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Emergence of Daptomycin-Nonsusceptible Methicillin-Resistant Staphylococcus aureus Clinical Isolates among Daptomycin-Naive Patients in Korea

  • Eun Young Nam
  • , Soo Jin Yang
  • , Eu Suk Kim*
  • , Jeong Eun Cho
  • , Kyung Hwa Park
  • , Sook In Jung
  • , Nara Yoon
  • , Dong Min Kim
  • , Chang Seop Lee
  • , Hee Chang Jang
  • , Yoonseon Park
  • , Kkot Sil Lee
  • , Yee Gyung Kwak
  • , Jae Hoon Lee
  • , Seong Yeon Park
  • , Joo Hee Hwang
  • , Moonsuk Kim
  • , Kyoung Ho Song
  • , Hong Bin Kim
  • *Corresponding author for this work
  • Seoul National University
  • Chung-Ang University
  • Chonnam National University
  • Chosun University
  • National Health Insurance Corporation Ilsan Hospital
  • Myongji Hospital
  • Inje University
  • Wonkwang University
  • Dongguk University

Research output: Contribution to journalJournal articlepeer-review

Abstract

This study was conducted to assess emergence of daptomycin-nonsusceptible (DAP-NS) phenotype in DAP-naive patients with invasive Staphylococcus aureus (ISA) infections in Korea. A total of 208 S. aureus clinical isolates were selected from a previous prospective study on ISA infections and evaluated for DAP-NS. Although DAP has never been introduced in Korea, five DAP-NS S. aureus strains (2.4%) were identified among 208 S. aureus strains collected from ISA infections. The DAP-NS phenotype was observed only in methicillin-resistant S. aureus (MRSA) strains, but not in methicillin-susceptible S. aureus strains. One DAP-NS MRSA strain belonged to sequence type 72 (ST72) and four were ST5 MRSA strains, three of which were heteroresistant vancomycin (VAN)-intermediate S. aureus. All these five DAP-NS MRSA strains were from healthcare-associated infections without prior exposure to VAN within 30 days. While the ST72 MRSA strain exhibited DAP-NS phenotype via charge repulsion mechanism, four ST5 DAP-NS S. aureus strains had charge-independent DAP-NS mechanism. None of the five DAP-NS strains displayed significant increase in cell wall thickness, indicating that altered cell wall thickness was not associated with the observed DAP-NS phenotype.

Original languageEnglish
Pages (from-to)534-541
Number of pages8
JournalMicrobial Drug Resistance
Volume24
Issue number5
DOIs
StatePublished - 2018.06

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • daptomycin resistance
  • Staphylococcus aureus
  • vancomycin

Quacquarelli Symonds(QS) Subject Topics

  • Medicine
  • Pharmacy & Pharmacology
  • Biological Sciences

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