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对39株侵袭性肺炎链球菌199序列型分离株进行全基因组测序,结果显示存在从19A血清型到15B血清型的转换。

Whole Genome Sequencing of 39 Invasive Streptococcus pneumoniae Sequence Type 199 Isolates Revealed Switches from Serotype 19A to 15B.

作者信息

Makarewicz Oliwia, Lucas Marie, Brandt Christian, Herrmann Leonie, Albersmeier Andreas, Rückert Christian, Blom Jochen, Goesmann Alexander, van der Linden Mark, Kalinowski Jörn, Pletz Mathias W

机构信息

Center for Infectious Diseases and Infection Control, Jena University Hospital, Jena, Germany.

Center for Biotechology, University of Bielefeld, Bielefeld, Germany.

出版信息

PLoS One. 2017 Jan 3;12(1):e0169370. doi: 10.1371/journal.pone.0169370. eCollection 2017.

Abstract

Streptococcus pneumoniae is a major pathogen that causes different invasive pneumococcal diseases (IPD). The pneumococcal polysaccharide capsule is a main virulence factor. More than 94 capsule types have been described, but only a limited number of capsule types accounted for the majority of IPD cases before the introduction of pneumococcal vaccines. After the introduction of the conjugated pneumococcal vaccine PCV7, which covered the seven most frequent serotypes in IPD in the USA, an increase in IPD caused by non-vaccine serotypes was observed, and serotype 19A, which belongs to sequence type (ST) 199, was among the most prevalent STs. After the introduction of the extended vaccine PCV13, which includes serotype 19A, serogroup 15B/C increased in IPD. Therefore, whole genome sequences of 39 isolates of ST199 from Germany (collected between 1998 and 2011) with serotype 19A (n = 24) and serogroup 15B/C (n = 15) were obtained using an Illumina platform and were analysed to identify capsular switches within ST199. Two 19A to 15B/C serotype switch events were identified. Both events occurred before the introduction of PCV7, which indicates that a capsular switch from 19A to 15B among ST199 isolates is not unusual and is not directly linked to the vaccination. The observed serotype replacement appears to be the result of a vacant niche due to the displacement of vaccine serotypes that is now successfully occupied by ST199 clones.

摘要

肺炎链球菌是一种引发不同侵袭性肺炎球菌疾病(IPD)的主要病原体。肺炎球菌多糖荚膜是主要的毒力因子。已描述的荚膜类型超过94种,但在肺炎球菌疫苗引入之前,只有有限数量的荚膜类型占IPD病例的大多数。引入覆盖美国IPD中七种最常见血清型的结合肺炎球菌疫苗PCV7后,观察到由非疫苗血清型引起的IPD增加,属于序列型(ST)199的19A血清型是最普遍的ST之一。引入包括19A血清型的扩展疫苗PCV13后,IPD中15B/C血清群增加。因此,使用Illumina平台获得了来自德国(1998年至2011年期间收集)的39株ST199分离株的全基因组序列,这些分离株具有19A血清型(n = 24)和15B/C血清群(n = 15),并进行分析以鉴定ST199内的荚膜转换。鉴定出两个从19A到15B/C血清型的转换事件。这两个事件都发生在PCV7引入之前,这表明ST199分离株中从19A到15B的荚膜转换并不罕见,且与疫苗接种没有直接关联。观察到的血清型替代似乎是由于疫苗血清型被取代后出现空缺生态位的结果,现在该生态位已被ST199克隆成功占据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/900b/5207522/96c95f7652c3/pone.0169370.g001.jpg

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