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Frequency of occurrence of physical defects in turkey poults / Częstotliwość występowania wad budowy piskląt indyczych

.E., Anderson J.W., Patterson R.A., Velleman S.G. (2008). Genetics of growth and reproduction in the turkey. 17. Changes in genetic parameters over forty generations of selection for increased sixteen-week body weight. Poultry Sci., 87: 1971-1979. Rosario C.C., Lopez C.C., Tellez I.G., Navarro O.A., Anderson R.C., Eslava C.C. (2004). Serotyping and virulence genes detection in Escherichia coli isolated from fertile and infertile eggs, dead-in-shell embryos, and chickens with yolk sac infection. Avian Diseases, 48: 791-802. Shanawany M

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Mouse duodenum as a model of inflammation induced by enterotoxigenic Escherichia coli K88

prevention strategies. Anim Health Res Rev 2005, 6, 17-39. 4. Julian R.M., Takuichi S., Andrew J.W., Tracey A.M., John C.F., Sarah J.H., William G.W.: Design and evalution of useful bacterium-specific PCR primers that amplify genes coding for bacterial 16S rRNA. Appl Environ Microb 1998, 64, 795-799. 5. Kerry K., Cooper J., Glenn S.: Virulence of Clostridium perfringens in an experimental model of poultry necrotic enteritis. Vet Microbiol 2010, 142, 323-328. 6. Kwang-il J., Malabi M., Venkatesan J., Shoshana B., Saul T

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Occurrence of reovirus (ARV) infections in poultry flocks in Poland in 2010–2017

References 1. Bayai K., Dandar E., Dorsey K.M., Mato T., Palya V.: The genomic constellation of a novel avian orthoreovirus strain associated with runting stunting syndrome in broilers. Virus Genes 2011, 42, 82–89. 2. Benavente J., Martinez-Costas J.: Avian reovirus: structure and biology. Virus Res 2007, 123, 1005–1019. 3. Goldenberg D., Pasmanik-Chor M., Pirak M., Kass N., Lublin A., Yeheskel A., Heller D., Pitcovski J.: Genetic and antigenic characterization of sigma C protein from avian reovirus. Avian Pathol 2010, 39, 189–199. 4

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Substitution in position 222 of haemagglutinin of pandemic influenza A (H1N1) viruses isolated from pigs in Poland

(H1N1) influenza viruses in ferrets and mice. Science 2009, 325, 484-487. 12. Mak D.B., Daly A.M., Armstrong P.K., Effler P.V.: Pandemic (H1N1) 2009 influenza vaccination coverage in Western Australia. Med J Aust 2010, 193, 401-404. 13. Melidou A., Gioula G., Exindari M., Chatzidimitriou D., Diza E., Malisiovas N.: Molecular and phylogenetic analysis of the haemagglutinin gene of pandemic influenza H1N1 2009 viruses associated with severe and fatal infections. Vet Res 2010, 151, 192-199. 14. Moussi A., Kacem M.A., Pozo

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Detection of classical genes and enterotoxins of Staphylococcus aureus isolated from raw milk in the south-east region of Poland

raw milk cheese. J. Dairy Sci 2005, 88, 3810-3817. 15. Kerouanton A., Hennekinne J.A., Letertre C., Petit L., Chesneau O., Brisabois A., De Buyser M.L.: Characterization of Staphylococcus aureus strains associated with food poisoning outbreaks in France. Int J Food Microbiol 2007, 115, 369-375. 16. Korpysa-Dzirba W., Osek J.: Identification of genes encoding classical staphylococcal enterotoxins in Staphylococcus aureus isolated from raw milk. Bull Vet Inst Pulawy 2011, 55, 55-58. 17. Loncarevic S., Jørgensen H

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Comparison of two multiplex PCR assays for the detection of Listeria spp. and Listeria monocytogenes in biological samples

.M., Barbuddhe S.B.: Detection of multiple virulence-associated genes in Listeria monocytogenes isolated from bovine mastitis cases. Int J Food Microbiol 2007, 113, 201-207. 24. Schuchat A., Swaminathan B., Broome C.V.: Epidemiology of human listeriosis. Clin Microbiol Rev 1991, 4, 169-183. 25. Swaminathan B., Gerner-Smidt P.: The epidemiology of human listeriosis. Microbes Infect 2007, 9, 1236-1243. 26. Van Gelder R.N.: Applications of the polymerase chain reaction to diagnosis of ophthalmic disease. Surv Ophthalmol 2001, 46

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Occurrence of extended spectrum β-lactamaseand AmpC-producing Escherichia coli in meat samples

: Controversies about extended-spectrum and AmpC beta-lactamases. Emerg Infect Dis 2001, 7, 333-336. 27. Van T., Chin J., Chapman T., Tran L., Coloe P.: Safety of raw meat and shellfish in Vietnam: an analysis of Escherichia coli isolates for antibiotic resistance and virulence genes. Int. J Food Microbiol 2008, 124, 217-223. 28. Warren R., Ensor V., O’Neill P., Butler V., Taylor J., Nye K., Harvey M., Livermore D., Woodford N., Havkey P.: Imported chicken meat as a potential source of quinolone-resistant Escherichia coli producing extended

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In Vitro Replication of Recombinant Marek’S Disease Viruses Constructed from Field Strains Lacking Meq and Vtr Oncogenes

.1371/journal.ppat.1002333. 8. Kim T., Mays J., Fadly A., Silva R.F.: Artificially inserting a reticuloendotheliosis virus long terminal repeat into a bacterial artificial chromosome clone of Marek's disease virus (MDV) alters expression of nearby MDV genes. Virus Genes 2011, 42 , 369 - 376. 9. Messerle M., Crnkovic I., Hammerschmidt W., Ziegler H., Koszinowski U.H.: Cloning and mutagenesis of a herpesvirus genome as an infectious bacterial artificial chromosome. Proc Nat Acad Sci USA 1997, 94 , 14759 - 14763. 10. Mays J

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Changes in Antibiotic Susceptibility Pattern of Atypical Staphylococcus Aureus Strains Isolated from Cows of the same Herd in 2008-2010

References 1. Bannerman T.L.: Staphylococcus, Micrococcus, and other catalase-positive cocci that grow aerobically. Manual of clinical microbiology. ASM Press, Washington DC, 2003. 2. Cabral da Silva Santos O., Mdenezes Barros E., Vasconcelos Paida Brito M.A., do Carmo de Freire Bastos M., Netto dos Santos K.R., Giambiagi-deMarval M.: Identification of coagulase-negative staphylococcifrom bovine mastitis using RFLP-PCR of the groEL gene. Vet Microbiol 2008, 130, 134-140. 3. Clinical and Laboratory

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Contribution of Pili of S. Pneumoniae in the Onset of Meningitis

:// . 3. Barocchi, M. A., Ries, J., Zogaj, X., Hemsley, C., Albiger, B., Kanth, A., et al., 2006: A pneumococcal pilus influences virulence and host inflammatory responses. In Proc. Natl. Acad. Sci. USA . 103, 2857—2862. (4 March 2015). 4. Burnaugh, A. M., Frantz, L. J. and King, S. J., 2008: Growth of Streptococcus pneumoniae on human glycoconjugates is dependent upon the sequential activity of bacterial exoglycosidases. J. Bacteriol. , 190, 221

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