| Literature DB >> 29467194 |
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.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