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利用 MALDI-TOF MS 鉴定与侵袭性 ST1、血清型 VI 组 B 链球菌相关的蛋白质组生物标志物。

Identification of a proteomic biomarker associated with invasive ST1, serotype VI Group B Streptococcus by MALDI-TOF MS.

机构信息

School of Medicine, China Medical University, Taichung, Taiwan; Department of Pediatric Infectious Diseases, China Medical University Children's Hospital, Taichung, Taiwan.

Department of Laboratory Medicine, Linkou Chang-Gung Memorial Hospital, Taoyuan, Taiwan; Department of Medical Research, China Medical University Hospital, Taichung, Taiwan; Department of Medical Biotechnology and Laboratory Science, Chang Gung University, Kwei-Shan, Taoyuan, Taiwan.

出版信息

J Microbiol Immunol Infect. 2019 Feb;52(1):81-89. doi: 10.1016/j.jmii.2017.11.007. Epub 2017 Dec 30.

DOI:10.1016/j.jmii.2017.11.007
PMID:29317173
Abstract

BACKGROUND

Group B Streptococcus (GBS) is an important invasive pathogen in neonates, pregnant women and the elderly. Serotype VI GBS, which has been rarely reported globally, has emerged as a significant pathogen in Asia. However, traditional serologic latex agglutination (LA) methods may fail to type isolates that lack of or low expression of CPS.

METHODS

A total of 104 GBS strains were analyzed by MALDI-TOF MS. Multiplex PCR and multilocus sequence typing (MLST) were also performed to confirm their strains. The protein markers were purified with gel electrophoresis and LC-column, followed by identification with nanoLC-MS/MS analysis.

RESULTS

Protein peak of 6251-Da was appeared in most (20/24, 92%) serotypes VI (94% ST-1 or single locus variant of ST-1), and protein peak of 6891-Da was appeared in most serotypes III (15/18, 83%) and Ib (19/23, 83%) strains. The protein peak of 6251-Da and 6891-Da were identified as CsbD family protein and UPF0337 protein gbs0600, respectively.

CONCLUSIONS

The protein peak of 6251 Da may play a role of emergence of ST-1 clone, serotype VI GBS in central Taiwan and could be useful in rapid identifying invasive serotype VI from III isolates, which is hardly achieved by LA.

摘要

背景

B 群链球菌(GBS)是新生儿、孕妇和老年人中一种重要的侵袭性病原体。全球鲜有报道的血清型 VI GBS 已成为亚洲的重要病原体。然而,传统的乳胶凝集(LA)血清学方法可能无法对缺乏或低表达荚膜多糖(CPS)的分离株进行分型。

方法

采用 MALDI-TOF MS 对 104 株 GBS 菌株进行分析。还进行了多重 PCR 和多位点序列分型(MLST)以确认其菌株。采用凝胶电泳和 LC 柱纯化蛋白标志物,然后进行 nanoLC-MS/MS 分析鉴定。

结果

大多数血清型 VI(94% ST-1 或 ST-1 的单一基因座变异体,20/24,92%)菌株出现 6251-Da 蛋白峰,大多数血清型 III(15/18,83%)和 Ib(19/23,83%)菌株出现 6891-Da 蛋白峰。6251-Da 和 6891-Da 蛋白峰分别被鉴定为 CsbD 家族蛋白和 UPF0337 蛋白 gbs0600。

结论

6251-Da 蛋白峰可能在台湾中部 ST-1 克隆、血清型 VI GBS 的出现中发挥作用,可用于快速鉴定 LA 难以实现的侵袭性血清型 VI 与 III 分离株。

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