Institute of Infection and Global Health, Department of Clinical Infection, Microbiology, and Immunology, University of Liverpool, Liverpool, United Kingdom.
Malawi-Liverpool-Wellcome Trust Clinical Research Programme, University of Malawi, College of Medicine, Blantyre, Malawi.
mBio. 2020 Dec 8;11(6):e00814-20. doi: 10.1128/mBio.00814-20.
is a frequent colonizer of the human nasopharynx and a major cause of life-threating invasive infections such as pneumonia, meningitis and sepsis. Over 1 million people die every year due to invasive pneumococcal disease (IPD), mainly in developing countries. Serotype 1 is a common cause of IPD; however, unlike other serotypes, it is rarely found in the carrier state in the nasopharynx, which is often considered a prerequisite for disease. The aim of this study was to understand this dichotomy. We used murine models of carriage and IPD to characterize the pathogenesis of African serotype 1 (sequence type 217) pneumococcal strains obtained from the Queen Elizabeth Central Hospital in Blantyre, Malawi. We found that ST217 pneumococcal strains were highly virulent in a mouse model of invasive pneumonia, but in contrast to the generally accepted assumption, can also successfully establish nasopharyngeal carriage. Interestingly, we found that cocolonizing serotypes may proliferate in the presence of serotype 1, suggesting that acquisition of serotype 1 carriage could increase the risk of developing IPD by other serotypes. RNA sequencing analysis confirmed that key virulence genes associated with inflammation and tissue invasiveness were upregulated in serotype 1. These data reveal important new insights into serotype 1 pathogenesis, with implications for carriage potential and risk of invasive disease through interactions with other cocolonizing serotypes, an often-overlooked factor in transmission and disease progression. The pneumococcus causes serious diseases such as pneumonia, sepsis, and meningitis and is a major cause of morbidity and mortality worldwide. Serotype 1 accounts for the majority of invasive pneumococcal disease cases in sub-Saharan Africa but is rarely found during nasopharyngeal carriage. Understanding the mechanisms leading to nasopharyngeal carriage and invasive disease by this serotype can help reduce its burden on health care systems worldwide. In this study, we also uncovered the potential impact of serotype 1 on disease progression of other coinfecting serotypes, which can have important implications for vaccine efficacy. Understanding the interactions between different serotypes during nasopharyngeal carriage may lead to improved intervention methods and therapies to reduce pneumococcal invasive disease levels.
是人类鼻咽部的常见定植菌,也是导致肺炎、脑膜炎和败血症等危及生命的侵袭性感染的主要原因。每年有超过 100 万人死于侵袭性肺炎球菌病(IPD),主要在发展中国家。血清型 1 是 IPD 的常见原因;然而,与其他血清型不同,它很少在鼻咽部的携带状态中被发现,而鼻咽部的携带状态通常被认为是疾病的前提。本研究旨在了解这种二分法。我们使用来自马拉维布兰太尔伊丽莎白女王中央医院的非洲血清型 1(序列型 217)肺炎球菌株的携带和 IPD 小鼠模型来表征其发病机制。我们发现 ST217 肺炎球菌株在侵袭性肺炎的小鼠模型中具有高度毒力,但与普遍接受的假设相反,它也可以成功建立鼻咽部携带。有趣的是,我们发现共定植的血清型可能在血清型 1 的存在下增殖,这表明获得血清型 1 携带可能会增加其他血清型发生 IPD 的风险。RNA 测序分析证实,与炎症和组织侵袭相关的关键毒力基因在血清型 1 中上调。这些数据揭示了血清型 1 发病机制的重要新见解,这对携带潜力和通过与其他共定植血清型的相互作用(在传播和疾病进展中经常被忽视的一个因素)导致侵袭性疾病的风险具有重要意义。肺炎球菌会导致严重疾病,如肺炎、败血症和脑膜炎,是全球发病率和死亡率的主要原因。血清型 1 占撒哈拉以南非洲侵袭性肺炎球菌病病例的大多数,但在鼻咽部携带时很少被发现。了解导致该血清型鼻咽部携带和侵袭性疾病的机制可以帮助减轻其对全球卫生保健系统的负担。在这项研究中,我们还发现了血清型 1 对其他共感染血清型疾病进展的潜在影响,这对疫苗效力具有重要意义。了解不同血清型在鼻咽部携带期间的相互作用可能会导致改善干预方法和治疗方法,以降低肺炎球菌侵袭性疾病的水平。