A prospective surveillance study to determine the prevalence of 16S rRNA methyltransferase-producing Gram-negative bacteria in the UK

被引:13
|
作者
Taylor, Emma [1 ,2 ]
Bal, Abhijit M. [3 ]
Balakrishnan, Indran [4 ]
Brown, Nicholas M. [5 ]
Burns, Phillipa [6 ,18 ]
Clark, Marilyn [7 ]
Diggle, Mathew [8 ,19 ]
Donaldson, Hugo [9 ]
Eltringham, Ian [10 ]
Folb, Jonathan [11 ]
Gadsby, Naomi [12 ]
Macleod, Mairi [13 ]
Ratnaraja, Natasha V. D. V. [14 ,20 ]
Williams, Cheryl [15 ]
Wootton, Mandy [16 ]
Sriskandan, Shiranee [1 ,17 ]
Woodford, Neil [1 ,2 ]
Hopkins, Katie L. [1 ,2 ]
机构
[1] Hammersmith Hosp, Hlth Protect Res Unit NIHR HPRU Healthcare Associ, Natl Inst Hlth Res, Imperial Coll London, Du Cane Rd, London W12 0NN, England
[2] Publ Hlth England, Antimicrobial Resistance & Healthcare Associated, Natl Infect Serv, London NW9 5EQ, England
[3] Univ Hosp Crosshouse NHS Ayrshire & Arran, Microbiol, Kilmarnock KA2 0BE, Scotland
[4] Royal Free London NHS Fdn Trust, Pond St, London NW3 2QG, England
[5] Cambridge Univ Hosp NHS Fdn Trust, Clin Microbiol & Publ Hlth Lab, Cambridge CB2 0QW, England
[6] Manchester Univ NHS Fdn Trust, Manchester Royal Infirm, Manchester Med Microbiol Partnership, Oxford Rd, Manchester M13 9WL, Lancs, England
[7] Ninewells Hosp, Dept Med Microbiol, Dundee DD2 1SY, Scotland
[8] Nottingham Univ Hosp Natl Hlth Serv Trust, Hucknall Rd, Nottingham NG5 1PB, England
[9] Imperial Coll Healthcare NHS Trust, Charing Cross Hosp, Fulham Palace Rd, London W6 8RF, England
[10] Kings Coll Hosp NHS Fdn Trust, Microbiol Dept, Denmark Hill, London SE5 9RS, England
[11] Liverpool Univ Hosp NHS Fdn Trust, Prescot St, Liverpool L7 8XP, Merseyside, England
[12] Royal Infirm Edinburgh NHS Trust, Dept Lab Med, Med Microbiol, 51 Little France Cres, Edinburgh EH16 4SA, Midlothian, Scotland
[13] Glasgow Royal Infirm Hosp, Clin Microbiol, Level 4 New Lister Bldg,10-16 Alexandra Parade, Glasgow G31 2ER, Lanark, Scotland
[14] Sandwell & West Birmingham NHS Trust, Dept Microbiol, Dudley Rd, Birmingham B18 7QH, W Midlands, England
[15] Royal Oldham Hosp, Microbiol Lab, Pathol Lab, First Floor,Rochdale Rd, Oldham OL1 2JH, England
[16] Univ Hosp Wales, Publ Hlth Wales Microbiol Cardiff, Cardiff CF14 4XW, Wales
[17] Imperial Coll London, MRC Ctr Mol Bacteriol & Infect, London SW7 2DD, England
[18] Hull Royal Infirm, Hull Univ Teaching Hosp, Dept Infect, Anlaby Rd, Kingston Upon Hull HU3 2JZ, N Humberside, England
[19] Univ Alberta Hosp, ProvLab Alberta Precis Labs, 2B1-03 WMC,8440-112 St, Edmonton, AB T6G 2J2, Canada
[20] Univ Hosp Coventry & Warwickshire NHS Trust, Univ Hosp, Clifford Bridge Rd, Coventry CV2 2DX, W Midlands, England
关键词
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;
D O I
10.1093/jac/dkab186
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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 (bla(KPC), bla(NDM), bla(OXA)(-48-like) and bla(VIM)). 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.
引用
收藏
页码:2428 / 2436
页数:9
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