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猪链球菌活疫苗抑制链球菌中毒性休克样综合征并提供与序列型无关的保护。

A Streptococcus suis Live Vaccine Suppresses Streptococcal Toxic Shock-Like Syndrome and Provides Sequence Type-Independent Protection.

机构信息

Bio-Medical Center, Key Laboratory of Environment Correlative Dietology, College of Food Science and Technology, Huazhong Agricultural University, Wuhan, Hubei, People's Republic of China.

State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, Hubei, People's Republic of China.

出版信息

J Infect Dis. 2019 Jan 9;219(3):448-458. doi: 10.1093/infdis/jiy512.

Abstract

BACKGROUND

Streptococcus suis is an encapsulated zoonotic pathogen. Increasing antimicrobial resistance invokes the need for effective vaccines. Despite many attempts to develop an effective vaccine, none is currently available.

METHODS

A capsular polysaccharide (CPS)-expressing attenuated mutant 2015033 was constructed by deleting 5 virulence-associated factors (sly, scpA, ssnA, fhb, and ssads) in an infective S. suis strain SC19. The safety and immune effect of 2015033 were determined both in vitro and in vivo.

RESULTS

Deletion of 5 genes did not impact the growth ability and CPS generation of 2015033, and the mutant exhibited no cytotoxicity in different cell models. 2015033 was more easily eliminated by innate immunity both in vitro and in vivo. In addition, 2015033 showed a diminished invasive ability in different mouse organs (brain, lung, and liver) and avirulent properties in mice associated with weak inflammation-inducing ability. Immunization with 2015033 triggered T cell-dependent immunity, suppressed streptococcal toxic shock-like syndrome, and conferred sequence type-independent protection to mice during infection.

CONCLUSIONS

This study presents the feasibility of the strategy of multigene deletion for the development of promising live vaccines against invasive encapsulated pathogens.

摘要

背景

猪链球菌(Streptococcus suis)是一种具荚膜的人畜共患病病原体。不断增加的抗生素耐药性,促使我们需要开发有效的疫苗。尽管已经进行了许多尝试来开发有效的疫苗,但目前尚无可用的疫苗。

方法

通过删除感染性猪链球菌菌株 SC19 中的 5 个与毒力相关的因子(sly、scpA、ssnA、fhb 和 ssads),构建了表达荚膜多糖(CPS)的减毒突变体 2015033。在体外和体内均测定了 2015033 的安全性和免疫效果。

结果

5 个基因的缺失并未影响 2015033 的生长能力和 CPS 的产生,且该突变体在不同细胞模型中均无细胞毒性。2015033 在体外和体内均更容易被先天免疫清除。此外,2015033 在不同小鼠器官(脑、肺和肝)中的侵袭能力减弱,且其致炎症能力较弱,导致其毒力降低。2015033 免疫接种可引发 T 细胞依赖性免疫,抑制链球菌中毒性休克样综合征,并在感染期间为小鼠提供与序列型无关的保护。

结论

本研究提出了利用多基因缺失策略开发针对侵袭性荚膜病原体的有前途的活疫苗的可行性。

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