Ching-Hsi Hsiao, Eugene Yu-Chuan Kang, Ya-Tung Liu, Hung-Chi Chen, Lung-Kun Yeh, David H K Ma, Kuo-Hsuan Hung, Yhu-Chering Huang
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引用次数: 0
Abstract
Background: Methicillin-resistant Staphylococcus aureus (MRSA) is a major cause of ocular infections, with evolving molecular epidemiology observed in systemic infections in Taiwan. However, longitudinal data on clonal distribution and antibiotic susceptibility in ocular MRSA isolates remain limited.
Material and methods: Patients with culture-proven S. aureus ocular infection at Chang Gung Memorial Hospital between 2013 and 2022 were included. MRSA isolates were characterized by pulsed-field gel electrophoresis, multilocus sequence typing, and staphylococcal cassette chromosome mec typing, and Panton-Valentine leucocidin genes detection. Antibiotic susceptibility was examined using disk diffusion method and E-test. Temporal trends were analyzed using chi-square tests for trend.
Results: A total of 154 MRSA ocular isolates were identified. The predominant clone complex (CC) was CC59 (80/154, 52.0%), followed by CC8 (30/154, 19.5%) and CC45 (25/154, 16.2%). Over the decade, CC59 declined while CC8 increased significantly (P = 0.005 and P = 0.002, respectively), paralleling nationwide systemic MRSA trends. CC8 isolates were more frequently associated with eyelid disorders than CC59 (50.0% vs 28.8%; P = 0.045). CC59 isolates remained highly susceptible to fluoroquinolones (> 95%), while CC8 demonstrated marked resistance (≤ 11% susceptible; P < 0.0001). All isolates were susceptible to vancomycin and teicoplanin.
Conclusions: Ocular MRSA infections in Taiwan demonstrate longitudinal changes in clonal distribution, characterized by declining CC59 and increasing CC8, and a concurrent increase in fluoroquinolone-resistant CC8. This evolution may compromise fluoroquinolone-based empirical therapy, a cornerstone of first-line treatment for ocular infections, and highlights the importance of continued molecular surveillance.
期刊介绍:
Biomedical Journal publishes 6 peer-reviewed issues per year in all fields of clinical and biomedical sciences for an internationally diverse authorship. Unlike most open access journals, which are free to readers but not authors, Biomedical Journal does not charge for subscription, submission, processing or publication of manuscripts, nor for color reproduction of photographs.
Clinical studies, accounts of clinical trials, biomarker studies, and characterization of human pathogens are within the scope of the journal, as well as basic studies in model species such as Escherichia coli, Caenorhabditis elegans, Drosophila melanogaster, and Mus musculus revealing the function of molecules, cells, and tissues relevant for human health. However, articles on other species can be published if they contribute to our understanding of basic mechanisms of biology.
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