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Identification of bacterial pathogens and determination of their antibacterial resistance profiles in some cultured fish in Turkey

genotypic antimicrobial resistance of Lactococcus sp. strains isolated from rainbow trout ( Oncorhynchus mykiss ). Bull Vet Inst Pulawy 2015, 59, 37–42. 26. Van T.T.H., Chin J., Chapman T., Tran L.T., Coloe P.J.: Safety of raw meat and shellfish in Vietnam: an analysis of Escherichia coli isolations for antibiotic resistance and virulence genes. Int J Food Microbiol 2008, 124, 217–223. 27. Zhang X.X., Zhang T., Fang H.H.P.: Antibiotic resistance genes in water environment. Appl Microbiol Biotechnol 2009, 82, 397−414.

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Parapoxvirus orf virus infection induces an increase in interleukin-8, tumour necrosis factor-α, and decorin in goat skin fibroblast cells

., Ledgerwood E.C., Hibma M.H., Fleming S.B., Whelan E.M., Mercer A.A.: A novel Bcl-2-like inhibitor of apoptosis is encoded by the parapoxvirus ORF virus. J Virol 2007, 81, 7178–7188. 27. Zhang K., Liu.Y., Shang Y., Liu X., Cai X.: Major virulence factors of orf virus and their mechanism for immune evasion. Austin J Infect Dis 2014, 1, 5. 28. Zhao C.X., Zhao Y.T., Wang P.H., Xiao X., Wang D.W.: Influences of recombinant adeno-associated virus-mediated Decorin gene transfection on cell cycle and apoptosis of SiHa cells. Ai Zheng 2005, 24, 28–32.

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Sensitivity enhancement of nucleic acid detection by lateral flow strip test using UV crosslink method

detection of infectious spleen and kidney necrosis virus by loop-mediated isothermal amplification combined with a lateral flow dipstick. Archives of Virology. 2010; 155:385-9. 7. Odenthal KJ, Gooding JJ. An introduction to electrochemical DNAbiosensors. Analyst. 2007; 132: 603-10. 8. Noguera P, Posthuma-Trumpie G, van Tuil M, van der Wal F, de Boer A, Moers A, et al. Carbon nanoparticles in lateral flow methods to detect genes encoding virulence factors of Shiga toxin-producing Escherichia coli. Analytical and Bioanalytical Chemistry. 2011

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Microbiome and antimicrobial resistance genes in microbiota of cloacal samples from European herring gulls (Larus argentatus)

. Seputiene V., Bogdaite A., Ruzauskas M., Suziedeliene E.: Antibiotic resistance genes and virulence factors in Enterococcus faecium and Enterococcus faecalis from diseased farm animals: pigs, cattle and poultry. Pol J Vet Sci 2012, 15, 431–438, doi: 10.2478/v10181-012-0067-6. 19. Seputiene V., Povilonis J., Ruzauskas M., Virgailis M., Zlabys P., Suziedeliene E.: Quinolone resistance among Salmonella enterica and Escherichia coli in Lithuania. Biologija, 2006, 3, 74–78. 20. Shobrak M.Y., Abo-Amer A.E.: Role of wild birds as carriers of multi

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Evaluation of real-time PCR based on SYBR Green I fluorescent dye for detection of Bacillus anthracis strains in biological samples

References 1. Adone R., Pasquali P., La Rosa G., Marianelli C., Muscillo M., Fasanella A., Francia M., Ciuchini F.: Sequence analysis of the genes encoding for the major virulence factors of Bacillus anthracis vaccine strain Carbosap. J Appl Microbiol 2002, 93, 117–121. 2. Bentahir M., Ambroise J., Delcorps C., Pilo P., Gala J.L.: Sensitive and specific recombinase polymerase amplification for fast screening, detection, and identification of Bacillus anthracis in a field setting. Appl Environ Microbiol 2018, 84, 1–13. 3. Beyer W., Turnbull P

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A step forward into respiratory genetics: overview contribution of genetics in respiratory diseases

. Novel CFTR mutations in a Korean infant with cystic fibrosis and pancreatic insufficiency. J Korean Med Sci. 2010; 25:163-5. 6. Collins F. Genetics terminology for respiratory physicians. Paediatr Respir Rev. 2009; 10:124-33. 7. Fu J, Festen EA, Wijmenga C. Multi-ethnic studies in complex traits. Hum Mol Genet. 2011; 20:R206-13. 8. Ober C, Hoffjan S. Asthma genetics 2006: the long and winding road to gene discovery. Genes Immun. 2006; 7:95-100. 9. Moffatt MF, Kabesch M, Liang L, Dixon AL, Strachan D

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Occurrence of enterococci in mastitic cow’s milk and their antimicrobial resistance

Portugal. RCPV 2014, 109, 79–88. 30. Rüegsegger F., Ruf J., Tschour A., Sigrist Y., Rooskopf M., Hässig M.: Antimicrobial susceptibility of mastitis pathogens of dairy cows in Switzerland. Schw Arch Tier 2014, 156, 483–488. 31. Xiaohu W.U., Zhang Q., Ma Y., Zhang Y., Kan W., Zhao X.: Prevalence of virulence genes and resistance to antibiotics in pathogenic enterococci isolated from mastitic cows. J Vet Med. Sci 2016, 78, 1663–1683. 32. Zdolec N., Dobranić V., Butković I., Koturić A., Filipović I., Medvid V.: Antimicrobial susceptibility of milk bacteria

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Elevated intracellular levels of iron in host cells promotes Burkholderia pseudomallei infection

expression in Caco-2 human intestinal cells. J Nutr. 2001; 131:1452-8. 8. Bullen JJ, Ward CG, Wallis SN. Virulence and the role of iron in Pseudomonas aeruginosa infection. Infect Immun. 1974; 10:443-50. 9. Wuthiekanun V, Smith MD, Dance DA, White NJ. Isolation of Pseudomonas pseudomallei from soil in north-eastern Thailand. Trans R Soc Trop Med Hyg. 1995; 89:41-3. 10. Schaible UE, Kaufmann SH. Iron and microbial infection. Nat Rev Microbiol. 2004; 2:946-53. 11. Loprasert S, Sallabhan R, Whangsuk W, Mongkolsuk

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Characterisation of newly emerged isolates of classical swine fever virus in China, 2014–2015

-Strain Vaccination. Front Microbiol 2016, 7, 85. 9. Ji W., Niu D.D., Si H.L., Ding N.Z., He C.Q.: Vaccination influences the evolution of classical swine fever virus. Infect Genet Evol 2014, 25, 69–77. 10. Jiang D.L., Gong W.J., Li R.C., Liu G.H., Hu Y.F., Ge M., Wang S.Q., Yu X.L., Tu C.: Phylogenetic analysis using E2 gene of classical swine fever virus reveals a new subgenotype in China. Infect Genet Evol 2013, 17, 231–238. 11. Leifer I., Ruggli N., Blome S.: Approaches to define the viral genetic basis of classical swine fever virus virulence. Virology 2013

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Characterisation of Staphylococcus aureus and Staphylococcus aureus – like strains isolated from table eggs

-248. 4. Brakstad O.G., Maeland J.A., Tveten Y.: Multiplex polymerase chain reaction for detection of genes for Staphylococcus aureus thermonuclease and methicillin resistance and correlation with oxacillin resistance. APMIS 1993, 101, 681-688. 5. Bystroń J., Podkowik M., Piasecki T., Wieliczko A., Molenda J., Bania J.: Genotypes and enterotoxin gene content of S. aureus isolates from poultry. Vet Microbiol 2010, 144, 498-501. 6. Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing

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