Linezolid-resistant Enterococcus faecalis ST16 harbouring optrA on a Tn6674-like element isolated from surface water. (June 2021)

• Record Type: Journal Article
• Authors: Nüesch-Inderbinen, Magdalena; Raschle, Susanne; Stevens, Marc J.A.; Schmitt, Kira; Stephan, Roger
• Is Part Of: Journal of global antimicrobial resistance. Volume 25(2021)
• Page Start: 89
• Page End: 92
• Publication Date: 2021-06
• Subjects: Linezolid-resistant -- Enterococcus faecalis ST16 -- optrA -- Surface water; Drug resistance -- Periodicals; Drug resistance -- Periodicals; Drug resistance; Periodicals; 616.9041
• DOI: 10.1016/j.jgar.2021.02.029
• Languages: English
• ISSNs: 2213-7165

Abstract

Highlights: Linezolid-resistant Enterococcus faecalis ST16 strain F102 was recovered from surface water. E. faecalis F102 carried the optrA gene on a Tn 6674 -like element. E. faecalis ST16 harboured a large number of antimicrobial resistance genes and virulence genes. The aquatic environment is important in view of dissemination of antimicrobial-resistant bacteria. ABSTRACT: Objectives: The objective of this work was to characterise an optrA -carrying Enterococcus faecalis ST16 isolate recovered from a river water sample in Switzerland. Methods: Linezolid-resistant E. faecalis F102 was recovered from surface water in Switzerland and was subjected to comprehensive genotypic characterisation and analysis of the genetic environment of the oxazolidinone/phenicol resistance gene optrA . Whole-genome sequencing (WGS) was performed to detect linezolid resistance mechanisms, including mutations in 23S rRNA and ribosomal protein genes as well as acquired resistance genes. The isolate was further characterised by multilocus sequence typing (MLST) and identification of virulence genes. Results: WGS detected the presence of optrA identical to the original optrA gene from E. faecalis E349. Analysis of the genetic environment revealed the association of optrA with fexA and a Tn 6674 -like transposon in co-existence with spc and erm (A) resistance genes. Sequence alignment indicated that the genetic environment of optrA was identical to a Tn 6674 -like variant from E. faecalis previously isolated from diseased and healthy humans and food-producing animals in the Asia-Pacific region. Enterococcus faecalis F102 did not contain any mutations in 23S rRNA or in genes encoding ribosomal proteins L3, L4 and L22. A total of 14 other resistance genes and 16 virulence genes were detected. Enterococcus faecalis F102 was assigned in silico to ST16. Conclusion: The spread of optrA -carrying E. faecalis ST16 with a high pathogenic potential in surface water is a worrisome aspect from a public-health perspective.