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Prevalence of pathogens from Mollicutes class in cattle affected by respiratory diseases and molecular characteristics of Mycoplasma bovis field strains

.10.057. 15. Manso-Silván L., Dupuy V., Lysnyansky I., Ozdemir U., Thiaucourt F.: Phylogeny and molecular typing of Mycoplasma agalactiae and Mycoplasma bovis by multilocus sequencing. Vet Microbiol 2012, 161, 104-112, doi: 10.1016/j.vetmic.2012.07.015. 16. McAuliffe L., Ellis R.J., Lawes J.R., Ayling R.D., Nicholas R.A.J.: 16S rDNA PCR and denaturing gradient gel electrophoresis; a single generic test for detecting and differentiating Mycoplasma species. J Med Microbiol 2005, 54, 731-739. 17. McAuliffe L., Kokotovic B., Ayling R

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Multiplex real-time PCRs for detection of Salmonella, Listeria monocytogenes, and verotoxigenic Escherichia coli in carcasses of slaughtered animals

References 1. Alarcón B., García-Cañas V., Cifuentes A., González R., Aznar R.: Simultaneous and sensitive detection of three foodborne pathogens by multiplex PCR, capillary gel electrophoresis, and laser-induced fluorescence. J Agric Food Chem 2004, 52, 7180–7186. 2. Beutin L., Miko A., Krause G., Pries K., Haby S., Steege K., Albrecht N.: Identification of human-pathogenic strains of Shiga toxin producing Escherichia coli from food by a combination of serotyping and molecular typing of Shiga toxin genes. Appl Environ Microbiol 2007, 73, 4769

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Epidemiology and antibiogram of Riemerella anatipestifer isolated from waterfowl slaughterhouses in Taiwan

.L., Wang S.T., Chu C., Wang S.H.: Comparison of four molecular typing methods for Riemerella anatipestifer . Taiwan Vet J 2015, 41, 177–185. 5. Chen Y.P., Lee S.H., Chou C.H., Tsai H.J.: Detection of florfenicol resistance genes in Riemerella anatipestifer isolated from ducks and geese. Vet Microbiol 2012, 154, 325–331. 6. Chen Y.P., Lee S.H., Tsai H.J.: Serotyping of Riemerellar anatipestifer isolates from waterfowl in Taiwan between 2008 and 2012. Exp Rep Taiwan AHRI 2013, 48, 21–28. 7. Chu C.Y., Liu C.H., Liou J.J., Lee J.W., Cheng L

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Reduced susceptibility to disinfectants of Acinetobacter baumannii biofilms on glass and ceramic

interim standard definitions for acquired resistance. Clin Microbiol Infect 2012;18:268-81. doi: 10.1111/j.1469-0691.2011.03570 25. Célia Maria Carvalho Pereira Araújo Romão, Faria YN, Pereira LR, Asensi MD. Susceptibility of clinical isolates of multiresistant Pseudomonas aeruginosa to a hospital disinfectant and molecular typing. Mem Inst Oswaldo Cruz 2005;100:541-8. doi: 10.1590/S0074-02762005000500015 26. Pour NK, Dusane DH, Dhakephalkar PK, Zamin FR, Zinjarde SS, Chopade BA. Biofilm formation by Acinetobacter baumannii strains

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Mechanisms of Resistance to Quinolones and Epidemiological Significance of Salmonella spp.

tetracycline resistance of Salmonella enterica subspecies enterica serovar Infantis isolated from poultry in the northern part of Serbia. Acta Vet Beograd 2015, 65:548-556. 47. Velhner M, Kozoderović G, Jelesić Z: Antibiotic resistance to fluoroqionoles in Salmonella spp.: Recent findings in Serbia and brief overview of resistance mechanisms and molecular typing methods, Proceedings “One Health-New Challenges” First International Symposium of Veterinary Medicine, Hotel “Premier Aqua”, Vrdnik, May 21-23, 2015, 468-472.

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Antibiotic susceptibility and resistance profiles of Romanian Clostridioides difficile isolates

antibiotic consumption. J Gastrointestin Liver Dis. 2014b;23(3):342-3. 27. Florea D, Huhulescu S, Indra A, Badicut I, Rafila A, Otelea D, et al. PCR coupled with mass-spectrometry for detection of Clostridium difficile virulence markers during the emergence of ribotype 027 in Bucharest area. Rev Romana Med Lab. 2015;23(4):449-55. DOI:10.1515/rrlm-2015-0044 28. Macovei IS, Lemeni D, Usein CR, Șerban R, Niculcea A, Popescu GA, et al. The use of PCR Ribotyping for molecular typing of clinically significant Clostridium difficile Romanian

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Intestinal parasites of pets and other house-kept animals in Moscow

. J ., 177(1): 18 – 25. DOI: 10.1016/j. tvjl.2007.09.022 U mur , S., M eral , Y, B olukbas , C., G urler , A., A cici , M. (2017): First clinical Strongyloides stercoralis case in a dog in Turkey. Turk. J. Vet. Anim. Sci ., 4(1): 312 – 315. DOI: 10.3906/vet-1606-2 U pjohn , M., C obb , C., M onger , J.,G eurden , T., C laerebout , E., F ox , M. (2010): Prevalence, molecular typing and risk factor analysis for Giardia duodenalis infections in dogs in a central London rescue shelter. Vet. Parasitol ., 172(3 – 4): 341 – 346. DOI: 10.1016/j. vetpar

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Antibiotic resistance, multidrug resistance and enterobacterial repetitive intergenic consensus polymerase chain reaction profiles of clinically important Klebsiella species

Reservoirs of drug resistant bacterial genomes and extrachromosomal DNA segments are a growing problem and cause emergence of new multidrug resistant (MDR) strains [ 1 ]. Antibiotic resistance of Klebsiella infections are causing increasing morbidity and mortality, and an increase in health care costs worldwide. In epidemiological research, not only phenotypical analysis, but also genotypical analysis is conducted by using various molecular typing methods such as plasmid profiling, ribotyping, and polymerase chain reaction (PCR) to find genetic

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Bovine Tuberculosis in the Republic of Macedonia: Postmortem, Microbiological and Molecular Study in Slaughtered Reactor Cattle

.B., Goria, M., Loda, D., Garrone, A., Benedetto, A., Mondo, A., Tisato, E., Zanoni, M., Zoppi, S., Dondo, A., Tagliabue, S., Bonora, S., Zanardi, G., Pacciarini, M.L. (2009). Molecular typing of Mycobacterium bovis strains isolated in Italy from 2000 to 2006 and evaluation of variablenumber- tandem-repeats for a geographic optimized genotyping. J Clin Microbiol. 47 (3): 636-644. PMid:19144792 PMCid:PMC2650904 44. Prodinger, W.M., Brandstätter, A., Naumann, L., Pacciarini, M., Kubica, T., Boschiroli, M.L., Aranaz, A

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Mycobacteriosis in Pigs – An Underrated Threat

;31(6):537-50. 46. Iwamoto T, Nakajima C, Nishiuchi Y, Kato T, Yoshida S, Nakanishi N, Tamaru A, Tamura Y, Suzuki Y, Nasu M. Genetic diversity of Mycobacterium avium subsp. hominissuis strains isolated from humans, pigs, and human living environment. Infect Genet Evol. 2012;12(4):846-52. 47. Ogawa K, Ichikawa K, Hasegawa Y, Inagaki T, Yagi T, Nakagawa T, Moriyama M, Adachi T. Molecular typing and genetic characterization of Mycobacterium avium subspecies hominissuis isolates from humans and swine in Japan. J Med Microbiol. 2016; 48. Starkova DA

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