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. 2023 Feb 23:11:e14859.
doi: 10.7717/peerj.14859. eCollection 2023.

Epidemiological profiles and pathogenicity of Vancomycin-resistant Enterococcus faecium clinical isolates in Taiwan

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Epidemiological profiles and pathogenicity of Vancomycin-resistant Enterococcus faecium clinical isolates in Taiwan

Pei-Yun Lin et al. PeerJ. .

Abstract

The emerging Vancomycin-resistant Enterococcus faecium (VRE-fm) is an opportunistic pathogen causing nosocomial infections. The identification of VRE-fm is important for successful prevention and control in healthcare settings. VRE-fm clinical isolates obtained from regional hospitals in northern Taiwan were characterized for antimicrobial susceptibility, virulence genes and biofilm production. Most isolates exhibited multi-drug resistance and carried the virulence genes, esp and hyl. While all isolates produce biofilms, those isolates that carried esp exhibited greater biofilm production. Isolates with different virulence gene carriages were examined for pathogenicity by using a nematode model, Caenorhabditis elegans, for determining microbial-host interactions. The survival assay showed that C. elegans was susceptible to Linezolid-resistant VRE-fm isolates with hyl. Combining the molecular epidemiological profiles regarding pathogenesis in C. elegans can serve as a guide for physicians in limiting opportunistic infections caused by VRE-fm.

Keywords: Biofilm; Caenorhabditis elegans; Vancomycin-resistant Enterococcus faecium; Virulence genes.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Figure 1
Figure 1. Distribution of virulence gene carriages in VRE-fm isolates with different antibiotic resistance.
ND: non-detected.
Figure 2
Figure 2. Survival analysis of Linezolid-resistant/susceptible VRE-fm in the C. elegans host.
(A) Survival analyses were assayed for the C. elegans challenged by the indicated Linezolid-resistant VRE-fm (n = 132 (OP50), 58 (D11), 55 (D12), 43 (B51), 33 (A68), 46 (A126); *P < 0.05, ***P < 0.001, ns, P > 0.05). (B) Lethality of C. elegans at the 8th day after being infected were derived from (A). Percentage of each condition as indicated. (C) Survival analysis was assayed for C. elegans challenged by the Linezolid-susceptible VRE-fm A127 (n = 48) compared to the E. coli OP50 control (n = 53, P = 0.88).

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