Yoon Eun-Jeong, Lee Hyukmin, Kim Dokyun, Shin Jong Hee, Shin Jeong Hwan, Jeong Seok Hoon
Department of Laboratory Medicine, Research Institute of Bacterial Resistance, Yonsei University College of Medicine, Seoul, South Korea.
Department of Laboratory Medicine, Chonnam National University Medical School, Gwangju, South Korea.
Front Microbiol. 2019 Mar 29;10:540. doi: 10.3389/fmicb.2019.00540. eCollection 2019.
The aim of this work was to assess a novel pseudo-staphylococcal cassette chromosome (ΨSCC) element in methicillin-resistant (MRSA) blood isolates. Community-associated MRSA E16SA093 and healthcare-associated MRSA F17SA003 isolates were recovered from the blood specimens of patients with bacteremia in 2016 and in 2017, respectively. Antimicrobial susceptibility was determined the disk diffusion method, and SCC typing was conducted by multiplex polymerase chain reaction. Whole genome sequencing was carried out by single molecule real-time long-read sequencing. Both isolates belonged to sequence type 72 and -type I, and they were negative for Panton-Valentine leukocidin and toxic shock syndrome toxin. The -types of E16SA093 and F17SA003 were t324 and t2460, respectively. They had a SCC IV-like element devoid of the cassette chromosome recombinase () gene complex, designated as ΨSCC . The element was manufactured from SCC type IV and the deletion of the gene complex and a 7.0- and 31.9-kb portion of each chromosome. The deficiency of the gene complex in the SCC unit is likely resulting in mobility loss, which would be an adaptive evolutionary mechanism. The dissemination of this clone should be monitored closely.
这项工作的目的是评估耐甲氧西林金黄色葡萄球菌(MRSA)血液分离株中的一种新型假葡萄球菌盒式染色体(ΨSCC)元件。社区获得性MRSA E16SA093和医疗保健相关MRSA F17SA003分离株分别于2016年和2017年从菌血症患者的血液标本中分离得到。采用纸片扩散法测定抗菌药物敏感性,通过多重聚合酶链反应进行SCC分型。通过单分子实时长读测序进行全基因组测序。两种分离株均属于序列类型72和I型,并且它们的杀白细胞素和中毒性休克综合征毒素均为阴性。E16SA093和F17SA003的类型分别为t324和t2460。它们有一个类似SCC IV的元件,缺乏盒式染色体重组酶()基因复合体,命名为ΨSCC 。该元件由IV型SCC制造,缺失了基因复合体以及每条染色体的7.0和31.9 kb部分。SCC单元中基因复合体的缺失可能导致移动性丧失,这将是一种适应性进化机制。应密切监测该克隆的传播。