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Commercial Biocides Induce Transfer of Prophage Φ13 from Human Strains of Staphylococcus aureus to Livestock CC398

Human strains of Staphylococcus aureus commonly carry the bacteriophage ΦSa3 that encodes immune evasion factors. Recently, this prophage has been found in livestock-associated, methicillin resistant S. aureus (MRSA) CC398 strains where it may promote human colonization. Here, we have addressed if e...

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Autores principales: Tang, Yuanyue, Nielsen, Lene N., Hvitved, Annemette, Haaber, Jakob K., Wirtz, Christiane, Andersen, Paal S., Larsen, Jesper, Wolz, Christiane, Ingmer, Hanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726172/
https://www.ncbi.nlm.nih.gov/pubmed/29270158
http://dx.doi.org/10.3389/fmicb.2017.02418
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author Tang, Yuanyue
Nielsen, Lene N.
Hvitved, Annemette
Haaber, Jakob K.
Wirtz, Christiane
Andersen, Paal S.
Larsen, Jesper
Wolz, Christiane
Ingmer, Hanne
author_facet Tang, Yuanyue
Nielsen, Lene N.
Hvitved, Annemette
Haaber, Jakob K.
Wirtz, Christiane
Andersen, Paal S.
Larsen, Jesper
Wolz, Christiane
Ingmer, Hanne
author_sort Tang, Yuanyue
collection PubMed
description Human strains of Staphylococcus aureus commonly carry the bacteriophage ΦSa3 that encodes immune evasion factors. Recently, this prophage has been found in livestock-associated, methicillin resistant S. aureus (MRSA) CC398 strains where it may promote human colonization. Here, we have addressed if exposure to biocidal products induces phage transfer, and find that during co-culture, Φ13 from strain 8325, belonging to ΦSa3 group, is induced and transferred from a human strain to LA-MRSA CC398 when exposed to sub-lethal concentrations of commercial biocides containing hydrogen peroxide. Integration of ΦSa3 in LA-MRSA CC398 occurs at multiple positions and the integration site influences the stability of the prophage. We did not observe integration in hlb encoding β-hemolysin that contains the preferred ΦSa3 attachment site in human strains, and we demonstrate that this is due to allelic variation in CC398 strains that disrupts the phage attachment site, but not the expression of β-hemolysin. Our results show that hydrogen peroxide present in biocidal products stimulate transfer of ΦSa3 from human to LA-MRSA CC398 strains and that in these strains prophage stability depends on the integration site. Knowledge of ΦSa3 transfer and stability between human and livestock strains may lead to new intervention measures directed at reducing human infection by LA-MRSA strains.
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spelling pubmed-57261722017-12-21 Commercial Biocides Induce Transfer of Prophage Φ13 from Human Strains of Staphylococcus aureus to Livestock CC398 Tang, Yuanyue Nielsen, Lene N. Hvitved, Annemette Haaber, Jakob K. Wirtz, Christiane Andersen, Paal S. Larsen, Jesper Wolz, Christiane Ingmer, Hanne Front Microbiol Microbiology Human strains of Staphylococcus aureus commonly carry the bacteriophage ΦSa3 that encodes immune evasion factors. Recently, this prophage has been found in livestock-associated, methicillin resistant S. aureus (MRSA) CC398 strains where it may promote human colonization. Here, we have addressed if exposure to biocidal products induces phage transfer, and find that during co-culture, Φ13 from strain 8325, belonging to ΦSa3 group, is induced and transferred from a human strain to LA-MRSA CC398 when exposed to sub-lethal concentrations of commercial biocides containing hydrogen peroxide. Integration of ΦSa3 in LA-MRSA CC398 occurs at multiple positions and the integration site influences the stability of the prophage. We did not observe integration in hlb encoding β-hemolysin that contains the preferred ΦSa3 attachment site in human strains, and we demonstrate that this is due to allelic variation in CC398 strains that disrupts the phage attachment site, but not the expression of β-hemolysin. Our results show that hydrogen peroxide present in biocidal products stimulate transfer of ΦSa3 from human to LA-MRSA CC398 strains and that in these strains prophage stability depends on the integration site. Knowledge of ΦSa3 transfer and stability between human and livestock strains may lead to new intervention measures directed at reducing human infection by LA-MRSA strains. Frontiers Media S.A. 2017-12-07 /pmc/articles/PMC5726172/ /pubmed/29270158 http://dx.doi.org/10.3389/fmicb.2017.02418 Text en Copyright © 2017 Tang, Nielsen, Hvitved, Haaber, Wirtz, Andersen, Larsen, Wolz and Ingmer. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Tang, Yuanyue
Nielsen, Lene N.
Hvitved, Annemette
Haaber, Jakob K.
Wirtz, Christiane
Andersen, Paal S.
Larsen, Jesper
Wolz, Christiane
Ingmer, Hanne
Commercial Biocides Induce Transfer of Prophage Φ13 from Human Strains of Staphylococcus aureus to Livestock CC398
title Commercial Biocides Induce Transfer of Prophage Φ13 from Human Strains of Staphylococcus aureus to Livestock CC398
title_full Commercial Biocides Induce Transfer of Prophage Φ13 from Human Strains of Staphylococcus aureus to Livestock CC398
title_fullStr Commercial Biocides Induce Transfer of Prophage Φ13 from Human Strains of Staphylococcus aureus to Livestock CC398
title_full_unstemmed Commercial Biocides Induce Transfer of Prophage Φ13 from Human Strains of Staphylococcus aureus to Livestock CC398
title_short Commercial Biocides Induce Transfer of Prophage Φ13 from Human Strains of Staphylococcus aureus to Livestock CC398
title_sort commercial biocides induce transfer of prophage φ13 from human strains of staphylococcus aureus to livestock cc398
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726172/
https://www.ncbi.nlm.nih.gov/pubmed/29270158
http://dx.doi.org/10.3389/fmicb.2017.02418
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