Senok Abiola C, Somily Ali M, Slickers Peter, Raji Muhabat A, Garaween Ghada, Shibl Atef, Monecke Stefan, Ehricht Ralf
Department of Basic Science, College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Department of Pathology and Laboratory Medicine, College of Medicine, King Khalid University Hospital and King Saud University, Riyadh, Saudi Arabia.
Infect Drug Resist. 2017 Oct 4;10:307-315. doi: 10.2147/IDR.S145394. eCollection 2017.
Methicillin resistant 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.
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.
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 , , and a helicase, another one included , , and 1 had and . 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 gene. Two copies of this insertion element were present with 1 located in the SCC element and another inserted into the gene. A short 3 kb region, which lacks any bacteriophage structural genes and site-specific DNA integrase, was inserted into the gene. The and the 5'-part of the gene are replaced by a copy of the paralogs from giving rise to a new chimeric paralog in .
CC15-MRSA shows a novel SCCV/SCC composite element. Its variant of 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.
耐甲氧西林CC15菌株(CC15-MRSA)在文献中仅有零星报道。本研究旨在描述这种罕见的MRSA菌株的基因组成。
对2013年至2014年期间在沙特阿拉伯利雅得收集的4株CC15-MRSA分离株进行研究。其中2株分离自临床感染,2株分离自零售肉类产品。使用Illumina HiSeq2500基因组分析仪进行全基因组测序。
所有CC15-MRSA分离株的多位点序列分型谱为ST1535,即13-13-1-1-81-11-13,它是ST15的单一位点变体。在与SCC元件相关的6个重叠群中,一个包含重组酶基因、和一个解旋酶,另一个包含、,还有一个包含和。SCC元件有5个转座酶基因,即3个相同的tnpIS431旁系同源物和2个相同的tnpIS256旁系同源物。基于tnpIS256的插入元件的两个相同拷贝位于基因两侧。该插入元件的两个拷贝存在,一个位于SCC元件中,另一个插入到基因中。一个短的3 kb区域插入到基因中,该区域缺乏任何噬菌体结构基因和位点特异性DNA整合酶。基因的和5'部分被来自的旁系同源物的一个拷贝取代,在中产生了一个新的嵌合旁系同源物。
CC15-MRSA显示出一种新型的SCCV/SCC复合元件。其变体可能促进了外来移动遗传元件的摄取,从而促进了CC15-MRSA的出现。需要密切监测以监测更多CC15 MRSA菌株的传播和出现。