Methicillin-resistant Staphylococcus aureus (MRSA) nasal carriage among patients with diabetes at the Korle Bu Teaching Hospital.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 13 01 2021
accepted: 20 08 2021
entrez: 17 9 2021
pubmed: 18 9 2021
medline: 19 11 2021
Statut: epublish

Résumé

To investigate the epidemiology of S. aureus and MRSA nasal carriage among people with diabetes at the Korle Bu Teaching Hospital in Accra, including the prevalence, predictors of carriage, and antibiotic resistance. This study was cross-sectional, involving 300 diabetes patients and 106 non-diabetic individuals. Swab specimens of the nares were obtained from the participants and bacteriologically-cultured. Identification and characterization of S. aureus and MRSA were based on standard bacteriological methods; antimicrobial susceptibility testing was by the Kirby-Bauer method. The prevalence of staphylococcal carriage, the diabetes group relative to the non-diabetes group, were 31.0% and 10.4% (S. aureus), and 3.3% and 0.0% (MRSA). Presence of diabetes predisposed to S. aureus carriage, but not MRSA nor coagulase-negative staphylococci (CoNS) carriage (OR = 3.88; p < 0.0001). Colonization with CoNS was protective of S. aureus (OR = 0.039, p < 0.001) and MRSA (OR = 0.115, p = 0.043) colonization among the diabetics. The antimicrobial resistance patterns recorded among the S. aureus isolated from the diabetic individuals relative to the non-diabetics were as follows: penicillin (95% vs. 91%), tetracycline (37% vs. 27%), cotrimoxazole (30% vs. 36%), erythromycin (17% vs. 0%), norfloxacin (13% vs. 0%), clindamycin (12% vs. 0%), gentamicin (9% vs. 0%), fusidic acid (10% vs. 9%), linezolid (4% vs. 0%), and rifampicin (5% vs. 0%). The proportion of multidrug resistant S. aureus was 41% (n = 38) in the diabetes group and 0% in the non-diabetes group; this difference was statistically significant (p = 0.01). The presence of diabetes predisposed the participants to S. aureus carriage by almost four folds, but not MRSA carriage. Colonization with CoNS was protective of S. aureus and MRSA carriage in the diabetes group. Finally, linezolid remains a good therapeutic agent for anti-MRSA therapy.

Identifiants

pubmed: 34534230
doi: 10.1371/journal.pone.0257004
pii: PONE-D-21-01107
pmc: PMC8448364
doi:

Substances chimiques

Anti-Bacterial Agents 0
Gentamicins 0
Penicillins 0
Clindamycin 3U02EL437C
Fusidic Acid 59XE10C19C
Erythromycin 63937KV33D
Trimethoprim, Sulfamethoxazole Drug Combination 8064-90-2
Tetracycline F8VB5M810T
Linezolid ISQ9I6J12J
Norfloxacin N0F8P22L1P
Rifampin VJT6J7R4TR

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0257004

Déclaration de conflit d'intérêts

FCNK and M-MO are affiliated with FleRhoLife Research Consult, but this firm didnot provide financial support nor play a role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

Références

J Antimicrob Chemother. 2004 Mar;53(3):474-9
pubmed: 14762054
J Microbiol Immunol Infect. 2020 Apr;53(2):292-299
pubmed: 29907536
J Antimicrob Chemother. 2012 Feb;67(2):326-9
pubmed: 22146878
AIDS Res Ther. 2012 Nov 06;9(1):33
pubmed: 23126233
Pathogens. 2019 Mar 17;8(1):
pubmed: 30884909
Am J Infect Control. 2013 Nov;41(11):1100-1
pubmed: 23663856
Clin Microbiol Rev. 1997 Jul;10(3):505-20
pubmed: 9227864
Epidemiol Infect. 1995 Aug;115(1):51-60
pubmed: 7641838
Diagn Microbiol Infect Dis. 2013 Jul;76(3):372-4
pubmed: 23602786
Cell Host Microbe. 2017 Dec 13;22(6):746-756.e5
pubmed: 29199097
Am J Infect Control. 2015 Apr 1;43(4):329-35
pubmed: 25687358
Bacteriol Rev. 1963 Mar;27:56-71
pubmed: 14000926
Epidemiol Infect. 2013 Jun;141(6):1166-79
pubmed: 22929058
J Clin Microbiol. 2007 Apr;45(4):1350-2
pubmed: 17287335
J Acquir Immune Defic Syndr. 2008 Aug 15;48(5):567-71
pubmed: 18645516
J Glob Antimicrob Resist. 2013 Dec;1(4):189-193
pubmed: 27873611
J Bacteriol. 2014 Oct;196(19):3482-93
pubmed: 25070736
Infect Immun. 2004 Nov;72(11):6685-8
pubmed: 15501803
BMC Res Notes. 2013 Aug 27;6:336
pubmed: 23981343
Ren Fail. 2002 Nov;24(6):763-77
pubmed: 12472199
Diabet Med. 2000 Jun;17(6):487-8
pubmed: 10975221
J Antimicrob Chemother. 2012 May;67(5):1267-70
pubmed: 22311935
Vet Dermatol. 2013 Oct;24(5):538-e128
pubmed: 23869430
N Engl J Med. 2006 Aug 17;355(7):666-74
pubmed: 16914702
Am J Infect Control. 2012 May;40(4):365-8
pubmed: 21864943
Int J Antimicrob Agents. 2013 Nov;42(5):450-5
pubmed: 23993067
Clin Microbiol Rev. 1997 Oct;10(4):781-91
pubmed: 9336672
Nat Rev Microbiol. 2009 Sep;7(9):629-41
pubmed: 19680247
J Int Assoc Provid AIDS Care. 2016 Mar-Apr;15(2):141-7
pubmed: 25331220
Antimicrob Agents Chemother. 2011 Apr;55(4):1598-605
pubmed: 21220533
Pan Afr Med J. 2017 Feb 02;26:60
pubmed: 28451037
Lancet Infect Dis. 2005 Dec;5(12):751-62
pubmed: 16310147
Nature. 2010 May 20;465(7296):346-9
pubmed: 20485435
Pathogens. 2020 Apr 28;9(5):
pubmed: 32354004
Infect Drug Resist. 2018 Oct 11;11:1757-1765
pubmed: 30349333
Lancet. 2004 Jun 5;363(9424):1871-2
pubmed: 15183627
J Diabetes Investig. 2017 May;8(3):383-391
pubmed: 27808480
J Diabetes Complications. 2015 Nov-Dec;29(8):1092-7
pubmed: 26243688
BMC Res Notes. 2015 Dec 01;8:742
pubmed: 26628056
Public Health Rep. 2007 Mar-Apr;122(2):160-6
pubmed: 17357358
Annu Rev Biochem. 2015;84:577-601
pubmed: 26034890
Clin Infect Dis. 2012 Sep;55 Suppl 3:S173-80
pubmed: 22903949
PLoS One. 2014 Apr 23;9(4):e96119
pubmed: 24760001
J Med Microbiol. 1995 Feb;42(2):127-32
pubmed: 7869348
N Engl J Med. 2001 Jan 4;344(1):11-6
pubmed: 11136954
Nat Rev Microbiol. 2005 Dec;3(12):948-58
pubmed: 16322743
J Infect Dev Ctries. 2016 May 31;10(5):453-6
pubmed: 27249519
BMJ Open. 2013 Mar 05;3(3):
pubmed: 23468471

Auteurs

Ramzy B Anafo (RB)

Department of Medical Microbiology, University of Ghana Medical School, Korle Bu, Accra, Ghana.

Yacoba Atiase (Y)

Department of Medicine, University of Ghana Medical School, Korle Bu, Accra, Ghana.

Fleischer C N Kotey (FCN)

Department of Medical Microbiology, University of Ghana Medical School, Korle Bu, Accra, Ghana.
FleRhoLife Research Consult, Teshie, Accra, Ghana.

Nicholas T K D Dayie (NTKD)

Department of Medical Microbiology, University of Ghana Medical School, Korle Bu, Accra, Ghana.

Patience B Tetteh-Quarcoo (PB)

Department of Medical Microbiology, University of Ghana Medical School, Korle Bu, Accra, Ghana.

Samuel Duodu (S)

Department of Biochemistry, Cell and Molecular Biology and West African Centre for Cell Biology of Infectious Pathogens, University of Ghana, Legon, Accra, Ghana.

Mary-Magdalene Osei (MM)

Department of Medical Microbiology, University of Ghana Medical School, Korle Bu, Accra, Ghana.
FleRhoLife Research Consult, Teshie, Accra, Ghana.

Khalid J Alzahrani (KJ)

Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Taif University, Taif, Saudi Arabia.

Eric S Donkor (ES)

Department of Medical Microbiology, University of Ghana Medical School, Korle Bu, Accra, Ghana.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH