4.6 Article

Methicillin-Resistant Staphylococcus aureus (MRSA) Clonal Replacement in a Malaysian Teaching Hospital: Findings from an Eight-Year Interval Molecular Surveillance

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ANTIBIOTICS-BASEL
卷 10, 期 3, 页码 -

出版社

MDPI
DOI: 10.3390/antibiotics10030320

关键词

MRSA; molecular surveillance; SCCmec typing; toxin typing; spa typing; antimicrobial susceptibility

资金

  1. Universiti Kebangsaan Malaysia [GUP-2020-079, GGPM-2016066]
  2. Faculty of Medicine, Universiti Kebangsaan Malaysia [FF-2017-081]
  3. [GP-2019-K016842]

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Periodic surveillance of hospital-acquired pathogens is crucial for antimicrobial control and infection prevention. The second MRSA surveillance at HCTM in 2017 found a dominant strain resistant to multiple antibiotics, suggesting clonal replacement in the hospital within 8 years. Ongoing investigation of the new MRSA clone's phenotype changes is underway.
Periodical surveillance on nosocomial pathogens is important for antimicrobial stewardship and infection control. The first methicillin-resistant Staphylococcus aureus (MRSA) molecular surveillance in Hospital Canselor Tuanku Muhriz (HCTM), a Malaysian teaching hospital, was performed in 2009. The dominant clone was identified as an MRSA carrying SCCmec type III-SCCmercury with ccrC and sea+cna toxin genes. In this study, we report the findings of the second HCTM MRSA surveillance carried out in 2017, after an interval of 8 years. Antibiotic susceptibility testing, SCCmec, toxin gene, and spa typing were performed for 222 MRSA strains isolated in 2017. Most strains were resistant to ciprofloxacin, erythromycin, clindamycin, cefoxitin, and penicillin (n = 126, 56.8%), belong to SCCmec type IV (n = 205, 92.3%), spa type t032 (n = 160, 72.1%) and harboured seg+sei toxin genes (n = 172, 77.5%). There was significant association between resistance of the aforementioned antibiotics with SCCmec type IV (p < 0.05), t032 (p < 0.001), and seg+sei carriage (p < 0.05). Results from this second MRSA surveillance revealed the occurrence of clonal replacement in HCTM during an interval of not more than 8 years. Investigation of the corresponding phenotype changes in this new dominant MRSA clone is currently on-going.

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