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A prospective surveillance study to determine the prevalence of 16S rRNA methyltransferase-producing Gram-negative bacteria in the UK.
Taylor, Emma; Bal, Abhijit M; Balakrishnan, Indran; Brown, Nicholas M; Burns, Phillipa; Clark, Marilyn; Diggle, Mathew; Donaldson, Hugo; Eltringham, Ian; Folb, Jonathan; Gadsby, Naomi; Macleod, Mairi; Ratnaraja, Natasha V D V; Williams, Cheryl; Wootton, Mandy; Sriskandan, Shiranee; Woodford, Neil; Hopkins, Katie L.
Afiliación
  • Taylor E; National Institute for Health Research Health Protection Research Unit (NIHR HPRU) in Healthcare Associated Infections and Antimicrobial Resistance at Imperial College London, Hammersmith Hospital, Du Cane Road, London, W12 0NN, UK.
  • Bal AM; Antimicrobial Resistance and Healthcare Associated Infections (AMRHAI) Reference Unit, National Infection Service, Public Health England, London, NW9 5EQ, UK.
  • Balakrishnan I; Microbiology, University Hospital Crosshouse, NHS Ayrshire and Arran, Kilmarnock, KA2 0BE, UK.
  • Brown NM; Royal Free London NHS Foundation Trust, Pond St, London, NW3 2QG, UK.
  • Burns P; Clinical Microbiology and Public Health Laboratory Cambridge University Hospitals NHS Foundation Trust, Cambridge, CB2 0QW, UK.
  • Clark M; Manchester Medical Microbiology Partnership, Manchester University NHS Foundation Trust, Manchester Royal Infirmary, Oxford Rd, Manchester, M13 9WL, UK.
  • Diggle M; Department of Medical Microbiology, Ninewells Hospital, Dundee, DD2 1SY, UK.
  • Donaldson H; Nottingham University Hospitals National Health Service Trust, Hucknall Rd, Nottingham, NG5 1PB, UK.
  • Eltringham I; Imperial College Healthcare NHS Trust, Charing Cross Hospital, Fulham Palace Road, London, W6 8RF, UK.
  • Folb J; Microbiology Department, King's College Hospital NHS Foundation Trust, Denmark Hill, London, SE5 9RS, UK.
  • Gadsby N; Liverpool University Hospitals NHS Foundation Trust, Prescot St, Liverpool, L7 8XP, UK.
  • Macleod M; Medical Microbiology, Department of Laboratory Medicine, Royal Infirmary of Edinburgh, 51 Little France Cres, Edinburgh, EH16 4SA, UK.
  • Ratnaraja NVDV; Clinical Microbiology, Glasgow Royal Infirmary Hospital, Level 4 New Lister Building, 10-16 Alexandra Parade, Glasgow, G31 2ER, UK.
  • Williams C; Department of Microbiology, Sandwell and West Birmingham NHS Trust, Dudley Road, Birmingham, B18 7QH, UK.
  • Wootton M; Microbiology Laboratory, First Floor, Pathology Laboratory, Royal Oldham Hospital, Rochdale Road, Oldham, OL1 2JH, UK.
  • Sriskandan S; Public Health Wales Microbiology Cardiff, University Hospital of Wales, Cardiff, CF14 4XW, UK.
  • Woodford N; National Institute for Health Research Health Protection Research Unit (NIHR HPRU) in Healthcare Associated Infections and Antimicrobial Resistance at Imperial College London, Hammersmith Hospital, Du Cane Road, London, W12 0NN, UK.
  • Hopkins KL; MRC Centre for Molecular Bacteriology & Infection, Imperial College London, London, SW7 2DD, UK.
J Antimicrob Chemother ; 76(9): 2428-2436, 2021 08 12.
Article en En | MEDLINE | ID: mdl-34142130
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Farmacorresistencia Bacteriana / Bacterias Gramnegativas Tipo de estudio: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Humans / Male País/Región como asunto: Europa Idioma: En Revista: J Antimicrob Chemother Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Farmacorresistencia Bacteriana / Bacterias Gramnegativas Tipo de estudio: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Humans / Male País/Región como asunto: Europa Idioma: En Revista: J Antimicrob Chemother Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido