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Phenotypic and molecular characterization of Staphylococcus aureus from mobile phones in Nigeria
The presence of Staphylococcus aureus, a normal human flora on cellphones of different professionals in Ile-Ife was investigated with a view to determining their antibiotic susceptibility profile and nature of resistance and virulence genes. One hundred swab samples were collected aseptically from m...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AIMS Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10462460/ https://www.ncbi.nlm.nih.gov/pubmed/37649800 http://dx.doi.org/10.3934/microbiol.2023021 |
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author | Oluduro, Anthonia O. Adesiyan, Yetunde M. Omoboye, Olumide O. Odeyemi, Adebowale T. |
author_facet | Oluduro, Anthonia O. Adesiyan, Yetunde M. Omoboye, Olumide O. Odeyemi, Adebowale T. |
author_sort | Oluduro, Anthonia O. |
collection | PubMed |
description | The presence of Staphylococcus aureus, a normal human flora on cellphones of different professionals in Ile-Ife was investigated with a view to determining their antibiotic susceptibility profile and nature of resistance and virulence genes. One hundred swab samples were collected aseptically from mobile phones of various users based on their profession. Surfaces of the mobile phones were swabbed and the streak plate method was used to isolate colonies showing characteristic golden yellow on mannitol salt agar plates. These isolates were further identified using standard microbiological methods. The antibiotic susceptibility of the isolates was determined using Kirby-Bauer's disk diffusion technique. Molecular detection of nuc, mecA and pvl genes in some isolates was carried out by polymerase chain reaction technique. All the 36 isolates obtained in this study were 100% resistant to amoxicillin and augmentin; the isolates also displayed 55.6%, 44.4% and 41.7% resistance to ceftriazone, erythromycin and chloramphenicol, respectively. Based on resistance to oxacillin, prevalence of methicillin resistant Staphylococcus aureus (MRSA) was 11.1%. Only one S. aureus was positive for plasmid analysis. MecA gene was genetically confirmed in four (4) out of the 16 suspected phenotypic MRSA strains, nuc gene was confirmed in all 28 isolates investigated, while there was no pvl gene in the strains investigated. Mobile phones harbor multiple antibiotics resistant S. aureus, which are responsible for important diseases in humans and could be difficult to manage with antibiotics thereby posing serious health risks. |
format | Online Article Text |
id | pubmed-10462460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | AIMS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-104624602023-08-30 Phenotypic and molecular characterization of Staphylococcus aureus from mobile phones in Nigeria Oluduro, Anthonia O. Adesiyan, Yetunde M. Omoboye, Olumide O. Odeyemi, Adebowale T. AIMS Microbiol Research Article The presence of Staphylococcus aureus, a normal human flora on cellphones of different professionals in Ile-Ife was investigated with a view to determining their antibiotic susceptibility profile and nature of resistance and virulence genes. One hundred swab samples were collected aseptically from mobile phones of various users based on their profession. Surfaces of the mobile phones were swabbed and the streak plate method was used to isolate colonies showing characteristic golden yellow on mannitol salt agar plates. These isolates were further identified using standard microbiological methods. The antibiotic susceptibility of the isolates was determined using Kirby-Bauer's disk diffusion technique. Molecular detection of nuc, mecA and pvl genes in some isolates was carried out by polymerase chain reaction technique. All the 36 isolates obtained in this study were 100% resistant to amoxicillin and augmentin; the isolates also displayed 55.6%, 44.4% and 41.7% resistance to ceftriazone, erythromycin and chloramphenicol, respectively. Based on resistance to oxacillin, prevalence of methicillin resistant Staphylococcus aureus (MRSA) was 11.1%. Only one S. aureus was positive for plasmid analysis. MecA gene was genetically confirmed in four (4) out of the 16 suspected phenotypic MRSA strains, nuc gene was confirmed in all 28 isolates investigated, while there was no pvl gene in the strains investigated. Mobile phones harbor multiple antibiotics resistant S. aureus, which are responsible for important diseases in humans and could be difficult to manage with antibiotics thereby posing serious health risks. AIMS Press 2023-04-23 /pmc/articles/PMC10462460/ /pubmed/37649800 http://dx.doi.org/10.3934/microbiol.2023021 Text en © 2023 the Author(s), licensee AIMS Press https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ) |
spellingShingle | Research Article Oluduro, Anthonia O. Adesiyan, Yetunde M. Omoboye, Olumide O. Odeyemi, Adebowale T. Phenotypic and molecular characterization of Staphylococcus aureus from mobile phones in Nigeria |
title | Phenotypic and molecular characterization of Staphylococcus aureus from mobile phones in Nigeria |
title_full | Phenotypic and molecular characterization of Staphylococcus aureus from mobile phones in Nigeria |
title_fullStr | Phenotypic and molecular characterization of Staphylococcus aureus from mobile phones in Nigeria |
title_full_unstemmed | Phenotypic and molecular characterization of Staphylococcus aureus from mobile phones in Nigeria |
title_short | Phenotypic and molecular characterization of Staphylococcus aureus from mobile phones in Nigeria |
title_sort | phenotypic and molecular characterization of staphylococcus aureus from mobile phones in nigeria |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10462460/ https://www.ncbi.nlm.nih.gov/pubmed/37649800 http://dx.doi.org/10.3934/microbiol.2023021 |
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