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Characterization of a lytic Pseudomonas aeruginosa phage vB_PaeP_ASP23 and functional analysis of its lysin LysASP and holin HolASP

In this study, we isolated a lytic Pseudomonas aeruginosa phage (vB_PaeP_ASP23) from the sewage of a mink farm, characterized its complete genome and analyzed the function of its putative lysin and holin. Morphological characterization and genome annotation showed that phage ASP23 belonged to the Kr...

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Autores principales: Cui, Jiaqi, Shi, Xiaojie, Wang, Xinwei, Sun, Huzhi, Yan, Yanxin, Zhao, Feiyang, Zhang, Can, Liu, Wenhua, Zou, Ling, Han, Lei, Pan, Qiang, Ren, Huiying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045481/
https://www.ncbi.nlm.nih.gov/pubmed/36998407
http://dx.doi.org/10.3389/fmicb.2023.1093668
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author Cui, Jiaqi
Shi, Xiaojie
Wang, Xinwei
Sun, Huzhi
Yan, Yanxin
Zhao, Feiyang
Zhang, Can
Liu, Wenhua
Zou, Ling
Han, Lei
Pan, Qiang
Ren, Huiying
author_facet Cui, Jiaqi
Shi, Xiaojie
Wang, Xinwei
Sun, Huzhi
Yan, Yanxin
Zhao, Feiyang
Zhang, Can
Liu, Wenhua
Zou, Ling
Han, Lei
Pan, Qiang
Ren, Huiying
author_sort Cui, Jiaqi
collection PubMed
description In this study, we isolated a lytic Pseudomonas aeruginosa phage (vB_PaeP_ASP23) from the sewage of a mink farm, characterized its complete genome and analyzed the function of its putative lysin and holin. Morphological characterization and genome annotation showed that phage ASP23 belonged to the Krylovirinae family genus Phikmvvirus, and it had a latent period of 10 min and a burst size of 140 pfu/infected cell. In minks challenged with P. aeruginosa, phage ASP23 significantly reduced bacterial counts in the liver, lung, and blood. The whole-genome sequencing showed that its genome was a 42,735-bp linear and double-stranded DNA (dsDNA), with a G + C content of 62.15%. Its genome contained 54 predicted open reading frames (ORFs), 25 of which had known functions. The lysin of phage ASP23 (LysASP), in combination with EDTA, showed high lytic activity against P. aeruginosa L64. The holin of phage ASP23 was synthesized by M13 phage display technology, to produce recombinant phages (HolASP). Though HolASP exhibited a narrow lytic spectrum, it was effective against Staphylococcus aureus and Bacillus subtilis. However, these two bacteria were insensitive to LysASP. The findings highlight the potential of phage ASP23 to be used in the development of new antibacterial agents.
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spelling pubmed-100454812023-03-29 Characterization of a lytic Pseudomonas aeruginosa phage vB_PaeP_ASP23 and functional analysis of its lysin LysASP and holin HolASP Cui, Jiaqi Shi, Xiaojie Wang, Xinwei Sun, Huzhi Yan, Yanxin Zhao, Feiyang Zhang, Can Liu, Wenhua Zou, Ling Han, Lei Pan, Qiang Ren, Huiying Front Microbiol Microbiology In this study, we isolated a lytic Pseudomonas aeruginosa phage (vB_PaeP_ASP23) from the sewage of a mink farm, characterized its complete genome and analyzed the function of its putative lysin and holin. Morphological characterization and genome annotation showed that phage ASP23 belonged to the Krylovirinae family genus Phikmvvirus, and it had a latent period of 10 min and a burst size of 140 pfu/infected cell. In minks challenged with P. aeruginosa, phage ASP23 significantly reduced bacterial counts in the liver, lung, and blood. The whole-genome sequencing showed that its genome was a 42,735-bp linear and double-stranded DNA (dsDNA), with a G + C content of 62.15%. Its genome contained 54 predicted open reading frames (ORFs), 25 of which had known functions. The lysin of phage ASP23 (LysASP), in combination with EDTA, showed high lytic activity against P. aeruginosa L64. The holin of phage ASP23 was synthesized by M13 phage display technology, to produce recombinant phages (HolASP). Though HolASP exhibited a narrow lytic spectrum, it was effective against Staphylococcus aureus and Bacillus subtilis. However, these two bacteria were insensitive to LysASP. The findings highlight the potential of phage ASP23 to be used in the development of new antibacterial agents. Frontiers Media S.A. 2023-03-15 /pmc/articles/PMC10045481/ /pubmed/36998407 http://dx.doi.org/10.3389/fmicb.2023.1093668 Text en Copyright © 2023 Cui, Shi, Wang, Sun, Yan, Zhao, Zhang, Liu, Zou, Han, Pan and Ren. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Cui, Jiaqi
Shi, Xiaojie
Wang, Xinwei
Sun, Huzhi
Yan, Yanxin
Zhao, Feiyang
Zhang, Can
Liu, Wenhua
Zou, Ling
Han, Lei
Pan, Qiang
Ren, Huiying
Characterization of a lytic Pseudomonas aeruginosa phage vB_PaeP_ASP23 and functional analysis of its lysin LysASP and holin HolASP
title Characterization of a lytic Pseudomonas aeruginosa phage vB_PaeP_ASP23 and functional analysis of its lysin LysASP and holin HolASP
title_full Characterization of a lytic Pseudomonas aeruginosa phage vB_PaeP_ASP23 and functional analysis of its lysin LysASP and holin HolASP
title_fullStr Characterization of a lytic Pseudomonas aeruginosa phage vB_PaeP_ASP23 and functional analysis of its lysin LysASP and holin HolASP
title_full_unstemmed Characterization of a lytic Pseudomonas aeruginosa phage vB_PaeP_ASP23 and functional analysis of its lysin LysASP and holin HolASP
title_short Characterization of a lytic Pseudomonas aeruginosa phage vB_PaeP_ASP23 and functional analysis of its lysin LysASP and holin HolASP
title_sort characterization of a lytic pseudomonas aeruginosa phage vb_paep_asp23 and functional analysis of its lysin lysasp and holin holasp
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045481/
https://www.ncbi.nlm.nih.gov/pubmed/36998407
http://dx.doi.org/10.3389/fmicb.2023.1093668
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