Staphylococcus aureus colonization and acquisition of skin and soft tissue infection among Royal Marines recruits: a prospective cohort study.


Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 28 04 2019
revised: 03 07 2019
accepted: 13 07 2019
pubmed: 30 7 2019
medline: 2 10 2020
entrez: 30 7 2019
Statut: ppublish

Résumé

Skin and soft tissue infections (SSTIs) are a serious health issue for military personnel. Of particular importance are those caused by methicillin-resistant Staphylococcus aureus and Panton-Valentine leucocidin (PVL)-positive S. aureus (PVL-SA), as they have been associated with outbreaks of SSTIs. A prospective observational study was conducted in Royal Marine (RM) recruits to investigate the prevalence of PVL-SA carriage and any association with SSTIs. A total of 1012 RM recruits were followed through a 32-week training programme, with nose and throat swabs obtained at weeks 1, 6, 15 and 32. S. aureus isolates were characterized by antibiotic susceptibility testing, spa typing, presence of mecA/C and PVL genes. Retrospective review of the clinical notes for SSTI acquisition was conducted. S. aureus colonization decreased from Week 1 to Week 32 (41% to 26%, p < 0.0001). Of 1168 S. aureus isolates, three out of 1168 (0.3%) were MRSA and ten out of 1168 (0.9%) PVL-positive (all MSSA) and 169 out of 1168 (14.5%) were resistant to clindamycin. Isolates showed genetic diversity with 238 different spa types associated with 25 multi-locus sequence type (MLST) clonal complexes. SSTIs were seen in 35% (351/989) of recruits with 3 training days lost per recruit. SSTI acquisition rate was reduced amongst persistent carriers (p < 0.0283). Nose and throat carriage of MRSA and PVL-SA was low among recruits, despite a high incidence of SSTIs being reported, particularly cellulitis. Carriage strains were predominantly MSSA with a marked diversity of genotypes. Persistent nose and/or throat carriage was not associated with SSTI acquisition. Putative person-to-person transmission within troops was identified based on spa typing requiring further research to confirm and explore potential transmission routes.

Identifiants

pubmed: 31357012
pii: S1198-743X(19)30403-3
doi: 10.1016/j.cmi.2019.07.014
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

381.e1-381.e6

Subventions

Organisme : Medical Research Council
ID : MR/R015600/1
Pays : United Kingdom

Informations de copyright

Copyright © 2019. Published by Elsevier Ltd.

Auteurs

E Jauneikaite (E)

Department of Medicine, Imperial College London, London, UK; NIHR Health Protection Research Unit in Antimicrobial Resistance and Healthcare-associated Infections, Imperial College London, London, UK; Department of Infectious Disease Epidemiology, Imperial College London, London, UK.

T Ferguson (T)

Department of Medicine, Imperial College London, London, UK.

M Mosavie (M)

Department of Medicine, Imperial College London, London, UK; NIHR Health Protection Research Unit in Antimicrobial Resistance and Healthcare-associated Infections, Imperial College London, London, UK.

J L Fallowfield (JL)

Institute of Naval Medicine, Alverstoke, UK.

T Davey (T)

Institute of Naval Medicine, Alverstoke, UK.

N Thorpe (N)

Institute of Naval Medicine, Alverstoke, UK.

A Allsopp (A)

Institute of Naval Medicine, Alverstoke, UK.

A M Shaw (AM)

Institute of Naval Medicine, Alverstoke, UK.

D Fudge (D)

Academic Department of Military Medicine, Royal Centre for Defence Medicine (Research and Academia), Birmingham, UK.

M K O'Shea (MK)

Academic Department of Military Medicine, Royal Centre for Defence Medicine (Research and Academia), Birmingham, UK; Institute of Microbiology and Infection, The University of Birmingham, Birmingham, UK.

D Wilson (D)

Academic Department of Military Medicine, Royal Centre for Defence Medicine (Research and Academia), Birmingham, UK.

M Morgan (M)

Department of Microbiology, Royal Devon and Exeter Hospital, Exeter, UK.

B Pichon (B)

Healthcare Associated Infections and Antimicrobial Resistance Division, National Infection Service, Public Health England, London, UK.

A M Kearns (AM)

Healthcare Associated Infections and Antimicrobial Resistance Division, National Infection Service, Public Health England, London, UK.

S Sriskandan (S)

Department of Medicine, Imperial College London, London, UK; NIHR Health Protection Research Unit in Antimicrobial Resistance and Healthcare-associated Infections, Imperial College London, London, UK.

L E Lamb (LE)

Department of Medicine, Imperial College London, London, UK; Academic Department of Military Medicine, Royal Centre for Defence Medicine (Research and Academia), Birmingham, UK; Royal Free London NHS Foundation Trust, London, UK. Electronic address: lucylamb@nhs.net.

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Classifications MeSH