Investigating a rare methicillin-resistant Staphylococcus aureus strain: first description of genome sequencing and molecular characterization of CC15-MRSA

被引:17
作者
Senok, Abiola C. [1 ]
Somily, Ali M. [2 ,3 ]
Slickers, Peter [4 ,5 ]
Raji, Muhabat A. [6 ]
Garaween, Ghada [6 ]
Shibl, Atef [6 ]
Monecke, Stefan [4 ,5 ,7 ]
Ehricht, Ralf [4 ,5 ]
机构
[1] Mohammed Bin Rashid Univ Med & Hlth Sci, Dept Basic Sci, Coll Med, Dubai, U Arab Emirates
[2] King Khalid Univ Hosp, Dept Pathol & Lab Med, Coll Med, Riyadh, Saudi Arabia
[3] King Saud Univ, Riyadh, Saudi Arabia
[4] Alere Technol GmbH, Jena, Germany
[5] InfectoGnost Res Campus, Jena, Germany
[6] Alfaisal Univ, Dept Microbiol & Immunol, Coll Med, Riyadh, Saudi Arabia
[7] Tech Univ Dresden, IMMH, Dresden, Germany
来源
INFECTION AND DRUG RESISTANCE | 2017年 / 10卷
关键词
whole genome sequencing; MRSA; MLST; clonal complex; SCCmec; Saudi Arabia; RESTRICTION; INFECTIONS; PROTEIN;
D O I
10.2147/IDR.S145394
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Purpose: Methicillin resistant Staphylococcus aureus CC15 strains (CC15-MRSA) have only been sporadically described in literature. This study was carried out to describe the genetic make-up for this rare MRSA strain. Methods: Four CC15-MRSA isolates collected in Riyadh, Saudi Arabia, between 2013 and 2014 were studied. Two isolates were from clinical infection and 2 from retail meat products. Whole genome sequencing was carried out using Illumina HiSeq2500 genome analyzer. Results: All the CC15-MRSA isolates had the multilocus sequence typing profile ST1535, 13-13-1-1-81-11-13, which is a single locus variant of ST15. Of the 6 contigs related to the SCC element, one comprised a recombinase gene ccrAA, ccrC-PM1, fusC and a helicase, another one included mvaS, dru, mecA and 1 had yobV and Q4LAG7. The SCC element had 5 transposase genes, namely 3 identical paralogs of tnpIS431 and 2 identical paralogs of tnpIS256. Two identical copies of a tnpIS256-based insertion element flank the aacA-aphD gene. Two copies of this insertion element were present with 1 located in the SCC element and another inserted into the sasC gene. A short 3 kb region, which lacks any bacteriophage structural genes and site-specific DNA integrase, was inserted into the hlb gene. The hsdM and the 5'-part of the hsdS gene are replaced by a copy of the hsdM/hsdS paralogs from nSa beta giving rise to a new chimeric paralog of hsdS in nSa alpha. Conclusion: CC15-MRSA shows a novel SCCmecV/SCCfus composite element. Its variant of hsdM/hsdS probably facilitated uptake of foreign mobile genetic elements that promoted emergence of CC15-MRSA. Close surveillance is needed to monitor spread and emergence of further CC15 MRSA strains.
引用
收藏
页码:307 / 315
页数:9
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