Yamamoto Takeshi, Kida Yutaka, Sakamoto Yuichi, Kuwano Koichi
Division of Microbiology, Department of Infectious Medicine, Kurume University School of Medicine, Kurume, 830-0011, Japan.
Cell Microbiol. 2017 Mar;19(3). doi: 10.1111/cmi.12666. Epub 2016 Oct 4.
Neutrophils play an important role in antimicrobial defense as the first line of innate immune system. Recently, the release of neutrophil extracellular traps (NETs) has been identified as a killing mechanism of neutrophils against invading microbes. Mycoplasma pneumoniae, a causative agent of respiratory infection, has been shown to be resistant to in vitro killing by neutrophils, suggesting that the bacterium might circumvent bactericidal activity of NETs. In this study, we investigated whether M. pneumoniae possesses resistance mechanisms against the NETs-mediated killing of neutrophils and found that the bacterium degrades the NETs induced upon M. pneumoniae infection. The NETs-degrading ability of M. pneumoniae required the production of a secreted nuclease, Mpn491, capable of using Mg as a cofactor for its hydrolytic activity. Moreover, the inactivation of the nuclease resulted in increased susceptibility of M. pneumoniae to the NETs-mediated killing of neutrophils. The results suggest that M. pneumoniae employs Mpn491 as a means for evading the killing mechanism of neutrophils.
中性粒细胞作为固有免疫系统的第一道防线,在抗菌防御中发挥着重要作用。最近,中性粒细胞胞外陷阱(NETs)的释放已被确定为中性粒细胞对抗入侵微生物的一种杀伤机制。肺炎支原体是呼吸道感染的病原体,已被证明对中性粒细胞的体外杀伤具有抗性,这表明该细菌可能规避NETs的杀菌活性。在本研究中,我们调查了肺炎支原体是否具有针对NETs介导的中性粒细胞杀伤的抗性机制,发现该细菌可降解肺炎支原体感染后诱导产生的NETs。肺炎支原体的NETs降解能力需要分泌一种核酸酶Mpn491,该酶能够利用镁作为其水解活性的辅因子。此外,核酸酶的失活导致肺炎支原体对NETs介导的中性粒细胞杀伤的敏感性增加。结果表明,肺炎支原体利用Mpn491作为逃避中性粒细胞杀伤机制的一种手段。