Department of Immunology & Infectious Diseases, Montana State University, Bozeman, MT, USA.
Virulence. 2012 Jan-Feb;3(1):29-42. doi: 10.4161/viru.3.1.18447. Epub 2012 Jan 1.
Generation of a live attenuated vaccine for bacterial pathogens often requires prior knowledge of the pathogen's virulence factors. We hypothesized an alternative approach of heterologous gene expression would make a wild-type (wt) pathogen more susceptible to host cell killing, thus, resulting in immunization. As proof of concept, the heterologous expression of enterotoxigenic E. coli (ETEC) colonization factor antigen I (CFA/I) was tested to attenuate Salmonella. The overexpression of CFA/I resulted in significant attenuation of wt Salmonella. In-depth studies revealed the attenuation depended on the co-expression of chaperone (CfaA) and usher (CfaC) proteins. Remarkably, the CfaAC-attenuated Salmonella conferred protection against wt Salmonella challenge. Mechanistic study indicated CfaAC made Salmonella outer membranes permeable, causing Salmonella to be vulnerable to host destruction. Thus, enhancing bacterial permeability via CfaAC represents an alternative method to attenuate pathogens despite the presence of unknown virulence factors.
针对细菌病原体的活疫苗的生成通常需要对病原体的毒力因子有预先的了解。我们假设,一种异源基因表达的方法可以使野生型(wt)病原体更容易受到宿主细胞杀伤,从而导致免疫。作为概念验证,我们测试了肠致病性大肠杆菌(ETEC)定植因子抗原 I(CFA/I)的异源表达,以减轻沙门氏菌的毒力。CFA/I 的过度表达导致 wt 沙门氏菌的显著减毒。深入的研究表明,这种减毒依赖于伴侣蛋白(CfaA)和 usher 蛋白(CfaC)的共表达。值得注意的是,CfaAC 减毒的沙门氏菌赋予了对 wt 沙门氏菌攻击的保护作用。机制研究表明,CfaAC 使沙门氏菌的外膜具有渗透性,使沙门氏菌易受宿主破坏。因此,尽管存在未知的毒力因子,通过 CfaAC 增强细菌通透性代表了一种减毒病原体的替代方法。