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推测性新型血清型和疫苗效力降低的可能性:5405 株肺炎球菌基因组中揭示的荚膜基因座多样性。

Putatively novel serotypes and the potential for reduced vaccine effectiveness: capsular locus diversity revealed among 5405 pneumococcal genomes.

机构信息

1​Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.

2​Department of Zoology, University of Oxford, Oxford, United Kingdom.

出版信息

Microb Genom. 2016 Oct 1;2(10):000090. doi: 10.1099/mgen.0.000090.

Abstract

The pneumococcus is a leading global pathogen and a key virulence factor possessed by the majority of pneumococci is an antigenic polysaccharide capsule ('serotype'), which is encoded by the capsular () locus. Approximately 100 different serotypes are known, but the extent of sequence diversity within the loci of individual serotypes is not well understood. Investigating serotype-specific sequence variation is crucial to the design of sequence-based serotyping methodology, understanding pneumococcal conjugate vaccine (PCV) effectiveness and the design of future PCVs. The availability of large genome datasets makes it possible to assess population-level variation among pneumococcal serotypes and in this study 5405 pneumococcal genomes were used to investigate locus diversity among 49 different serotypes. Pneumococci had been recovered between 1916 and 2014 from people of all ages living in 51 countries. Serotypes were deduced bioinformatically, locus sequences were extracted and variation was assessed within the locus, in the context of pneumococcal genetic lineages. Overall, locus sequence diversity varied markedly: low to moderate diversity was revealed among serogroups/types 1, 3, 7, 9, 11 and 22; whereas serogroups/types 6, 19, 23, 14, 15, 18, 33 and 35 displayed high diversity. Putative novel and/or hybrid loci were identified among all serogroups/types apart from 1, 3 and 9. This study demonstrated that locus sequence diversity varied widely between serogroups/types. Investigation of the biochemical structure of the polysaccharide capsule of major variants, particularly PCV-related serotypes and those that appear to be novel or hybrids, is warranted.

摘要

肺炎球菌是一种主要的全球病原体,大多数肺炎球菌所具有的一个关键毒力因子是一种抗原性多糖荚膜(“血清型”),它由荚膜()基因座编码。已知大约有 100 种不同的血清型,但单个血清型的 基因座内序列多样性的程度尚不清楚。研究血清型特异性序列变异对于基于序列的血清分型方法的设计、了解肺炎球菌结合疫苗(PCV)的有效性以及未来 PCV 的设计至关重要。大量基因组数据集的可用性使得评估肺炎球菌血清型之间的群体水平变异成为可能,在这项研究中,使用了 5405 个肺炎球菌基因组来研究 49 个不同血清型中的 基因座多样性。这些肺炎球菌是从 51 个国家的所有年龄段的人群中于 1916 年至 2014 年间分离出来的。通过生物信息学推断血清型,提取 基因座序列,并在肺炎球菌遗传谱系的背景下评估 基因座内的变异。总体而言,基因座序列多样性差异显著:血清组/型 1、3、7、9、11 和 22 中显示出低到中等多样性;而血清组/型 6、19、23、14、15、18、33 和 35 则显示出高度多样性。除了血清组/型 1、3 和 9 之外,所有血清组/型中都发现了假定的新型和/或杂交 基因座。本研究表明,基因座序列多样性在血清组/型之间差异很大。有必要对主要变体(特别是与 PCV 相关的血清型以及那些似乎是新型或杂交的变体)的多糖荚膜的生化结构进行调查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c412/5359407/aa10fef1a8bb/mgen-02-90-f001.jpg

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