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Characterization and genome analysis of six novel Vibrio parahaemolyticus phages associated with acute hepatopancreatic necrosis disease (AHPND)

Vibrio parahaemolyticus causes acute hepatopancreatic necrosis disease (AHPND) in farmed shrimp. Due to its damage potential, which could be as high as a 100% mortality rate, bacteriophages have emerged as a promising natural control intervention other than antibiotics, yet multiple roadblocks need...

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Autores principales: Orozco-Ochoa, Alma Karen, González-Gómez, Jean Pierre, Castro-del Campo, Nohelia, Lira-Morales, Juan Daniel, Martínez-Rodríguez, Célida Isabel, Gomez-Gil, Bruno, Chaidez, Cristóbal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10194199/
https://www.ncbi.nlm.nih.gov/pubmed/36272541
http://dx.doi.org/10.1016/j.virusres.2022.198973
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author Orozco-Ochoa, Alma Karen
González-Gómez, Jean Pierre
Castro-del Campo, Nohelia
Lira-Morales, Juan Daniel
Martínez-Rodríguez, Célida Isabel
Gomez-Gil, Bruno
Chaidez, Cristóbal
author_facet Orozco-Ochoa, Alma Karen
González-Gómez, Jean Pierre
Castro-del Campo, Nohelia
Lira-Morales, Juan Daniel
Martínez-Rodríguez, Célida Isabel
Gomez-Gil, Bruno
Chaidez, Cristóbal
author_sort Orozco-Ochoa, Alma Karen
collection PubMed
description Vibrio parahaemolyticus causes acute hepatopancreatic necrosis disease (AHPND) in farmed shrimp. Due to its damage potential, which could be as high as a 100% mortality rate, bacteriophages have emerged as a promising natural control intervention other than antibiotics, yet multiple roadblocks need to be overcome. In this study, six bacteriophages isolated from seafood samples, seawater, and estuary water in Sinaloa, Mexico, demonstrated a narrow host range among Mexican AHPND-causing V. parahaemolyticus. All bacteriophages are composed of a double-stranded DNA genome with lengths ranging between 43,268 and 57,805 bp. All six phages exhibited latency periods of 10–30 min and burst sizes of 34–168 viral particles per infected cell. The optimal MOI for bacteriophage propagation was 0.01–1. No transfer RNA (tRNA), virulence, or resistance genes were found in either genome, and the life cycle of these phages was classified as virulent by the PhageAI platform. Phylogenetic and comparative genomics analyzes assigned phages M3, C2, M9, and M83 as new species not yet reported within the genus Maculvirus, Autographiviridae family. ALK and CHI phages were assigned as new members of a new genus not yet classified within the subfamily Queuovirinae. The findings highlight the potential of CHI, ALK, M3, C2, M9, and M83 as promising alternatives against AHPND-causing V. parahaemolyticus from Mexico.
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spelling pubmed-101941992023-05-19 Characterization and genome analysis of six novel Vibrio parahaemolyticus phages associated with acute hepatopancreatic necrosis disease (AHPND) Orozco-Ochoa, Alma Karen González-Gómez, Jean Pierre Castro-del Campo, Nohelia Lira-Morales, Juan Daniel Martínez-Rodríguez, Célida Isabel Gomez-Gil, Bruno Chaidez, Cristóbal Virus Res Article Vibrio parahaemolyticus causes acute hepatopancreatic necrosis disease (AHPND) in farmed shrimp. Due to its damage potential, which could be as high as a 100% mortality rate, bacteriophages have emerged as a promising natural control intervention other than antibiotics, yet multiple roadblocks need to be overcome. In this study, six bacteriophages isolated from seafood samples, seawater, and estuary water in Sinaloa, Mexico, demonstrated a narrow host range among Mexican AHPND-causing V. parahaemolyticus. All bacteriophages are composed of a double-stranded DNA genome with lengths ranging between 43,268 and 57,805 bp. All six phages exhibited latency periods of 10–30 min and burst sizes of 34–168 viral particles per infected cell. The optimal MOI for bacteriophage propagation was 0.01–1. No transfer RNA (tRNA), virulence, or resistance genes were found in either genome, and the life cycle of these phages was classified as virulent by the PhageAI platform. Phylogenetic and comparative genomics analyzes assigned phages M3, C2, M9, and M83 as new species not yet reported within the genus Maculvirus, Autographiviridae family. ALK and CHI phages were assigned as new members of a new genus not yet classified within the subfamily Queuovirinae. The findings highlight the potential of CHI, ALK, M3, C2, M9, and M83 as promising alternatives against AHPND-causing V. parahaemolyticus from Mexico. Elsevier 2022-10-20 /pmc/articles/PMC10194199/ /pubmed/36272541 http://dx.doi.org/10.1016/j.virusres.2022.198973 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Orozco-Ochoa, Alma Karen
González-Gómez, Jean Pierre
Castro-del Campo, Nohelia
Lira-Morales, Juan Daniel
Martínez-Rodríguez, Célida Isabel
Gomez-Gil, Bruno
Chaidez, Cristóbal
Characterization and genome analysis of six novel Vibrio parahaemolyticus phages associated with acute hepatopancreatic necrosis disease (AHPND)
title Characterization and genome analysis of six novel Vibrio parahaemolyticus phages associated with acute hepatopancreatic necrosis disease (AHPND)
title_full Characterization and genome analysis of six novel Vibrio parahaemolyticus phages associated with acute hepatopancreatic necrosis disease (AHPND)
title_fullStr Characterization and genome analysis of six novel Vibrio parahaemolyticus phages associated with acute hepatopancreatic necrosis disease (AHPND)
title_full_unstemmed Characterization and genome analysis of six novel Vibrio parahaemolyticus phages associated with acute hepatopancreatic necrosis disease (AHPND)
title_short Characterization and genome analysis of six novel Vibrio parahaemolyticus phages associated with acute hepatopancreatic necrosis disease (AHPND)
title_sort characterization and genome analysis of six novel vibrio parahaemolyticus phages associated with acute hepatopancreatic necrosis disease (ahpnd)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10194199/
https://www.ncbi.nlm.nih.gov/pubmed/36272541
http://dx.doi.org/10.1016/j.virusres.2022.198973
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