4.7 Article

Yersinia pestis Requires the 2-Component Regulatory System OmpR-EnvZ to Resist Innate Immunity During the Early and Late Stages of Plague

期刊

JOURNAL OF INFECTIOUS DISEASES
卷 210, 期 9, 页码 1367-1375

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiu274

关键词

Yersiniosis; plague; Yersinia; innate immunity; two-component systems; polymorphonuclear leukocyte

资金

  1. Institut National de la Sante et de la Recherche Medicale
  2. Institut Pasteur de Lille
  3. Universite Lille Nord de France
  4. Centre National de la Recherche Scientifique
  5. Region Nord Pas de Calais
  6. European Regional Development Fund as part of the Action de recherche concertee d'initiative regionale program [10090077-Presage 35712]
  7. European Community (ERC-STG INTRACELLTB grant) [260901]
  8. Agence Nationale de Recherche
  9. Feder ([D-AL] Equipex Imaginex BioMed-Bioimaging Center of Lille) [12001407]
  10. Direction Generale de l'Armement
  11. Fondation pour la Recherche Medicale
  12. European Research Council (ERC) [260901] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Plague is transmitted by fleas or contaminated aerosols. To successfully produce disease, the causal agent (Yersinia pestis) must rapidly sense and respond to rapid variations in its environment. Here, we investigated the role of 2-component regulatory systems (2CSs) in plague because the latter are known to be key players in bacterial adaptation to environmental change. Along with the previously studied PhoP-PhoQ system, OmpR-EnvZ was the only one of Y. pestis' 23 other 2CSs required for production of bubonic, septicemic, and pneumonic plague. In vitro, OmpR-EnvZ was needed to counter serum complement and leukocytes but was not required for the secretion of antiphagocyte exotoxins. In vivo, Y. pestis lacking OmpR-EnvZ did not induce an early immune response in the skin and was fully virulent in neutropenic mice. We conclude that, throughout the course of Y. pestis infection, OmpR-EnvZ is required to counter toxic effectors secreted by polymorphonuclear leukocytes in the tissues.

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