# High-Risk VREfm Clones and Resistance Determinants in a Thai Hospital

**Authors:** Peechanika Chopjitt, Rada Kansaen, Sumontha Chaisaeng, Sawarod Phongchaiwasin, Parichart Boueroy, Piroon Jenjaroenpun, Thidathip Wongsurawat, Anusak Kerdsin, Nuchsupha Sunthamala

PMC · DOI: 10.3390/antibiotics14030229 · 2025-02-24

## TL;DR

This study identifies high-risk clones and resistance patterns of vancomycin-resistant Enterococcus faecium causing bloodstream infections in a Thai hospital.

## Contribution

The study reveals the genomic and phenotypic features of VREfm clones and their resistance determinants in Thailand.

## Key findings

- Most isolates belonged to clonal complex 17, with ST17 being the most common.
- All isolates carried the vanA gene and showed resistance to multiple antibiotics.
- Virulence genes like acm and esp were detected, linked to biofilm formation.

## Abstract

Background/Objective: Vancomycin-resistant enterococci (VRE), particularly Enterococcus faecium (VREfm), are significant healthcare-associated infections, especially bloodstream infections (BSIs). Method: This study explored the genotypic and phenotypic characteristics of 29 VREfm isolates causing BSIs in Thailand. Bacterial species, sequence types (STs), virulence genes, and vancomycin antimicrobial-resistance genes were identified by multiplex PCR, multilocus sequence typing, and whole-genome sequencing (WGS). Antibiotic susceptibility was determined by disk diffusion, while an E-test or broth microdilution were used for daptomycin, teicoplanin, linezolid, and tigecycline. Biofilm formation was assessed using a microtiter plate assay. Results: All isolates harbored the vanA gene and exhibited resistance to ampicillin, erythromycin, norfloxacin, vancomycin, and rifampin. Resistance to ciprofloxacin, tigecycline, and nitrofurantoin was widespread as well. All isolates remained susceptible to chloramphenicol and linezolid. The majority of isolates belonged to clonal complex 17, with ST17 being predominant (21/29, 72.4%), followed by ST80 (6/29, 20.7%), ST761 (1/29, 3.4%), and ST117 (1/29, 3.4%). WGS analysis confirmed the presence of various antimicrobial resistance genes, including aac(6′)-Ii, ant-Ia, erm(B), and vanA. Additionally, virulence genes such as acm (collagen adhesin) and esp (enterococcal surface protein), which are involved in biofilm formation, were detected. Conclusion: This study provides insights into the genomic characteristics and clonal dissemination of invasive VREfm in Thailand, which is crucial for infection control and public health surveillance.

## Linked entities

- **Genes:** vanA (vanillate O-demethylase oxygenase) [NCBI Gene 877879], erm(B) (23S rRNA (adenine(2058)-N(6))-methyltransferase Erm(B)) [NCBI Gene 8154416], acm (collagen-binding MSCRAMM adhesin Acm) [NCBI Gene 66455089], PTPRVP (protein tyrosine phosphatase receptor type V, pseudogene) [NCBI Gene 148713]
- **Chemicals:** vancomycin (PubChem CID 14969), ampicillin (PubChem CID 6249), erythromycin (PubChem CID 12560), norfloxacin (PubChem CID 4539), rifampin (PubChem CID 135398735), ciprofloxacin (PubChem CID 2764), tigecycline (PubChem CID 54686904), nitrofurantoin (PubChem CID 6604200), chloramphenicol (PubChem CID 5959), linezolid (PubChem CID 3929), daptomycin (PubChem CID 21585658), teicoplanin (PubChem CID 133065662)
- **Species:** Enterococcus faecium (taxon 1352)

## Full-text entities

- **Genes:** vanA [NCBI Gene 13874695], erm(B [NCBI Gene 15414719]
- **Diseases:** BSIs (MESH:D018805), infection (MESH:D007239), VRE (MESH:D060467)
- **Chemicals:** nitrofurantoin (MESH:D009582), linezolid (MESH:D000069349), teicoplanin (MESH:D017334), erythromycin (MESH:D004917), ampicillin (MESH:D000667), tigecycline (MESH:D000078304), rifampin (MESH:D012293), ciprofloxacin (MESH:D002939), norfloxacin (MESH:D009643), chloramphenicol (MESH:D002701), daptomycin (MESH:D017576), Vancomycin (MESH:D014640)
- **Species:** Enterococcus faecium (species) [taxon 1352]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11939153/full.md

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Source: https://tomesphere.com/paper/PMC11939153