Suppr超能文献

用于肺炎支原体分子分型的多位点序列分型方案的开发

Development of a Multilocus Sequence Typing Scheme for Molecular Typing of Mycoplasma pneumoniae.

作者信息

Brown Rebecca J, Holden Matthew T G, Spiller O Brad, Chalker Victoria J

机构信息

Cardiff University, School of Medicine, Department of Child Health, University Hospital of Wales, Cardiff, United Kingdom Bacteriology Reference Department, Public Health England, London, United Kingdom.

University of St. Andrews, School of Medicine, Medical & Biological Sciences, North Haugh, St. Andrews, United Kingdom.

出版信息

J Clin Microbiol. 2015 Oct;53(10):3195-203. doi: 10.1128/JCM.01301-15. Epub 2015 Jul 22.

Abstract

Mycoplasma pneumoniae is a major human respiratory pathogen causing both upper and lower respiratory disease in humans of all ages, and it can also result in other serious extrapulmonary sequelae. A multilocus sequence typing (MLST) scheme for M. pneumoniae was developed based on the sequences of eight housekeeping genes (ppa, pgm, gyrB, gmk, glyA, atpA, arcC, and adk) and applied to 55 M. pneumoniae clinical isolates and the two type strains M129 and FH. A total of 12 sequence types (STs) resulted for 57 M. pneumoniae isolates tested, with a discriminatory index of 0.21 STs per isolate. The MLST loci used in this scheme were shown to be stable in 10 strains following 10 sequential subculture passages. Phylogenetic analysis of concatenated sequences of the eight loci indicated two distinct genetic clusters that were directly linked to multilocus variable-number tandem repeat analysis (MLVA) type. Genetic MLST clustering was confirmed by genomic sequence analysis, indicating that the MLST scheme developed in this study is representative of the genome. Furthermore, this MLST scheme was shown to be more discriminatory than both MLVA and P1 typing for the M. pneumoniae isolates examined, providing a method for further and more detailed analysis of observed epidemic peaks of M. pneumoniae infection. This scheme is supported by a public Web-based database (http://pubmlst.org/mpneumoniae).

摘要

肺炎支原体是一种主要的人类呼吸道病原体,可导致各年龄段人群的上、下呼吸道疾病,还可引发其他严重的肺外后遗症。基于八个管家基因(ppa、pgm、gyrB、gmk、glyA、atpA、arcC和adk)的序列开发了一种肺炎支原体多位点序列分型(MLST)方案,并应用于55株肺炎支原体临床分离株以及两株标准菌株M129和FH。对57株测试的肺炎支原体分离株共产生了12种序列类型(STs),每个分离株的鉴别指数为0.21 STs。该方案中使用的MLST位点在10株菌株连续传代10次后显示稳定。对八个位点的串联序列进行系统发育分析表明,有两个不同的遗传簇,它们与多位点可变数目串联重复分析(MLVA)类型直接相关。通过基因组序列分析证实了遗传MLST聚类,表明本研究中开发的MLST方案代表了基因组。此外,对于所检测的肺炎支原体分离株,该MLST方案显示出比MLVA和P1分型更具鉴别力,为进一步更详细地分析观察到的肺炎支原体感染流行高峰提供了一种方法。该方案得到了一个基于网络的公共数据库(http://pubmlst.org/mpneumoniae)的支持。

相似文献

5
Multilocus sequence typing of Mycoplasma agalactiae.牛支原体多位点序列分型。
J Med Microbiol. 2011 Jun;60(Pt 6):803-811. doi: 10.1099/jmm.0.028159-0. Epub 2011 Mar 3.
9
Periodic Genotype Shifts in Clinically Prevalent Strains in Japan.日本临床流行株中的周期性基因型转变。
Front Cell Infect Microbiol. 2020 Aug 6;10:385. doi: 10.3389/fcimb.2020.00385. eCollection 2020.

引用本文的文献

8
The Association between Genotype and Cutaneous Disease.基因型与皮肤疾病之间的关联。
Microorganisms. 2023 Jan 13;11(1):205. doi: 10.3390/microorganisms11010205.

本文引用的文献

7
Macrolide-resistant Mycoplasma pneumoniae in adults in Zhejiang, China.中国浙江成人中对大环内酯类耐药的肺炎支原体
Antimicrob Agents Chemother. 2015 Feb;59(2):1048-51. doi: 10.1128/AAC.04308-14. Epub 2014 Dec 1.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验