Cooperative Role of Antibodies against Heat-Labile Toxin and the EtpA Adhesin in Preventing Toxin Delivery and Intestinal Colonization by Enterotoxigenic Escherichia coli

被引:29
作者
Roy, Koushik [1 ]
Hamilton, David J. [2 ]
Fleckensteina, James M. [1 ,3 ,4 ]
机构
[1] Univ Tennessee, Ctr Hlth Sci, Dept Med, Memphis, TN 38163 USA
[2] Univ Tennessee, Ctr Hlth Sci, Dept Comparat Med, Memphis, TN 38163 USA
[3] Univ Tennessee, Ctr Hlth Sci, Dept Mol Sci, Memphis, TN 38163 USA
[4] Vet Affairs Med Ctr, Med Serv, Memphis, TN USA
基金
美国国家卫生研究院;
关键词
BORDETELLA-PERTUSSIS INFECTION; TISSUE-CULTURE CELLS; ENHANCED TOXICITY; IMMUNE-RESPONSES; PROTEINS; VIRULENCE; VACCINES; MODEL; VACCINATION; COMMENSAL;
D O I
10.1128/CVI.00351-12
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Enterotoxigenic Escherichia coli (ETEC) is an important cause of diarrheal disease in developing countries, where it is responsible for hundreds of thousands of deaths each year. Vaccine development for ETEC has been hindered by the heterogeneity of known molecular targets and the lack of broad-based sustained protection afforded by existing vaccine strategies. In an effort to explore the potential role of novel antigens in ETEC vaccines, we examined the ability of antibodies directed against the ETEC heat-labile toxin (LT) and the recently described EtpA adhesin to prevent intestinal colonization in vivo and toxin delivery to epithelial cells in vitro. We demonstrate that EtpA is required for the optimal delivery of LT and that antibodies against this adhesin play at least an additive role in preventing delivery of LT to target intestinal cells when combined with antibodies against either the A or B subunits of the toxin. Moreover, vaccination with a combination of LT and EtpA significantly impaired intestinal colonization. Together, these results suggest that the incorporation of recently identified molecules such as EtpA could be used to enhance current approaches to ETEC vaccine development.
引用
收藏
页码:1603 / 1608
页数:6
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