Genomic insight into Enterococcus faecium biofilm formation isolated from catheter associated urinary tract infection

Authors

  • Ayu Rahayu Department of Microbiology, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia
  • Sayyidah Auliany Aminy Department of Microbiology, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia
  • Dian Asti Umaroh Department of Biology, Faculty of Mathematics and Natural Sciences, Universitas Tanjungpura, Pontianak, Indonesia
  • Niar Gusnaniar Indonesian Biofilm Research Collaboration Center, Yogyakarta, Indonesia
  • Akhirta Atikana Indonesian Biofilm Research Collaboration Center, Yogyakarta, Indonesia
  • Puspita Lisdiyanti Indonesian Biofilm Research Collaboration Center, Yogyakarta, Indonesia
  • Estelle Perraud Laboratoire Ecologie et Biologie des Interactions, Université de Poitiers, Poitiers, France
  • Christine Imbert Laboratory of Parasitology and Mycology, Poitiers University Hospital, Poitiers, France
  • Titik Nuryastuti Department of Microbiology, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia

DOI:

https://doi.org/10.18502/ijm.v18i5.22866

Keywords:

Enterococcus faecium; Biofilms; Drug resistance; Microbial; Genome; Bacterial; Catheter-related infections

Abstract

Background and Objectives: Enterococcus faecium is a major nosocomial pathogen frequently associated with catheter-re- lated infections and biofilm-mediated antimicrobial resistance. This study aimed to investigate the genomic determinants and structural characteristics underlying biofilm formation in a clinical E. faecium isolate recovered from a catheter-associated urinary tract infection (CAUTI).

Materials and Methods: A clinical isolate, E. faecium MFKCC-BF.UR33, was subjected to whole-genome sequencing and comprehensive genome annotation to identify biofilm-associated and antimicrobial resistance genes. Phylogenetic analysis was performed to determine its relatedness to reference clinical strains. Structural modeling of selected biofilm-associated proteins was conducted using AlphaFold2 to assess their three-dimensional conformations and potential as therapeutic tar- gets.

Results: Whole-genome sequencing revealed a 3.32 Mb genome with a G+C content of 37.35%, comprising 2,321 predicted coding sequences and no detectable plasmids. Genome annotation identified several biofilm-associated genes, including sgrA, acm, fss3, scm, and efbA, as well as antimicrobial resistance genes (antA/B, tetM, tetL, efmA, and liaFSR). Phylogeneticanalysis placed the isolate within the E. faecium clade, closely related to other clinical reference strains. Structural modeling demonstrated high-confidence 3D structures for Fss3 and EfbA proteins.

Conclusion: The integration of genomic and structural analyses provides insights into the genetic and structural basis of biofilm formation in E. faecium and establishes a foundation for future functional and structure-based investigations.

Published

2026-10-04

Issue

Section

Articles