Cargando…
Complex Routes of Nosocomial Vancomycin-Resistant Enterococcus faecium Transmission Revealed by Genome Sequencing
BACKGROUND. Vancomycin-resistant Enterococcus faecium (VREfm) is a leading cause of nosocomial infection. Here, we describe the utility of whole-genome sequencing in defining nosocomial VREfm transmission. METHODS. A retrospective study at a single hospital in the United Kingdom identified 342 patie...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5439346/ https://www.ncbi.nlm.nih.gov/pubmed/28362945 http://dx.doi.org/10.1093/cid/ciw872 |
_version_ | 1783237930451468288 |
---|---|
author | Raven, Kathy E. Gouliouris, Theodore Brodrick, Hayley Coll, Francesc Brown, Nicholas M. Reynolds, Rosy Reuter, Sandra Török, M. Estée Parkhill, Julian Peacock, Sharon J. |
author_facet | Raven, Kathy E. Gouliouris, Theodore Brodrick, Hayley Coll, Francesc Brown, Nicholas M. Reynolds, Rosy Reuter, Sandra Török, M. Estée Parkhill, Julian Peacock, Sharon J. |
author_sort | Raven, Kathy E. |
collection | PubMed |
description | BACKGROUND. Vancomycin-resistant Enterococcus faecium (VREfm) is a leading cause of nosocomial infection. Here, we describe the utility of whole-genome sequencing in defining nosocomial VREfm transmission. METHODS. A retrospective study at a single hospital in the United Kingdom identified 342 patients with E. faecium bloodstream infection over 7 years. Of these, 293 patients had a stored isolate and formed the basis for the study. The first stored isolate from each case was sequenced (200 VREfm [197 vanA, 2 vanB, and 1 isolate containing both vanA and vanB], 93 vancomycin-susceptible E. faecium) and epidemiological data were collected. Genomes were also available for E. faecium associated with bloodstream infections in 15 patients in neighboring hospitals, and 456 patients across the United Kingdom and Ireland. RESULTS. The majority of infections in the 293 patients were hospital-acquired (n = 249) or healthcare-associated (n = 42). Phylogenetic analysis showed that 291 of 293 isolates resided in a hospital-associated clade that contained numerous discrete clusters of closely related isolates, indicative of multiple introductions into the hospital followed by clonal expansion associated with transmission. Fine-scale analysis of 6 exemplar phylogenetic clusters containing isolates from 93 patients (32%) identified complex transmission routes that spanned numerous wards and years, extending beyond the detection of conventional infection control. These contained both vancomycin-resistant and -susceptible isolates. We also identified closely related isolates from patients at Cambridge University Hospitals NHS Foundation Trust and regional and national hospitals, suggesting interhospital transmission. CONCLUSIONS. These findings provide important insights for infection control practice and signpost areas for interventions. We conclude that sequencing represents a powerful tool for the enhanced surveillance and control of nosocomial E. faecium transmission and infection. |
format | Online Article Text |
id | pubmed-5439346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54393462017-05-25 Complex Routes of Nosocomial Vancomycin-Resistant Enterococcus faecium Transmission Revealed by Genome Sequencing Raven, Kathy E. Gouliouris, Theodore Brodrick, Hayley Coll, Francesc Brown, Nicholas M. Reynolds, Rosy Reuter, Sandra Török, M. Estée Parkhill, Julian Peacock, Sharon J. Clin Infect Dis Major Article BACKGROUND. Vancomycin-resistant Enterococcus faecium (VREfm) is a leading cause of nosocomial infection. Here, we describe the utility of whole-genome sequencing in defining nosocomial VREfm transmission. METHODS. A retrospective study at a single hospital in the United Kingdom identified 342 patients with E. faecium bloodstream infection over 7 years. Of these, 293 patients had a stored isolate and formed the basis for the study. The first stored isolate from each case was sequenced (200 VREfm [197 vanA, 2 vanB, and 1 isolate containing both vanA and vanB], 93 vancomycin-susceptible E. faecium) and epidemiological data were collected. Genomes were also available for E. faecium associated with bloodstream infections in 15 patients in neighboring hospitals, and 456 patients across the United Kingdom and Ireland. RESULTS. The majority of infections in the 293 patients were hospital-acquired (n = 249) or healthcare-associated (n = 42). Phylogenetic analysis showed that 291 of 293 isolates resided in a hospital-associated clade that contained numerous discrete clusters of closely related isolates, indicative of multiple introductions into the hospital followed by clonal expansion associated with transmission. Fine-scale analysis of 6 exemplar phylogenetic clusters containing isolates from 93 patients (32%) identified complex transmission routes that spanned numerous wards and years, extending beyond the detection of conventional infection control. These contained both vancomycin-resistant and -susceptible isolates. We also identified closely related isolates from patients at Cambridge University Hospitals NHS Foundation Trust and regional and national hospitals, suggesting interhospital transmission. CONCLUSIONS. These findings provide important insights for infection control practice and signpost areas for interventions. We conclude that sequencing represents a powerful tool for the enhanced surveillance and control of nosocomial E. faecium transmission and infection. Oxford University Press 2017-04-01 2017-02-23 /pmc/articles/PMC5439346/ /pubmed/28362945 http://dx.doi.org/10.1093/cid/ciw872 Text en © The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Major Article Raven, Kathy E. Gouliouris, Theodore Brodrick, Hayley Coll, Francesc Brown, Nicholas M. Reynolds, Rosy Reuter, Sandra Török, M. Estée Parkhill, Julian Peacock, Sharon J. Complex Routes of Nosocomial Vancomycin-Resistant Enterococcus faecium Transmission Revealed by Genome Sequencing |
title | Complex Routes of Nosocomial Vancomycin-Resistant Enterococcus faecium Transmission Revealed by Genome Sequencing |
title_full | Complex Routes of Nosocomial Vancomycin-Resistant Enterococcus faecium Transmission Revealed by Genome Sequencing |
title_fullStr | Complex Routes of Nosocomial Vancomycin-Resistant Enterococcus faecium Transmission Revealed by Genome Sequencing |
title_full_unstemmed | Complex Routes of Nosocomial Vancomycin-Resistant Enterococcus faecium Transmission Revealed by Genome Sequencing |
title_short | Complex Routes of Nosocomial Vancomycin-Resistant Enterococcus faecium Transmission Revealed by Genome Sequencing |
title_sort | complex routes of nosocomial vancomycin-resistant enterococcus faecium transmission revealed by genome sequencing |
topic | Major Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5439346/ https://www.ncbi.nlm.nih.gov/pubmed/28362945 http://dx.doi.org/10.1093/cid/ciw872 |
work_keys_str_mv | AT ravenkathye complexroutesofnosocomialvancomycinresistantenterococcusfaeciumtransmissionrevealedbygenomesequencing AT gouliouristheodore complexroutesofnosocomialvancomycinresistantenterococcusfaeciumtransmissionrevealedbygenomesequencing AT brodrickhayley complexroutesofnosocomialvancomycinresistantenterococcusfaeciumtransmissionrevealedbygenomesequencing AT collfrancesc complexroutesofnosocomialvancomycinresistantenterococcusfaeciumtransmissionrevealedbygenomesequencing AT brownnicholasm complexroutesofnosocomialvancomycinresistantenterococcusfaeciumtransmissionrevealedbygenomesequencing AT reynoldsrosy complexroutesofnosocomialvancomycinresistantenterococcusfaeciumtransmissionrevealedbygenomesequencing AT reutersandra complexroutesofnosocomialvancomycinresistantenterococcusfaeciumtransmissionrevealedbygenomesequencing AT torokmestee complexroutesofnosocomialvancomycinresistantenterococcusfaeciumtransmissionrevealedbygenomesequencing AT parkhilljulian complexroutesofnosocomialvancomycinresistantenterococcusfaeciumtransmissionrevealedbygenomesequencing AT peacocksharonj complexroutesofnosocomialvancomycinresistantenterococcusfaeciumtransmissionrevealedbygenomesequencing |