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Статті в журналах з теми "Plant viruses Control"
Bradamante, Gabriele, Ortrun Mittelsten Scheid, and Marco Incarbone. "Under siege: virus control in plant meristems and progeny." Plant Cell 33, no. 8 (May 20, 2021): 2523–37. http://dx.doi.org/10.1093/plcell/koab140.
Повний текст джерелаFalk, Bryce W., and Shahideh Nouri. "Special Issue: “Plant Virus Pathogenesis and Disease Control”." Viruses 12, no. 9 (September 21, 2020): 1049. http://dx.doi.org/10.3390/v12091049.
Повний текст джерелаDreher, Theo W., and W. Allen Miller. "Translational control in positive strand RNA plant viruses." Virology 344, no. 1 (January 2006): 185–97. http://dx.doi.org/10.1016/j.virol.2005.09.031.
Повний текст джерелаNavas-Castillo, Jesús, and Elvira Fiallo-Olivé. "Special Issue “Plant Viruses: From Ecology to Control”." Microorganisms 9, no. 6 (May 25, 2021): 1136. http://dx.doi.org/10.3390/microorganisms9061136.
Повний текст джерелаV, Maksimov I., Sorokan A. V, Burkhanova G. F, Veselova S. V, Alekseev V. Yu, Shein M. Yu, Avalbaev A. M, et al. "Mechanisms of Plant Tolerance to RNA Viruses Induced by Plant-Growth-Promoting Microorganisms." Plants 8, no. 12 (December 5, 2019): 575. http://dx.doi.org/10.3390/plants8120575.
Повний текст джерелаTapio, Eeva, Katri Bremer, and Jari P. T. Valkonen. "Viruses and their significance in agricultural and horticultural crops in Finland." Agricultural and Food Science 6, no. 4 (December 1, 1997): 323–36. http://dx.doi.org/10.23986/afsci.72795.
Повний текст джерелаZettler, F. William. "Viruses of Orchids and Their Control." Plant Disease 74, no. 9 (1990): 621. http://dx.doi.org/10.1094/pd-74-0621.
Повний текст джерелаBosque-Pérez, N. A., J. M. Thresh, R. A. C. Jones, U. Melcher, A. Fereres, P. L. Kumar, S. M. Gray, and H. Lecoq. "Ecology, evolution and control of plant viruses and their vectors." Virus Research 186 (June 2014): 1–2. http://dx.doi.org/10.1016/j.virusres.2014.04.001.
Повний текст джерелаRoenhorst, J. W., M. Botermans, and J. T. J. Verhoeven. "Quality control in bioassays used in screening for plant viruses." EPPO Bulletin 43, no. 2 (July 16, 2013): 244–49. http://dx.doi.org/10.1111/epp.12034.
Повний текст джерелаLee, Ga Hyung, and Choong-Min Ryu. "Spraying of Leaf-Colonizing Bacillus amyloliquefaciens Protects Pepper from Cucumber mosaic virus." Plant Disease 100, no. 10 (October 2016): 2099–105. http://dx.doi.org/10.1094/pdis-03-16-0314-re.
Повний текст джерелаДисертації з теми "Plant viruses Control"
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.
Повний текст джерелаENGLISH 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.
Giampan, José Segundo. "Infectividade e proteção de três estirpes fracas do Papaya ringspot virus em plantas de melancia." Universidade de São Paulo, 2003. http://www.teses.usp.br/teses/disponiveis/11/11135/tde-25022003-134805/.
Повний текст джерелаThe purpose of this work was to evaluate the infectivity of three mild strains of Papaya ringspot virus - type W (PRSV-W) on watermelon (Citrullus lanatus). The effect of the origin of the mild strain, the concentration of the inoculum, the species of the source of the inoculum and the age of the test-plant on the infectivity of mechanically inoculated watermelon were also evaluated. The protective effect of these mild strains on preimmunized watermelon plants was evaluated under greenhouse and field conditions. Mild strains were selected from blisters formed on mosaic leaves of naturally infected watermelon plants. The infectivity of the selected mild strain was compared with that of mild strains PRSV-W-1 and PRSV-W-2, which were previously obtained from blisters formed on mosaic leaves of zucchini squash (Cucurbita pepo cv. Caserta). A severe strain isolated from zucchini squash (PRSV-W-C) was used as control. The effect of the concentration and the species source of inoculum of the mild strains on the infectivity of watermelon plants was studied with inoculum extracted from 4, 8, 12 and 16 leaf discs of zucchini squash and watermelon plants, separately infected with the mild and severe strains, diluted in 2 mL of phosphate buffer. Four stages of development of watermelon plants, starting at the cotyledonal stage, were tested for the infectivity with the mild strains. Inocula were prepared with extracts of 12 leaf discs diluted in 2 mL of phosphate buffer. The protective effect of the mild strain selected from blisters on mosaic leaves of watermelon plants was evaluated on preimmunized plants challenge inoculated with severe strain PRSV-W-C, under greenhouse and field conditions. Watermelon plants preimmunized with mild strains PRSV-W-1 and PRSV-W-2 and unprotected plants were also included in the field trial. Protection was evaluated based on plant simptons, yield and sugar content in the fruits. One mild strain, named PRSV-W-3, was obtained from blisters on mosaic leaves of watermelon plants. The rate of infection of watermelon plants with mild strain PRSV-W-3 was similar to that with mild strains PRSV-W-1 and PRSV-W-2 in all infectivity tests, independently of the concentration of the inoculum, species source of the inoculum and stage of development of the inoculated test-plant, reaching 100% in some cases. Rate of infectivity with severe strain PRSV-W-C was always 100%. Apparently, the infectivity of the mild strains on watermelon was more directly related with the intensity of the abrasion produced by mechanical inoculation than with the above studied variables. The selected mild strain PRSV-W-3 protected watermelon plants against superinfection with the severe strain in the greenhouse tests. Protection was also effective under field conditions. Yield of plants preimmunized with all three mild strains and unprotected plants were statistically similar. The sugar content and the quality of the pulp of the fruits were similar for all treatments.
Mkhize, Thokozani M. "The detection of cherry leaf-roll nepovirus and the use of molecular markers for germplasm identification in walnuts (Juglans regia L.)." Thesis, Stellenbosch : Stellenbosch University, 2003. http://hdl.handle.net/10019.1/53624.
Повний текст джерелаENGLISH ABSTRACT: The aim of this study was to combine two common diagnostic tools: serological kits and genetic fingerprinting to identify cherry leaf-roll nepovirus (CLRV), and to establish a marker system to characterize walnut germplasm. The detection of plant viruses is difficult. Restrictions are imposed for quarantine purposes on the importation of plant material from foreign countries. Modern techniques such as a PCR based screening method for CLRV are required to ensure material do not harbour viruses. A primer pair was designed to amplify a 430 bp non-coding homologous region. For the choice of primers, consensus sequences were considered and areas where the sequence data shared 98.5% homology, were chosen. The sensitivity of this detection method was 100-fold higher when compared to the ELISA. The PCR fragment was verified by nucleotide sequencing. AFLP technology was used to identify polymorphic fragments for 6 walnut cultivars and a rootstock, and SCARs were developed from AFLP specific bands. The AFLP technique distinguished all the walnut cultivars and the rootstock. However, conversion of AFLP fragments to SCAR markers for the development of a simple robust technique for cultivar discrimination, was not successful. Using 27 AFLP primer combinations, polymorphic fragments as high as 47.8% were scored. The reason for the lack of efficient conversion was as the result of the AFLP technique. The SCAR primers were generated from sequences internal to the AFLP primers but the specificity of the markers was in the AFLP primers not the internal sequence. In this study using AFLP, walnut cultivars were found to be closely related. The AFLP primer pairs used, provided polymorphic fragments. From these fragments, 7 SCAR markers were developed. It was expected that these SCARs derived from the AFLP markers would detect slight differences between cultivars. The Paradox SCAR marker was the only one that could divide the cultivars into two groups. When Chandler SCAR products were digested with the restriction enzyme Rsal, the same banding pattern as that of Paradox SCAR products was observed.
AFRIKAANSE OPSOMMING: Die doel van hierdie studie was om twee algemene opsporingstegnieke te kombineer: serologiese toetsstelle en genetiese vingerafdrukke om cherry leaf-roll nepovirus (CLRV) te eien en om In merkersisteem te ontwikkel wat okkerneut kiemplasma kan karakteriseer. Die opsporing van plant virusse is baie moeilik. As gevolg van kwarantyn vereistes, word daar beperkinge geplaas word op die invoer van plant materiaal vanuit die buiteland. Moderne tegnieke soos hierdie een wat op PKR berus, word benodig om te verseker dat CLRV nie in plantmateriaal teenwoordig is nie. In Stel inleiers is ontwerp wat In 430 bp nie-koderende homoloë area amplifiseer. Hiervoor is konsensus volgordes bestudeer en slegs die volgordes wat 98,5% homologie getoon het, is gekies. In vergelyking met ELISA was die sensitiwiteit van hierdie deteksie metode 100 maal beter. DNA volgordebepaling is op die resulterende fragment gedoen om die PKR produk te verifieer. AFLP tegnologie is gebruik om polimorfiese fraqmente vir 6 okkerneut kultivars en 'n onderstok te identifiseer en SCARs is uit hierdie fragmente ontwikkel. Die AFLP tegniek kon tussen al die okkerneut kultivars en die onderstok onderskei. Die omskakeling van die AFLP fragmente in SCAR merkers om sodoende In eenvoudige kragtige tegniek vir kultivar onderskeiding te ontwikkel, was egter nie suksesvol nie. Met die gebruik van 27 AFLP inleier kombinasies, kon polimorfiese fragmente van so hoog as 47.8% verkry word. Die rede hoekom omskakeling onsuksesvol was lê by die aard van die AFLP tegniek. Die SCAR inleiers is ontwikkel uit volyordes intern tot die AFLP inleiers, maar die spesifisiteit van die merkers het juis in die AFLP inleiers gelê en nie in die interne volgordes nie. In hierdie studie, met die gebruik van AFLP, is gevind dat okkerneut kultivars baie naby verwant is. Die AFLP inleierstelle wat gebruik is, het polimorfiese fragmente gelewer. Uit hierdie fragmente is 7 SCAR merkers ontwikkel. Daar is verwag dat die SCARs wat uit die AFLP merkers ontwikkel is, klein verskille tussen kultivars sou opspoor. Dit was egter net die Paradox SCAR merker wat die kultivars in twee groepe kon verdeel. Restriksie ensiem vertering met Rsalop die Chandler SCAR produkte het dieselfde bandpatrone as die van die Paradox SCAR produkte gelewer.
Li, Sizhun. "SnRK1-eIF4E Interaction in Translational Control and Antiviral Defense." The Ohio State University, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=osu1417694518.
Повний текст джерелаBeltrame, André Boldrin. "Efeito de cianobactérias e algas eucarióticas na resistência de plantas de fumo contra o Tobacco mosaic virus (TMV)." Universidade de São Paulo, 2006. http://www.teses.usp.br/teses/disponiveis/11/11135/tde-02032006-155032/.
Повний текст джерелаAlgae produce several different compounds that show biological activity, including ones with antiviral activity or that act as phytoalexin inducers. Thus, it was investigated the reduction of Tobacco mosaic virus (TMV) symptoms on tobacco plants treated with cyanobacteria or eukaryotic algae, and it was studied the way of action of algae on the studied pathosystem. When the tobacco plants were treated two days before the inoculation, it was verified that the suspension of 004/02, 008/02, 061/02 Anabaena sp., and Nostoc sp. 61 strains as well as the intracellular preparation of 004/02 strain (4 C) and the medium filtrated from 061/02 strain (61 M) reduced TMV symptoms on tobacco plants, cultivar TNN. Furthermore, it was studied the direct effect of the algae suspensions on virus particles. The results showed that Anabaena sp., Nostoc sp. 21, Nostoc sp. 61 and 090/02 strains have compounds with direct activity on TMV. To try to elucidate the way of the action of algae, on the studied pathosystem, several biochemical parameters were investigated. It was seen that the preparation 4 C increase peroxidase activity and all treatments decrease β-1,3-glucanase activity on tobacco leaves from the forth day on after the treatment. Moreover, 008/02 and 061/02 strains and the 61 M preparation caused higher superoxide accumulation, and the preparation 4 C decreased hydrogen peroxide accumulation when compared to the controls distilled water and BG 11 medium 37 hour after virus inoculation. In this way, the algae could be a biocontrol agents, because it shows direct action on phytopathogens and/or change the metabolism of the plants, that could be associated with the synthesis of deffence compounds.
Du, Preez Jacques. "The construction of an infectious clone of grapevine virus A (GV A)." Thesis, Link to the online version, 2005. http://hdl.handle.net/10019/1012.
Повний текст джерелаNovaes, Quelmo Silva de. "Seleção de estirpes fracas do Passion Fruit Woodiness Virus e tentativas de premunização para o controle do endurecimento dos frutos do maracujazeiro." Universidade de São Paulo, 2002. http://www.teses.usp.br/teses/disponiveis/11/11135/tde-03122002-080324/.
Повний текст джерелаThe main purpose of this work was to select mild strains of Passion fruit woodiness virus (PWV) and to evaluate their protective effect in passion flower (Passiflora edulis f. flavicarpa Deg.) challenged with a severe strain of the virus. Three mild strains were selected from outstanding plants found in orchards severely affected by the virus (F-101, F-102 and F-103) and three others were obtained from blisters formed in passion flower leaves with mosaic (F-99, F-144 and F-145). The protective effect of the mild strains was evaluated in passion flower under greenhouse and field conditions. Plants preimmunized with mild strains F-101, F-102 and F-144, under greenhouse conditions, showed partial protection after challenge inoculation with the severe strain PWV-SP. Total absence of protection was observed in passion flower preimmunized with all six mild strains and challenged with PWV-SP in the first field experiment. Due to these results, two hypotheses were raised to explain the intensification of symptoms in passion flower preimmunized with mild strains and challenged with the severe strain of the virus: a) the occurrence of low concentration and/or irregular distribution of the mild strains in the tissues of the preimmunized plants allow the infection and establishment of the later inoculated severe strain and b) the selected mild strains belong to a different species of Potyvirus, serologically related to PWV, but that do not offer protection against the severe strain of PWV. The first hypothesis was studied in a field experiment with passion flower preimmunized with mild strains F-101 and F-144, separately, and cultivated under screenhouse. Before the challenge inoculation, leaf samples were taken from five leaves of all protected plants and the concentration of the mild strains was estimated by indirect DAS-ELISA. A group of plants was challenged in three expanded leaves of the vine and another group was challenged with viruliferous aphids placed on the tip of the vine. All preimmunized plants showed severe symptoms of the disease, four months after the challenge inoculation. A great variation was observed in the concentration of the mild strains in the tissues of different leaves of the same plant. The ELISA test was not able to detect the mild strains in extracts of 205 out of 300 leaf disks. The second hypothesis was tested with crotalaria plants (Crotalaria juncea L.) preimmunized with mild strains F-101 and F-144 and analysis of the nucleotide sequence of the coat protein gene of the F-101, F-103 and PWV-SP strains. All preimmunized crotalaria plants were protected against the infection and/or manifestation of the symptoms caused by the severe strain PWV-SP. Quantitative studies of the mild strains in crotalaria revealed a larger uniformity in the concentration of the virus in the leaves. The analysis of the nucleotide sequence of the coat protein gene pointed out identity of 99.7% among the mild strains. The severe strain shared 97.5 % identity with both mild strains, showing that they are all strains of the same virus. These results showed that preimmunization does not seem to be an appropriate alternative for the control of the passion fruit woodiness disease in passion flower due to the breakdown in protection. Failure in protection seems to be related to the low concentration and/or irregular distribution of the mild strains in the leaves of the passion flower, which allow the occurrence of infection sites available for superinfection with the severe strain.
Gouvêa, Marina Mengardo. "Efeito de inseticidas no controle das transmissões primária e secundária do Tomato severe rugose virus (ToSRV) para tomateiro por Bemisia tabaci biótipo B." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/11/11135/tde-20102015-152947/.
Повний текст джерелаThe severe mosaic, caused by ToSRV begomovirus, is a major disease of tomato. This study evaluated the efficacy of four insecticides, sprayed cyazypyr, drench cyazypyr, sprayed spiromesifen and thiamethoxam on controlling primary and secondary infections by ToSRV to tomato plants, transmitted by Bemisia tabaci biotype B. Treatments were confined separately in proof insects cages, which were: control, represented by healthy and infected tomato plants sprayed with water and aviruliferous insects releasing; primary infection, simulated by healthy tomato plants with insecticide spraying and viruliferous insects releasing, and secondary infection, simulated with healthy tomato plants and ToSRV infected tomato plants, sprayed with insecticide, and aviruliferous insects releasing. None of the insecticides was effective in controlling primary infection. In the case of secondary infection simulation, 4% and 16% of the tomato plants treated with soil and foliar cyazypyr insecticides, respectively, were infected; against 84% and 74% of infected tomato plants in their respective controls. For treatments with thiamethoxam and spiromesifen insecticides spraying, in secondary infection simulation, 58% and 62% of tomato plants were infected, respectively, versus 66% and 74% of infected plants in their respective controls. The rational use of insecticides to reduce secondary infection associated with elimination of external sources of inoculum may contribute to disease management.
Willekens, Jeroen. "Mechanism of vector resistance in groundnut to control groundnut rosette virus disease in Sub-Saharan Africa." Thesis, University of Greenwich, 2003. http://gala.gre.ac.uk/6344/.
Повний текст джерелаMarques, Míriam de Almeida. "Óleos vegetais e óleo mineral na mortalidade da Bemisia tabaci biótipo B e na transmissão do vírus do mosaico dourado no feijoeiro." Universidade Federal de Goiás, 2011. http://repositorio.bc.ufg.br/tede/handle/tede/3577.
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As an alternative to synthetic insecticides, mineral oils and vegetable oils have been shown to be promising in controlling Bemisia tabaci biotype B. This study aimed to evaluate the effect of mineral and vegetable oils on eggs, nymphs and adults of B. tabaci biotype B, in the transmission of the bean golden mosaic virus and on dry production. The experiments were conducted at screenhouse at Embrapa Rice and Beans, Santo Antônio de Goiás, Goiás. The following oils in the concentration of 1% were used: Assist® mineral oil, Neem Max® neem oil, Veget'oil® vegetable oil, Citrole® orange oil, Castor Oil®, Sesame Oil®. The two last oils were emulsified with detergent Zupp® at 2%. Thiamethoxam at 200 g pc/ha (GD - dispersible granule) was used as a standard for comparison of chemical insecticide and distilled water as control. In all experiments, the experimental unit consisted of a polyethylene pot (34 cm diameter x 12 cm) containing two seedlings of common bean cv. Pearl. The experimental design was completely randomized with four replications / treatment. In the first experiment was evaluated the effect of oils on the mortality of eggs of B. tabaci. The second experiment was conducted to verify that the treatment of eggs with the oils would affect first instar nymphs. In the third experiment was evaluated the mortality of nymphs of the second to fourth instar after spraying of oil on the second instar nymphs. In these experiments, seedlings of bean cv. Pearl infested with eggs or nymphs of the whitefly were sprayed with 250 μL of each treatment on the abaxial surface of leaves. In the fourth experiment, four seedlings infested with adults and distributed in one m2 were sprayed with 30 ml of treatment. In the fifth experiment the effect of oils on adult mortality, the incidence of bean golden mosaic virus and crop production were evaluated by spraying only vegetable oils before the infestation of the seedlings with adults. All treatments caused mortality of eggs lesser or equal to 9.5%. Vegetable oils, when applied to eggs, caused mortality of newly-hatched nymphs lesser or equal to 22.3%. All treatments caused significant mortality of second instar nymphs, ranging from 46.5% for thiamethoxan to 81.6% for to castor oil. The treatments also affected the development of the nymphs until the fourth instar. Mortalities of nymphs greater than 80% were observed with castor, neem, sesame and orange oils. Only castor, sesame and mineral oils caused significant adult mortalities of 41.2%, 25.7% and 38.0%, respectively, one day after spraying. The orange, castor, neem and sesame oils, when sprayed prior to insect infestation of beans seedlings, caused mortality of whitefly adults ranging from 32.1% to 53.6%, one day after application. The castor and orange oils reduced the incidence of golden mosaic virus in bean. Castor oil favored greater pod yield, while the lowest pod yield was observed on sesame oil. The total number of seeds, mean number of seeds per pod and seed weight was not increased with the use of vegetable oils. The use vegetable and mineral oils have the potential to control B. tabaci biotype B.
Como alternativa aos inseticidas sintéticos, óleos vegetais e óleos minerais têm se revelado promissores no controle da Bemisia tabaci biótipo B. Esse trabalho teve como objetivo avaliar o efeito de óleos vegetais e mineral sobre ovos, ninfas e adultos da B. tabaci biótipo B e sobre a transmissão do vírus do mosaico dourado no feijoeiro e na sua produtividade. Os experimentos foram conduzidos em casa telada na Embrapa Arroz e Feijão, Santo Antônio de Goiás, Goiás. Utilizaram-se os seguintes óleos na concentração de 1%: óleo mineral Assist®, óleo de nim Max Neem®, óleo vegetal Veget’oil®, óleo de laranja Citrole®, óleo de Mamona®, óleo de Gergelim®, sendo os dois últimos emulsificados com detergente neutro Zupp® a 2%. Como padrão de comparação de inseticida químico utilizou-se o thiamethoxam a 200 g p.c./ha (granulado dispersível-GD) e como testemunha água destilada. Em todos os experimentos, a unidade experimental foi constituída por um vaso de polietileno (34 cm de diâmetro x 12 cm de altura) contendo duas plântulas do feijoeiro comum cv. Pérola. O delineamento experimental utilizado foi o inteiramente casualizado com quatro repetições/tratamento. No primeiro experimento foi avaliado o efeito dos óleos sobre a mortalidade dos ovos da B. tabaci. O segundo experimento foi instalado para verificar se o tratamento de ovos com os óleos afetaria as ninfas de primeiro ínstar da mosca-branca. No terceiro experimento foi avaliada a mortalidade de ninfas do segundo ao quarto ínstar após a pulverização dos óleos sobre ninfas do segundo ínstar. Nestes experimentos, plântulas de feijão cv. Pérola infestadas com ovos ou ninfas da mosca-branca foram pulverizadas com 250 μL de cada tratamento na face abaxial das folhas. No quarto experimento, quatro plântulas infestadas com adultos e distribuídas em um m2 foram pulverizadas com 30 ml dos tratamentos. No quinto experimento avaliou-se o efeito dos óleos na mortalidade dos adultos, na incidência do vírus do mosaico dourado do feijoeiro e na produtividade dessa cultura, pulverizando-se apenas os óleos vegetais antes da infestação dos adultos nas plântulas. Todos os tratamentos causaram mortalidade de ovos menor ou igual a 9,5%. Os óleos vegetais quando aplicados sobre os ovos, apresentaram efeito residual, causando mortalidade de ninfas recém-eclodidas menor ou igual a 22,3%. Todos os tratamentos causaram mortalidades significativas de ninfas do segundo ínstar, variando de 46,5% para o thiamethoxan até 81,6% para o óleo de mamona. Os tratamentos também afetaram o desenvolvimento das ninfas até o quarto ínstar. Foram observadas mortalidades de ninfas maiores que 80% com o óleo de mamona, nim, gergelim e laranja. Somente os óleos de mamona, gergelim e mineral causaram mortalidades significativas de adultos de 41,2%, 25,7% e 38%, respectivamente, um dia após a pulverização. Os óleos vegetais de laranja, mamona, nim e gergelim, quando pulverizados antes da infestação do inseto em plântulas de feijão, causaram mortalidade de adultos da mosca-branca variando de 32,1% a 53,6%, um dia após aplicação. Os óleos de mamona e laranja reduziram a incidência do vírus do mosaico dourado no feijoeiro. O óleo de mamona favoreceu maior produção de vagens, enquanto que o gergelim proporcionou menores valores de produção. O número total de grãos, número de grãos por vagem e massa de grãos, não foi incrementado com o uso de óleos vegetais. O uso de óleos vegetal e mineral apresenta potencial no controle da B. tabaci biótipo B.
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