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抑制立氏立克次体的一氧化氮。

Nitric Oxide Inhibition of Rickettsia rickettsii.

机构信息

Host-Parasite Interactions Section, Laboratory of Bacteriology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, USA.

出版信息

Infect Immun. 2021 Nov 16;89(12):e0037121. doi: 10.1128/IAI.00371-21. Epub 2021 Sep 7.

Abstract

Rickettsia rickettsii, the causative agent of Rocky Mountain spotted fever, is an enzootic, obligate, intracellular bacterial pathogen. Nitric oxide (NO) synthesized by the inducible NO synthase (iNOS) is a potent antimicrobial component of innate immunity and has been implicated in the control of virulent spp. in diverse cell types. In this study, we examined the antibacterial role of NO on R. rickettsii. Our results indicate that NO challenge dramatically reduces R. rickettsii adhesion through the disruption of bacterial energetics. Additionally, NO-treated R. rickettsii cells were unable to synthesize protein or replicate in permissive cells. Activated, NO-producing macrophages restricted R. rickettsii infections, but inhibition of iNOS ablated the inhibition of bacterial growth. These data indicate that NO is a potent antirickettsial effector of innate immunity that targets energy generation in these pathogenic bacteria to prevent growth and subversion of infected host cells.

摘要

落矶山斑点热的病原体立氏立克次体(Rickettsia rickettsii)是一种地方性、专性、细胞内细菌病原体。诱导型一氧化氮合酶(iNOS)合成的一氧化氮(NO)是先天免疫中一种强大的抗菌成分,并被认为在控制多种细胞类型中的毒力 spp 方面发挥作用。在这项研究中,我们研究了 NO 对立氏立克次体的抗菌作用。我们的结果表明,NO 挑战通过破坏细菌的能量代谢,显著降低了立氏立克次体的黏附能力。此外,NO 处理的立氏立克次体细胞无法在允许的细胞中合成蛋白质或复制。活化的、产生 NO 的巨噬细胞限制了立氏立克次体的感染,但抑制 iNOS 会消除对细菌生长的抑制作用。这些数据表明,NO 是先天免疫的一种强大的抗立克次体效应因子,它针对这些致病性细菌的能量产生,以防止受感染宿主细胞的生长和颠覆。

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