Molecular characterization of methicillin-susceptible/resistant Staphylococcus aureus (MSSA/MRSA) from bloodstream infections in northern Japan : the dominance of CC1-MRSA-IV, the emergence of human-associated ST398 and livestock-associated CC20 and CC97 MSSA.

IF 3.7 3区 医学 Q2 INFECTIOUS DISEASES
Meiji Soe Aung, Masako Osada, Noriko Urushibara, Mitsuyo Kawaguchiya, Nobuhide Ohashi, Mina Hirose, Masahiko Ito, Kazuki Yamada, Kousuke Tada, Nobumichi Kobayashi
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引用次数: 0

Abstract

Objectives: Staphylococcus aureus is a major cause of bloodstream infections. The recent epidemiological features and antimicrobial resistance trend were analyzed for methicillin-resistant and susceptible S. aureus (MRSA/MSSA) isolates from blood samples in northern Japan.

Methods: S. aureus isolates from blood culture were screened by MALDI-TOF and genotyped by the schemes of MLST, coa, agr, spa, and SCCmec types. Antimicrobial resistance genes and virulence factors were detected by multiplex/uniplex PCR. Antimicrobial susceptibility was examined using a broth microdilution test.

Results: A total of 301 isolates (163 MRSA and 138 MSSA) were isolated from bloodstream infections in 2023 (From Apr. to Dec.). The MRSA isolates were classified into three groups, i.e., CC1-SCCmec-IV (CC1-IV) (52%), CC5-II (36%), and CC8-IV (12%). The prevalence of CC1 was significantly higher than those in our previous studies (2017-2021). Four CC8-IVa isolates with PVL genes on ΦSa2usa were considered to be the USA300 clone (ST8/spa-t008/coa IIIa/agr I) or its variants that were genotyped as those closely related to ST8/t008 or lacking ACME. In contrast, MSSA was genetically highly divergent and classified into 22 STs, with CC1 (ST1, ST188) being the most common (25%). It was notable that 29 MSSA isolates (21%) were classified into livestock-associated (LA) genotypes, ST20, ST97, and CC398 (ST398, ST291). Genetic characterization of the CC398 isolates suggested that these belong to human-adapted MSSA clones.

Conclusions: The present study revealed the increasing trend of CC1 MRSA surpassing CC5, and the emergence of MSSA representing human-adapted CC398, and LA types ST97 and ST20 from bloodstream infections in Japan.

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来源期刊
Journal of global antimicrobial resistance
Journal of global antimicrobial resistance INFECTIOUS DISEASES-PHARMACOLOGY & PHARMACY
CiteScore
8.70
自引率
2.20%
发文量
285
审稿时长
34 weeks
期刊介绍: The Journal of Global Antimicrobial Resistance (JGAR) is a quarterly online journal run by an international Editorial Board that focuses on the global spread of antibiotic-resistant microbes. JGAR is a dedicated journal for all professionals working in research, health care, the environment and animal infection control, aiming to track the resistance threat worldwide and provides a single voice devoted to antimicrobial resistance (AMR). Featuring peer-reviewed and up to date research articles, reviews, short notes and hot topics JGAR covers the key topics related to antibacterial, antiviral, antifungal and antiparasitic resistance.
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