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Lookup NU author(s): Ahmed Alhejaili, Manuel BanzhafORCiD
This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).
Copyright © 2025 Alhejaili, Zhou, Halawa, Huang, Fallatah, Hirayban, Iftikhar, AlAsmari, Milner, Banzhaf, Alzaidi, Rajeh, Al-Otaiby, Alabbad, Bukhari, Aljurayyan, Aljasham, Alzeyadi, Alajel, Alanazi, Alghoribi, Almutairi, Pain, Senok, Moradigaravand and Al Salem.Objectives: Staphylococcus aureus is a leading cause of hospital-acquired infections worldwide. Over recent decades, methicillin-resistant Staphylococcus aureus (MRSA), which is resistant to multiple antimicrobials, has emerged as a significant pathogenic strain in both hospital and community settings. The rapid emergence and dissemination of MRSA clones are driven by a dynamic and evolving population, spreading swiftly across regions on epidemiological time scales. Despite the vast geographical expanse and diverse demographics of the Kingdom of Saudi Arabia and the broader West Asia region, the population diversity of MRSA in hospitals in these areas remains underexplored. Methods: We conducted a large-scale genomic analysis of a systematic Staphylococcus aureus collection obtained from 34 hospitals across all provinces of KSA, from diverse body sites between 2022 and 2024. The dataset comprised 581 MRSA and 31 methicillin-susceptible Staphylococcus aureus (MSSA) isolates, all subjected to whole-genome sequencing. A combination of phylogenetic and population genomics approaches was utilized to analyze the genomic data. Hybrid sequencing approach was employed to retrieve the complete plasmid content. Results: The population displayed remarkable diversity, comprising 48 distinct sequence types (STs), with the majority harboring community-associated SCCmec loci (types IVa, V/VII, and VI). Virulence factors associated with community-acquired MRSA (CA-MRSA), including Panton-Valentine Leukocidin (PVL) genes, were identified in 12 distinct STs. Dominant clones, including ST8-t008 (USA300), ST88-t690, ST672-t3841, ST6-t304, and ST5-t311, were associated with infections at various body sites and were widely disseminated across the country. Linezolid and vancomycin resistance were mediated by cfr-carrying plasmids and mutations in the vraR gene (involved in cell-wall stress response) and the murF gene (involved in peptidoglycan biosynthesis) in five isolates, respectively. Phylodynamic analysis revealed rapid expansion of the dominant clones, with their emergence estimated to have occurred 10–20 years ago. Plasmidome analysis uncovered a diverse repertoire of blaZ-containing plasmids and the sharing of erm(C)-encoding plasmids among major clades. The acquisition of plasmids coincided with clonal expansion. Conclusions: Our results highlight the recent concurrent expansion and geographical dissemination of CA-MRSA clones across hospitals. These findings also underscore the interplay between clonal spread and horizontal gene transfer in shaping the resistance landscape of MRSA.
Author(s): Alhejaili AY, Zhou G, Halawa H, Huang J, Fallatah O, Hirayban R, Iftikhar S, AlAsmari A, Milner M, Banzhaf M, Alzaidi AA, Rajeh AA, Al-Otaiby MA, Alabbad SS, Bukhari D, Aljurayyan AN, Aljasham AT, Alzeyadi ZA, Alajel SM, Alanazi RH, Alghoribi M, Almutairi MM, Pain A, Senok A, Moradigaravand D, Al Salem W
Publication type: Article
Publication status: Published
Journal: Frontiers in Microbiology
Year: 2025
Volume: 16
Online publication date: 13/06/2025
Acceptance date: 21/05/2025
Date deposited: 22/07/2025
ISSN (electronic): 1664-302X
Publisher: Frontiers Media SA
URL: https://doi.org/10.3389/fmicb.2025.1602985
DOI: 10.3389/fmicb.2025.1602985
Data Access Statement: The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material.
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