Nasal carriage of sequence type 22 MRSA and livestock-associated ST398 clones in Tangier, Morocco

Introduction: This study aimed to provide data of Staphylococcus aureus and methicillin-resistant Staphylococcus aureus (MRSA) nasal carriage as well as to determine the genetic lineages of this circulating MRSA in the Tangier community. Methodology:  Between 2012 and 2013 two subpopulations con...

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Main Authors: Nadira Mourabit, Abdelhay Arakrak, Mohammed Bakkali, Amin Laglaoui
Format: Article
Language:English
Published: The Journal of Infection in Developing Countries 2017-07-01
Series:Journal of Infection in Developing Countries
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Online Access:https://jidc.org/index.php/journal/article/view/9235
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author Nadira Mourabit
Abdelhay Arakrak
Mohammed Bakkali
Amin Laglaoui
author_facet Nadira Mourabit
Abdelhay Arakrak
Mohammed Bakkali
Amin Laglaoui
author_sort Nadira Mourabit
collection DOAJ
description Introduction: This study aimed to provide data of Staphylococcus aureus and methicillin-resistant Staphylococcus aureus (MRSA) nasal carriage as well as to determine the genetic lineages of this circulating MRSA in the Tangier community. Methodology:  Between 2012 and 2013 two subpopulations consisting of randomly chosen healthy volunteers and outpatients in 11 healthcare facilities were screened. The antibiotic resistance phenotype was determined by disk diffusion. Toxin Panton-Valentin Leukocidin (PVL), toxic shock syndrome toxin-1 gene (tst), and mecA were detected by polymerase chain reaction (PCR). Nasal swabs were obtained from persons with no identified risk factors for MRSA acquisition. MRSA molecular typing was performed by pulsed-field gel electrophoresis (PFGE), staphylococcal chromosomal cassette mec, and Staphylococcus protein A (spa) typing. Results: A total of400 subjects (33.3%) were nasally colonized with S. aureus, and 17 (1.4%) were nasal carriers of MRSA. The analysis did not identify age, gender, and the two subpopulations as predictors for MRSA colonization. MRSA were more likely to harbor the tst gene (p < 0.05). This work highlighted a low prevalence of nasal MRSA carriage, with 52.94% belonging to sequence type (ST) ST22. The remaining isolates were distributed as singletons (ST8, ST1, and ST398), whereas approximately one-third of MRSA was not identified, including three novel spa-types (t13247, t13248, and t13249). Conclusions: Although we highlighted the current clones present in the Tangier community, they are limited in space and time. Therefore, further studies would be required to obtain a comprehensive picture of the dissemination of MRSA in the community, hospital, and livestock.
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spelling doaj-art-40eecafb2fed4a7c8697c34cdc9a48a52025-08-20T02:57:01ZengThe Journal of Infection in Developing CountriesJournal of Infection in Developing Countries1972-26802017-07-01110710.3855/jidc.9235Nasal carriage of sequence type 22 MRSA and livestock-associated ST398 clones in Tangier, MoroccoNadira Mourabit0Abdelhay Arakrak1Mohammed Bakkali2Amin Laglaoui3Faculté des Sciences et Techniques, Tangier, MoroccoFaculté des Sciences et Techniques, Tangier, MoroccoFaculté des Sciences et Techniques, Tangier, MoroccoFaculté des Sciences et Techniques, Tangier, Morocco Introduction: This study aimed to provide data of Staphylococcus aureus and methicillin-resistant Staphylococcus aureus (MRSA) nasal carriage as well as to determine the genetic lineages of this circulating MRSA in the Tangier community. Methodology:  Between 2012 and 2013 two subpopulations consisting of randomly chosen healthy volunteers and outpatients in 11 healthcare facilities were screened. The antibiotic resistance phenotype was determined by disk diffusion. Toxin Panton-Valentin Leukocidin (PVL), toxic shock syndrome toxin-1 gene (tst), and mecA were detected by polymerase chain reaction (PCR). Nasal swabs were obtained from persons with no identified risk factors for MRSA acquisition. MRSA molecular typing was performed by pulsed-field gel electrophoresis (PFGE), staphylococcal chromosomal cassette mec, and Staphylococcus protein A (spa) typing. Results: A total of400 subjects (33.3%) were nasally colonized with S. aureus, and 17 (1.4%) were nasal carriers of MRSA. The analysis did not identify age, gender, and the two subpopulations as predictors for MRSA colonization. MRSA were more likely to harbor the tst gene (p < 0.05). This work highlighted a low prevalence of nasal MRSA carriage, with 52.94% belonging to sequence type (ST) ST22. The remaining isolates were distributed as singletons (ST8, ST1, and ST398), whereas approximately one-third of MRSA was not identified, including three novel spa-types (t13247, t13248, and t13249). Conclusions: Although we highlighted the current clones present in the Tangier community, they are limited in space and time. Therefore, further studies would be required to obtain a comprehensive picture of the dissemination of MRSA in the community, hospital, and livestock. https://jidc.org/index.php/journal/article/view/9235Staphylococcus aureusNasal carriagenasal carriageST22MRSAST398
spellingShingle Nadira Mourabit
Abdelhay Arakrak
Mohammed Bakkali
Amin Laglaoui
Nasal carriage of sequence type 22 MRSA and livestock-associated ST398 clones in Tangier, Morocco
Journal of Infection in Developing Countries
Staphylococcus aureus
Nasal carriage
nasal carriage
ST22
MRSA
ST398
title Nasal carriage of sequence type 22 MRSA and livestock-associated ST398 clones in Tangier, Morocco
title_full Nasal carriage of sequence type 22 MRSA and livestock-associated ST398 clones in Tangier, Morocco
title_fullStr Nasal carriage of sequence type 22 MRSA and livestock-associated ST398 clones in Tangier, Morocco
title_full_unstemmed Nasal carriage of sequence type 22 MRSA and livestock-associated ST398 clones in Tangier, Morocco
title_short Nasal carriage of sequence type 22 MRSA and livestock-associated ST398 clones in Tangier, Morocco
title_sort nasal carriage of sequence type 22 mrsa and livestock associated st398 clones in tangier morocco
topic Staphylococcus aureus
Nasal carriage
nasal carriage
ST22
MRSA
ST398
url https://jidc.org/index.php/journal/article/view/9235
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AT abdelhayarakrak nasalcarriageofsequencetype22mrsaandlivestockassociatedst398clonesintangiermorocco
AT mohammedbakkali nasalcarriageofsequencetype22mrsaandlivestockassociatedst398clonesintangiermorocco
AT aminlaglaoui nasalcarriageofsequencetype22mrsaandlivestockassociatedst398clonesintangiermorocco