Kerr Alison R, Wei Xiao-Qing, Andrew Peter W, Mitchell Tim J
Division of Infection and Immunity, IBLS, University of Glasgow, Glasgow G12 8QQ, Scotland, UK.
Microb Pathog. 2004 Jun;36(6):303-10. doi: 10.1016/j.micpath.2004.02.001.
Nitric oxide (NO) is known to be involved in the immune response against a range of organisms. Little is known about the effects of nitric oxide in pneumococcal infections. We have now investigated the role of nitric oxide in local and systemic infections caused by Streptococcus pneumoniae in NOS2 deficient mice. Although a deficiency in NO does not affect survival of mice during pneumococcal pneumonia, NO does control pneumococcal viability within the lung airways and tissue. Bronchoalveolar lavage fluid (BALF) from NOS2-deficient mice contained significantly elevated TNF activity, IFNgamma and total protein during mid/late infection. Incubation of S. pneumoniae with the NO donor SNAP revealed a direct anti-pneumococcal effect for NO in vitro. Deficiency in NOS2 did not affect bacteraemia following intranasal infection. In contrast NOS2-deficient mice were significantly less susceptible to intravenous infection with S. pneumoniae than were wild type mice and were able to control pneumococcal viability within the bloodstream. Our results indicate that NO is required within the lungs for anti-bacterial activity during the pneumococcal pneumonia but during Gram-positive bacteraemia NO is associated with increased bacterial loads and reduced survival.
已知一氧化氮(NO)参与针对多种生物体的免疫反应。关于一氧化氮在肺炎球菌感染中的作用知之甚少。我们现在研究了一氧化氮在NOS2缺陷小鼠中由肺炎链球菌引起的局部和全身感染中的作用。尽管NO缺乏并不影响肺炎球菌肺炎期间小鼠的存活,但NO确实能控制肺气道和组织内肺炎球菌的活力。在感染中期/后期,NOS2缺陷小鼠的支气管肺泡灌洗液(BALF)中TNF活性、IFNγ和总蛋白显著升高。肺炎链球菌与NO供体SNAP孵育显示NO在体外具有直接的抗肺炎球菌作用。NOS2缺乏并不影响鼻内感染后的菌血症。相反,与野生型小鼠相比,NOS2缺陷小鼠对肺炎链球菌静脉感染的易感性显著降低,并且能够控制血液中肺炎球菌的活力。我们的结果表明,在肺炎球菌肺炎期间,肺部需要NO来发挥抗菌活性,但在革兰氏阳性菌血症期间,NO与细菌载量增加和存活率降低有关。