Geno K Aaron, Gilbert Gwendolyn L, Song Joon Young, Skovsted Ian C, Klugman Keith P, Jones Christopher, Konradsen Helle B, Nahm Moon H
Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Centre for Infectious Diseases and Microbiology, Institute of Clinical Pathology & Medical Research, Westmead Hospital, Wentworthville, New South Wales, Australia Marie Bashir Institute for Infectious Diseases and Biosecurity, University of Sydney, Sydney, New South Wales, Australia.
Clin Microbiol Rev. 2015 Jul;28(3):871-99. doi: 10.1128/CMR.00024-15.
Streptococcus pneumoniae (the pneumococcus) is an important human pathogen. Its virulence is largely due to its polysaccharide capsule, which shields it from the host immune system, and because of this, the capsule has been extensively studied. Studies of the capsule led to the identification of DNA as the genetic material, identification of many different capsular serotypes, and identification of the serotype-specific nature of protection by adaptive immunity. Recent studies have led to the determination of capsular polysaccharide structures for many serotypes using advanced analytical technologies, complete elucidation of genetic basis for the capsular types, and the development of highly effective pneumococcal conjugate vaccines. Conjugate vaccine use has altered the serotype distribution by either serotype replacement or switching, and this has increased the need to serotype pneumococci. Due to great advances in molecular technologies and our understanding of the pneumococcal genome, molecular approaches have become powerful tools to predict pneumococcal serotypes. In addition, more-precise and -efficient serotyping methods that directly detect polysaccharide structures are emerging. These improvements in our capabilities will greatly enhance future investigations of pneumococcal epidemiology and diseases and the biology of colonization and innate immunity to pneumococcal capsules.
肺炎链球菌是一种重要的人类病原体。其毒力很大程度上归因于其多糖荚膜,该荚膜可使其免受宿主免疫系统的攻击,正因如此,对荚膜进行了广泛研究。对荚膜的研究促成了DNA作为遗传物质的确定、多种不同荚膜血清型的鉴定以及适应性免疫保护血清型特异性本质的鉴定。最近的研究利用先进分析技术确定了许多血清型的荚膜多糖结构,完全阐明了荚膜类型的遗传基础,并开发出了高效的肺炎球菌结合疫苗。结合疫苗的使用通过血清型替代或转换改变了血清型分布,这增加了对肺炎球菌进行血清分型的需求。由于分子技术的巨大进步以及我们对肺炎球菌基因组的了解,分子方法已成为预测肺炎球菌血清型的有力工具。此外,直接检测多糖结构的更精确、高效的血清分型方法也不断涌现。我们能力的这些提升将极大地促进未来对肺炎球菌流行病学、疾病以及肺炎球菌荚膜定植生物学和固有免疫的研究。