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首页> 外文期刊>Journal of Clinical Microbiology >Characterization of a Shiga Toxin-, Intimin-, and Enterotoxin Hemolysin-Producing Escherichia coli ONT:H25 Strain Commonly Isolated from Healthy Cattle
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Characterization of a Shiga Toxin-, Intimin-, and Enterotoxin Hemolysin-Producing Escherichia coli ONT:H25 Strain Commonly Isolated from Healthy Cattle

机译:通常从健康牛中分离出的滋贺毒素,内膜素和肠毒素溶血素生产大肠杆菌ONT:H25菌株的表征

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摘要

Among bovine fecal and recto-anal mucosal swab samples cultured in our laboratory for Escherichia coli O157:H7, we frequently isolated E. coli organisms that were phenotypically similar to the O157:H7 serotype as non-sorbitol fermenting and negative for β-glucuronidase activity but serotyped O nontypeable:H25 (ONT:H25). This study determined the prevalence and virulence properties of the E. coli ONT:H25 isolates. Among dairy and feedlot cattle (n = 170) sampled in Washington, Idaho, and Alberta, Canada, the percentage of animals culture positive for E. coli ONT:H25 ranged from 7.5% to 22.5%, compared to the prevalence of E. coli O157:H7 that ranged from 0% to 15%. A longitudinal 8-month study of dairy heifers (n = 40) showed that 0 to 15% of the heifers were culture positive for E. coli O157:H7, while 15 to 22.5% of the animals were culture positive for E. coli ONT:H25. As determined by a multiplex PCR, the E. coli ONT:H25 isolates carried a combination of virulence genes characteristic of the enterohemorrhagic E. coli, including intimin, translocated intimin receptor, Stx2, and hemolysin (eae-β, tir, stx2vh-a, and hly). E. coli ONT:H25 isolates from diverse geographic locations and over time were fingerprinted by separating XbaI-restricted chromosomal DNA by pulsed-field gel electrophoresis (PFGE) separation. Two strains of E. coli ONT:H25 were highly similar by PFGE pattern. Experimental inoculation of cattle showed that E. coli ONT:H25, like E. coli O157:H7, colonized the bovine recto-anal junction mucosa for more than 4 weeks following a single rectal application of bacteria.
机译:在我们实验室为大肠杆菌 O157:H7培养的牛粪便和直肠肛门粘膜拭子样本中,我们经常分离出 E。表型与O157:H7血清型相似的非山梨醇发酵菌,β-葡萄糖醛酸苷酶活性为阴性,但血清型为O nontypeable:H25(ONT:H25)。这项研究确定了 E的流行和毒力特性。大肠杆菌ONT:H25分离株。在加拿大华盛顿,爱达荷州和加拿大艾伯塔省抽样的奶牛场和饲养场牛( n = 170)中, E阳性的动物百分比。与 E的患病率相比,大肠埃希菌ONT:H25的变化范围为7.5%至22.5%。大肠杆菌O157:H7的范围从0%到15%。对奶牛小母牛( n = 40)进行的为期8个月的纵向研究表明,0至15%的小母牛对 E呈阳性培养。大肠杆菌O157:H7,而15%至22.5%的动物对E E培养呈阳性。大肠菌 ONT:H25。如通过多重PCR确定的, E。大肠杆菌ONT:H25分离株带有肠出血性 E特有的毒力基因组合。大肠菌,包括内膜素,易位的内膜素受体,Stx2和溶血素( eae-β, tir stx 2vh -a hly )。 E。通过脉冲场凝胶电泳(PFGE)分离XbaI限制性染色体DNA,鉴定了来自不同地理位置和时间的大肠杆菌ONT:H25分离株。两株 E。大肠埃希菌ONT:H25在PFGE模式上具有高度相似性。牛的实验性接种显示出 E。大肠菌 ONT:H25,例如 E。一次直肠应用细菌后,O157:H7大肠埃希菌在牛的直肠-肛门交界处的粘膜上定居了超过4周。

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