Genomic Epidemiology of Vancomycin-Resistant Enterococcus faecium (VREfm) in Latin America: Revisiting The Global VRE Population Structure
Little is known about the population structure of vancomycin-resistant Enterococcus faecium (VR Efm ) in Latin America (LATAM). Here, we provide a complete genomic characterization of 55 representative Latin American VR Efm recovered from 1998–2015 in 5 countries. The LATAM VR Efm population is stru...
Gespeichert in:
Veröffentlicht in: | Scientific reports 2020-03, Vol.10 (1), p.5636-5636, Article 5636 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Little is known about the population structure of vancomycin-resistant
Enterococcus faecium
(VR
Efm
) in Latin America (LATAM). Here, we provide a complete genomic characterization of 55 representative Latin American VR
Efm
recovered from 1998–2015 in 5 countries. The LATAM VR
Efm
population is structured into two main clinical clades without geographical clustering. Using the LATAM genomes, we reconstructed the global population of VR
Efm
by including 285 genomes from 36 countries spanning from 1946 to 2017. In contrast to previous studies, our results show an early branching of animal related isolates and a further split of clinical isolates into two sub-clades within clade A. The overall phylogenomic structure of clade A was highly dependent on recombination (54% of the genome) and the split between clades A and B was estimated to have occurred more than 2,765 years ago. Furthermore, our molecular clock calculations suggest the branching of animal isolates and clinical clades occurred ~502 years ago whereas the split within the clinical clade occurred ~302 years ago (previous studies showed a more recent split between clinical an animal branches around ~74 years ago). By including isolates from Latin America, we present novel insights into the population structure of VR
Efm
and revisit the evolution of these pathogens. |
---|---|
ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-020-62371-7 |