The Redox-Sensing Regulator Rex Contributes to the Virulence and Oxidative Stress Response of Streptococcus suis Serotype 2

serotype 2 (SS2) is an important zoonotic pathogen responsible for septicemia and meningitis. The redox-sensing regulator Rex has been reported to play critical roles in the metabolism regulation, oxidative stress response, and virulence of various pathogens. In this study, we identified and charact...

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Veröffentlicht in:Frontiers in cellular and infection microbiology 2018-09, Vol.8, p.317-317
Hauptverfasser: Zhu, Haodan, Wang, Yong, Ni, Yanxiu, Zhou, Junming, Han, Lixiao, Yu, Zhengyu, Mao, Aihua, Wang, Dandan, Fan, Hongjie, He, Kongwang
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Sprache:eng
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Zusammenfassung:serotype 2 (SS2) is an important zoonotic pathogen responsible for septicemia and meningitis. The redox-sensing regulator Rex has been reported to play critical roles in the metabolism regulation, oxidative stress response, and virulence of various pathogens. In this study, we identified and characterized a Rex ortholog in the SS2 virulent strain SS2-1 that is involved in bacterial pathogenicity and stress environment susceptibility. Our data show that the Rex-knockout mutant strain Δrex exhibited impaired growth in medium with hydrogen peroxide or a low pH compared with the wildtype strain SS2-1 and the complementary strain CΔrex. In addition, Δrex showed a decreased level of survival in whole blood and in RAW264.7 macrophages. Further analyses revealed that Rex deficiency significantly attenuated bacterial virulence in an animal model. A comparative proteome analysis found that the expression levels of several proteins involved in virulence and oxidative stress were significantly different in Δrex compared with SS2-1. Electrophoretic mobility shift assays revealed that recombinant Rex specifically bound to the promoters of target genes in a manner that was modulated by NADH and NAD . Taken together, our data suggest that Rex plays critical roles in the virulence and oxidative stress response of SS2.
ISSN:2235-2988
2235-2988
DOI:10.3389/fcimb.2018.00317