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Panton-Valentine leukocidin in community and hospital-acquired Staphylococcus aureus strains

Staphylococcus aureus causes serious hospital-acquired (HA) and community-acquired (CA) infections. Skin and soft-tissue infections especially are sometimes caused by strains harbouring Panton-Valentine leukocidin (PVL). PVL belongs to a family of bi-component leukocidal toxins produced by staphyloc...

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Autores principales: Özekinci, Tuncer, Dal, Tuba, Yanık, Keramettin, Özcan, Nida, Can, Şükran, Tekin, Alicem, Yıldırım, Halil İbrahim, Kandemir, İdris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433891/
https://www.ncbi.nlm.nih.gov/pubmed/26019595
http://dx.doi.org/10.1080/13102818.2014.976457
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author Özekinci, Tuncer
Dal, Tuba
Yanık, Keramettin
Özcan, Nida
Can, Şükran
Tekin, Alicem
Yıldırım, Halil İbrahim
Kandemir, İdris
author_facet Özekinci, Tuncer
Dal, Tuba
Yanık, Keramettin
Özcan, Nida
Can, Şükran
Tekin, Alicem
Yıldırım, Halil İbrahim
Kandemir, İdris
author_sort Özekinci, Tuncer
collection PubMed
description Staphylococcus aureus causes serious hospital-acquired (HA) and community-acquired (CA) infections. Skin and soft-tissue infections especially are sometimes caused by strains harbouring Panton-Valentine leukocidin (PVL). PVL belongs to a family of bi-component leukocidal toxins produced by staphylococci. It is a pore-forming toxin encoded by lukF-PV and lukS-PV. A total of 70 S. aureus strains: 38 (54%) methicillin-resistant (MRSA) and 32 (46%) methicillin-susceptible (MSSA), were isolated from patients admitted to Dicle University Hospital (Turkey). Identification of S. aureus and antibiotics-susceptibility testing were performed with PHOENIX 100. PVL genes and mecA genes were detected by polymerase chain reaction. Of the 70 studied strains, 36 ones (51%) were community acquired and 34 ones (49%) were hospital acquired . A total of 38 (54%) strains were positive for mecA (mecA (+)), of which 32 ones (84%) were HA. Of the mecA (−) strains, 30 (94%) were CA. Of the 70 studied strains, 12 (17%) strains were PVL(+): 8 (22%) of the 36 CA strains and 4 (12%) of the 34 HA strains. Of the 12 PVL(+) strains, 4 strains were mecA (+). The PVL positivity rate was 25% in MSSA, whereas 10.5% in MRSA. Of the overall PVL(+) strains, seven strains were obtained from wounds; four ones from skin abscess; and one from blood culture. Taken together, the obtained results showed a substantial level of PVL genes in the studied region. Although PVL is known as a common virulence factor of CA MRSA, HA MRSA isolates in our study showed a considerable rate of PVL positivity.
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spelling pubmed-44338912015-05-25 Panton-Valentine leukocidin in community and hospital-acquired Staphylococcus aureus strains Özekinci, Tuncer Dal, Tuba Yanık, Keramettin Özcan, Nida Can, Şükran Tekin, Alicem Yıldırım, Halil İbrahim Kandemir, İdris Biotechnol Biotechnol Equip Article; Medical Biotechnology Staphylococcus aureus causes serious hospital-acquired (HA) and community-acquired (CA) infections. Skin and soft-tissue infections especially are sometimes caused by strains harbouring Panton-Valentine leukocidin (PVL). PVL belongs to a family of bi-component leukocidal toxins produced by staphylococci. It is a pore-forming toxin encoded by lukF-PV and lukS-PV. A total of 70 S. aureus strains: 38 (54%) methicillin-resistant (MRSA) and 32 (46%) methicillin-susceptible (MSSA), were isolated from patients admitted to Dicle University Hospital (Turkey). Identification of S. aureus and antibiotics-susceptibility testing were performed with PHOENIX 100. PVL genes and mecA genes were detected by polymerase chain reaction. Of the 70 studied strains, 36 ones (51%) were community acquired and 34 ones (49%) were hospital acquired . A total of 38 (54%) strains were positive for mecA (mecA (+)), of which 32 ones (84%) were HA. Of the mecA (−) strains, 30 (94%) were CA. Of the 70 studied strains, 12 (17%) strains were PVL(+): 8 (22%) of the 36 CA strains and 4 (12%) of the 34 HA strains. Of the 12 PVL(+) strains, 4 strains were mecA (+). The PVL positivity rate was 25% in MSSA, whereas 10.5% in MRSA. Of the overall PVL(+) strains, seven strains were obtained from wounds; four ones from skin abscess; and one from blood culture. Taken together, the obtained results showed a substantial level of PVL genes in the studied region. Although PVL is known as a common virulence factor of CA MRSA, HA MRSA isolates in our study showed a considerable rate of PVL positivity. Taylor & Francis 2014-11-02 2014-11-07 /pmc/articles/PMC4433891/ /pubmed/26019595 http://dx.doi.org/10.1080/13102818.2014.976457 Text en © 2014 The Author(s). Published by Taylor & Francis. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Article; Medical Biotechnology
Özekinci, Tuncer
Dal, Tuba
Yanık, Keramettin
Özcan, Nida
Can, Şükran
Tekin, Alicem
Yıldırım, Halil İbrahim
Kandemir, İdris
Panton-Valentine leukocidin in community and hospital-acquired Staphylococcus aureus strains
title Panton-Valentine leukocidin in community and hospital-acquired Staphylococcus aureus strains
title_full Panton-Valentine leukocidin in community and hospital-acquired Staphylococcus aureus strains
title_fullStr Panton-Valentine leukocidin in community and hospital-acquired Staphylococcus aureus strains
title_full_unstemmed Panton-Valentine leukocidin in community and hospital-acquired Staphylococcus aureus strains
title_short Panton-Valentine leukocidin in community and hospital-acquired Staphylococcus aureus strains
title_sort panton-valentine leukocidin in community and hospital-acquired staphylococcus aureus strains
topic Article; Medical Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433891/
https://www.ncbi.nlm.nih.gov/pubmed/26019595
http://dx.doi.org/10.1080/13102818.2014.976457
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