelaide.edu.au/theses/09PH/09phb713.pdf.
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Bibliography: leaves 78-90. Designed to localize viroids at the histological and subcellular level and to determine with which cellular compartments the different viroids are associated. The majority of the work, in both the viroid and the phytoplasma studies involved the development of different methods and techniques.
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Van, Dyk Kerien. "Fungi associated with root and crown rot of wheat and barley in Tanzania." Diss., University of Pretoria, 2003. http://hdl.handle.net/2263/25941.
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Truter, Mariette. "Etiology and alternative control of potato rhizoctoniasis in South Africa." Pretoria : [s.n.], 2005. http://upetd.up.ac.za/thesis/available/etd-04122005-112047.
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Schuh, Casey Steven. "Revisiting Management Practices for Diseases of Spring Barley in North Dakota." Thesis, North Dakota State University, 2018. https://hdl.handle.net/10365/28723.
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Common barley diseases observed in North Dakota include net blotch, spot blotch, leaf and stripe rust, bacterial leaf streak, and Fusarium head blight. The first objective of this research was to determine the effect of variety and fungicide timing on disease development of barley under conventionally tilled systems. Five field trials were performed in 2016-2017 to test the effect of common varieties and fungicide applications on foliar disease of barley. Overall, varietal selection had a greater effect on the level of foliar disease observed than fungicide application. The second objective focused on the efficacy and timing of adepidyn and prothioconazole + tebuconazole on Fusarium head blight. An inoculated greenhouse experiment was performed the fall of 2017 to determine the effectiveness of fungicide timing at half-spike, full-spike, and five days after full-spike. The protectant capabilities of the fungicides were greater than their curative properties.
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Herrmann, Revital. "Characterization and efficacy testing of novel antifungal peptides in transgenic rice." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file 2.08 Mb., 254 p, 2006. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&res_dat=xri:pqdiss&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:3220793.
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Waters, Brian M. "Iron nutrition in plants and yeast : studies on the FRO1 gene of Pisum sativum and the FET4 gene of Sacharomyces [sic] cerevisiae /." free to MU campus, to others for purchase, 2002. http://wwwlib.umi.com/cr/mo/fullcit?p3060158.
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Stone, Bethany. "The effects of boron deficiency and aluminum toxicity on plant magnesium /." free to MU campus, to others for purchase, 2001. http://wwwlib.umi.com/cr/mo/fullcit?p3036861.
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Yam, Jianying. "The search for bioactive compounds in tropical plants to target hormone imbalance associated diseases /." Basel : [s.n.], 2008. http://edoc.unibas.ch/diss/DissB_8163.
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Lowe, Rohan George Thomas. "Sporulation of Stagonospora nodorum /." Access via Murdoch University Digital Theses Project, 2006. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20071101.221432.
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Wang, An Qi. "Screening of hepatoprotective constituents from herbal medicines and investigation on the underlying mechanisms." Thesis, University of Macau, 2017. http://umaclib3.umac.mo/record=b3690819.
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Soetopo, Lita. "Resistance to cereal cyst nematode (Heterodera avenae Wall.) in barley /." Title page, contents and abstract only, 1986. http://web4.library.adelaide.edu.au/theses/09PH/09phs6812.pdf.
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Visser, Marike. "Small RNA profiling of virus-infected apple plants." Thesis, Stellenbosch : Stellenbosch University, 2014. http://hdl.handle.net/10019.1/95828.
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Thesis (PhD)--Stellenbosch University, 2014.ENGLISH ABSTRACT: Apple stem grooving virus (ASGV) is globally associated with latent infection in commercial apple trees. Little is known about this plant-‐virus interaction. This study made use of next-‐generation sequencing to investigate the effect of virus-‐infection on the expression of the different small RNA (sRNA) species namely, miRNAs, nat-‐siRNAs, phasiRNAs, rasiRNAs, tRNA-‐derived sRNAs and vsiRNAs. Broad and narrow size-‐range datasets were generated using sRNA libraries prepared from total and size-‐selected RNA, respectively. Through bioinformatic data analyses, 130 genomic loci were predicted to give rise to miRNAs, 85 of which were novel MIR genes. Targets were predicted for the majority of miRNAs, a few of which could be validated with a publicly available degradome dataset. Cis-‐ and trans-‐natural antisense transcripts (NATs) were identified, of which only the latter were highly enriched for sRNAs in their overlapping regions. Transcript as well as genomic regions were also identified that can give rise to phasiRNAs. For 25 of these loci an in-‐phase miRNA target site was identified, half of which could be validated with the degradome dataset. Nearly all apple repeat sequences in Repbase were associated with sRNA synthesis. sRNAs derived from both ends of mature tRNAs were identified. These sRNAs corresponded to tRFs and tRNA-‐halves. Reads associated with tRNA-‐halves were prominent in the broad range datasets. sRNAs, originating from the central regions of tRNAs, were also observed. Analysis of the vsiRNAs suggested the presence of two ASGV genetic variants in two of the samples, while the third sample was infected with only one variant. Comparison of the vsiRNA profiles generated from the two datasets highlighted the influence of library preparation on the interpretation of results. Differential expression analysis of the identified apple sRNA species showed no variation between healthy and infected plants, except for the tRNA-‐derived sRNAs, which did show altered expression levels. Taken together, the various sRNA species characterised in this study significantly extended the existing knowledge of apple sRNAs and provide a broad platform for future functional studies in apple. This study also presents the first and most comprehensive report on sRNAs involved in ASGV infection in apple.
AFRIKAANSE OPSOMMING: Appel gleufstam virus (ASGV) word wêreldwyd geassosieer met latente infeksie in kommersiële appelbome. Min inligting oor hierdie plant-‐virus interaksie is beskikbaar. Hierdie studie het van volgende-‐generasie volgordebepaling gebruik gemaak om die effek van virusinfeksie op die uitdrukking van verskillende klein RNA (sRNA) spesies, nl. miRNAs, nat-‐siRNAs, phasiRNAs, rasiRNAs, tRNA-‐afkomstige sRNAs en vsiRNAs, te ondersoek. Datastelle met breë en smal grootte-‐verspreiding is gegenereer m.b.v. sRNA biblioteke wat onderskeidelik voorberei is vanaf totale RNA en RNA van ‘n bepaalde grootte. Deur middel van bioinformatiese data-‐ontleding is 130 genomiese loci voorspel wat aanleiding kan gee tot miRNAs, waarvan 85 nuwe MIR gene is. Teikens is voorspel vir die meerderheid van die miRNAs en 'n aantal daarvan kon bevestig word m.b.v. 'n publiek-‐beskikbare degradoom datastel. Cis-‐ en trans-‐natuurlike antisense transkripte (NATs) is geïdentifiseer, waarvan slegs die laasgenoemde verryk was vir sRNAs in hul oorvleuelende areas. Transkrip sowel as genomiese areas, wat aanleiding kan gee tot phasiRNAs, is ook geïdentifiseer. Vir 25 van hierdie loci is 'n in-‐fase miRNA teiken geïdentifiseer, waarvan die helfte bevestig kon word met die degradoom datastel. Byna al die appel herhalende volgordes in Repbase was geassosieer met sRNA sintese. sRNAs afkomstig van beide kante van volwasse tRNAs is geïdentifiseer. Hierdie sRNAs het ooreengestem met tRFs en tRNA-‐helftes. Volgordes geassosieer met tRNA-‐helftes was prominent in die breë grootte-‐verspreiding datastelle. sRNAs, afkomstig van die sentrale dele van tRNAs, is ook waargeneem. Ontleding van die vsiRNAs het die teenwoordigheid van twee ASGV genetiese variante in twee van die monsters aangetoon, terwyl die derde monster met slegs een variant geïnfekteer was. Die vergelyking van vsiRNA profiele, gegenereer vanaf die twee datasteltipes, beklemtoon die invloed van biblioteek voorbereiding op die interpretasie van resultate. Ontleding van die differensiële uitdrukking van die geïdentifiseerde appel sRNA spesies het geen verskil tussen gesonde en geïnfekteerde plante getoon nie, behalwe vir die tRNA-‐afkomstige sRNAs, wat wel verandering die vlak van uitdrukking getoon het. Die verskillende sRNA spesies wat in hierdie studie geïdentifiseer is, het die bestaande kennis van appel sRNAs aansienlik uitgebrei en bied 'n breë platform vir toekomstige funksionele studies in appel. Hierdie studie bied ook die eerste, en mees omvattende verslag oor sRNAs betrokke in ASGV infeksie in appel.
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Beltran, Oscar. "Investigation of the anti-mycobacterial and cytotoxic effect of three medicinal plants used in the traditional treatment of tuberculosis in northern Mexico and the southwest U.S." To access this resource online via ProQuest Dissertations and Theses @ UTEP, 2008. http://0-proquest.umi.com.lib.utep.edu/login?COPT=REJTPTU0YmImSU5UPTAmVkVSPTI=&clientId=2515.
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Soriano, Imelda Rizalina. "Novel inducible phytochemical defences against plant parasitic nematodes /." Title page, table of contents and summary only, 2004. http://web4.library.adelaide.edu.au/theses/09PH/09phs7141.pdf.
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Thompson, Winston Mark Obed. "Studies of Bemisia tabaci (Gennadius) (Homoptera: Aleyrodidae) and interactions with host plants and viral diseases." Thesis, University of Greenwich, 2001. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.503681.
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Meyer, Jacolene Bee. "Banana streak badnavirus (BSV) in South Africa incidence, transmission and the development of an antibody based detection system /." Pretoria : [s.n.], 2005. http://upetd.up.ac.za/thesis/available/etd-02092007-171659.
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Pangga, Ireneo B. "Effects of elevated CO2 on plant architecture of Stylosanthes scabra and epidemiology of anthracnose disease /." [St. Lucia, Qld.], 2001. http://www.library.uq.edu.au/pdfserve.php?image=thesisabs/absthe16215.pdf.
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Zhang, Chao. "Anti-liver cancer effect of polyphyllin VII and its molecular mechanisms." Thesis, University of Macau, 2017. http://umaclib3.umac.mo/record=b3690802.
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Tan, Kar-Chun. "Role of signal transduction in the pathogenicity of Stagonospora nodorum on wheat." Tan, Kar-Chun (2007) Role of signal transduction in the pathogenicity of Stagonospora nodorum on wheat. PhD thesis, Murdoch University, 2007. http://researchrepository.murdoch.edu.au/425/.
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The fungus Stagonospora nodorum is the causal agent of leaf and glume blotch disease on wheat and is an emerging model for the study of the interaction between plants and necrotrophic fungal pathogens. Signal transduction plays a critical role during infection by allowing the pathogen to sense and appropriately respond to environmental changes. The role of signal transduction in the pathogenicity of S. nodorum was analysed by the targeted inactivation of genes encoding a G[alpha] subunit (Gna1) and a mitogen-activated protein kinase (Mak2). Strains carrying the inactivated genes were impaired in virulence and demonstrated a host of phenotypic impairments such as abolished sporulation. Therefore, it was hypothesised that Gna1 and Mak2 regulate downstream effector molecules that are critical for pathogenic development. A 2D gel-based proteomic approach was used to compare the extracellular and intracellular proteomes of the wild-type fungus and signalling mutants for differences in protein abundance. Tandem mass spectrometry (LC-MS/MS) analysis and patternmatching against the S. nodorum genome sequence led to the identification of 26 genes from 34 differentially abundant protein spots. These genes possess probable roles in protein cycling, plant cell wall degradation, stress response, nucleotide metabolism, proteolysis, quinate and secondary metabolism. A putative short-chain dehydrogenase gene (Sch1) was identified and its expression was shown to be reduced in both signalling mutants. The transcript level of Sch1 increased during the latter period of infection coinciding with pycnidiation. Sch1 was inactivated by targeted gene deletion. Mutants were able to effectively colonise the host but asexual sporulation was dramatically reduced and pycnidial ontogeny was severely disrupted. Furthermore, the sch1 mutants showed alterations in the metabolome. GC-MS analysis identified a metabolite which accumulated in the sch1 mutants. Computational and database analyses indicated that the compound possesses a cyclic carbon backbone. Based on these findings, Sch1 may be a suitable target for fungicides that inhibit asexual sporulation and the accumulated compound may be used to design novel antifungal compounds. 2D SDS-PAGE analysis identified increased abundance of another putative short-chain dehydrogenase (Sch2) and a nitroreductase in the sch1-deleted background. It was also shown that Sch2 was regulated by Gna1.
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Groenewald, Michelle. "Characterization and control of Phaeomoniella chlamydospora in grapevines." Thesis, Stellenbosch : Stellenbosch University, 2000. http://hdl.handle.net/10019.1/51650.
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Thesis (MScAgric)--University of Stellenbosch, 2000.ENGLISH ABSTRACT: Petri grapevme decline, also known as black goo, slow die-back and Phaeoacremonium grapevine decline, causes significant losses of young vines worldwide. Species of Phaeoacremonium, Phaeomoniella chlamydospora and related genera are associated with this grapevine disease. This study investigates the Phaeoacremonium-complex and Phaeomoniella chlamydospora, focussing on the species isolated from grapevines. Fungicide sensitivity of Pa. chlamydospora and the possibility of employing molecular techniques for the detection of Pa. chlamydospora in grapevines were also investigated. In an overview of the literature on Petri grapevine decline the disease history and the relatedness of Petri grapevine decline to esca is discussed. Petri grapvine decline occurs in propagation material or young vines. Infected material can appear asymptomatic and therefore the possibilities of molecular techniques for identification were also investigated in the literature. In South Africa Pa. chlamydospora is the dominant organism causing Petri grapevine decline and therefore different fungicides were evaluated to control this fungus. Six isolates of Pa. chlamydospora, from Stellenbosch, Wellington, Somerset West and Malmesbury of Western Cape province, South Africa, were screened against twelve fungicides testing their effect on mycelial inhibition in vitro. These fungicides included benomyl, chlorothalonil, fenarimol, fosetyl-Al, iprodione, kresoxim-methyl, mancozeb, metalaxyl, prochloraz manganese chloride, quintozene, tebuconazole and thiram. Results provided the base-line sensitivity of South African isolates of Pa. chlamydospora. Benomyl, fenarimol, kresoxim-methyl, prochloraz manganese chloride and tebuconazole were the most effective (with EC50 values ranging from 0.01 to 0.05 ug/ml) for inhibiting mycelial growth of Pa. chlamydospora in vitro. This in vitro test gave a good indication of which fungicides could be selected for further studies in glasshouses and nurseries. The molecular phylogeny of Phaeoacremonium and Phaeomoniella isolates from grapevines of South Africa, or isolates obtained from the Centraalbureau voor Schimmelcultures (CBS) in the Netherland, were investigated. Sequence data were created from the rONA region and partial B-tubulin gene of 33 of these isolates using the PCR technique. This sequence data were analysed with PAUP* version 4.Ob2a. An analysis of the sequence data confirmed the genus Phaeomoniella to be distinct from Phaeoacremonium (Pm.) based on DNA phylogeny. Although morphologically similar, the species status of Pm. aleophi/um and Pm. angustius was confirmed with DNA phylogeny and cultural characteristics. Pm. aleophilum has an optimum growth rate at 30°C and the ability to grow at 35°C, where as Pm. angustius has an optimum growth rate at 25°C and cannot grow at 35°C_ Pm. viticola was shown to be synonymous with Pm. angustius, and a new species, Pm. mortoniae, was newly described from grapevine occurring in California. Futhermore, Pm. aleophilum was newly reported from South Africa and grapevine isolates thought to be Pm. inflatipes were all re-identified as Pm. aleophilum. These findings therefore also shed some doubt on the possible role of Pm. inflatipes in Petri grapevine decline. It was confirmed that Pa. chlamydospora, Pm. aleophilum and Pm. angustius are the species involved in Petri grapevine decline. Pm. mortoniae was isolated from grapevines, but its pathogenicity should still be confirmed and the role of Pm. injlatipes in Petri grapevine decline remains unclear. Pa. chlamydospora has been routinely isolated from symptomless propagation and nursery material. Because the disease can take years to develop, it is crucial that healthy propagation material is used at planting. Pa. chlamydospora is a slowgrowing fungus, and positive identification from symptomless grapevine tissue can take up to 4 wks. The possibility of employing molecular techniques for the detection of Pa. chlamydospora in apparently healthy grapevines was investigated. Speciesspecific primers (PCLI and PCL2) based on the regions ITSI and ITS2 were designed for Pa. chlamydospora. These primers were highly sensitive and amplification was achieved from genomic DNA of Pa. chlamydospora from as low as 16 pg. Phaeoacremonium spp., related genera and common fungal taxa from grapevines were tested with these primers, but positive amplification was achieved for Pa. chlamydospora only. The presence of Pa. chlamydospora in symptomless grapevine tissue culture plants was confirmed by PCR within 24 hours. These primers therefore allow rapid and accurate identification of Pa. c~lamydospora. Testing on a larger scale with nursery material should be conducted to determine the feasibility of using these species-specific primers in the grapevine industry.
AFRIKAANSE OPSOMMING: Petri-terugsterwing van jong wingerde, ook algemeen bekend as "black goo" en Phaeoacremonium-terugsterwing, veroorsaak wêreldwyd groot geldelike verliese in die wingerdbedryf. Spesies van Phaeoacremonium, Phaeomoniella chlamydospora en verwante genera word met hierdie wingerdsiekte geassosieer. In die tesis word In oorsig gegee van die geskiedenis van hierdie siekte, die verwantskap tussen Petriterugsterwing en esca, en moontlike maniere van siektebestuur. Swamme wat by die siektekompleks betrokke is, kan in simptoomlose plantweefsel voorkom en daarom is die moontlikhede van die gebruik van molekulêre tegnieke vir swamidentifikasie in oënskou geneem. In Suid-Afrika is Pa. chlamydospora die dominante swam wat met Petriterugsterwing geassosieerword, gevolglik is verskillende fungisiedes vir die chemiese beheer van Pa. chlamydospora geëvalueer. Ses isolate van Pa. chlamydospora, versamel vanaf verskillende areas in die Wes-Kaap provinsie, is in dié studie gebruik. Benomyl, chlorothalonil, fenarimol, fosetyl-Al, iprodione, kresoxim-methyl, mancozeb, metalaxyl, prochloraz manganese chloride, quintozene, tebuconazole en thiram se effek op miselium inhibisie van Pa. chlamydospora is in vitro geëvalueer. Benomyl, fenarimol, kresoxim-methyl, prochloraz manganese chloride en tebuconazole was die mees effektiewe middels. Die effektiewe konsentrasie waarby 50% van die miselium groei geïnhibeer is (EKso),was tussen 0.01 en 0.05 ug/ml vir die mees effektiewe groep middels. Benomyl, fenarimol, kresoxim-methyl, prochloraz manganese chloride en tebuconazole het in vitro goeie potensiaal getoon, en verder toetse moet in vivo uitgevoer word. 'n Molekulêre studie is van Phaeoacremonium en Phaeomoniella isolate; verkry uit Suid-Afrikaanse wingerde, of vanaf die "Centraalbureau voor Schimmelcultures" (CBS) van Nederland; gedoen. Deur van die PKR tegniek gebruik te maak, is die basispaaropeenvolgingsdata van 33 isolate, van die ITSl, 5.8S, ITS2 rDNA area en die gedeeltelike B-tubullen geen verkry. Gekombineerde molekulêre data het die teorie ondersteun dat Phaeomoniella (Herpotrichiellaceae) gedistansieerd is van Phaeoacremonium (Magnaporthaceae). Pm. aleophilum en Pm. angustius was morfologies moeilik onderskeibaar, maar kon op grond van molekulêre data en kulturele eienskappe onderskei word. Pm. aleophilum se optimum groeitemperatuur was by 30°C en die swam besit die vermoë om by 35°C te groei. Pm. angus/ius se optimum groeitemperatuur was by 25°C, maar het nie by 35°C gegroei nie. 'n Studie van molekulêre en kulturele eienskappe het getoon dat Pm. angus/ius en Pm. viticola sinoniem is. 'n Nuwe spesie, Pm. mortoniae, wat uit wingerde van Kalifornie geïsoleer is, is beskrywe. Verder is Pm. aleophilum die eerste keer in Suid-Afrikaanse wingerde aangetref en Pm. tnflatipes isolate, wat vanuit wingerde geïsoleer is, is almal met molekulêre data gewys om Pm. aleophilum te wees. Hierdie bevindinge trek die rol van Pm. inflatipes in Petri-terugsterwing van wingerde in twyfel. Phaeomoniella chlamydospora IS m voortplantingsmateriaal en kwekerystokkies opgespoor. Omdat dit jare kan duur voordat siektesimptome ontwikkel, is dit belangrik om vroegtydig te weet of jong stokkies met Pa. chlamydospora geïnfekteer is. Pa. chlamydospora groei baie stadig en positiewe identifikasie van simptoomlose infeksies duur tot vier weke. Die toepassing van molekulêre tegnieke vir die vinnige identifikasie van Pa. chlamydospora in wingerde is dus ondersoek. Spesie-spesifieke oligonukleotiedes (PCU en PCL2) is vir Pa. chlamydospora ontwerp. Hierdie oligonukleotiedes is uiters sensitief en genomiese DNA van Pa. chlamydospora is van so laag as 16 pg geamplifiseer. Phaeoacremonium spp., verwante genera en algemene swamme vanuit wingerdmateriaal is met die oligonukleotiedes getoets, maar positiewe amplifikasie was slegs met Pa. chlamydospora moontlik. Die teenwoordigheid van Pa. chlamydospora is binne 24 uur in asimptomatiese wingerd weefselkultuurplantjies bevestig. Hierdie oligonukleotiedes identifiseer Pa. chlamydospora vinnig en akkuraat en toetsing op 'n groter skaal moet vervolgens met kwekerymateriaal onderneem word.
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Du, Preez Izak Frederik. "Infection pathways of Botrytis cinerea on selected wine grape cultivars." Thesis, Stellenbosch : Stellenbosch University, 2002. http://hdl.handle.net/10019.1/52889.
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Thesis (MScAgric)--University of StellenboschENGLISH ABSTRACT: An understanding of the infection pathways of Botrytis cinerea in grape bunches will help to combat this devastating pathogen of grape. Many studies have been done to determine the possible infection pathways of B. cinerea. Most of these studies made use of artificial inoculations that deposit groups of conidia on the plant surface. The deposition of clusters of conidia is not a common phenomenon in nature. The aim of this study was to investigate the infection pathways of (i) naturally- as well as (ii) artificially inoculated B. cinerea conidia during all the phenological stages of three wine grape cultivars, and to compare the (iii) pathogenicity and virulence, on grape and nectarine fruit, of isolates obtained from different host plants. In the natural infection study the occurrence of Botrytis cinerea and subsequent disease expression at different positions in bunches of wine grapes (cultivars Chenin Blanc, Shiraz and Chardonnay) was determined from 1999 to 2001. Different techniques were used to detect viable inoculum at different positions (rachises, laterals, pedicels, and the peicel end, cheek and style end of berries) in bunches. Isolations were made on Kerssies' B. cinerea selective medium, or bunches were used untreated, or treated with paraquat. Paraquat was used to terminate host resistance and to promote the development of the pathogen from the tissues. The material was used untreated to detect the pathogen on the surface, or were surface-sterilized to detect mycelia (latent infection) in the tissue. In the artificial inoculation study, bunches of wine grapes (cultivars Chenin Blanc, Chardonnay and Shiraz) at pea size, bunch closure, and harvest were dusted with dry conidia of Botrytis cinerea in a settling tower and incubated for 24 h at high relative humidity (±93%). Following incubation, the bunches were divided in two groups. The one group was surface-sterilised in 70% ethanol for 5 s, the other group was left untreated. Bunches of the sterile group, and from the untreated group were used for isolation. From each bunch rachis segments, laterals, pedicels and berry skin segments (from the pedicel-end and cheek) were removed. The sections were placed in Petri dishes on Kerssies' B. cinerea selective medium and on a water agar medium supplemented with paraquat, and incubated at 22°C under diurnal light. Occupation by the pathogen was positively identified by the formation of sporulating colonies of B. cinerea on the different tissues. Lastly, in the virulence and pathogenicity experiment on grape and nectarine fruit Botrytis cinerea isolates, which were obtained from different host plants, were compared by simulating natural infection. Cold-stored fruit, considered highly susceptible to B. cinerea were therefore inoculated with single, airborne conidia of the pathogen. Different tests were conducted to assess surface penetration and lesion formation. Isolations were made from fruit skins on Kerssies' B. cinerea selective medium. Nectarine fruit were treated with paraquat, and grape berries were frozen for 1 h at -12°C. Paraquat and freezing were used to terminate host resistance and to promote the development of the pathogen from the tissues. In the natural infection studies B. cinerea occurred in a consistent pattern in bunches of the three cultivars. B. cinerea consistently developed from the tissue of the rachis, laterals, pedicel and pedicel-end, but not from the berry cheek. The rachis, lateral and pedicel contained much higher levels of B. cinerea than any position on the berry. Furthermore, the pathogen consistenly occurred at relatively high levels on the rachises throughout the season. Collectively, the data showed that in the Western Cape province, B. cinerea occured more regularly in wine grape bunches during the early part of the season, than later in the season. The data of the artificial studies confirmed the findings made with the natural infection studies. In these experiments the pathogen resided more often on the structural bunch parts than on the berries. Overall, the isolation studies revealed that conidia occurred predominantly on the rachis. The incidence of B. cinerea was furthermore constantly high in the inner bunch after each inoculation, and in bunches of different maturities. The data therefore indicated that, when available, conidia penetrated loose and tight clustered bunches in a similar way. Finally, in the virulence and pathogenicity experiments the results showed clearly that no host specialisation exists in the B. cinerea isolates used in this study. From these studies it is clear that in the Western Cape province B. cinerea occurs more readily in the inner structural parts of the bunches and more so during the earlier parts of the season. These findings should be considered when planning and implementing disease control programmes.
AFRIKAANSE OPSOMMING: INFEKSIEWEË VAN BOTRYTIS CINEREA OP GESELEKTEERDE WYNDRUIF KULTIVARS Indiepte kennis van die infeksieweë van Botrytis cinerea op druiwetrosse word benodig vir die beheer van dié vernietigende patogeen van druiwe. Vele studies is al gedoen om die moontlike infeksieweë van die swam op druiwe trosse te ondersoek. Die meeste van die studies het gebruik gemaak van kunsmatige inokulasie tegnieke waar die konidia van die swam in groepe op die korreloppervlak gedeponeer is. In die natuur is dit 'n rare verskynsel dat konidia in groepe op die korreloppervlak land. Die doel van die studie was om die infeksieweë van B. cinerea op drie wyndruif kultivars te ondersoek wat (i) natuurlik- en (ii) kunsmatig geïnokuleer is met konidia gedurende al die fenologiese stadia, en om die (iii) virulensie en patogenisisteit van isolate wat van verskillende gashere verkry is, op druiwe en nektariens te vergelyk. In die natuurlik-geïnokuleerde druiwe is die voorkoms van B. cinerea en die gevolglike siektevoorkoms op verkillende posisies in trosse van wyndruiwe (Chenin Blanc, Chardonnay, Shiraz) gedurende 1999 tot 2001 bepaal. Verskillende tegnieke is gebruik om lewensvatbare inokulum by verskillende posisies (ragis, lateraal, pedisel en pedisel-end van die korrel) in die tros waar te neem. Isolasies is op Kerssies' B. cinerea selektiewe medium gemaak, of trosse is onbehandeld gebruik, of behandel met paraquat. Paraquat is gebruik om die gasheer se natuurlike weerstand te verlaag en om die ontwikkeling van die patogeen te bevorder. Die plantmateriaal is onbehandeld gelaat om die patogeen op die oppervlak waar te neem, of die oppervlak is gesteriliseer om die latente myselium in die weefsel waar te neem. In die kunsmatige inokulasiestudies is trosse, van wyndruiwe (Chenin Blanc, Chardonnay, Shiraz), geïnokuleer met droë spore, van B. cinerea, in 'n inokulasietoring en die plantmateriaal is dan geinkubeer vir 24 h by 'n hoë relatiewe humiditeit (93%). Na die inkubasie proses is die trosse in twee groepe verdeel. Die een groep druiwe het oppervlak sterilisasie ondergaan in 70% etanol vir 5 s, en die ander groep was onbehandeld gelaat. Trosse van die onbehandelde en gesteriliseerde groep druiwe is gebruik vir isolasies. Vanuit elke tros is daar segmente van die ragis, laterale, pediselle en korrels (van die pedisel-end en wang gedeeltes) geïsoleer. Die segmente is in Petri bakkies met Kerssies' B. cinerea selektiewe medium en op water agar medium, wat paraquat bevat het, geïsoleer en geïnkubeer onder 'n 12 h dagligperiode teen 22°C. Die patogeen is positief geïdentifiseer deur sporuierende kolonies op die onderskeie weefseltipes. Laastens, in die virulensie- en patogenisiteitsproewe op druiwe en nektariens is verskillende isolate van B. cinerea, verkry vanaf verskillende gasheerplante, vergelyk deur natuurlike inokulasie toestande na te boots. Koue opgebergde vrugte, wat beskou word as hoogs vatbaar vir die infeksie van B. cinerea, is geïnokuleer met droë, enkel luggedraagde spore van die patogeen. Verskillende toetse is gedoen om die oppervlak penetrerende en letselvormende vermoëns van die onderskeie isolate te toets. Isolasies is van die skille van die vrugte gemaak en op Kerssies' B. cinerea selektiewe medium geplaas. Die nektarienvrugte is met paraquat behandel en die druifkorrels is gevries vir 1 h teen -12°C. Paraquat en bevriesing is gebruik om die gasheer se weerstand te verlaag en om die ontwikkeling van die patogeen te bevorder. In die natuurlik-geïnokuleerde studies het B. cinerea 'n konstante patroon getoon in die trosse van die drie verskillende wyndruif kultivars. B. cinerea het konstant ontwikkel uit die ragis, laterale, pedisel en pedisel-end, maar selde uit die korrelwang. Die ragis, lateral en pedisel dele het baie hoër vlakke van van die swam bevat as enige deel op die korrel. Die patogeen het ook konstant volop deur die hele seisoen op die ragis voorgekom. Gesamentlik wys die data dat, B. cinerea in wyndruiwe, in die Wes Kaap provinsie, meer geredelik vroeër in die seisoen voorkom, eerder as later. Data van die kunsmatige inokulasiestudies het die bevindinge van die natuurlike inokulasiestudies tot 'n groot mate bevestig. In dié studies het die patogeen meer geredelik die strukturele dele van die tros, eerder as op die korrels, bewoon. Oor die algemeen het die isolasieproewe gewys dat die konidia meer op die ragis voorkom as op enige ander deel. Die voorkoms van B. cinerea was ook oor die algemeen baie hoër in die strukturele dele van die tros, as op die korrel self. Die verskynsel het onder trosse van verskillende ontwikkelingsvlakke voorgekom. Die data het dus ook gewys dat konidia, wanner dit beskikbaar is, minder- sowel as meer kompakte trosse op 'n soortgelyke manier penetreer. Laastens, in die virulensie en patogenisiteitseksperimente het die resultate duidelik gewys dat daar geen gasheer spesifieke gedrag onder B. cinerea isolate is nie. In die studies het dit duidelik na vore gekom dat, B. cinerea meer geredelik in die strukturele binne dele van die wyndruif tros, in die Wes Kaap provinsie voorkom. En so ook eerder aan die begin van die seisoen, as later in die seisoen. Dié kennis moet in aanmerking geneem word by die beplanning en implementering van siektebeheerprogramme.
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Presello, Daniel A. "Studies on breeding of maize for resistance to ear rots caused by Fusarium spp. and on the occurrence of viruses in maize in eastern Canada." Thesis, McGill University, 2001. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=38260.
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Responses from pedigree selection for resistance to gibberella ear rot were assessed in four maize (Zea mays L.) populations, two selected after inoculation of Fusarium graminearum (Schwabe) macroconidia into the silk channel and two selected after inoculation into developing kernels. Responses were significant in both populations selected for silk resistance and in one of the populations selected for kernel resistance. Selection was more effective in later generations and genetic gains were associated with among-family selection but not with within-family selection. Results obtained here indicate that responses to selection could be more efficiently obtained by applying high selection intensities in advanced generations, by managing earlier generations as bulks and by reducing the number of plants per family. In another experiment, a wide sample of Argentine maize germplasm was evaluated for silk and kernel resistance to gibberella ear rot and to fusarium ear rot (caused by F. verticillioides (Saccardo) Nirenberg [=F. moniliforme (Sheldon)]. Several entries exhibited disease resistance in comparison with local check hybrids, particularly for fusarium ear rot, the most prevalent ear rot in Argentina. Results obtained in this study suggested the presence of general mechanisms controlling silk and kernel resistance to both diseases. In a supplementary study, viral diseases were surveyed in maize fields from the provinces of Ontario and Quebec in 1999 and 2000. Barley yellow dwarf was found in 1999. Sugarcane mosaic, maize dwarf mosaic and wheat streak mosaic were found in 2000. These diseases were not important for grain-maize planted in May, the most prevalent kind of maize crop in these provinces. Some of these diseases, such as sugarcane maize mosaic and maize dwarf mosaic were found important only in maize fields planted during or after the month of June, and this is of commercial relevance only for sweet corn.
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Nicol, Julie. "The distribution, pathogenicity and population dynamics of Pratylenchus thornei on wheat in South Australia." Title page, contents and summary only, 1996. http://web4.library.adelaide.edu.au/theses/09PH/09phn634.pdf.
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Bibliography: leaves 224-236. The study aimed to determine the distribution of both P. thornei and P. neglectus in South Australia. Also to study the field and laboratory population dynamics of P. thornei in relation to wheat yields, to determine its host range on a variety of cereal and non-leguminous hosts and to identify possible sources of nematode resistant wheat cultivars/varieties. Preliminary experiments studied the involvement of root rotting fungi with the nematode in wheat disease.
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Shrestha, Roshi. "A physiological and genetic mapping study of tolerance to root-knot nematode in rice." Thesis, Available from the University of Aberdeen Library and Historic Collections Digital Resources, 2008. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=24807.
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Maree, H. J. (Hans Jacob). "The expression of Dianthin 30, a ribosome inactivating protein." Thesis, Stellenbosch : Stellenbosch University, 2003. http://hdl.handle.net/10019.1/53633.
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Thesis (MSc)--Stellenbosch University, 2003.ENGLISH ABSTRACT: Ribosome inactivating proteins (RIPs) are currently classified as rRNA N-glycosidases, but also have polynucleotide: adenosine glycosidase activity. RIPs are believed to have anti-viral and anti-fungal properties, but the exact mechanism of these proteins still need to be elucidated.The mechanism of resistance however, appears to be independent of the pathogen. For resistance the RIP terminates virus infected plant cells and stops the reproduction and spread of the virus. Transgenic plants containing RIPs should thus be resistant to a wide range of viruses. The ultimate goal of the larger project of which this forms part is the development of virus resistant plants. To monitor the expression of a RIP in a transgenic plant a detection method had to be developed. Antibody detection of the RIP was decided upon as the most cost effective method. The RIP, Dianthin 30 from Dianthus caryophyllus (carnation), was used and expressed in bacterial and insect expression systems. The bacterial expression experiments were done using the pET expression system in BL21(DE3)pLysS cells. The expression in this system yielded recombinant protein at a very low concentration. Expression experiments were also performed in insect tissue culture with the baculovirus vector BAC-TO-BAC™.With this system the expression was also too low to be used for the production of antibodies. A Dianthin 30 specific peptide was then designed and then produced by Bio-Synthesis. This peptide was then used to raise antibodies to detect Dianthin 30. These antibodies were tested on Dianthus caryophyllus proteins. To establish if this detection method was effective to monitor the expression in plants, tobacco plants were transformed with Agrobacterium tumefaciens containing Dianthin 30 in the pART27 plant expression vector. The putative transformed plants were analysed with peR and Southern blots.
AFRIKAANSE OPSOMMING: Tans word Ribosomale-inaktiverende proteïene (RIPs) geklassifiseer as rRNA N-glikosidase wat ook polinukleotied: adenosien glikosidase aktiwiteit bevat. Daar word geglo dat RIPs anti-virale en anti-fungus eienskappe bevat, maar die meganisme van beskerming word nog nie ten volle verstaan nie. Dit is wel bewys dat die meganisme van weerstand onafhanklik is van die patogeen. Virus geinfekteerde plantselle word deur die RIP gedood om die voortplanting en verspreiding te bekamp en sodoende word weerstand bewerkstellig. Transgeniese plante wat dan 'n RIP bevat sal dus weerstandbiedend wees teen 'n wye spektrum virusse. Die hoofdoel van die breër projek, waarvan die projek deel uitmaak: is die ontwikkeling van virusbestande plante. Om die uitdrukking van die RIP in die transgeniese plante te kontroleer, moes 'n deteksie metode ontwikkel word. Die mees koste effektiewe deteksie metode is met teenliggame. Die RIP, Dianthin 30 from Dianthus caryophyllus (angelier) was gebruik vir uitdrukking in bakteriele- en insekweefselkultuur. Die bakteriele uitdrukkingseksperimente was gedoen met die pET uitdrukkings sisteem III BL21(DE3)pLysS selle. Die uitdrukking in die sisteem het slegs rekombinante proteïene gelewer in uiters lae konsentrasies. Uitdrukkingseksperimente was ook gedoen in insekweefselkultuur met die baculovirus vektor BAC-To- BACTM. Met die sisteem was die uitdrukking ook veels te laag om bruikbaar te wees vir die produksie van teenliggame. Daar is toe 'n peptied ontwerp wat Dianthin 30 kan verteenwoordig vir die produksie van teenliggame. Die teenliggame is getoets teen Dianthus caryophyllus proteïene. Om vas te stel of die deteksiemetode wel die uitdrukking van Dianthin 30 sal kan monitor, is tabak ook getransformeer met Dianthin 30. Die transformasies is gedoen met die hulp van Agrobacterium tumefaciens en die pART27 plant uitdrukkings vektor. Die plante is getoets met die polimerase ketting reaksie en Southern klad tegnieke.
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Van, der Walt Susanna Johanna. "Feeding by larvae of the American bollworm, Heliothis armigera (Hübner) (Lepidoptera: Noctuidae) on cotton plants." Thesis, Rhodes University, 1988. http://hdl.handle.net/10962/d1004386.
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H. armigera larvae are a key stage for pest management in conmercial irrigated cotton crops in South Africa. Effective survey methods for detecting larval populations in the field require an understanding of the biology of the larvae, particularly their feeding habits. Their feeding is central to the development of pest threshold levels for the implementation of integrated control programmes. This applies to routine surveys for the larvae as well as to the damage they cause. Biological characteristics of the larvae are described with the emphasis on the identification of the larval instars, which were consistently five in number in both field and laboratory populations. The distribution of H. armigera larvae on cotton plants in the field was examined, but was found to more or less random; had there been a clear preference for any height zones or compass direction this would have been an obvious avenue for improving the survey methods currently in use. Details of field and laboratory investigations of the selection of feeding sites by the larvae are given. The study confirmed a clear preference by the larvae for cotton buds, flowers and bolls (in the thesis collectively called "fruiting forms"), over leaves. There were indications that the larvae selected flowers more readily than buds or bolls. This "preference", however, is shown to be of no practical value for refining survey methods. Damage levels to cotton due to B. armigera are discussed. Both direct losses and indirect losses due to the abortion of fruiting forms are considered. These criteria are inadequate since they do not take into account the ability of cotton plants to compensate for these losses. It is concluded that this compensation by cotton plants should be taken into account in further studies of the pest status of B. armigera.
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Kamanga, Melvin Chalochapasi. "Biological activities of medical plants traditionally used in the Eastern Cape to treat pneumonia." Thesis, Nelson Mandela Metropolitan University, 2013. http://hdl.handle.net/10948/d1020051.
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Infectious diseases such as pneumonia still pose a major global health concern. Currently, the world is facing widespread emergence of acquired bacterial resistance to antibiotics which constitute one of the chief causes of infectious diseases. The accumulation of different antibiotic resistance mechanisms within the same strains has induced the appearance of the so called “superbugs”, or “multiple-drug resistant bacteria”. Due to antibiotic resistance, attention is currently being drawn towards biologically active components isolated from plant species commonly used as herbal medicine, as they may offer a new source of antibacterial, antifungal and antiviral activities. This is the basis of this study. In this study four medicinal plants namely, Cassia abbreviata, Geranium incanum, Pelargonium hortorum and Tecoma capensis were investigated for their antimicrobial potential. In vitro antimicrobial activity using agar disc diffusion method, agar dilution method and broth microdilution plate determination of minimum inhibitory concentration (MIC), were carried out against ATCC (American Type Culture Collection) strains and clinical isolates known to cause pneumonia. Aqueous, methanol and acetone extracts from the selected plants were thus tested against strains of Streptococcus pneumoniae, Haemophilus influenzae, Staphylococcus aureus, Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii, Escherichia coli and Candida albicans. The plants exhibited pronounced antimicrobial activity and were more active against Gram-positive bacteria than Gram-negative bacteria. During agar disc diffusion method, the highest inhibition zone was demonstrated by the acetone extract of P. hortorum (IZ=22mm and AI=0.73) against the reference strain of S. pneumoniae (ATCC 49619). The range of zones of inhibition in diameter across strains of S. pneumoniae and H. influenzae was 7mm to 22mm with activity index range of 0.23 to 0.74. The lowest MIC produced by medicinal plants in the study during agar disc diffusion method against S. pneumoniae and H. influenzae strains, was 2.5mg/ml. In broth microdilution plate assay, the lowest MIC demonstrated by C. abbreviata, T. capensis and P. hortorum extracts on tested bacteria was 0.031mg/ml and that of G. incanum was 0.063mg/ml. Candida albicans strains were only inhibited at 20mg/ml by the study plants. The highest activity among the individual extracts was shown by P. hortorum methanol extract which inhibited 71% of the studied bacteria. T. capensis methanol extract was the least and inhibited only 17% of the tested bacteria. The strains of Klebsiella pneumoniae showed the highest resistance to medicinal plants employed in this study. Traditional preparation of selected medicinal plants did not show any significant antimicrobial activity. Bioactive analysis of compounds on study plants was carried out using standard methods which revealed the presence of anthraquinones, flavonoids, phytosterol, saponins, tannins and triterpenoids. Comparison of the inhibitory effect of the plant extracts against some broad spectrum antibiotics revealed that the tested medicinal plants showed greater antimicrobial activity than standard antibiotics. However, there was no correlation between the antibiotic susceptibility patterns of the bacteria and the effects of the plants, signifying that plants probably function through different mechanisms. Bioautographic findings on thin-layer chromatography plate, exhibited clear zones of inhibition of bacterial growth with the Rf value range of 0.09 to 0.94. Anti-mutagenic activity was assayed by the Ames mutagenicity test in the plate-incorporation method using histidine mutants of S. typhimurium strains TA 100. The selected plant extracts at 2.5mg/ml and 5mg/ml did not induce mutagenesis in the absence of liver-metabolizing enzymes. The study results indicated that the selected plants are capable of inhibiting the growth of the studied pathogenic microorganisms to a varied degree. The leaves of G. incanum, P. hortorum, T. capensis as well as the stem bark of C. abbreviata could be novel sources of antimicrobial agents that might have broad spectrum activity. The anti-mutagenic properties of the studied medicinal plants may also provide additional health supplemental value to the other claimed therapeutic properties of the plants.