Literature DB >> 29467194

Identification and Characterization of Clostridium difficile Sequence Type 37 Genotype by Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry.

Ruxin Li1, Di Xiao2, Jing Yang1, Suju Sun3, Samuel Kaplan4, Zhirong Li1, Yanan Niu1, Cuixin Qiang1, Yu Zhai1, Xiaoming Wang1, Xingzhen Zhao1, Baoxin Zhao1, Martin Welker5, David H Pincus6, Dazhi Jin7, Mini Kamboj4, Guanghui Zheng8, Guojun Zhang8, Jianzhong Zhang2, Yi-Wei Tang9,10, Jianhong Zhao11.   

Abstract

Clostridium difficile multilocus sequence type 37 (ST37), which mainly corresponds to ribotype 017, has been a dominant genotype circulating in China. In this study, we report the use of matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) to analyze and characterize 204 C. difficile clinical isolates, including 49 ST37 and 155 non-ST37 isolates collected in China and other countries. The distributions of two major protein peaks (m/z 3,242 and 3,286) were significantly different between ST37 and non-ST37 prototype strains and clinical isolates. This difference was reproducible when analysis was performed on different colonies in different runs. This finding was repeated and confirmed by both bioMérieux Vitek MS and Bruker Microflex LT systems on isolates recovered from a variety of geographic regions worldwide. The combination of the two peaks was present in 47 of 49 ST37 isolates, resulting in a sensitivity of 95.9%. In contrast, the peak combination was absent in 153 of 155 non-ST37 isolates, resulting in a specificity of 98.7%. Our results suggest that MALDI-TOF MS is a rapid and reliable tool to identify C. difficile genotype ST37. Work is in progress to characterize the two molecules having peaks at m/z 3,242 and 3,286, which appear to be specific to C. difficile genotype ST37.
Copyright © 2018 American Society for Microbiology.

Entities:  

Keywords:  Clostridium difficile; MALDI-TOF MS; genotype ST37; m/z 3,242; m/z 3,286

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Year:  2018        PMID: 29467194      PMCID: PMC5925732          DOI: 10.1128/JCM.01990-17

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  38 in total

1.  Real-time cellular analysis coupled with a specimen enrichment accurately detects and quantifies Clostridium difficile toxins in stool.

Authors:  Bin Huang; Dazhi Jin; Jing Zhang; Janet Y Sun; Xiaobo Wang; Jeffrey Stiles; Xiao Xu; Mini Kamboj; N Esther Babady; Yi-Wei Tang
Journal:  J Clin Microbiol       Date:  2014-01-22       Impact factor: 5.948

2.  Matrix-assisted laser desorption ionization-time of flight mass spectrometry identifies Pseudomonas aeruginosa high-risk clones.

Authors:  Nadège Cabrolier; Marlène Sauget; Xavier Bertrand; Didier Hocquet
Journal:  J Clin Microbiol       Date:  2015-02-04       Impact factor: 5.948

3.  Molecular Epidemiology of Clostridium difficile Infection in Hospitalized Patients in Eastern China.

Authors:  Dazhi Jin; Yun Luo; Chen Huang; Jian Cai; Julian Ye; Yi Zheng; Liqian Wang; Peng Zhao; Anbing Liu; Weijia Fang; Xianjun Wang; Shichang Xia; Jianmin Jiang; Yi-Wei Tang
Journal:  J Clin Microbiol       Date:  2016-12-14       Impact factor: 5.948

4.  The role of toxin A and toxin B in Clostridium difficile infection.

Authors:  Sarah A Kuehne; Stephen T Cartman; John T Heap; Michelle L Kelly; Alan Cockayne; Nigel P Minton
Journal:  Nature       Date:  2010-09-15       Impact factor: 49.962

5.  High-throughput identification of bacteria and yeast by matrix-assisted laser desorption ionization-time of flight mass spectrometry in conventional medical microbiology laboratories.

Authors:  S Q van Veen; E C J Claas; Ed J Kuijper
Journal:  J Clin Microbiol       Date:  2010-01-06       Impact factor: 5.948

Review 6.  Clostridium difficile infection: new developments in epidemiology and pathogenesis.

Authors:  Maja Rupnik; Mark H Wilcox; Dale N Gerding
Journal:  Nat Rev Microbiol       Date:  2009-07       Impact factor: 60.633

7.  Association between PCR ribotypes and antimicrobial susceptibility among Clostridium difficile isolates from healthcare-associated infections in South Korea.

Authors:  Jieun Kim; Jung Oak Kang; Hyunjoo Pai; Tae Yeal Choi
Journal:  Int J Antimicrob Agents       Date:  2012-05-11       Impact factor: 5.283

Review 8.  The Clostridium difficile PCR ribotype 027 lineage: a pathogen on the move.

Authors:  E Valiente; M D Cairns; B W Wren
Journal:  Clin Microbiol Infect       Date:  2014-04-28       Impact factor: 8.067

9.  Molecular Characterization of Clostridium difficile Isolates from Human Subjects and the Environment.

Authors:  Tian-tian Tian; Jian-hong Zhao; Jing Yang; Cui-xin Qiang; Zhi-rong Li; Jing Chen; Kai-yue Xu; Qing-qing Ciu; Ru-xin Li
Journal:  PLoS One       Date:  2016-03-24       Impact factor: 3.240

10.  Molecular Epidemiology and Antimicrobial Susceptibility of Clostridium difficile Isolates from a University Teaching Hospital in China.

Authors:  Jing-Wei Cheng; Meng Xiao; Timothy Kudinha; Fanrong Kong; Zhi-Peng Xu; Lin-Ying Sun; Li Zhang; Xin Fan; Xiu-Li Xie; Ying-Chun Xu
Journal:  Front Microbiol       Date:  2016-10-17       Impact factor: 5.640

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  1 in total

1.  MALDI-TOF mass spectrometry-based serotyping of V. parahaemolyticus isolated from the Zhejiang province of China.

Authors:  Ping Li; Wenwen Xin; Susu Xia; Yun Luo; Zhongwen Chen; Dazhi Jin; Shan Gao; Hao Yang; Bin Ji; Henghui Wang; Yong Yan; Lin Kang; Jinglin Wang
Journal:  BMC Microbiol       Date:  2018-11-13       Impact factor: 3.605

  1 in total

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