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Isolation and molecular characterisation of Achromobacter phage phiAxp-3, an N4-like bacteriophage
Achromobacter xylosoxidans, an opportunistic pathogen, is responsible for various nosocomial and community-acquired infections. We isolated phiAxp-3, an N4-like bacteriophage that infects A. xylosoxidans, from hospital waste and studied its genomic and biological properties. Transmission electron mi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837373/ https://www.ncbi.nlm.nih.gov/pubmed/27094846 http://dx.doi.org/10.1038/srep24776 |
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author | Ma, Yanyan Li, Erna Qi, Zhizhen Li, Huan Wei, Xiao Lin, Weishi Zhao, Ruixiang Jiang, Aimin Yang, Huiying Yin, Zhe Yuan, Jing Zhao, Xiangna |
author_facet | Ma, Yanyan Li, Erna Qi, Zhizhen Li, Huan Wei, Xiao Lin, Weishi Zhao, Ruixiang Jiang, Aimin Yang, Huiying Yin, Zhe Yuan, Jing Zhao, Xiangna |
author_sort | Ma, Yanyan |
collection | PubMed |
description | Achromobacter xylosoxidans, an opportunistic pathogen, is responsible for various nosocomial and community-acquired infections. We isolated phiAxp-3, an N4-like bacteriophage that infects A. xylosoxidans, from hospital waste and studied its genomic and biological properties. Transmission electron microscopy revealed that, with a 67-nm diameter icosahedral head and a 20-nm non-contractile tail, phiAxp-3 has features characteristic of Podoviridae bacteriophages (order Caudovirales). With a burst size of 9000 plaque-forming units and a latent period of 80 min, phiAxp-3 had a host range limited to only four A. xylosoxidans strains of the 35 strains that were tested. The 72,825 bp phiAxp-3 DNA genome, with 416-bp terminal redundant ends, contains 80 predicted open reading frames, none of which are related to virulence or drug resistance. Genome sequence comparisons place phiAxp-3 more closely with JWAlpha and JWDelta Achromobacter phages than with other N4 viruses. Using proteomics, we identified 25 viral proteins from purified phiAxp-3 particles. Notably, investigation of the phage phiAxp-3 receptor on the surface of the host cell revealed that lipopolysaccharide serves as the receptor for the adsorption of phage phiAxp-3. Our findings advance current knowledge about A. xylosoxidans phages in an age where alternative therapies to combat antibiotic-resistant bacteria are urgently needed. |
format | Online Article Text |
id | pubmed-4837373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48373732016-04-27 Isolation and molecular characterisation of Achromobacter phage phiAxp-3, an N4-like bacteriophage Ma, Yanyan Li, Erna Qi, Zhizhen Li, Huan Wei, Xiao Lin, Weishi Zhao, Ruixiang Jiang, Aimin Yang, Huiying Yin, Zhe Yuan, Jing Zhao, Xiangna Sci Rep Article Achromobacter xylosoxidans, an opportunistic pathogen, is responsible for various nosocomial and community-acquired infections. We isolated phiAxp-3, an N4-like bacteriophage that infects A. xylosoxidans, from hospital waste and studied its genomic and biological properties. Transmission electron microscopy revealed that, with a 67-nm diameter icosahedral head and a 20-nm non-contractile tail, phiAxp-3 has features characteristic of Podoviridae bacteriophages (order Caudovirales). With a burst size of 9000 plaque-forming units and a latent period of 80 min, phiAxp-3 had a host range limited to only four A. xylosoxidans strains of the 35 strains that were tested. The 72,825 bp phiAxp-3 DNA genome, with 416-bp terminal redundant ends, contains 80 predicted open reading frames, none of which are related to virulence or drug resistance. Genome sequence comparisons place phiAxp-3 more closely with JWAlpha and JWDelta Achromobacter phages than with other N4 viruses. Using proteomics, we identified 25 viral proteins from purified phiAxp-3 particles. Notably, investigation of the phage phiAxp-3 receptor on the surface of the host cell revealed that lipopolysaccharide serves as the receptor for the adsorption of phage phiAxp-3. Our findings advance current knowledge about A. xylosoxidans phages in an age where alternative therapies to combat antibiotic-resistant bacteria are urgently needed. Nature Publishing Group 2016-04-20 /pmc/articles/PMC4837373/ /pubmed/27094846 http://dx.doi.org/10.1038/srep24776 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ma, Yanyan Li, Erna Qi, Zhizhen Li, Huan Wei, Xiao Lin, Weishi Zhao, Ruixiang Jiang, Aimin Yang, Huiying Yin, Zhe Yuan, Jing Zhao, Xiangna Isolation and molecular characterisation of Achromobacter phage phiAxp-3, an N4-like bacteriophage |
title | Isolation and molecular characterisation of Achromobacter phage phiAxp-3, an N4-like bacteriophage |
title_full | Isolation and molecular characterisation of Achromobacter phage phiAxp-3, an N4-like bacteriophage |
title_fullStr | Isolation and molecular characterisation of Achromobacter phage phiAxp-3, an N4-like bacteriophage |
title_full_unstemmed | Isolation and molecular characterisation of Achromobacter phage phiAxp-3, an N4-like bacteriophage |
title_short | Isolation and molecular characterisation of Achromobacter phage phiAxp-3, an N4-like bacteriophage |
title_sort | isolation and molecular characterisation of achromobacter phage phiaxp-3, an n4-like bacteriophage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837373/ https://www.ncbi.nlm.nih.gov/pubmed/27094846 http://dx.doi.org/10.1038/srep24776 |
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