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Comparative analysis of Mycobacterium avium subsp. paratuberculosis isolates from cattle, sheep and goats by short sequence repeat and pulsed-field gel electrophoresis typing

机译:鸟分枝杆菌亚种的比较分析。通过短序列重复和脉冲场凝胶电泳分型从牛,绵羊和山羊分离出副结核病

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Background Mycobacterium avium subsp. paratuberculosis (Map) causes the chronic enteritis called paratuberculosis mainly in cattle, sheep and goats. Evidences that point out an association between Map and Crohn's Disease in humans are increasing. Strain differentiation among Map isolates has proved to be difficult and has limited the study of the molecular epidemiology of paratuberculosis. In order to asses the usefulness of the PCR based short sequence repeat (SSR) analysis of locus 1 and locus 8 in the epidemiological tracing of paratuberculosis strains we here compare for the first time the results of SSR and SnaBI-SpeI pulsed-field gel electrophoresis (PFGE) typing methods in a set of 268 Map isolates from different hosts (cattle, sheep, goats, bison, deer and wild boar). Results A total of nineteen different multi-locus SSR (SSR1_SSR8) types were identified amongst the 268 isolates compared to the 37 multiplex profiles differentiated by the SnaBI-SpeI PFGE. SSR type 7_4 was the predominant genotype (51.2% of all isolates and 54.3% of cattle isolates), but combined with PFGE results the abundance of the most prevalent genotype (7_4&{2-1}) dropped down to 37.7%. SSR types 7_3 and 14_3 were significantly spread amongst isolates recovered from small ruminants. The comparison of SSR1_SSR8 and SnaBI-SpeI PFGE typing of these isolates has shown that both methods perform at similar discriminatory level. These were 0.691 and 0.693, respectively for SSR and PFGE as indicated Simpson's Index of Diversity, and 0.82 when calculated for combined SSR and PFGE genotypes. Overall, SSR1_SSR8 analysis seemed to detect higher levels of within-farm strain diversity and seemed to give higher year-related information. Combination of both typing methods revealed 20 multi-type farms out of the 33 bovine farms studied with more than one isolate. Conclusion The particular SSR and PFGE typing approaches described here are in general agreement but they showed some discrepancies that might reflect differing evolutionary processes of Map strains. Both methods are able to reciprocally complement their results and neither should be replaced with the other if sufficient material and time is available. Overall, the results of our comparative analyses suggest that, based on current methodologies available, a combined approach that includes SSR and PFGE seems to provide the highest level of discrimination for Map strain typing with meaningful epidemiological information.
机译:背景鸟分枝杆菌亚种。副结核病(Map)导致慢性肠炎,称为副结核病,主要发生在牛,绵羊和山羊身上。越来越多的证据表明Map与人类克罗恩病之间的关联。已经证明Map分离株之间的菌株分化是困难的,并且限制了副结核病分子流行病学的研究。为了评估基于PCR的1号和8号位点的短序列重复(SSR)分析在副结核病菌株的流行病学追踪中的有用性,我们在此首次比较SSR和SnaBI-SpeI脉冲场凝胶电泳的结果(PFGE)分型方法,来自不同宿主(牛,羊,山羊,野牛,鹿和野猪)的268种地图分离物中。结果与SnaBI-SpeI PFGE区分的37个多重谱相比,在268个分离株中总共鉴定出19种不同的多位点SSR(SSR1_SSR8)类型。 SSR 7_4型是主要的基因型(所有分离株的51.2%,牛分离株的54.3%),但结合PFGE结果,最流行的基因型(7_4&{2-1})的丰度下降到37.7%。 SSR类型7_3和14_3在从小反刍动物中回收的分离株中显着分布。这些分离株的SSR1_SSR8和SnaBI-SpeI PFGE分型的比较显示,两种方法在相似的判别水平上均表现良好。如Simpson的多样性指数所示,SSR和PFGE分别为0.691和0.693,而SSR和PFGE组合基因型的计算结果分别为0.82和0.82。总体而言,SSR1_SSR8分析似乎可以检测出较高水平的农场内菌株多样性,并且可以提供与年份相关的更高信息。两种分型方法的组合揭示了在研究的33个牛场中有20个多类型场,其中有一个以上的分离株。结论此处描述的特定SSR和PFGE分型方法总体上是一致的,但它们显示出一些差异,可能反映了Map菌株的不同进化过程。两种方法都可以相互补充其结果,并且如果有足够的材料和时间可用,则不应将任何一种方法替换为另一种方法。总体而言,我们的比较分析结果表明,基于当前可用的方法,结合SSR和PFGE的组合方法似乎可以为Map菌株的分类提供最高水平的识别,并提供有意义的流行病学信息。

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