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首页> 外文期刊>Iranian journal of public health. >Genetic Diversity among Yersinia enterocolitica Isolated from Chicken and Fish in and around Coimbatore City, India
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Genetic Diversity among Yersinia enterocolitica Isolated from Chicken and Fish in and around Coimbatore City, India

机译:印度哥印拜陀市及其周边地区鸡和鱼中分离的小肠结肠炎耶尔森氏菌的遗传多样性

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摘要

Background: Yersinia enterocolitica is rapidly emerging worldwide as an enteric pathogen and has become a major cause of diarrhea even in developed countries. The aim of this study was to characterize and genetic diversity analysis among Y. enterocolitica strains isolated from fish and chicken sources.Methods: From 44 strains, 55% (24 strains) found to be positive for Y. enterocolitica by colony morphology, biochemical tests and 16S rRNA. We investigate the diversity of Y. enterocolitica by hemolytic activity, antimicrobial resistance, RAPD, ERIC and REP-PCRs PCR, profiling of outermembrane proteins and lipopolysaccarides. Results: Forty one percent of the strains were found to be the producers of haemolysin at 37 °C but not at 28 °C. All the isolates were exhibiting multi-drug resistance and found sensitive to chloramphenicol, and resistant to ciprofloxacin and amoxicillin. Eight, eleven and twelve different genotypic patterns were observed in RAPD, ERIC and REP-PCRs respectively. Five isolates have produced high molecular weight protein (HMWP) with a molecular weight of 150 - 220 kDa. Mostly LPS produce identical profiles, 22 strains have produced smooth LPS, while 2 strains have produced the rough LPS pattern.Conclusion: Genotyping tools strongly confirm the co-existence wide genetic diversity among the strains tested. By using any or the combination of these molecular tools, epidemiological investigation on Y. enterocolitica could be elucidated effectively. These results showed that the REP-PCR is more informative and discriminative than other for analysis of Y. enterocolitica diversity.
机译:背景:小肠结肠炎耶尔森菌作为一种肠道病原体在世界范围内正在迅速兴起,甚至在发达国家也已成为引起腹泻的主要原因。本研究的目的是对分离自鱼类和鸡源的小肠结肠炎耶尔森氏菌进行表征和遗传多样性分析。方法:从44个菌株中,通过菌落形态学,生化检测发现55%(24个菌株)肠小肠结肠炎耶尔森氏菌呈阳性。和16S rRNA。我们通过溶血活性,抗菌素耐药性,RAPD,ERIC和REP-PCRs PCR,外膜蛋白和脂多糖的分布来研究小肠结肠炎耶尔森氏菌的多样性。结果:发现在37°C而不是28°C时有41%的菌株是溶血素的产生者。所有分离株均表现出多药耐药性,对氯霉素敏感,对环丙沙星和阿莫西林耐药。在RAPD,ERIC和REP-PCR中分别观察到八种,十一种和十二种不同的基因型。五个分离物已生产出分子量为150-220 kDa的高分子量蛋白(HMWP)。大多数情况下,LPS产生相同的谱图,22个菌株产生了平滑的LPS,而2个菌株产生了粗糙的LPS模式。结论:基因分型工具强有力地证实了所测试菌株之间广泛存在的遗传多样性。通过使用这些分子工具中的任何一个或组合,可以有效地阐明小肠结肠炎耶尔森氏菌的流行病学调查。这些结果表明,REP-PCR在分析小肠结肠炎耶尔森氏菌多样性方面比其他方法更具参考价值。

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