The potential Salmonella aroA- vaccine strain is safe and effective in young BALB/c mice

被引:5
作者
Burns-Guydish, Stacy M.
Zhao, Hui
Stevenson, David K.
Contag, Christopher H.
机构
[1] Stanford Univ, Sch Med, Div Neonatal & Dev Med, Dept Pediat, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Radiol, Stanford, CA 94305 USA
关键词
age-related susceptibility; neonates; Salmonella; aroA; phoP; biophotonic imaging; molecular imaging;
D O I
10.1159/000097128
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Due to the increased susceptibility of neonates to pathogens including those with mutations, the use of live vaccine strategies in the human population may present a potential risk to the young. Objectives: The specific aim of this study was to assess the risk that prospective Salmonella enterica serovar Typhimurium vaccine strains pose for the neonate and determine whether the strains are an effective vaccine by assessing the adaptive immune response. Methods: To evaluate the susceptibility of young mice to potential vaccine strains, S. typhimurium aroA(-) and Delta phoP mutant strains were labeled by chromosomal insertion of the lux operon-this serves as a readily traceable marker of infection using noninvasive imaging methods. BALB/c mice ages 1, 2, 4, and 6 weeks of age were fed the bioluminescent aroA(-) or Delta phoP strains and the course of infection was monitored by in vivo bioluminescence imaging. In addition, blood samples were collected post-inoculation to assess the IgG response of mice to S. typhimurium LPS. Results: Young BALB/c mice were not susceptible to the aroA strain in contrast to their susceptibility to the Delta phoP strain at a dose of 10(9) colony forming units. Delivery by oral feeding of the aroA(-) and Delta phoP strains in young mice also produced a robust IgG anti-LPS response. Conclusion: Here, we report that young 2-week-old mice orally fed the bioluminescent aroA(-) S. typhimurium strain were not susceptible to infection and elicited a protective immune response. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:114 / 120
页数:7
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