Draft genome sequence of a multidrug-resistant beta-lactamase OXA-357-producing Acinetobacter pittii ST865 clinical isolate from China

Worldwide increasing emergence of carbapenem-resistant Acinetobacter spp. has rendered the limited availability of effective antimicrobial agents and has become a major public health concern. In this study, we report the draft genome sequence of A. pittii TCM156, a multidrug-resistant isolate that h...

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Detalles Bibliográficos
Autores principales: Wang, Jianfeng, Chen, Yan, Wu, Liyan, Chen, Yu, Xu, Liqun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Genome Announcements
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470435/
https://www.ncbi.nlm.nih.gov/pubmed/28034597
http://dx.doi.org/10.1016/j.bjm.2016.10.020
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author Wang, Jianfeng
Chen, Yan
Wu, Liyan
Chen, Yu
Xu, Liqun
author_facet Wang, Jianfeng
Chen, Yan
Wu, Liyan
Chen, Yu
Xu, Liqun
author_sort Wang, Jianfeng
collection PubMed
description Worldwide increasing emergence of carbapenem-resistant Acinetobacter spp. has rendered the limited availability of effective antimicrobial agents and has become a major public health concern. In this study, we report the draft genome sequence of A. pittii TCM156, a multidrug-resistant isolate that harbored the bla(OXA-357) gene. The genome sequence was further analyzed by various bioinformatics methods. The genome size was estimated to be 3,807,313 bp with 3508 predicted coding regions and G + C content is 38.7%. These findings have raised awareness of the possible emergence of OXA-type enzyme-producing A. pittii isolate in China.
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spelling pubmed-54704352017-06-23 Draft genome sequence of a multidrug-resistant beta-lactamase OXA-357-producing Acinetobacter pittii ST865 clinical isolate from China Wang, Jianfeng Chen, Yan Wu, Liyan Chen, Yu Xu, Liqun Braz J Microbiol Genome Announcements Worldwide increasing emergence of carbapenem-resistant Acinetobacter spp. has rendered the limited availability of effective antimicrobial agents and has become a major public health concern. In this study, we report the draft genome sequence of A. pittii TCM156, a multidrug-resistant isolate that harbored the bla(OXA-357) gene. The genome sequence was further analyzed by various bioinformatics methods. The genome size was estimated to be 3,807,313 bp with 3508 predicted coding regions and G + C content is 38.7%. These findings have raised awareness of the possible emergence of OXA-type enzyme-producing A. pittii isolate in China. Elsevier 2016-12-14 /pmc/articles/PMC5470435/ /pubmed/28034597 http://dx.doi.org/10.1016/j.bjm.2016.10.020 Text en © 2016 Sociedade Brasileira de Microbiologia. Published by Elsevier Editora Ltda. 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 Genome Announcements
Wang, Jianfeng
Chen, Yan
Wu, Liyan
Chen, Yu
Xu, Liqun
Draft genome sequence of a multidrug-resistant beta-lactamase OXA-357-producing Acinetobacter pittii ST865 clinical isolate from China
title Draft genome sequence of a multidrug-resistant beta-lactamase OXA-357-producing Acinetobacter pittii ST865 clinical isolate from China
title_full Draft genome sequence of a multidrug-resistant beta-lactamase OXA-357-producing Acinetobacter pittii ST865 clinical isolate from China
title_fullStr Draft genome sequence of a multidrug-resistant beta-lactamase OXA-357-producing Acinetobacter pittii ST865 clinical isolate from China
title_full_unstemmed Draft genome sequence of a multidrug-resistant beta-lactamase OXA-357-producing Acinetobacter pittii ST865 clinical isolate from China
title_short Draft genome sequence of a multidrug-resistant beta-lactamase OXA-357-producing Acinetobacter pittii ST865 clinical isolate from China
title_sort draft genome sequence of a multidrug-resistant beta-lactamase oxa-357-producing acinetobacter pittii st865 clinical isolate from china
topic Genome Announcements
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470435/
https://www.ncbi.nlm.nih.gov/pubmed/28034597
http://dx.doi.org/10.1016/j.bjm.2016.10.020
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