Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
National Reference Center for Streptococci, University Hospital RWTH, Aachen, Germany.
J Clin Microbiol. 2021 Jun 18;59(7):e0054021. doi: 10.1128/JCM.00540-21.
Pneumococcal capsules are important in pneumococcal pathogenesis and vaccine development. Although conjugate vaccines have brought about a significant reduction in invasive pneumococcal disease (IPD) caused by vaccine serotypes, the relative serotype prevalence has shifted with the dramatic emergence of serotype 24F in some countries. Here, we describe 14 isolates (13 IPD and 1 non-IPD) expressing a new capsule type, 24C, which resembles 24F but has a novel serological profile. We also describe the antigenic, biochemical, and genetic basis of 24F and 24C and the related serotypes 24A and 24B. Structural studies show that 24B, 24C, and 24F have identical polysaccharide backbones [β-Rib(1→4)-α-Rha-(1→3)-β-GlcNAc-(1→4)-β-Rha-(1→4)-β-Glc] but with different side chains, as follows: 24F has arabinitol-phosphate and 24B has ribitol-phosphate. 24C has a mixture of 24F and 24B repeating units, with the ratio of ribitol to arabinitol being strain dependent. In contrast, the 24A capsule has a backbone without β-Rib but with arabinitol-phosphate and phosphocholine side chains. These structures indicate that factor-sera 24d and 24e recognize arabinitol and ribitol, respectively, which explains the serology of serogroup 24, including those of 24C. The structures can be genetically described by the bispecificity of , which is capable of transferring arabinitol or ribitol when arabinitol is limiting. Arabinitol is likely not produced in 24B but is produced in reduced amounts in 24C due to various mutations in or genes. Our findings demonstrate how pneumococci modulate their capsule structure and immunologic properties with small genetic changes, thereby evading host immune responses. Our findings also suggest a potential for new capsule types within serogroup 24.
肺炎球菌荚膜在肺炎球菌发病机制和疫苗开发中起着重要作用。尽管结合疫苗的使用显著降低了疫苗血清型引起的侵袭性肺炎球菌病(IPD),但由于某些国家 24F 血清型的急剧出现,相对血清型流行率已经发生了变化。在这里,我们描述了 14 株(13 株 IPD 和 1 株非 IPD)表达一种新的荚膜型 24C,它类似于 24F,但具有新的血清学特征。我们还描述了 24F 和 24C 以及相关血清型 24A 和 24B 的抗原性、生化和遗传基础。结构研究表明,24B、24C 和 24F 具有相同的多糖骨架[β-Rib(1→4)-α-Rha-(1→3)-β-GlcNAc-(1→4)-β-Rha-(1→4)-β-Glc],但侧链不同,如下所示:24F 具有阿拉伯糖醇磷酸盐,24B 具有核糖醇磷酸盐。24C 具有 24F 和 24B 重复单元的混合物,核糖醇与阿拉伯糖醇的比例取决于菌株。相比之下,24A 荚膜没有β-Rib,但具有阿拉伯糖醇磷酸盐和磷酰胆碱侧链。这些结构表明因子血清 24d 和 24e 分别识别阿拉伯糖醇和核糖醇,这解释了血清组 24 的血清学,包括 24C。这些结构可以通过基因的双特异性来遗传描述,当阿拉伯糖醇有限时, 能够转移阿拉伯糖醇或核糖醇。由于 或 基因的各种突变,24B 中可能不产生阿拉伯糖醇,但在 24C 中产生的阿拉伯糖醇量减少。我们的研究结果表明,肺炎球菌如何通过微小的遗传变化来调节荚膜结构和免疫特性,从而逃避宿主免疫反应。我们的研究结果还表明,血清组 24 内可能存在新的荚膜型。