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Molecular characterization of Panton-Valentine leukocidin (PVL) toxin–encoding phages from South India
A total of 19 methicillin-resistant Staphylococcus aureus (MRSA) isolates were investigated for Panton-Valentine leukocidin (PVL) toxin, PVL gene sequence variation and PVL-encoding phages. Whole genome sequencing was performed for all isolates. Analysis of MRSA isolates (n = 19) confirmed that most...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682882/ https://www.ncbi.nlm.nih.gov/pubmed/29158906 http://dx.doi.org/10.1016/j.nmni.2017.08.005 |
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author | Yamuna, D.B. Francis, Y.I. Priya Doss, G. Balaji, V. |
author_facet | Yamuna, D.B. Francis, Y.I. Priya Doss, G. Balaji, V. |
author_sort | Yamuna, D.B. |
collection | PubMed |
description | A total of 19 methicillin-resistant Staphylococcus aureus (MRSA) isolates were investigated for Panton-Valentine leukocidin (PVL) toxin, PVL gene sequence variation and PVL-encoding phages. Whole genome sequencing was performed for all isolates. Analysis of MRSA isolates (n = 19) confirmed that most MRSA (n = 11) were positive for the PVL gene and were multidrug resistant. ST772-MRSA-V was the predominant PVL-positive MRSA clone, although all of them were found to carry the ΦIND772PVL phage in the genome. This study provides insights into the evolution of a new lineage of PVL-MRSA and highlights the potential risk of the emergence of multidrug-resistant community-acquired MRSA with high virulence. |
format | Online Article Text |
id | pubmed-5682882 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-56828822017-11-20 Molecular characterization of Panton-Valentine leukocidin (PVL) toxin–encoding phages from South India Yamuna, D.B. Francis, Y.I. Priya Doss, G. Balaji, V. New Microbes New Infect New Resistant Microbes in Human A total of 19 methicillin-resistant Staphylococcus aureus (MRSA) isolates were investigated for Panton-Valentine leukocidin (PVL) toxin, PVL gene sequence variation and PVL-encoding phages. Whole genome sequencing was performed for all isolates. Analysis of MRSA isolates (n = 19) confirmed that most MRSA (n = 11) were positive for the PVL gene and were multidrug resistant. ST772-MRSA-V was the predominant PVL-positive MRSA clone, although all of them were found to carry the ΦIND772PVL phage in the genome. This study provides insights into the evolution of a new lineage of PVL-MRSA and highlights the potential risk of the emergence of multidrug-resistant community-acquired MRSA with high virulence. Elsevier 2017-08-25 /pmc/articles/PMC5682882/ /pubmed/29158906 http://dx.doi.org/10.1016/j.nmni.2017.08.005 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | New Resistant Microbes in Human Yamuna, D.B. Francis, Y.I. Priya Doss, G. Balaji, V. Molecular characterization of Panton-Valentine leukocidin (PVL) toxin–encoding phages from South India |
title | Molecular characterization of Panton-Valentine leukocidin (PVL) toxin–encoding phages from South India |
title_full | Molecular characterization of Panton-Valentine leukocidin (PVL) toxin–encoding phages from South India |
title_fullStr | Molecular characterization of Panton-Valentine leukocidin (PVL) toxin–encoding phages from South India |
title_full_unstemmed | Molecular characterization of Panton-Valentine leukocidin (PVL) toxin–encoding phages from South India |
title_short | Molecular characterization of Panton-Valentine leukocidin (PVL) toxin–encoding phages from South India |
title_sort | molecular characterization of panton-valentine leukocidin (pvl) toxin–encoding phages from south india |
topic | New Resistant Microbes in Human |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682882/ https://www.ncbi.nlm.nih.gov/pubmed/29158906 http://dx.doi.org/10.1016/j.nmni.2017.08.005 |
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