Imperial College London

ProfessorShiraneeSriskandan

Faculty of MedicineDepartment of Infectious Disease

Professor of Infectious Diseases
 
 
 
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Contact

 

s.sriskandan

 
 
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Assistant

 

Ms Teyanna Gaeta +44 (0)20 3313 1943

 
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Location

 

8N21ACWBCommonwealth BuildingHammersmith Campus

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Summary

 

Publications

Citation

BibTex format

@article{Taylor:2021:jac/dkab186,
author = {Taylor, E and Bal, AM and Balakrishnan, I and Brown, NM and Burns, P and Clark, M and Diggle, M and Donaldson, H and Eltringham, I and Folb, J and Gadsby, N and Macleod, M and Ratnaraja, NVDV and Williams, C and Wootton, M and Sriskandan, S and Woodford, N and Hopkins, KL},
doi = {jac/dkab186},
journal = {Journal of Antimicrobial Chemotherapy},
pages = {2428--2436},
title = {A prospective surveillance study to determine the prevalence of 16S rRNA methyltransferase-producing Gram-negative bacteria in the UK},
url = {http://dx.doi.org/10.1093/jac/dkab186},
volume = {76},
year = {2021}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - 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% (79/71063). 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.
AU - Taylor,E
AU - Bal,AM
AU - Balakrishnan,I
AU - Brown,NM
AU - Burns,P
AU - Clark,M
AU - Diggle,M
AU - Donaldson,H
AU - Eltringham,I
AU - Folb,J
AU - Gadsby,N
AU - Macleod,M
AU - Ratnaraja,NVDV
AU - Williams,C
AU - Wootton,M
AU - Sriskandan,S
AU - Woodford,N
AU - Hopkins,KL
DO - jac/dkab186
EP - 2436
PY - 2021///
SN - 0305-7453
SP - 2428
TI - A prospective surveillance study to determine the prevalence of 16S rRNA methyltransferase-producing Gram-negative bacteria in the UK
T2 - Journal of Antimicrobial Chemotherapy
UR - http://dx.doi.org/10.1093/jac/dkab186
UR - https://www.ncbi.nlm.nih.gov/pubmed/34142130
UR - http://hdl.handle.net/10044/1/89939
VL - 76
ER -