Daptomycin treatment impacts resistance in off-target populations of vancomycin-resistant Enterococcus faecium.
Adaptation, Physiological
/ drug effects
Adult
Anti-Bacterial Agents
/ therapeutic use
Cohort Studies
Daptomycin
/ pharmacology
Drug Resistance, Bacterial
/ drug effects
Enterococcus faecium
/ drug effects
Female
Humans
Male
Microbial Sensitivity Tests
Phylogeny
Vancomycin
/ pharmacology
Vancomycin-Resistant Enterococci
/ drug effects
Journal
PLoS biology
ISSN: 1545-7885
Titre abrégé: PLoS Biol
Pays: United States
ID NLM: 101183755
Informations de publication
Date de publication:
12 2020
12 2020
Historique:
received:
31
01
2020
accepted:
30
11
2020
revised:
31
12
2020
pubmed:
18
12
2020
medline:
3
2
2021
entrez:
17
12
2020
Statut:
epublish
Résumé
The antimicrobial resistance crisis has persisted despite broad attempts at intervention. It has been proposed that an important driver of resistance is selection imposed on bacterial populations that are not the intended target of antimicrobial therapy. But to date, there has been limited quantitative measure of the mean and variance of resistance following antibiotic exposure. Here we focus on the important nosocomial pathogen Enterococcus faecium in a hospital system where resistance to daptomycin is evolving despite standard interventions. We hypothesized that the intravenous use of daptomycin generates off-target selection for resistance in transmissible gastrointestinal (carriage) populations of E. faecium. We performed a cohort study in which the daptomycin resistance of E. faecium isolated from rectal swabs from daptomycin-exposed patients was compared to a control group of patients exposed to linezolid, a drug with similar indications. In the daptomycin-exposed group, daptomycin resistance of E. faecium from the off-target population was on average 50% higher than resistance in the control group (n = 428 clones from 22 patients). There was also greater phenotypic diversity in daptomycin resistance within daptomycin-exposed patients. In patients where multiple samples over time were available, a wide variability in temporal dynamics were observed, from long-term maintenance of resistance to rapid return to sensitivity after daptomycin treatment stopped. Sequencing of isolates from a subset of patients supports the argument that selection occurs within patients. Our results demonstrate that off-target gastrointestinal populations rapidly respond to intravenous antibiotic exposure. Focusing on the off-target evolutionary dynamics may offer novel avenues to slow the spread of antibiotic resistance.
Identifiants
pubmed: 33332354
doi: 10.1371/journal.pbio.3000987
pii: PBIOLOGY-D-20-00242
pmc: PMC7775125
doi:
Substances chimiques
Anti-Bacterial Agents
0
Vancomycin
6Q205EH1VU
Daptomycin
NWQ5N31VKK
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e3000987Subventions
Organisme : NIAID NIH HHS
ID : K08 AI119182
Pays : United States
Organisme : NIAID NIH HHS
ID : L30 AI113834
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI143852
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM070449
Pays : United States
Déclaration de conflit d'intérêts
I have read the journal's policy and the authors of this manuscript have the following competing interests: A.F.R reports consulting with Foamix Inc and unrestricted grants from Merck, outside the submitted work. All other authors declare that no competing interests exist.
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