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首页> 外文期刊>Pesquisa Veterinaria Brasileira >Typing of avian pathogenic Escherichia coli strains by REP-PCR
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Typing of avian pathogenic Escherichia coli strains by REP-PCR

机译:通过REP-PCR对禽病原性大肠杆菌菌株进行分型

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摘要

In the present study the repetitive extragenic palindromic (REP) polymerase chain reaction (PCR) technique was used to establish the clonal variability of 49 avian Escherichia coli (APEC) strains isolated from different outbreak cases of septicemia (n=24), swollen head syndrome (n=14) and omphalitis (n=11). Thirty commensal strains isolated from poultry with no signs of these illnesses were used as control strains. The purified DNA of these strains produced electrophoretic profiles ranging from 0 to 15 bands with molecular sizes varying from 100 bp to 6.1 kb, allowing the grouping of the 79 strains into a dendrogram containing 49 REP-types. Although REP-PCR showed good discriminating power it was not able to group the strains either into specific pathogenic classes or to differentiate between pathogenic and non-pathogenic strains. On the contrary, we recently demonstrated that other techniques such as ERIC-PCR and isoenzyme profiles are appropriate to discriminate between commensal and APEC strains and also to group these strains into specific pathogenic classes. In conclusion, REP-PCR seems to be a technique neither efficient nor universal for APEC strains discrimination. However, the population clonal structure obtained with the use of REP-PCR must not be ignored particularly if one takes into account that the APEC pathogenic mechanisms are not completely understood yet. Index
机译:在本研究中,使用重复性外源性回文(REP)聚合酶链反应(PCR)技术来确定从不同的败血病暴发病例(n = 24),头肿综合征中分离出的49株禽大肠杆菌(APEC)菌株的克隆变异性(n = 14)和眼炎(n = 11)。从家禽中分离出的三十种没有这些疾病迹象的普通菌株用作对照菌株。这些菌株的纯化DNA产生了从0到15条带的电泳图谱,分子大小从100 bp到6.1 kb不等,从而将79个菌株分组为包含49个REP型的树状图。尽管REP-PCR表现出良好的区分能力,但无法将菌株分为特定的致病类别,也无法区分致病菌株和非致病菌株。相反,我们最近证明,其他技术(例如ERIC-PCR和同工酶谱)适用于区分共生和APEC菌株,并将这些菌株归为特定的病原体类别。总之,REP-PCR似乎对APEC菌株的鉴别既不高效也不通用。但是,使用REP-PCR获得的种群克隆结构一定不能忽略,特别是如果考虑到尚未完全理解APEC的致病机制。指数

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