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Observations on the pathogenic properties of the K88, Hly and Ent plasmids of Escherichia coli with particular reference to porcine diarrhoea.关于大肠杆菌K88、Hly和Ent质粒致病特性的观察,特别涉及猪腹泻。
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用产肠毒素大肠杆菌对兔进行口服免疫可预防肠道内攻击。

Oral immunization of rabbits with enterotoxigenic Escherichia coli protects against intraintestinal challenge.

作者信息

Sack R B, Kline R L, Spira W M

机构信息

Department of Medicine, Francis Scott Key Medical Center, Baltimore, Maryland 21224.

出版信息

Infect Immun. 1988 Feb;56(2):387-94. doi: 10.1128/iai.56.2.387-394.1988.

DOI:10.1128/iai.56.2.387-394.1988
PMID:3276624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC259293/
Abstract

The development of a successful oral vaccine against enterotoxigenic Escherichia coli depends upon the identification of appropriate protective antigens which can be delivered effectively to intestinal mucosa. We have determined in a modified RITARD model the relative protection against intraintestinal challenge afforded by oral immunization with live enterotoxigenic E. coli carrying different candidate antigens. Studies were done with both wild-type strains and genetically manipulated strains of enterotoxigenic E. coli (parent strain E1392/75 2A) which carried plasmids containing intact heat-labile toxin (LT) gene sequences or various mutations of the LT genes. Immunizations were done by orogastric tube inoculation on days 0, 7, and 14; challenges were done on day 33. Protection against diarrhea with a homologous challenge was found to be 84 to 100% (P less than 0.01). Protection against diarrhea with challenges in which specific antigens could be tested included the following: (i) O and H antigens (O6:H16), 87 to 100% protection with different E. coli strains with identical O and H antigens (P less than 0.01) but no protection against a heterologous challenge; (ii) LT or the B subunit of LT only, approximately 50% protection (P less than 0.02). These findings suggest that O antigens are highly protective in this model but afford only serotype-specific protection and that the B subunit (with or without the A subunit) affords less protection but confers cross-protection against heterologous strains producing LT. This model should be useful in further defining appropriate protective antigens for candidate enterotoxigenic E. coli vaccine strains.

摘要

研发一种成功的抗产肠毒素大肠杆菌口服疫苗,取决于能否鉴定出可有效递送至肠黏膜的合适保护性抗原。我们已在改良的RITARD模型中确定,用携带不同候选抗原的产肠毒素大肠杆菌进行口服免疫,对肠内攻击的相对保护作用。研究使用了野生型菌株和产肠毒素大肠杆菌(亲本菌株E1392/75 2A)的基因工程菌株,这些菌株携带含有完整热不稳定毒素(LT)基因序列或LT基因各种突变的质粒。于第0、7和14天通过经口胃管接种进行免疫;于第33天进行攻击。发现用同源攻击预防腹泻的保护率为84%至100%(P<0.01)。用可测试特定抗原的攻击预防腹泻的保护情况如下:(i)O抗原和H抗原(O6:H16),具有相同O抗原和H抗原的不同大肠杆菌菌株的保护率为87%至100%(P<0.01),但对异源攻击无保护作用;(ii)仅LT或LT的B亚基,约50%的保护率(P<0.02)。这些发现表明,O抗原在该模型中具有高度保护作用,但仅提供血清型特异性保护,且B亚基(无论有无A亚基)提供的保护作用较小,但可赋予针对产生LT的异源菌株的交叉保护作用。该模型应有助于进一步确定候选产肠毒素大肠杆菌疫苗株的合适保护性抗原。