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Phage ϕC2 Mediates Transduction of Tn6215, Encoding Erythromycin Resistance, between Clostridium difficile Strains
In this work, we show that Clostridium difficile phage ϕC2 transduces erm(B), which confers erythromycin resistance, from a donor to a recipient strain at a frequency of 10(−6) per PFU. The transductants were lysogenic for ϕC2 and contained the erm(B) gene in a novel transposon, Tn6215. This element...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Microbiology
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870246/ https://www.ncbi.nlm.nih.gov/pubmed/24255122 http://dx.doi.org/10.1128/mBio.00840-13 |
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author | Goh, Shan Hussain, Haitham Chang, Barbara J. Emmett, Warren Riley, Thomas V. Mullany, Peter |
author_facet | Goh, Shan Hussain, Haitham Chang, Barbara J. Emmett, Warren Riley, Thomas V. Mullany, Peter |
author_sort | Goh, Shan |
collection | PubMed |
description | In this work, we show that Clostridium difficile phage ϕC2 transduces erm(B), which confers erythromycin resistance, from a donor to a recipient strain at a frequency of 10(−6) per PFU. The transductants were lysogenic for ϕC2 and contained the erm(B) gene in a novel transposon, Tn6215. This element is 13,008 bp in length and contains 17 putative open reading frames (ORFs). It could also be transferred at a lower frequency by filter mating. |
format | Online Article Text |
id | pubmed-3870246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American Society of Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-38702462013-12-26 Phage ϕC2 Mediates Transduction of Tn6215, Encoding Erythromycin Resistance, between Clostridium difficile Strains Goh, Shan Hussain, Haitham Chang, Barbara J. Emmett, Warren Riley, Thomas V. Mullany, Peter mBio Research Article In this work, we show that Clostridium difficile phage ϕC2 transduces erm(B), which confers erythromycin resistance, from a donor to a recipient strain at a frequency of 10(−6) per PFU. The transductants were lysogenic for ϕC2 and contained the erm(B) gene in a novel transposon, Tn6215. This element is 13,008 bp in length and contains 17 putative open reading frames (ORFs). It could also be transferred at a lower frequency by filter mating. American Society of Microbiology 2013-11-19 /pmc/articles/PMC3870246/ /pubmed/24255122 http://dx.doi.org/10.1128/mBio.00840-13 Text en Copyright © 2013 Goh et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Goh, Shan Hussain, Haitham Chang, Barbara J. Emmett, Warren Riley, Thomas V. Mullany, Peter Phage ϕC2 Mediates Transduction of Tn6215, Encoding Erythromycin Resistance, between Clostridium difficile Strains |
title | Phage ϕC2 Mediates Transduction of Tn6215, Encoding Erythromycin Resistance, between Clostridium difficile Strains |
title_full | Phage ϕC2 Mediates Transduction of Tn6215, Encoding Erythromycin Resistance, between Clostridium difficile Strains |
title_fullStr | Phage ϕC2 Mediates Transduction of Tn6215, Encoding Erythromycin Resistance, between Clostridium difficile Strains |
title_full_unstemmed | Phage ϕC2 Mediates Transduction of Tn6215, Encoding Erythromycin Resistance, between Clostridium difficile Strains |
title_short | Phage ϕC2 Mediates Transduction of Tn6215, Encoding Erythromycin Resistance, between Clostridium difficile Strains |
title_sort | phage ϕc2 mediates transduction of tn6215, encoding erythromycin resistance, between clostridium difficile strains |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870246/ https://www.ncbi.nlm.nih.gov/pubmed/24255122 http://dx.doi.org/10.1128/mBio.00840-13 |
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