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西安某医院 11 年间骨关节感染中耐利奈唑胺金黄色葡萄球菌的分子特征及耐药性研究
Authors Zhou S, Zhou K , Yang P, Kong M, Liu H, Zhang R, Hou Z , Liu J
Received 3 December 2024
Accepted for publication 23 May 2025
Published 12 June 2025 Volume 2025:18 Pages 2987—2996
DOI https://doi.org/10.2147/IDR.S508027
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Zhi Ruan
Shan Zhou,1,* Ke Zhou,1,* Peihong Yang,1,* Meijuan Kong,1 Hao Liu,1 Rui Zhang,1 Zheng Hou,2 Jiayun Liu1
1Department of Clinical Laboratory, Xijing Hospital, Air Force Medical University, Xi’an, Shanxi, 710032, People’s Republic of China; 2Institute of Medical Research, Northwestern Polytechnical University, Xi’an, Shanxi, 710129, People’s Republic of China
*These authors contributed equally to this work
Correspondence: Jiayun Liu, Email jiayun@fmmu.edu.cn Zheng Hou, Email houzheng@nwpu.edu.cn; hzh_0001@163.com
Purpose: This study examines the distribution of pathogens and the characteristics of linezolid-resistant Staphylococcus aureus (LRSA) in osteoarticular infections (OAIs) over an 11-year period.
Methods: Identification and initial antimicrobial susceptibility testing were conducted using the VITEK2 compact system. Broth microdilution method (BMD) to confirm linezolid-resistant isolates. The results were interpreted according to the Clinical and Laboratory Standards Institute (CLSI) guideline. Polymerase chain reaction (PCR) screening identified linezolid-resistance-related genes and molecular typing loci.
Results: From 2012 to 2022, 2049 clinical isolates were collected, with S. aureus identified as the leading pathogen, constituting 38.90% (797/2049) of cases. Among the 797 S. aureus isolates, eight strains were initially identified as LRSA through VITEK2; however, only one isolate was confirmed as LRSA by BMD. For the eight strains, molecular typing revealed four spa types (t030, t037, t002, t437) and three MLST types, with ST239-t030 as the dominant clone. No transferable resistance genes (cfr, optrA, poxtA) were detected, but a G2576T mutation, associated with reduced linezolid sensitivity, was identified in two isolates (included the isolate confirmed as LRSA by BMD) subjected to extended linezolid therapy.
Conclusion: Our findings highlight the importance of accurate susceptibility testing and proactive monitoring of LRSA in the treatment of chronic OAIs to mitigate potential therapeutic challenges.
Keywords: Staphylococcus aureus, osteoarticular infections, antimicrobial resistance, linezolid