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Complete Genome Sequence of the MRSA Isolate HC1335 from ST239 Lineage Displaying a Truncated AgrC Histidine Kinase Receptor
Methicillin-resistant Staphylococcus aureus (MRSA) is still one of the most important hospital pathogen globally. The multiresistant isolates of the ST239-SCCmecIII lineage are spread over large geographic regions, colonizing and infecting hospital patients in virtually all continents. The balance b...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5174738/ https://www.ncbi.nlm.nih.gov/pubmed/27635055 http://dx.doi.org/10.1093/gbe/evw225 |
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author | Botelho, Ana M. N. Costa, Maiana O. C. Beltrame, Cristiana O. Ferreira, Fabienne A. Lima, Nicholas C. B. Costa, Bruno S. S. de Morais, Guilherme L. Souza, Rangel C. Almeida, Luiz G. P. Vasconcelos, Ana T. R. Nicolás, Marisa F. Figueiredo, Agnes M. S. |
author_facet | Botelho, Ana M. N. Costa, Maiana O. C. Beltrame, Cristiana O. Ferreira, Fabienne A. Lima, Nicholas C. B. Costa, Bruno S. S. de Morais, Guilherme L. Souza, Rangel C. Almeida, Luiz G. P. Vasconcelos, Ana T. R. Nicolás, Marisa F. Figueiredo, Agnes M. S. |
author_sort | Botelho, Ana M. N. |
collection | PubMed |
description | Methicillin-resistant Staphylococcus aureus (MRSA) is still one of the most important hospital pathogen globally. The multiresistant isolates of the ST239-SCCmecIII lineage are spread over large geographic regions, colonizing and infecting hospital patients in virtually all continents. The balance between fitness (adaptability) and virulence potential is likely to represent an important issue in the clonal shift dynamics leading the success of some specific MRSA clones over another. The accessory gene regulator (agr) is the master quorum sensing system of staphylococci playing a role in the global regulation of key virulence factors. Consequently, agr inactivation in S. aureus may represent a significant mechanism of genetic variability in the adaptation of this healthcare-associated pathogen. We report here the complete genome sequence of the methicillin-resistant S. aureus, isolate HC1335, a variant of the ST239 lineage, which presents a natural insertion of an IS256 transposase element in the agrC gene encoding AgrC histidine kinase receptor. |
format | Online Article Text |
id | pubmed-5174738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-51747382016-12-27 Complete Genome Sequence of the MRSA Isolate HC1335 from ST239 Lineage Displaying a Truncated AgrC Histidine Kinase Receptor Botelho, Ana M. N. Costa, Maiana O. C. Beltrame, Cristiana O. Ferreira, Fabienne A. Lima, Nicholas C. B. Costa, Bruno S. S. de Morais, Guilherme L. Souza, Rangel C. Almeida, Luiz G. P. Vasconcelos, Ana T. R. Nicolás, Marisa F. Figueiredo, Agnes M. S. Genome Biol Evol Research Article Methicillin-resistant Staphylococcus aureus (MRSA) is still one of the most important hospital pathogen globally. The multiresistant isolates of the ST239-SCCmecIII lineage are spread over large geographic regions, colonizing and infecting hospital patients in virtually all continents. The balance between fitness (adaptability) and virulence potential is likely to represent an important issue in the clonal shift dynamics leading the success of some specific MRSA clones over another. The accessory gene regulator (agr) is the master quorum sensing system of staphylococci playing a role in the global regulation of key virulence factors. Consequently, agr inactivation in S. aureus may represent a significant mechanism of genetic variability in the adaptation of this healthcare-associated pathogen. We report here the complete genome sequence of the methicillin-resistant S. aureus, isolate HC1335, a variant of the ST239 lineage, which presents a natural insertion of an IS256 transposase element in the agrC gene encoding AgrC histidine kinase receptor. Oxford University Press 2016-09-15 /pmc/articles/PMC5174738/ /pubmed/27635055 http://dx.doi.org/10.1093/gbe/evw225 Text en © The Author(s) 2016. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Botelho, Ana M. N. Costa, Maiana O. C. Beltrame, Cristiana O. Ferreira, Fabienne A. Lima, Nicholas C. B. Costa, Bruno S. S. de Morais, Guilherme L. Souza, Rangel C. Almeida, Luiz G. P. Vasconcelos, Ana T. R. Nicolás, Marisa F. Figueiredo, Agnes M. S. Complete Genome Sequence of the MRSA Isolate HC1335 from ST239 Lineage Displaying a Truncated AgrC Histidine Kinase Receptor |
title | Complete Genome Sequence of the MRSA Isolate HC1335 from ST239 Lineage Displaying a Truncated AgrC Histidine Kinase Receptor |
title_full | Complete Genome Sequence of the MRSA Isolate HC1335 from ST239 Lineage Displaying a Truncated AgrC Histidine Kinase Receptor |
title_fullStr | Complete Genome Sequence of the MRSA Isolate HC1335 from ST239 Lineage Displaying a Truncated AgrC Histidine Kinase Receptor |
title_full_unstemmed | Complete Genome Sequence of the MRSA Isolate HC1335 from ST239 Lineage Displaying a Truncated AgrC Histidine Kinase Receptor |
title_short | Complete Genome Sequence of the MRSA Isolate HC1335 from ST239 Lineage Displaying a Truncated AgrC Histidine Kinase Receptor |
title_sort | complete genome sequence of the mrsa isolate hc1335 from st239 lineage displaying a truncated agrc histidine kinase receptor |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5174738/ https://www.ncbi.nlm.nih.gov/pubmed/27635055 http://dx.doi.org/10.1093/gbe/evw225 |
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