首页> 美国卫生研究院文献>Infection and Immunity >Oral vaccination of weaned rabbits against enteropathogenic Escherichia coli-like E. coli O103 infection: use of heterologous strains harboring lipopolysaccharide or adhesin of pathogenic strains.
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Oral vaccination of weaned rabbits against enteropathogenic Escherichia coli-like E. coli O103 infection: use of heterologous strains harboring lipopolysaccharide or adhesin of pathogenic strains.

机译:断奶兔子的口服疫苗针对肠道致病性大肠埃希氏菌样大肠杆菌O103感染:使用携带病原体脂多糖或黏附素的异源菌株。

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摘要

To test the importance of lipopolysaccharide (LPS) and adhesin as major antigens in vaccination against rabbit enteropathogenic Escherichia coli (EPEC)-like E. coli O103 infection, we used two nonpathogenic wild-type strains to immunize rabbits at weaning. One of these strains (C127) harbors the O103 LPS but does not express the 32,000-molecular-weight adhesin that characterizes the highly pathogenic O103 strains. The other (C6) belongs to the O128 serogroup, which does not cross-react with the O103 serogroup, but expresses the adhesin. These strains were administered orally, either live or after Formalin inactivation. After vaccination, the animals were challenged with highly pathogenic O103 strain B10. Compared with rabbits vaccinated with the Formalin-killed homologous strain, rabbits vaccinated with killed C127 or C6 showed partial but significant protection. When given live, these strains colonized more or less heavily the digestive tract of the animals and provided nearly complete (C127) or complete (C6) protection against challenge. They induced a quick local immune response, as judged by fecal immunoglobulin A anti-LPS kinetics. Furthermore, strain C6 induced an ecological effect of "resistance to colonization" against challenge strain B10. This effect may have been due to the adhesin that is shared by both strains and to the production of a colicin. Strain C6 could inhibit in vitro the growth of highly pathogenic O103 strains. On the whole, our results show that adhesins and LPS are important, although probably not exclusive, protection-inducing components in rabbit EPEC-like colibacillosis and provide insight into possible protection of rabbits against EPEC-like E. coli infection with live strains.
机译:为了测试脂多糖(LPS)和黏附素作为主要抗原在针对兔肠道致病性大肠杆菌(EPEC)样大肠杆菌O103感染疫苗接种中的重要性,我们使用了两种非致病性野生型菌株在断奶时对兔进行免疫。这些菌株之一(C127)携带O103 LPS,但不表达高致病性O103菌株的32,000分子量粘附素。另一个(C6)属于O128血清群,它不与O103血清群交叉反应,但表达粘附素。这些菌株经口服或福尔马林灭活后口服。接种疫苗后,用高致病性的O103菌株B10攻击动物。与用福尔马林杀死的同源株接种的兔子相比,用灭活的C127或C6接种的兔子显示出部分但重要的保护作用。当活着时,这些菌株或多或少地在动物的消化道中定殖,并提供了几乎完整的(C127)或完整的(C6)抵抗攻击的保护。根据粪便免疫球蛋白A抗LPS动力学判断,它们诱导了快速的局部免疫反应。此外,菌株C6诱导了针对挑战菌株B10的“抗定殖”生态效应。这种作用可能是由于两种菌株共有的粘附素以及大肠菌素的产生。 C6菌株可在体外抑制高致病性O103菌株的生长。总体而言,我们的研究结果表明,粘附素和LPS在兔子EPEC样大肠杆菌病中是重要的(尽管不是唯一的)保护诱导成分,并为家兔对抗EPEC样大肠杆菌感染活菌株提供了可能的保护。

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