| Literature DB >> 28552322 |
Shunsuke Takadama1, Hidemasa Nakaminami1, Sae Aoki1, Megumi Akashi1, Takeaki Wajima1, Masami Ikeda2, Atsushi Mochida3, Fumiko Shimoe4, Kumiko Kimura5, Yasushi Matsuzaki6, Daisuke Sawamura6, Yoichi Inaba7, Tomohiro Oishi8, Osamu Nemoto9, Naoko Baba10, Norihisa Noguchi11.
Abstract
The prevalence of Panton-Valentine leukocidin gene (pvl)-positive community-acquired methicillin-resistant Staphylococcus aureus USA300 clone, which is designated as the ST8-staphylococcal cassette chromosome (SCC) mec type IV (ST8-IV) lineage, is a major public health concern worldwide. Thus, to elucidate the prevalence and characteristics of pvl-positive community-onset MRSA in Japan, we conducted a molecular epidemiological analysis for 854 S. aureus isolates obtained from outpatients with skin infections during 2013 and 2014. The isolation rate of MRSA was 25.6% (219 isolates), and the ratio of pvl-positive MRSA was 13.2% (29 isolates). Notably, the proportion (93.8%) of pvl-positive isolates was particularly high among MRSA isolates from Ishigaki island in Okinawa. Pulsed-field gel electrophoresis and multilocus sequence typing showed that the pulsotype C isolates (11 isolates) were typical USA300 clones with arginine catabolic mobile element (ACME) type I-CC8-IV lineages and prevalent on the main island of Japan (Honshu). Pulsotypes A (11 isolates) and B (four isolates) consisted of ACME-negative CC8-IV clones and were specific for Ishigaki island. Both USA300 and Okinawa-Ishigaki specific clones were associated with deep-seated skin infections, such as furuncle and cellulitis. Pulsotypes D (two isolates) and E (one isolate) were ACME-negative clonal complex (CC) 59-IV clones and were related to superficial skin infections, such as impetigo. Our findings revealed that pvl-positive MRSA associated with deep-seated skin infections are spreading in Japanese communities, particularly in Ishigaki, Okinawa.Entities:
Keywords: Community-acquired methicillin-resistant Staphylococcus aureus; Panton-Valentine leukocidin; USA300
Mesh:
Substances:
Year: 2017 PMID: 28552322 DOI: 10.1016/j.jiac.2017.04.016
Source DB: PubMed Journal: J Infect Chemother ISSN: 1341-321X Impact factor: 2.211