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Artigos de revistas sobre o assunto "Aviara"
Ubachukwu, N. N., e C. N. Emeribe. "The 2012 Flooding in Selected Parts of Isoko South, Delta State: Assessment of Socio-Economic Impacts". Mediterranean Journal of Social Sciences 8, n.º 1 (26 de janeiro de 2017): 353–58. http://dx.doi.org/10.5901/mjss.2017.v8n1p353.
Texto completo da fonteMeghann B. Humphries e Robert E. Ricklefs. "Alpha-globin variation does not predict avian malaria infection in the West Indian Bananaquit (Coereba flaveola)". Journal of Caribbean Ornithology 36 (6 de fevereiro de 2023): 1–16. http://dx.doi.org/10.55431/jco.2023.36.1-16.
Texto completo da fonteContent, Rob. "Aviary". Antioch Review 46, n.º 4 (1988): 488. http://dx.doi.org/10.2307/4611957.
Texto completo da fonteUnderwood, Susan O'Dell. "Aviary". Appalachian Heritage 31, n.º 1 (2003): 89–91. http://dx.doi.org/10.1353/aph.2003.0020.
Texto completo da fonteBelcher, Philip. "Aviary". Appalachian Heritage 45, n.º 2 (2017): 112. http://dx.doi.org/10.1353/aph.2017.0019.
Texto completo da fonteHuarcaya R., Freshia, Sonia Calle E., Juan Siuce M., André Sedano S., Jhonatan Huamaní P., Arturo García B., Luis Álvarez V. e Sofía Gonzales M. "Serotipificación y detección genética de Salmonella spp de origen aviar". Revista de Investigaciones Veterinarias del Perú 33, n.º 3 (29 de junho de 2022): e22893. http://dx.doi.org/10.15381/rivep.v33i3.22893.
Texto completo da fonteMaillé, Yves. "Tuberculinum aviare". Revista Médica de Homeopatía 4, n.º 3 (setembro de 2011): 111–15. http://dx.doi.org/10.1016/s1888-8526(11)70112-6.
Texto completo da fontePérez, Alberto A. "Influenza Aviar". El Hornero 29, n.º 1 (1 de agosto de 2014): 46–47. http://dx.doi.org/10.56178/eh.v29i1.626.
Texto completo da fonteBarrett, Paul. "The Mesozoic Aviary". American Scientist 95, n.º 6 (2007): 531. http://dx.doi.org/10.1511/2007.68.531.
Texto completo da fonteMachado, Aditi. "Outside the Aviary". New England Review 33, n.º 2 (2012): 6. http://dx.doi.org/10.1353/ner.2012.0041.
Texto completo da fonteTeses / dissertações sobre o assunto "Aviara"
Silveira, Flávio 1986. "Caracterização molecular de isolados brasileiros de Escherichia coli aviária". [s.n.], 2013. http://repositorio.unicamp.br/jspui/handle/REPOSIP/317368.
Texto completo da fonteDissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia
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Resumo: O resumo poderá ser visualizado no texto completo da tese digital
Abstract: The abstract is available with the full electronic document
Mestrado
Microbiologia
Mestre em Genética e Biologia Molecular
Macacu, Alina. "Modélisation du risque Influenza Aviaire dans l'écosystème de la Dombes, France". Thesis, Grenoble, 2014. http://www.theses.fr/2014GRENS008/document.
Texto completo da fonteAvian influenza is a contagious infectious disease caused by viruses of the family Orthomyxoviridae, influenza A viruses, affecting birds and known to cause extremely high mortality, especially in poultry. Highly pathogenic strains of avian influenza viruses cause severe and fatal disease in poultry and pose a risk to public health. In February 2006, France was hit by a highly pathogenic H5N1 avian influenza outbreak, affecting aquatic wildfowl in Dombes wetland. The Dombes is a wetland mosaic of more than a thousand ponds and an area of international ornithological importance, home to thousands of waterfowl. This is an area at risk for the spread of avian influenza viruses due to both the presence of wild birds on the ponds and the proximity of these populations to poultry farms that are present in the area. The main objective of this work is the modeling of the avian influenza risk in the Dombes region. This work is focused on the wildfowl and the risk of infection and transmission of infection by wild birds. As a first step, we have identified the specific characteristics of the Dombes area, which may affect the epidemiology of avian influenza in the region. The three main players in the Dombes ecosystem are the ponds, the wildfowl populations and the poultry farms. Secondly, the avian influenza risk in the Dombes was declined at two levels: 1) in the ecosystem of a single pond; and 2) within a network of ponds as characterized by 1), where the infection is spread from pond to pond. At the pond level, the avian influenza risk is modeled, on the one hand, by the persistence time of avian influenza viruses in the water of the pond, and, on the other hand, by the infection dynamics within wild bird populations by direct transmission between birds and indirectly through the water of the pond. At the ponds network, the risk analysis identifies spatial clusters of ponds at high risk of infection with avian influenza viruses. Concerning the risk of exposure of poultry farms to avian influenza viruses of wildfowl origin, it is calculated taking into account both the proximity of the farms to ponds likely to be infected and the probability of these ponds to become infected during an outbreak
Quel, Natália Galdi. "Escherichia coli Vacuolating Factor (ECVF) como fator associado a celulite aviária". Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/42/42132/tde-27062014-171721/.
Texto completo da fonteE. coli isolated from cellulitis lesions in broiler chickens produce a citotoxin, called ECVF (Escherichia coli Vacuolating Factor), which causes intense cytoplasm vacuolization in avian cells, but not in mammalian cells. The importance of ECVF in the pathogenesis of avian cellulitis was assessed in this study. Purified ECVF was inoculated subcutaneously in broiler chickens, and induced signs of inflammation on subcutaneous, adipose and connective tissues. In citotoxicity assays, we verified that ECVF induced cytoplasmic and nuclear alterations, which can affect cellular metabolism directly, such as chromatin condensation and nuclear fragmentation, intense cytoplasm vacuolization, and disorganization of cytoskeleton, leading to apoptosis. It was also verified the interaction of ECVF with proteins of avian cells, instead of those from mammalian cells, suggesting the specificity of this toxin to this cells. Our results, supported by data from previous studies, suggest an important role of ECVF in the pathogenesis of avian cellulitis.
Borzi, Mariana Monezi [UNESP]. "Produção da nucleoproteína recombinante do vírus da influenza aviária para aplicação no imunodiagnóstico". Universidade Estadual Paulista (UNESP), 2015. http://hdl.handle.net/11449/128008.
Texto completo da fonteA nucleoproteína (NP) do Vírus da Influenza Aviária (VIA) é um importante alvo antigênico no imunodiagnóstico desta doença, devido à sua baixa variabilidade entre as diferentes estirpes do VIA, resultando em uma elevada reatividade cruzada, e por ser também uma proteína altamente imunogênica para hospedeiros vertebrados. Neste estudo, o gene codificador da NP do VIA foi parcialmente clonado e expresso em Escherichia coli como uma proteína recombinante fusionada ao polipeptídeo SUMO e uma etiqueta de poli-histidina para seu uso no desenvolvimento de um ensaio de ELISA indireto para a detecção de anticorpos específicos contra o VIA. A NP recombinante foi expressada na fração solúvel e foi mais facilmente purificada. Após análise em relação aos seus principais sítios de antigenicidade e caracterização por meio de Western blotting, a NP recombinante foi utilizada como uma preparação antigênica no ELISA indireto para detecção de anticorpos contra o VIA presentes em amostras de soro de galinha. A análise comparativa do teste desenvolvido no presente estudo com um ELISA comercial apresentou valores de 95%, 97% e 96,7% de sensibilidade, especificidade e acurácia, respectivamente e um índice κappa de 0,88. Os resultados permitem concluir que a NP recombinante do VIA desenvolvida neste estudo possui características favoráveis para ser aplicada como antígeno no ELISA indireto, constituindo-se em um método sensível e específico para o imunodiagnóstico da Influenza Aviária em galinhas
The nucleoprotein (NP) of Avian Influenza Virus (AIV) is an important antigenic target for immunodiagnosis of this disease, due to its low variability among different AIV strains, resulting in high cross-reactivity, and the also highly immunogenic for vertebrate hosts. In this study, the gene enconding NP of AIV was cloned and expressed in Escherichia coli as a recombinant protein fused to SUMO polypeptide with a polyhistidine tag and used to develop an indirect ELISA for the detection of AIV-specific antibodies. The recombinant NP was expressed in the soluble fraction and easily purified. After Analysis of the main sites of antigenicity and characterization in Western-Blotting, the recombinant NP was optimized as an antigen preparation for indirect ELISA to detect anti-AIV antibodies in chicken serum samples. The comparative analysis of this ELISA with a commercial ELISA showed values of 95%, 97%, 96.7% of sensitivity, specificity and accuracy, respectively, and an agreement of k=0.88. In conclusion, the results indicated that the recombinant NP of AIV produced in this study is a good source of antigen for indirect ELISA and provides a sensitive and specific method for the immunodiagnosis of Avian Influenza in chickens
Maturana, Victor Gonçalves. "Subpatótipos de Escherichia coli patogênica para aves (APEC) podem estar associados às síndromes infecciosas infecciosas causadas no hospedeiro". [s.n.], 2010. http://repositorio.unicamp.br/jspui/handle/REPOSIP/317393.
Texto completo da fonteDissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia
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Resumo: Escherichia coli patogênica para aves (APEC) causa diferentes tipos de infecções sistêmicas extraintestinais nestes hospedeiros, coletivamente denominadas colibaciloses, causando grandes prejuízos econômicos à indústria aviária. Essas doenças incluem, dentre outras, septicemia, onfalite, celulite e síndrome da cabeça inchada. Entretanto, não há até o momento wna descrição de genes ou características que permitam classificar as linhagens aviárias em patótipos responsáveis por causar doenças específicas em seus hospedeiros, a semelhança do que ocorre para linhagens de E. co/i patogênicas para seres humanos. O objetivo deste estudo foi caracterizar linhagens de Escherichia coli de origem aviána representantes de 4 grupos, sendo um grupo de linhagens comensais (AFEC - stgla em inglês para "Avian Fecal Escherichia co/i") e três grupos de linhagens patogêmcas, causadoras de três sindromes diferentes em seus hospedeiros (septicemia, síndrome da cabeça inchada e onfalite). Para o trabalho, as características biológicas estudadas foram: adesão em células eucarióticas, formação de biofilme, produção de molécula sinalizadora de quorum sensing, presença de genes de ilhas de patogenicidade, dose de letalidade (LD50), grupo filogenético e presença de genes de virulência. A comparação entre as diferentes linhagens com base nestes traços genotípicos e fenotípicos, por meio de diferentes ferramentas de estatística multivariada além de redes complexas, permitiu inferir a estrutura populacional do grupo estudado. Os resultados indicam que APEC não constitui um grupo homogêneo, mas um conjunto estruturado de diferentes subgrupos, cada um associado a uma síndrome infecciosa específica causada no hospedeiro, possivelmente definindo diferentes patótipos ou subpatótipos dentro de linhagens APEC. Assim, sugerimos a existência de um subpatótipo associado à onfalite, com características de letal idade semelhantes as de linhagens AFEC, mas com um padrão de adesão diferente, que pode ser atribuído a uma especialização do grupo relacionada a colonização de um nicho particular, o saco da gema do ovo. E um subpatótipo associado à síndrome da cabeça inchada, igualmente adaptado à patogenicidade, mas com características mais "agressivas" evidenciadas pelos altos índices de letalidade, grande número de genes de virulência e altos índices de adesão. Linhagens associadas à septicemia, contudo, não constituem um grupo coeso, sugerindo tratar-se de uma miscelânea de linhagens que podem pertencer a diferentes subpatótipos e que em última instância geram a síndrome sistêmica (septicemia), devido à evolução do quadro clínico e/ou às condições imunológicas do hospedeiro. Este trabalho é pioneiro em demonstrar a existência de subpatótipos dentro de linhagens APEC, relacionando diferentes síndromes infecciosas com grupos específicos de linhagens as quais possuem características fenotípicas e genotípicas particulares. Tais resultados abrem novas possibilidades no estudo de genes responsáveis pelos diferentes processos de patogênese em APEC, bem como no desenvolvimento de vacinas. Talvez seja importante considerar estes subgrupos no desenvolvimento de vacinas, com o intuito de produzir vacinas com proteção cruzada, o que ainda não foi atingido com sucesso para linhagens APEC.
Abstract: Avian Pathogenic Escherichia coli (APEC) cause different types of systemic extraintestinal infections in poultry, which are collectively termed colibacillosis, imposing significant economic casses for the avian industry Among these diseases are septicaemia, omphalitis, cellulites and swollen head syndrome. However, to the date, there is no description of genes or characteristics which allow us to classify avian strains in pathotypes responsible for causing specific diseases in their hosts, as there are for human pathogenic E. co/i strains. In this study we aimed to characterize avian pathogenic E. co/i strains representing 4 groups, one of commensal strains (AFEC - Avian Fecal Escherichia co/i) and 3 groups of pathogenic strains responsible for causing 3 different syndromes in their hosts (septicaemia, omphalitis and swollen head syndrome). The biological characteristics studied were: adhesion to eukaryotic cells, biofilm formation, capacity of synthesizing quorum sensing s1gnaling molecule, presence of pathogenicity island, pathogenicity levels according to lethal dose (50%) assay, phylogenetic group and presence of virulence genes. The comparison between strains based on these genotypic and phenotypic traits, by different multivariate statistics tools and complex network, allowed us to infer. the population structure of the studied group. The results indicate that APEC do not constitute a unique homogeneous group, but a structured set of different subgroups, each one associated to a specific infectious syndrome inflicted to the host, possibly defining pathotypes or subpathotypes within APEC strains. Thus, we suggest the existence of a subpathotype associated to omphalitis, with lethality characteristics similar to AFEC strains, but with a different adhesion pattem, which may be due to a specialization related to the colonization of a particular niche, the egg's yolk sac. Anda subpathotype associated to the swollen head syndrome, equally adapted to pathogenicity, but with more "aggressive" characteristics demonstrated by the high lethality and adhesion levels. Septicaemic strains, however, do not constitute a cohesive group, which suggests a constellation of strains associated to different subpathotypes and capable of, eventually, cause a systemic syndrome (sepsis), due to the clinical evolution of the illness ami/or host immunological conditions. This work is pioneer in demonstrating the existence of subpathotypes within APEC strains, relating different infectious syndromes to specific groups of strains possessing particular genotypic and phenotypic characteristics. These results offer new possibilities in studying the genes responsible for different pathogenesis processes within APEC and for the vaccine developing. It may be important to consider these subgroups in the process of vaccine developing, in the efforts for obtain cross protection, which had not yet being accomplished successfully concerning APEC strains.
Mestrado
Genetica de Microorganismos
Mestre em Genética e Biologia Molecular
Rojas, Thaís Cabrera Galvão 1980. "Detecção de genes sob seleção positiva em linhagens de Escherichia coli patogênicas para aves (APEC) e para humanos". [s.n.], 2012. http://repositorio.unicamp.br/jspui/handle/REPOSIP/317369.
Texto completo da fonteTese (doutorado) - Universidade Estadual de Campinas, Instituto de Biologia
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Resumo: A bactéria Escherichia coli coloniza o trato intestinal de aves e humanos, de maneira comensal sem causar processos infecciosos. No entanto alguns clones adquiriram fatores de virulência específicos, permitindo o desenvolvimento de diferentes doenças como infecção do trato urinário, diarréia e meningite em humanos e colibacilose em aves. As linhagens que causam doença em aves são tipicamente denominadas APEC (Avian Pathogenic Escherichia coli). Neste trabalho foram sequenciados e anotados os genomas de quatro linhagens APECs (SCI-07, SEPT362, S17 e O8)que, juntamente com mais nove genomas referentes a linhagens de Escherichia coli patogênicas para aves e patogênicas para humanos foram utilizados para a busca de genes sob seleção positiva. Os genes homólogos foram agrupados,e posteriormente submetidos ao alinhamento de códons e das sequencias protéicas correspondentes. Uma árvore filogenética foi gerada para cada grupo de proteínas homólogas. Testes estatísticos determinaram qual entre os modelos de seleção neutra ou seleção positiva melhor explicou os dados existentes (alinhamentos de códons e árvores filogenéticas). Essas análises detectaram duzentas e cinquenta e quatro grupos de genes homólogos com evidência de seleção positiva. Para cada grupo foi realizado um teste de recombinação para verificar se o aumento na variação das sequencias não era devido à conversão gênica, resultando em cento e dezesseis grupos de genes homólogos sob seleção positiva. A proteína correspondente a um gene de cada grupo de genes homólogos foi identificada, por meio da ferramenta Blast. Diversos fatores de virulência, já conhecidos, e proteínas regulatórias puderem ser detectados. Os genes sob seleção positiva, também foram submetidos à anotação considerando o termo GO (Gene Ontology),apenas da categoria processo biológico. Dos cento e dezesseis genes apenas cinquenta e sete puderam ser identificados por meio dessa metodologia. O resultado da classificação dos genes dentro da classe GO, considerando o terceiro nível hierárquico,mostrou que a maioria dos genes anotados (31) tinha relação com o metabolismo primário.As proteínas cuja identificação, por meio do blast, não foi possível (proteínas hipotéticas)foram submetidas à análise de predição de localização subcelular e de peptídeo sinal. Essas análises revelaram que três proteínas desconhecidas (hypothetical proteinECIAI39_1028, hypothetical proteinZ0639e hypothetical proteinEC042_3791) são potenciais alvos para estudos que visam à busca de novos fatores de virulência de Escherichia coli patogênicas
Abstract: The bacterium Escherichia coli colonizesthe intestinal tract of birds and humans, in a commensal relationship without causing infection. However, some clones have acquired specific virulence factors allowing the development of various diseases such as urinary tract infection, diarrhea and meningitis in humans and colibacillosis in poultry. The strains that cause disease in birds are typically named APEC (Avian Pathogenic Escherichia coli). In this study we sequenced and annotated the genomes of four APECs strains (SCI-07, SEPT362, S17 and O8). These genomes and nine others avian pathogenic Escherichia coli and humans pathogenic strains genomes were used for studying genes under positive selection. The homologous genes were grouped and then subjected to codons and corresponding protein sequences alignment. A phylogenetic tree was generated for each group of homologous proteins. Statistical tests determined which among neutral or positive selection models best explains the existing data (codon alignments and phylogenetic trees). This analyzes detected two hundred fifty-four groups of homologous genes with positive selection evidence. For each group a recombination test was conducted to verify if the variation increase in the sequences was not due to gene conversion, resulting in one hundred and sixteen groups of homologous genes under positive selection. The protein corresponding to a gene of each group of homologous genes under positive selection was identified through Blast tool. Genes under positive selection were annotated considering the GO term (Gene Ontology), just for the biological process category. Only fifty-seven genes could be identified using this methodology. The gene classification within the GO classes, considering only the third hierarchical level showed that most of the annotated genes (31) were related with the primary metabolism. Proteins which blast identification was not possible (hypothetical proteins) were subjected to sub cellular localization and signal peptide prediction analyzes. These analyzes revealed that three unknown proteins (hypothetical protein ECIAI39_1028, hypothetical protein Z0639e hypothetical protein EC042_3791) are potential targets for studies, in order to search for new virulence factors of pathogenic Escherichia coli
Doutorado
Microbiologia
Doutora em Genética e Biologia Molecular
Scanavini, Luciana Simeoni. "Desenvolvimento de uma reação em cadeia pela polimerase para a detecção de coronavírus de perus (TCOV), por meio de um fragmento da região S2 de seu genoma". Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/10/10133/tde-02122013-160012/.
Texto completo da fonteTCOV was identified from field samples of birds with 13-84 days, from different regions of the country, and from organs such as intestine, kidneys and trachea, by polymerase chain reaction for 3\' UTR region and gene 3. The presence of this coronavirus in these different organs, not intestine, suggest a different strain, with similar phenotype observed in Infectious Bronchitis Virus (IBV). At the same time, a profile considering age of positive birds was designed by a Two sample T-test, which showed higher positivity in younger poults. Several TCOV sequences obtained from GenBank were aligned, and a genic segment was designed and submitted to different conditions in reaction in pursuit to develop a new PCR assay. A 436bp fragment was obtained, sequenced and presented 100% ID when compared to a TCOV complete sequence. The reaction featured good repetition, and reproduction as well, and some field samples did not turn out on positive results.
Matter, Leticia Beatriz. "Interação entre Escherichia coli patogência aviária (APEC) e células não fagocitárias". reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2011. http://hdl.handle.net/10183/60558.
Texto completo da fonteIn this work the interaction between avian pathogenic E. coli (APEC), the etiological agent of avian colibacillosis, and non-phagocytic cells was studied. APEC is an ExPEC (extraintestinal E. coli), a group that also includes UPEC (uropathogenic E. coli) and NMEC (E. coli neonatal meningitis). We analysed the behavior of 8 APEC strains - MT78, IMT2470, A2363, UEL31, UEL13, UEL17, IMT5155, UEL29 - against two non-phagocytic cell lines, avian fibroblasts (CEC-32) and human endothelial cells (Eahy926). Strains were genotyped for 33 virulence associated genes, and investigated the association capacity (adhesion and invasion), the invasion ability, intracellular multiplication, cytotoxicity and activation of caspases 3/7 of the strains after infecting avian fibroblasts. While all strains were able to adhere to avian fibroblasts, only the strain MT78 was able to invade them at levels comparable to the invasive bacterium Salmonella Typhymurium SL1344. APEC strains could not induce activation of caspases 3/7, nor were cytotoxic to fibroblasts. Since the invasive MT78 and the non-invasive IMT2470 strains presented very similar virulence genotypes, the expression of virulence genes of the bacteria grown in the absence and presence of avian fibroblasts by 3 h was analysed by RT-PCR. Results showed the expression of adhesins, siderophores and protectins/serum resistance structures for both strains in the two culture conditions, with and without fibroblasts. Analysis of the expression of fimH, ompA, ibeA and gimB by RT-qPCR revealed the repression of fimH in MT78, but the induction in IMT2470. In relation to ibeA and gimB invasins, they were induced in MT78 but repressed in IMT2470, while the ompA gene was expressed in both strains. The expression of invasins partly explains the invasive phenotype of MT78. It was also analysed the behaviour of the strains in relation to the association profile, invasion and intracellular multiplication when infecting EAhy926 human endothelial cells. The strains showed no ability to invade endothelial cells but showed a high level of association (up to 14 times higher than for fibroblasts cells for some strains). This study showed that the CEC-32 in vitro model is suitable for the study of cellular interaction between APEC and eukaryotic cells, and added more knowledge about the pathotype.
Zélé, Flore. "Interaction entre la bactérie endosymbiotique Wolbachia et le parasite responsable de la malaria aviaire, Plasmodium relictum, chez le moustique Culex pipiens". Thesis, Montpellier 2, 2012. http://www.theses.fr/2012MON20102.
Texto completo da fonteIn recent years, there has been a shift in the one host one parasite paradigm with the realization that, in the field, most hosts are co-infected with multiple parasites. Coinfections are particularly relevant when the host is a vector of diseases, because multiple infections can have drastic consequences for parasite transmission at both the ecological and evolutionary time scales. Wolbachia pipientis is the most common parasitic microorganism in insects and as such it is of special interest for understanding the role of coinfections in the outcome of parasite infections. This thesis investigates whether a natural Wolbachia infection can alter the quality of mosquitoes as vectors of malaria. To address this issue, we used a Wolbachia-mosquito-Plasmodium triad with a common evolutionary history. Our experimental system consists in the avian malaria parasite P. relictum SGS1 and its natural vector, the mosquito Cx. pipiens, which naturally harbours several wPip Wolbachia strains. First, we investigated the impact of different wPip groups on the prevalence and diversity on avian malaria in natural populations of Cx. pipiens mosquitoes in the Montpellier region. Second, using different isogenic laboratory mosquito strains harboring or not Wolbachia, we investigated the impact of the presence of Wolbachia on several mosquito and Plasmodium life history traits relevant for malaria transmission. We show that Wolbachia benefits both Cx. pipiens and Plasmodium: it enhances several mosquito life history traits, such as longevity and fecundity, increases their tolerance to P. relictum (i.e. compensates for a Plasmodium-induced mortality) and facilitates P. relictum infection both qualitatively (increases infection prevalence) and quantitatively (increases infection intensity). Although the mechanisms involved in the mosquito-Wolbachia-Plasmodium interaction remain elusive, these results suggest that Wolbachia may have important implications on the transmission of malaria in nature. This is consistent with the high prevalence and diversity of avian malaria parasites found in natural populations of Cx. pipiens. Further, these results suggest the need to reassess the use of Wolbachia as a way to fight pathogens and highlight the need to better understand parasite multipartite interactions
Cappelle, Julien. "Evaluation éco-épidémiologique du risque d'émergence du virus Influenza Aviaire Hautement Pathogène H5N1 dans le Delta Intérieur du Niger au Mali via l'avifaune sauvage". Doctoral thesis, Universite Libre de Bruxelles, 2010. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/210000.
Texto completo da fonte\
Doctorat en Sciences agronomiques et ingénierie biologique
info:eu-repo/semantics/nonPublished
Livros sobre o assunto "Aviara"
Cornel, Udrea, ed. Domnișoara aviara: Antologie de proză umoristică românească. Cluj-Napoca: Grinta, 2007.
Encontre o texto completo da fonteservice), SpringerLink (Online, ed. Introducing Aviary. New York: Friends of ED, 2009.
Encontre o texto completo da fontePeutz, Mike. Introducing Aviary. Berkeley, CA: Apress, 2009. http://dx.doi.org/10.1007/978-1-4302-7200-7.
Texto completo da fonteHall, Gaston. Alphabet aviary. Kenilworth: Ritchie, 1986.
Encontre o texto completo da fonteO'Dell, Kathleen. The aviary. New York: Alfred A. Knopf, 2011.
Encontre o texto completo da fonteill, Doty Andrea, ed. The children's aviary. West Hartford, Conn: Frog Books, 1998.
Encontre o texto completo da fonteAt the aviary. Plumstead, South Africa: Snailpress, 1995.
Encontre o texto completo da fonteGillian, Cummings. My dim aviary. [United States]: Black Lawrence Press, 2016.
Encontre o texto completo da fonteThe aviary gate. Bath: Windsor, 2008.
Encontre o texto completo da fonteKnowledge, forms, the aviary. Boise: Ahsahta Press, Boise State University, 2006.
Encontre o texto completo da fonteCapítulos de livros sobre o assunto "Aviara"
Peutz, Mike. "Welcome to the Aviary". In Introducing Aviary, 1–7. Berkeley, CA: Apress, 2009. http://dx.doi.org/10.1007/978-1-4302-7200-7_1.
Texto completo da fontePeutz, Mike. "Getting to Know Aviary.com". In Introducing Aviary, 555–89. Berkeley, CA: Apress, 2009. http://dx.doi.org/10.1007/978-1-4302-7200-7_10.
Texto completo da fontePeutz, Mike. "Creating Images with Phoenix". In Introducing Aviary, 9–77. Berkeley, CA: Apress, 2009. http://dx.doi.org/10.1007/978-1-4302-7200-7_2.
Texto completo da fontePeutz, Mike. "Image Manipulation with Phoenix". In Introducing Aviary, 79–151. Berkeley, CA: Apress, 2009. http://dx.doi.org/10.1007/978-1-4302-7200-7_3.
Texto completo da fontePeutz, Mike. "Raven—Vector Editing". In Introducing Aviary, 153–264. Berkeley, CA: Apress, 2009. http://dx.doi.org/10.1007/978-1-4302-7200-7_4.
Texto completo da fontePeutz, Mike. "Creating Images with Peacock". In Introducing Aviary, 265–358. Berkeley, CA: Apress, 2009. http://dx.doi.org/10.1007/978-1-4302-7200-7_5.
Texto completo da fontePeutz, Mike. "Creating Textures and Tiles in Peacock". In Introducing Aviary, 359–444. Berkeley, CA: Apress, 2009. http://dx.doi.org/10.1007/978-1-4302-7200-7_6.
Texto completo da fontePeutz, Mike. "Selecting and Managing Colors with Toucan". In Introducing Aviary, 445–74. Berkeley, CA: Apress, 2009. http://dx.doi.org/10.1007/978-1-4302-7200-7_7.
Texto completo da fontePeutz, Mike. "Screen Capture and Markup with Talon and Falcon". In Introducing Aviary, 475–504. Berkeley, CA: Apress, 2009. http://dx.doi.org/10.1007/978-1-4302-7200-7_8.
Texto completo da fontePeutz, Mike. "Application Switching". In Introducing Aviary, 505–53. Berkeley, CA: Apress, 2009. http://dx.doi.org/10.1007/978-1-4302-7200-7_9.
Texto completo da fonteTrabalhos de conferências sobre o assunto "Aviara"
DeLand, Trevor S., Ross E. Dudgeon, Michael W. Orth, Darrin M. Karcher e Roger C. Haut. "Effect of Housing System on Properties of Pullet Bones". In ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80631.
Texto completo da fonteArruda, Rafaela Oliveira de, e LUANA HELEN GONÇALVES SLAUTA. "CLAMIDIOSE AVIÁRIA". In II Congresso Brasileiro On-line de Clínica Médica Veterinária. Revista Multidisciplinar em Saúde, 2023. http://dx.doi.org/10.51161/convet2023/24812.
Texto completo da fonteAGUIAR, RAYANE OLIVEIRA PASCHOAL, e SHIHANE MOHAMAD COSTA MENDES. "Influenza aviária". In Congresso Iberoamericano de Saúde Pública Veterinária - 5ª Edição. Congresse.me, 2023. http://dx.doi.org/10.54265/beao9608.
Texto completo da fonteFattal, Laura. "Aviary Aspirations: Modeling Dance and Science Pedagogies". In AERA 2022. USA: AERA, 2022. http://dx.doi.org/10.3102/ip.22.1880276.
Texto completo da fonteFattal, Laura. "Aviary Aspirations: Modeling Dance and Science Pedagogies". In 2022 AERA Annual Meeting. Washington DC: AERA, 2022. http://dx.doi.org/10.3102/1880276.
Texto completo da fonteNorton, Thomas T. "Experimental myopia and emmetropization in mammals". In OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1991. http://dx.doi.org/10.1364/oam.1991.tuy3.
Texto completo da fonteGockley, Rachel, Michael Marotta, Carin Rogoff e Adrian Tang. "AVIVA". In CHI '06 extended abstracts. New York, New York, USA: ACM Press, 2006. http://dx.doi.org/10.1145/1125451.1125796.
Texto completo da fonteMARTINEZ, CRISTINA, MARIA TRIGUEZ e NURIA ZAMORA. "CELIACA SIN AVISAR". In 37 Congreso Nacional de la Sociedad Española de Pediatría y Atención Primaria - SEPEAP 2023. Grupo Pacífico, 2023. http://dx.doi.org/10.48158/sepeap2023.pd046.
Texto completo da fonteDeak, Michael D., e Scott C. McKenzie. "A COMPARISON OF NON-AVIAN THEROPOD AND BASAL AVIALAN LOCALITIES IN CHINA, GERMANY, AND ALBERTA WITH THE POTENTIAL FOR FEATHER PRESERVATION". In GSA Annual Meeting in Indianapolis, Indiana, USA - 2018. Geological Society of America, 2018. http://dx.doi.org/10.1130/abs/2018am-316030.
Texto completo da fonteMorgan Davis Hayes, Hongwei Xin, Hong Li, Timothy Shepherd, Yang Zhao e John Paul Stinn. "Bioenergetics of Hy-Line Brown Hens in Aviary Houses". In 2012 IX International Livestock Environment Symposium (ILES IX). St. Joseph, MI: American Society of Agricultural and Biological Engineers, 2012. http://dx.doi.org/10.13031/2013.41576.
Texto completo da fonteRelatórios de organizações sobre o assunto "Aviara"
Medici, André. Financial Support to Developing Countries to Face the Challenges Associated with Avian Influenza. Inter-American Development Bank, julho de 2006. http://dx.doi.org/10.18235/0006878.
Texto completo da fonteZhao, Yang, e Hongwei Xin. Ammonia Concentrations and Emissions of Aviary Hen Houses. Ames (Iowa): Iowa State University, janeiro de 2013. http://dx.doi.org/10.31274/ans_air-180814-740.
Texto completo da fonteJenkins, Jessica D., Rebecca L. Parsons, Morgan Hayes, Hongwei Xin e Suzanne T. Millman. Litter Use in an Aviary Laying Hen Housing System. Ames (Iowa): Iowa State University, janeiro de 2012. http://dx.doi.org/10.31274/ans_air-180814-1365.
Texto completo da fonteChai, Lilong, Hongwei Xin, Yang Zhao, Tong Wang e Michelle L. Soupir. Air Emissions Mitigation from Aviary Cage-free Hen Litter. Ames (Iowa): Iowa State University, janeiro de 2018. http://dx.doi.org/10.31274/ans_air-180814-390.
Texto completo da fonteMajo Masferrer, Natalia. La influenza aviar: una enfermedad en constante evolución. Sociedad Española de Bioquímica y Biología Molecular, março de 2024. http://dx.doi.org/10.18567/sebbmrev_219.202403.dc002.
Texto completo da fonteFalconi, César, e Alejandro Nin Pratt. Impacto económico potencial de la influenza aviar en el sector avícola de América Latina y el Caribe. Inter-American Development Bank, setembro de 2006. http://dx.doi.org/10.18235/0010293.
Texto completo da fonteFranzreb, Kathleen E. A Mobile Aviary Design to Allow the Soft Release of Cavity Nesting Birds. Asheville, NC: U.S. Department of Agriculture, Forest Service, Southern Research Station, 1997. http://dx.doi.org/10.2737/srs-rn-005.
Texto completo da fonteFranzreb, Kathleen E. A Mobile Aviary Design to Allow the Soft Release of Cavity Nesting Birds. Asheville, NC: U.S. Department of Agriculture, Forest Service, Southern Research Station, 1997. http://dx.doi.org/10.2737/srs-rn-5.
Texto completo da fonteHapner, Ralph W. Avian Influenza/Pandemic Influenza Program. Fort Belvoir, VA: Defense Technical Information Center, outubro de 2007. http://dx.doi.org/10.21236/ada501658.
Texto completo da fonteBradley, David Sherman. Avian Diagnostic and Therapeutic Antibodies. Office of Scientific and Technical Information (OSTI), dezembro de 2012. http://dx.doi.org/10.2172/1114116.
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