Absence of the mecC gene in methicillin-resistant Staphylococcus aureus isolated from various clinical samples: The first multi-centered study in Turkey.


Journal

Journal of infection and public health
ISSN: 1876-035X
Titre abrégé: J Infect Public Health
Pays: England
ID NLM: 101487384

Informations de publication

Date de publication:
Historique:
received: 24 10 2018
revised: 21 01 2019
accepted: 23 01 2019
pubmed: 13 2 2019
medline: 15 11 2019
entrez: 13 2 2019
Statut: ppublish

Résumé

mecA is a predefined gene causing methicillin resistance in Staphylococcus aureus (S. aureus) isolates; however, it has been shown that some methicillin-resistant S. aureus (MRSA) strains do not carry this gene. Recently, in isolates found to be MRSA-positive but mecA-negative, a new resistance gene called mecC, which is a homolog of mecA, has been reported. This study aimed to investigate the mecC and mecA genes in MRSA strains isolated from different geographic regions in Turkey. The sample of the study consisted of 494 MRSA strains isolated from seven geographical regions in Turkey between 2013 and 2016. The strains were obtained from 17 centers, comprising 13 university hospitals, three education and research hospitals, and one state hospital. Methicillin resistance in S. aureus strains was determined using the agar disk diffusion method with a cefoxitin disk and the agar dilution method with oxacillin. The mecC and mecA genes in MRSA strains was investigated by Polymerase Chain Reaction (PCR). Of the MRSA strains investigated, 47.9% were isolated from intensive care units. Concerning sample type, 36.7% were detected in the respiratory tract (tracheal aspirate, sputum, etc.), 24.8% in blood, 18.7% in skin and soft tissues, 9.3% in nasal swabs, 5.4% in urine, 4.1% in ears, and 1% in sterile body fluid. Using PCR, mecC was not identified in any of the S. aureus strains isolated from different clinical microbiology laboratories. mecA gene positivity was found in 315 of the MRSA strains (63.8%). Staphylococcal Cassette Chromosome mec (SCCmec) type was identified in 232 strains (46.9%), of which 136 (58.7%) were type II, 75 (32.4%) were type IV, 12 (5.1%) were type IIIb, six (2.5%) were type I, and three (1.3%) were type III. This is the first multi-centered study to investigate MRSA strains isolated from different regions in Turkey. The mecC gene was not detected in any of the MRSA strains. We believe that this study will constitute an important basis for monitoring possible future changes.

Sections du résumé

BACKGROUND BACKGROUND
mecA is a predefined gene causing methicillin resistance in Staphylococcus aureus (S. aureus) isolates; however, it has been shown that some methicillin-resistant S. aureus (MRSA) strains do not carry this gene. Recently, in isolates found to be MRSA-positive but mecA-negative, a new resistance gene called mecC, which is a homolog of mecA, has been reported. This study aimed to investigate the mecC and mecA genes in MRSA strains isolated from different geographic regions in Turkey.
METHODS METHODS
The sample of the study consisted of 494 MRSA strains isolated from seven geographical regions in Turkey between 2013 and 2016. The strains were obtained from 17 centers, comprising 13 university hospitals, three education and research hospitals, and one state hospital. Methicillin resistance in S. aureus strains was determined using the agar disk diffusion method with a cefoxitin disk and the agar dilution method with oxacillin. The mecC and mecA genes in MRSA strains was investigated by Polymerase Chain Reaction (PCR).
RESULTS RESULTS
Of the MRSA strains investigated, 47.9% were isolated from intensive care units. Concerning sample type, 36.7% were detected in the respiratory tract (tracheal aspirate, sputum, etc.), 24.8% in blood, 18.7% in skin and soft tissues, 9.3% in nasal swabs, 5.4% in urine, 4.1% in ears, and 1% in sterile body fluid. Using PCR, mecC was not identified in any of the S. aureus strains isolated from different clinical microbiology laboratories. mecA gene positivity was found in 315 of the MRSA strains (63.8%). Staphylococcal Cassette Chromosome mec (SCCmec) type was identified in 232 strains (46.9%), of which 136 (58.7%) were type II, 75 (32.4%) were type IV, 12 (5.1%) were type IIIb, six (2.5%) were type I, and three (1.3%) were type III.
CONCLUSION CONCLUSIONS
This is the first multi-centered study to investigate MRSA strains isolated from different regions in Turkey. The mecC gene was not detected in any of the MRSA strains. We believe that this study will constitute an important basis for monitoring possible future changes.

Identifiants

pubmed: 30745200
pii: S1876-0341(19)30065-6
doi: 10.1016/j.jiph.2019.01.063
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Bacterial Proteins 0
Penicillin-Binding Proteins 0
mecA protein, Staphylococcus aureus 0
Methicillin Q91FH1328A

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

528-533

Informations de copyright

Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

Aytekin Cikman (A)

Erzincan Binali Yildirim University, Faculty of Medicine, Department of Medical Microbiology, Erzincan, Turkey.

Merve Aydin (M)

Erzincan Binali Yildirim University, Faculty of Medicine, Department of Medical Microbiology, Erzincan, Turkey; KTO Karatay University, Faculty of Medicine, Department of Medical Microbiology, Konya, Turkey. Electronic address: merve.aydin@karatay.edu.tr.

Baris Gulhan (B)

Erzincan Binali Yildirim University, Faculty of Medicine, Department of Medical Microbiology, Erzincan, Turkey.

Faruk Karakecili (F)

Erzincan Binali Yildirim University, Faculty of Medicine, Department of Infectious Diseases and Clinical Microbiology, Erzincan, Turkey.

Muhammet G Kurtoglu (MG)

Abant Izzet Baysal University, Faculty of Medicine, Department of Medical Microbiology, Bolu, Turkey.

Serife Yuksekkaya (S)

Konya Training and Research Hospital, Microbiology Laboratory, Konya, Turkey.

Mehmet Parlak (M)

Yuzuncu Yil University, Faculty of Medicine, Department of Medical Microbiology, Van, Turkey.

Bilge S Gultepe (BS)

Bezmi-Alem University, Faculty of Medicine, Department of Medical Microbiology, Istanbul, Turkey.

Aysegul C Cicek (AC)

Recep Tayyip Erdogan University, Faculty of Medicine, Department of Medical Microbiology, Rize, Turkey.

Fulya B Bilman (FB)

Izmir Menemen State Hospital, Department of Medical Microbiology, Izmir, Turkey.

Ihsan H Ciftci (IH)

Sakarya University, Faculty of Medicine, Department of Medical Microbiology, Sakarya, Turkey.

Murat Kara (M)

Erzincan Binali Yildirim University, Faculty of Medicine, Department of Medical Microbiology, Erzincan, Turkey.

Selahattin Atmaca (S)

Dicle University, Faculty of Medicine, Department of Medical Microbiology, Diyarbakır, Turkey.

Tuncer Ozekinci (T)

Dicle University, Faculty of Medicine, Department of Medical Microbiology, Diyarbakır, Turkey.

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