A prospective surveillance study to determine the prevalence of 16S rRNA methyltransferase-producing Gram-negative bacteria in the UK
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Published version
Supporting information
Author(s)
Type
Journal Article
Abstract
OBJECTIVES: To determine the prevalence of 16S rRNA methyltransferase- (16S RMTase-) producing Gram-negative bacteria in patients in the UK and to identify potential risk factors for their acquisition. METHODS: A 6 month prospective surveillance study was conducted from 1 May to 31 October 2016, wherein 14 hospital laboratories submitted Acinetobacter baumannii, Enterobacterales and Pseudomonas aeruginosa isolates that displayed high-level amikacin resistance according to their testing methods, e.g. no zone of inhibition with amikacin discs. Isolates were linked to patient travel history, medical care abroad, and previous antibiotic exposure using a surveillance questionnaire. In the reference laboratory, isolates confirmed to grow on Mueller-Hinton agar supplemented with 256 mg/L amikacin were screened by PCR for 16S RMTase genes armA, rmtA-rmtH and npmA, and carbapenemase genes (blaKPC, blaNDM, blaOXA-48-like and blaVIM). STs and total antibiotic resistance gene complement were determined via WGS. Prevalence was determined using denominators for each bacterial species provided by participating hospital laboratories. RESULTS: Eighty-four isolates (44.7%), among 188 submitted isolates, exhibited high-level amikacin resistance (MIC >256 mg/L), and 79 (94.0%) of these harboured 16S RMTase genes. armA (54.4%, 43/79) was the most common, followed by rmtB (17.7%, 14/79), rmtF (13.9%, 11/79), rmtC (12.7%, 10/79) and armA + rmtF (1.3%, 1/79). The overall period prevalence of 16S RMTase-producing Gram-negative bacteria was 0.1% (79/71 063). Potential risk factors identified through multivariate statistical analysis included being male and polymyxin use. CONCLUSIONS: The UK prevalence of 16S RMTase-producing Gram-negative bacteria is low, but continued surveillance is needed to monitor their spread and inform intervention strategies.
Date Issued
2021-09-09
Date Acceptance
2021-05-06
Citation
Journal of Antimicrobial Chemotherapy, 2021, 76 (9), pp.2428-2436
ISSN
0305-7453
Publisher
Oxford University Press
Start Page
2428
End Page
2436
Journal / Book Title
Journal of Antimicrobial Chemotherapy
Volume
76
Issue
9
Copyright Statement
© Crown copyright 2021. This article contains public sector information licensed under the Open Government Licence v3.0 (http://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/)
Sponsor
National Institute for Health Research
National Institute for Health Research
Identifier
https://www.ncbi.nlm.nih.gov/pubmed/34142130
PII: 6303574
Grant Number
HPRU-2012-10047
HPRU-2012-10047
Subjects
Science & Technology
Life Sciences & Biomedicine
Infectious Diseases
Microbiology
Pharmacology & Pharmacy
CARBAPENEMASE-PRODUCING ENTEROBACTERIACEAE
VITRO ANTIMICROBIAL ACTIVITY
ESCHERICHIA-COLI STRAINS
SPECTRUM BETA-LACTAMASE
NUMBER TANDEM-REPEAT
AMINOGLYCOSIDE RESISTANCE
ACINETOBACTER-BAUMANNII
SIDEROPHORE CEPHALOSPORIN
PSEUDOMONAS-AERUGINOSA
METHYLASE GENES
Microbiology
0605 Microbiology
1108 Medical Microbiology
1115 Pharmacology and Pharmaceutical Sciences
Publication Status
Published
Coverage Spatial
England
Date Publish Online
2021-06-18