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Phenotypic and Genotypic Characterisation of Pasteurella Multocida Strains Isolated from Pigs in Poland

., Kang M.L., Yoo H.S.: Evaluation of the antimicrobial activity of the florfenicol against bacteria isolated from bovine and porcine respiratory disease. Vet Microbiol 2005, 106 , 73-77. 35. Tang X., Zhao Z., Hu J., Wu B., Cai X., He Q., Chen H.: Isolation, antimicrobial resistance, and virulence genes of Pasteurella multocida strains from swine in China. J Clin Microbiol 2009, 47 , 951-958. 36. Townsend K.M., Frost A.J., Lee C.W., Papadimitriou J.M., Dawkins H.J.: Development of PCR assays for species- and type

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Analysis of Cutaneous Microbiota of Piglets with Hereditary Melanoma

in vitro models of wound healing. PLoS ONE, 11, e0166176. doi: 10.1371/journal.pone.0166176. Nallapareddy SR, Murray BE (2008): Role of serum, a biological cue, in adherence of Enterococcus faecalis to extracellular matrix proteins, collagen, fibrinogen, and fibronectin. The Journal of Infectious Diseases, 197, 1728–1736. doi: 10.1086/588143. Nemeghaire S, Argudin MA, Fessler AT, Hauschild T, Schwarz S, Butaye P (2014): The ecological importance of the Staphylococcus sciuri species group as a reservoir for resistance and virulence genes. Veterinary

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Distribution of Antibiotic Resistance Genes in Enterococcus spp. Isolated from Mastitis Bovine Milk

of a genus- and species-specific multiplex PCR for identification of enterococci . J Clin Microbiol 2004, 42:(8):3558–3565. 13. Lanthier M, Scott A, Lapen D, Zhang Y, Topp E: Frequency of virulence genes and antibiotic resistances in Enterococcus spp. isolates from wastewater and feces of domesticated mammals and birds, and wildlife. Can J Microbiol 2010, 56:715–729. 14. CLSI: Performance standards for antimicrobial susceptibility testing. Twenty-First Informational Supplement. Clinical and Laboratory Standards Institute 2011, M02-A10 and M07-A08 vol

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Presence of Escherichia coli O157 and O157:H7 in raw milk and Van herby cheese

monocytogenes and Salmonella spp. in food from animal origin in Costa Rica. Arch Latinoam Nutr 2003, 53, 389-392. 25. Rey J., Sánchez S., Blanco J.E., Hermoso De Mendoza J., Hermoso De Mendoza M., Garcia A., Gil C., Tejero N., Rubio R., Alonso J.M.: Prevalence, serotypes and virulence genes of Shiga toxin-producing Escherichia coli isolated from ovine and caprine milk and other dairy products in Spain. Int J Food Microbiol 2006, 107, 212-217. 26. Riley L.W., Remis R.S., Helgerson S.D., McGee H.B., Wells J.G., Davis B.R., Hebert R.J., Olcott E

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Glycyrrhetinic acid and its derivatives in infectious diseases

, glycyrrhizin and its metabolites, J. Antimicrob. Chemother ., 54, 243, 2004. 26. Kumada H.: Long-term treatment of chronic hepatitis C with glycyrrhizin [Stronger Neo-Minophagen C (SNMC)] for preventing liver cirrhosis and hepatocellular carcinoma, Oncology , 62, 94, 2002. 27. Lacaille-Dubois M.A., Wagner H.: A review of the biological and pharmacological activities of saponins, Phytomedicine , 2, 363, 1996. 28. Long D.R. et al.: 18β-Glycyrrhetinic Acid Inhibits Methicillin-Resistant Staphylococcus aureus Survival and Attenuates Virulence Gene Expression

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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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Review of Research on Routes of Helicobacter pylori Infection

, Piqueres P, Alonso JL, et al . Survival and viability of Helicobacter pylori after inoculation into chlorinated drinking water. Water Res, 2007, 41:3490-3496. 33 Samra ZQ, Javaid U, Ghafoor S, et al . PCR assay targeting virulence genes of Helicobacter pylori isolated from drinking water and clinical samples in Lahore metropolitan, Pakistan. J Water Health, 2011, 9: 208-216. 34 Hulten K, Han SW, Enroth H, et al . Helicobacter pylori in the drinking water in Peru. Gastroenterology, 1996, 110:1031-1035. 35 Horiuchi T, Ohkusa T, Watanabe M, et al

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The Evaluation of Brucella Spp. Isolation Rates in Ruminant Abortion Cases by Using Different Selective Media

). Brucella: A pathogen without classic virulence genes. Vet. Microbiol. 129, 1-14. https://doi.org/10.1016/j.vetmic.2007.11.023 PMid:18226477 36. Poester, F.P., Samartino, L.E., Santos, R.L. (2013). Pathogenesis and pathology of Brucellosis in livestock. Revue scientifique et technique (International Office of Epizootics). 32 (1): 105-115. https://doi.org/10.20506/rst.32.1.2193 PMid:23837369 37. Sperry, J.F., Robertson, D.C. (1975). Inhibition of Growth by Erythritol Catabolism in Brucella abortus. J. Bacteriol. 124 (1): 391-397. PMid:170249 PMCid:PMC235907

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Austria-wide survey on resistant, potentially pathogenic bacteria at Austrian bathing sites, 2017

.0 (Joensen et al., 2015), and VirulenceFinder 2.0 ( Joensen et al., 2014 ) available from the Center for Genomic Epidemiology web server ( http://www.genomi-cepidemiology.org ) and the Comprehensive Antibiotic Resistance Database (CARD) ( Jia et al., 2017 ) were used to identify Escherichia coli serotypes and to search for the presence of plasmids, virulence genes, or genes conferring antibiotic resistance. 3 Results 3.1 Strain isolation and primary species identification The screening for antimicrobial-resistant bacteria yielded negative results in 23 of the 27

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Effects of newly developed synbiotic and commercial probiotic products on the haematological indices, serum cytokines, acute phase proteins concentration, and serum immunoglobulins amount in sows and growing pigs – a pilot study

Taras D., Vahjen W., Macha M., Simon O.: Performance, diarrhea incidence, and occurrence of Escherichia coli virulence genes during long-term administration of a probiotic Enterococcus faecium strain to sows and piglets. J Anim Sci 2006, 84, 607–617. Taras D. Vahjen W. Macha M. Simon O. Performance, diarrhea incidence, and occurrence of Escherichia coli virulence genes during long-term administration of a probiotic Enterococcus faecium strain to sows and piglets J Anim Sci 2006 84 607 – 617 29 Tian Z., Liu X., Dai R., Xiao Y., Wang X., Bi

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