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首页> 外文期刊>Journal of Clinical Microbiology >Genes coding for enterotoxins and verotoxins in porcine Escherichia coli strains belonging to different O:K:H serotypes: relationship with toxic phenotypes.
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Genes coding for enterotoxins and verotoxins in porcine Escherichia coli strains belonging to different O:K:H serotypes: relationship with toxic phenotypes.

机译:属于不同O:K:H血清型的猪大肠杆菌菌株中编码肠毒素和维毒素的基因:与毒性表型的关系。

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Seventy-four E. coli strains isolated from piglets with diarrhea or edema disease in Spain were serotyped and examined for production of heat-labile (LT) and heat-stable (ST) enterotoxins (LT-I, LT-II, STaH, STaP, and STb) and verotoxins (VT1, VT2, and VT2v = VTe) by phenotypic (Vero cell assay and infant mouse test) and genotypic (colony hybridization and PCR) methods. In general, an excellent correlation was found between the results obtained with a PCR approach and those determined with biological assays. DNA probes used in the hybridization also showed a very good agreement with phenotypic results, with the exception of a VT1 probe that initially produced 10 false-positive reactions. The gene coding for STb (58 strains) was the most prevalent gene detected by PCR, followed by those coding for STa (46 strains), LT (19 strains), VT2v (11 strains), and VT1 (1 strain). Apparently, in Spain three seropathotypes are predominant: (i) O149:K91:H10 K88+ LT-I+ STb+, (ii) O141:K85ab:H- P987+ STaP+, and (iii) O138:K81:H14 or H- STaP+ VT2v+. We conclude that PCR is a fast, specific, and practical method for the identification of enterotoxin and VT genes in clinical and epidemiological studies.
机译:对从西班牙腹泻或水肿病仔猪中分离的74株大肠杆菌进行血清分型,并检查其产生的热不稳定(LT)和热稳定(ST)肠毒素(LT-1,LT-2,STaH,STaP) ,以及STb)和Verotoxins(VT1,VT2和VT2v = VTe)通过表型(Vero细胞测定和婴儿小鼠试验)和基因型(菌落杂交和PCR)方法进行。通常,在通过PCR方法获得的结果与通过生物学分析确定的结果之间发现极好的相关性。杂交中使用的DNA探针与表型结果也显示出很好的一致性,除了VT1探针最初会产生10个假阳性反应。 PCR检测到的编码STb的基因(58个菌株)是最流行的基因,其次是编码STa的基因(46个菌株),LT(19个菌株),VT2v(11个菌株)和VT1(1个菌株)。显然,在西班牙,三种血清型是主要的:(i)O149:K91:H10 K88 + LT-1 + STb +,(ii)O141:K85ab:H- P987 + STaP +,和(iii)O138:K81:H14或H-STaP + VT2v +。我们得出结论,PCR是一种在临床和流行病学研究中鉴定肠毒素和VT基因的快速,特异性和实用的方法。

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