# Global genomic landscape of Staphylococcus lugdunensis: population structure, antimicrobial resistance, and virulence determinants

**Authors:** Donghong Yang, Pengcheng Du, Fang Wang, Shining Fu, Wentao Ni, Wen Xi, Ying Zhang, Chunyu Liu, Zhancheng Gao, Yukun He, Ran Li

PMC · DOI: 10.1128/aem.01893-25 · Applied and Environmental Microbiology · 2026-02-23

## TL;DR

This study explores the genetic diversity and antimicrobial resistance in Staphylococcus lugdunensis, highlighting its potential to cause severe infections and the need for targeted surveillance and treatment.

## Contribution

The study identifies novel plasmids and predominant high-risk lineages in S. lugdunensis, offering molecular targets for surveillance and therapy.

## Key findings

- 19 sequence types grouped into five clonal complexes were identified among 144 S. lugdunensis genomes.
- 76.2% of SCCmec-positive isolates were infection-associated, indicating a strong clinical link.
- Novel plasmids carrying multiple resistance genes were found in two ST3 isolates.

## Abstract

Staphylococcus lugdunensis, a coagulase-negative staphylococcus, has emerged as an opportunistic pathogen causing severe infections. It exhibits genetic diversity, with multiple sequence types, antimicrobial resistance (AMR) genes, and virulence factors. This study aimed to explore its genomic features and clinical implications. Six clinical isolates from Fujian, Beijing, and Wuhan were sequenced using Illumina and Oxford Nanopore platforms, and antimicrobial susceptibility was tested. Other 139 genomes were retrieved from GenBank. Multi-locus sequence typing, phylogenetic and recombination analyses, resistance/virulence gene detection, plasmid replicon identification, and staphylococcal cassette chromosome mec (SCCmec) typing were performed. Among 144 genomes, 19 sequence types (STs) were grouped into five clonal complexes (CCs), with CC3 (notably ST3) and ST27 predominating. Eighteen AMR genes were identified, with blaZ (37.5%), qacD (34.7%), and mecA (14.6%) most frequent. Seven isolates carried ≥5 AMR genes. Virulence genes, including cap8E and esxA, were widely distributed. SCCmec elements were identified in all mecA-positive isolates, with type V predominant in ST3 and type II in ST6. Importantly, 76.2% of SCCmec-positive isolates were infection-associated. Novel plasmids carrying multiple resistance genes were identified in two ST3 isolates. This study reveals extensive genetic diversity, widespread AMRs, and virulence determinants in S. lugdunensis, providing insights for surveillance and therapy.

This study highlights a direct public health threat: we found that infection-associated strains of S. lugdunensis frequently carry antimicrobial resistance genes and virulence factors, underscoring their potential to cause severe, hard-to-treat infections. It provides a genetic foundation for surveillance: the identification of predominant high-risk lineages and novel plasmids carrying multiple resistance genes offers crucial molecular targets for future tracking and monitoring of this emerging pathogen. It informs clinical decision-making: understanding the genetic basis of its resistance and virulence is a critical step toward developing more effective strategies for infection control and guiding targeted antibiotic therapy.

## Linked entities

- **Genes:** blaZ (penicillin-hydrolyzing class A beta-lactamase BlaZ) [NCBI Gene 48886948], mecA (adaptor protein controlling oligomerization of the AAA+ protein ClpC) [NCBI Gene 936406], cap8E (type 8 capsular polysaccharide synthesis protein Cap8E) [NCBI Gene 66838460], esxA (ESAT-6 protein EsxA) [NCBI Gene 886209]
- **Diseases:** infection (MONDO:0005550)
- **Species:** Staphylococcus lugdunensis (taxon 28035)

## Full-text entities

- **Diseases:** infection (MESH:D007239)
- **Chemicals:** mecA (MESH:C046756)
- **Species:** Staphylococcus lugdunensis (species) [taxon 28035]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12997805/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12997805/full.md

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Source: https://tomesphere.com/paper/PMC12997805