Genetic characterization of vancomycin-resistant Enterococcus faecium isolates from neutropenic patients in Tunisia: spread of the pandemic CC17 clone associated with high genetic diversity in Tn1546-like structures

Author:

Raddaoui Anis12ORCID,Chebbi Yosra12,Frigui Siwar12,Latorre Javier3,Ammeri Rim Werhani12,Abdejlil Nour Ben4,Torres Carmen3ORCID,Abbassi Mohamed Salah56ORCID,Achour Wafa12

Affiliation:

1. Laboratory Ward, National Bone Marrow Transplant Center , Tunis 1006 , Tunisia

2. Faculty of Medicine of Tunis, LR18ES39, University of Tunis El Manar , Tunis 1006 , Tunisia

3. Area de Bioquímica y Biología Molecular, Universidad de La Rioja , Logroño 26006 , Spain

4. Department of hematology and transplantationtion, National Bone Marrow Transplant Center , Tunis 1006 , Tunisia

5. Faculty of Medicine of Tunis, Laboratory of Antibiotic Resistance LR99ES09, University of Tunis El Manar , Tunis 1006 , Tunisia

6. Institute of Veterinary Research of Tunisia, University of Tunis El Manar , Tunis 1006, Tunisia

Abstract

Abstract Aims In Tunisia, limited research has focused on characterizing clinical vancomycin-resistant Enterococcus faecium (VREfm). This study aimed to bridge this knowledge gap by molecular characterization of antimicrobial resistance, determining the genetic elements mediating vancomycin-resistance, and whole-genome sequencing of one representative VREfm isolate Methods and results Over 6 years (2011–2016), a total of eighty VREfm isolates responsible for infection or colonization were identified from hospitalized patients, with the incidence rate increasing from 2% in 2011 to 27% in 2016. All of these strains harbored the vanA gene. The screening for antimicrobial resistance genes revealed the predominance of ermB, tetM, and aac(6′)-Ie-aph(2′’)-Ia genes and 81.2% of strains harbored the Tn1545. Pulsed-field gel electrophoresis identified seven clusters, with two major clusters (belonging to ST117 and ST80) persisting throughout the study period. Seven Tn1546 types were detected, with type VI (truncated transposon) being the most prevalent (57.5%). Whole-genome sequencing revealed a 3 028 373 bp chromosome and five plasmids. Mobile genetic elements and a type I CRISPR-cas locus were identified. Notably, the vanA gene was carried by the classic Tn1546 transposon with ISL3 insertion on a rep17pRUM plasmid. Conclusion A concerning trend in the prevalence of VREfm essentially attributed to CC17 persistence and to horizontal transfer of multiple genetic variants of truncated vanA-Tn1546.

Funder

Tunisian Ministry of Higher Education and Scientific Research

Publisher

Oxford University Press (OUP)

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