首页> 外文期刊>DTW:Deutsche Tierarztliche Wochenschrift >Duplex real-time PCR assays for rapid detection of virulence genes in E. coli isolated from post-weaning pigs and calves with diarrhoea.
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Duplex real-time PCR assays for rapid detection of virulence genes in E. coli isolated from post-weaning pigs and calves with diarrhoea.

机译:双重实时PCR分析法可快速检测从断奶后的猪和牛腹泻的大肠杆菌中分离的大肠杆菌中的毒力基因。

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Duplex real-time PCR assays were used as modules to cover partially automated detection of 12 genes encoding adhesins, enterotoxins and Shiga toxins in faecal E. coli isolates. For this a total of 194 E. coli isolates from pigs suffering from post-weaning diarrhoea (PWD), including 65 isolates with haemolytic activity, and 83 isolates from calves with diarrhoea were examined. Data obtained by PCR were compared with O-typing and with haemolytic activity as indirect virulence markers. E. coli O-types O139:K82, O141:K85, and O149:K91 accounted for 43.8% (n=85) of all porcine strains and for 55.4% (n=36) of the porcine strains, which exhibited haemolytic activity. These strains carried virulence genes by 65.9% (n=56) and 80.6% (haemolytic E. coli, n=29), respectively. The E. coli O-types O139:K82 and O141:K85 were significantly associated with the adhesin gene F18, and O149:K81 with the F4 gene. In this context, detection of the gene encoding F18 was coupled predominantly with the genes responsible for the production of the toxins ST-I, ST-II and Stx2, and the F4 gene with those of the enterotoxins ST-I, ST-II and LT. Both virulence patterns were detected more pronounced in E. coli strains with haemolytic activity. Fifty-six of a total of 83 E. coli isolates originating from calves were O-typed as O101 (O101:K28, O101:K30, O101:K32; n=29), O78:K80 (n=23), and O9:K35 (n=4). Most of the E. coli O78:K80 strains carried the F17 gene (69.6%, n=16). Virulence genes encoding for F4, F5 or ST-I were detected only in single cases. Intimin and Shiga toxin genes that are present in enterohaemorrhagic E. coli (EHEC) were not detected.
机译:双重实时PCR分析用作模块,以覆盖部分自动检测粪便大肠杆菌分离物中编码粘附素,肠毒素和志贺毒素的12个基因的功能。为此,对来自断奶后腹泻(PWD)的猪的194株大肠杆菌分离株进行了检查,其中包括65株具有溶血活性的分离株,以及犊牛与腹泻的83株分离株。将通过PCR获得的数据与O型分型和溶血活性作为间接毒力标记进行比较。大肠杆菌O型O139:K82,O141:K85和O149:K91占所有猪株的43.8%(n = 85),占表现出溶血活性的猪株的55.4%(n = 36)。这些菌株携带的毒力基因分别为65.9%(n = 56)和80.6%(溶血性大肠杆菌,n = 29)。大肠杆菌O型O139:K82和O141:K85与粘附素基因F18显着相关,而O149:K81与F4基因显着相关。在这种情况下,编码F18的基因的检测主要与负责产生毒素ST-1,ST-II和Stx2的基因偶联,以及将F4基因与肠毒素ST-1,ST-II和STx2的那些偶联。 LT。在具有溶血活性的大肠杆菌菌株中检​​测到两种毒力模式更为明显。在来自小牛的总共83株大肠杆菌中,有56种被O型分类为O101(O101:K28,O101:K30,O101:K32; n = 29),O78:K80(n = 23)和O9 :K35(n = 4)。大多数大肠杆菌O78:K80菌株携带F17基因(69.6%,n = 16)。仅在单个病例中检测到编码F4,F5或ST-1的毒力基因。没有检测到肠出血性大肠杆菌(EHEC)中存在的Intimin和Shiga毒素基因。

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