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Characterization and genome annotation of a newly detected bacteriophage infecting multidrug-resistant Acinetobacter baumannii
A novel virulent bacteriophage, φAbp2, infecting multidrug-resistant (MDR) Acinetobacter baumannii was isolated from the wastewater of a sewage management centre at Southwest Hospital, China. Transmission electron microscopy and phylogenetic analysis revealed that φAbp2 belongs to the subfamily Pedu...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6526140/ https://www.ncbi.nlm.nih.gov/pubmed/30900072 http://dx.doi.org/10.1007/s00705-019-04213-0 |
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author | Yang, Zichen Liu, Xinzhu Shi, Yunlong Yin, Supeng Shen, Wei Chen, Jing Chen, Yu Chen, Yajie You, Bo Gong, Yali Luo, Xiaoqiang Zhang, Cheng Yuan, Zhiqiang Peng, Yizhi |
author_facet | Yang, Zichen Liu, Xinzhu Shi, Yunlong Yin, Supeng Shen, Wei Chen, Jing Chen, Yu Chen, Yajie You, Bo Gong, Yali Luo, Xiaoqiang Zhang, Cheng Yuan, Zhiqiang Peng, Yizhi |
author_sort | Yang, Zichen |
collection | PubMed |
description | A novel virulent bacteriophage, φAbp2, infecting multidrug-resistant (MDR) Acinetobacter baumannii was isolated from the wastewater of a sewage management centre at Southwest Hospital, China. Transmission electron microscopy and phylogenetic analysis revealed that φAbp2 belongs to the subfamily Peduovirinae. A one-step growth curve demonstrated that φAbp2 had a latent period of 15 min, a lysis period of 35 min, and a burst size of 222 particles per infected host cell. Moreover, φAbp2 showed a relatively broad host range in local A. baumannii, and it also exhibited tolerance over a wider range of thermal and pH conditions. Genomic sequencing revealed that φAbp2 has a circular double-stranded DNA genome with no sequence similarity to our previously isolated φAbp1. Eighty-eight putative open reading frames (ORFs) encoding 41 proteins of known function and 47 of unknown function were identified, and the G/C content was 37.84%. φAbp2 is a new member of the subfamily Peduovirinae of the family Myoviridae. Its genome sequence is very similar to that of the A. baumannii phage LZ35. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00705-019-04213-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6526140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-65261402019-06-14 Characterization and genome annotation of a newly detected bacteriophage infecting multidrug-resistant Acinetobacter baumannii Yang, Zichen Liu, Xinzhu Shi, Yunlong Yin, Supeng Shen, Wei Chen, Jing Chen, Yu Chen, Yajie You, Bo Gong, Yali Luo, Xiaoqiang Zhang, Cheng Yuan, Zhiqiang Peng, Yizhi Arch Virol Original Article A novel virulent bacteriophage, φAbp2, infecting multidrug-resistant (MDR) Acinetobacter baumannii was isolated from the wastewater of a sewage management centre at Southwest Hospital, China. Transmission electron microscopy and phylogenetic analysis revealed that φAbp2 belongs to the subfamily Peduovirinae. A one-step growth curve demonstrated that φAbp2 had a latent period of 15 min, a lysis period of 35 min, and a burst size of 222 particles per infected host cell. Moreover, φAbp2 showed a relatively broad host range in local A. baumannii, and it also exhibited tolerance over a wider range of thermal and pH conditions. Genomic sequencing revealed that φAbp2 has a circular double-stranded DNA genome with no sequence similarity to our previously isolated φAbp1. Eighty-eight putative open reading frames (ORFs) encoding 41 proteins of known function and 47 of unknown function were identified, and the G/C content was 37.84%. φAbp2 is a new member of the subfamily Peduovirinae of the family Myoviridae. Its genome sequence is very similar to that of the A. baumannii phage LZ35. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00705-019-04213-0) contains supplementary material, which is available to authorized users. Springer Vienna 2019-03-21 2019 /pmc/articles/PMC6526140/ /pubmed/30900072 http://dx.doi.org/10.1007/s00705-019-04213-0 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Yang, Zichen Liu, Xinzhu Shi, Yunlong Yin, Supeng Shen, Wei Chen, Jing Chen, Yu Chen, Yajie You, Bo Gong, Yali Luo, Xiaoqiang Zhang, Cheng Yuan, Zhiqiang Peng, Yizhi Characterization and genome annotation of a newly detected bacteriophage infecting multidrug-resistant Acinetobacter baumannii |
title | Characterization and genome annotation of a newly detected bacteriophage infecting multidrug-resistant Acinetobacter baumannii |
title_full | Characterization and genome annotation of a newly detected bacteriophage infecting multidrug-resistant Acinetobacter baumannii |
title_fullStr | Characterization and genome annotation of a newly detected bacteriophage infecting multidrug-resistant Acinetobacter baumannii |
title_full_unstemmed | Characterization and genome annotation of a newly detected bacteriophage infecting multidrug-resistant Acinetobacter baumannii |
title_short | Characterization and genome annotation of a newly detected bacteriophage infecting multidrug-resistant Acinetobacter baumannii |
title_sort | characterization and genome annotation of a newly detected bacteriophage infecting multidrug-resistant acinetobacter baumannii |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6526140/ https://www.ncbi.nlm.nih.gov/pubmed/30900072 http://dx.doi.org/10.1007/s00705-019-04213-0 |
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