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Canker Development and Biocontrol Potential of CHV-1 Infected English Isolates of Cryphonectria parasitica Is Dependent on the Virus Concentration and the Compatibility of the Fungal Inoculums

Biological control of Cryphonectria parasitica fungus, causal agent of chestnut blight, by virus infection (hypovirulence) has been shown to be an effective control strategy against chestnut blight in Europe and some parts of North America. The most studied mycovirus is the Cryphonectria hypovirus 1...

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Autores principales: Romon-Ochoa, Pedro, Forster, Jack, Chitty, Ruth, Gorton, Caroline, Lewis, Alex, Eacock, Amy, Kupper, Quirin, Rigling, Daniel, Pérez-Sierra, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9785502/
https://www.ncbi.nlm.nih.gov/pubmed/36560682
http://dx.doi.org/10.3390/v14122678
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author Romon-Ochoa, Pedro
Forster, Jack
Chitty, Ruth
Gorton, Caroline
Lewis, Alex
Eacock, Amy
Kupper, Quirin
Rigling, Daniel
Pérez-Sierra, Ana
author_facet Romon-Ochoa, Pedro
Forster, Jack
Chitty, Ruth
Gorton, Caroline
Lewis, Alex
Eacock, Amy
Kupper, Quirin
Rigling, Daniel
Pérez-Sierra, Ana
author_sort Romon-Ochoa, Pedro
collection PubMed
description Biological control of Cryphonectria parasitica fungus, causal agent of chestnut blight, by virus infection (hypovirulence) has been shown to be an effective control strategy against chestnut blight in Europe and some parts of North America. The most studied mycovirus is the Cryphonectria hypovirus 1 (CHV-1) type species of the Hypoviridae family. To efficiently provide biocontrol, the virus must be able to induce hypovirulence in its fungal host in chestnut trees. Here, two different CHV-1 subtype I virus strains (E-5 and L-18), gained by transmissions, were tested for their hypovirulence induction, biocontrol potential, and transmission between vegetatively compatible (VCG) and incompatible fungal isolate groups in sweet chestnut seedlings and branches. Both strains of CHV-1 showed great biocontrol potential and could protect trees by efficiently transmitting CHV-1 by hyphal anastomosis between fungal isolates of the same VCG and converting virulent to hypovirulent cankers. The hypovirulent effect was positively correlated with the virus concentration, tested by four different reverse-transcription PCRs, two end-point and two real-time methods, one of which represents a newly developed real-time PCR for the detection and quantification of CHV-1.
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spelling pubmed-97855022022-12-24 Canker Development and Biocontrol Potential of CHV-1 Infected English Isolates of Cryphonectria parasitica Is Dependent on the Virus Concentration and the Compatibility of the Fungal Inoculums Romon-Ochoa, Pedro Forster, Jack Chitty, Ruth Gorton, Caroline Lewis, Alex Eacock, Amy Kupper, Quirin Rigling, Daniel Pérez-Sierra, Ana Viruses Article Biological control of Cryphonectria parasitica fungus, causal agent of chestnut blight, by virus infection (hypovirulence) has been shown to be an effective control strategy against chestnut blight in Europe and some parts of North America. The most studied mycovirus is the Cryphonectria hypovirus 1 (CHV-1) type species of the Hypoviridae family. To efficiently provide biocontrol, the virus must be able to induce hypovirulence in its fungal host in chestnut trees. Here, two different CHV-1 subtype I virus strains (E-5 and L-18), gained by transmissions, were tested for their hypovirulence induction, biocontrol potential, and transmission between vegetatively compatible (VCG) and incompatible fungal isolate groups in sweet chestnut seedlings and branches. Both strains of CHV-1 showed great biocontrol potential and could protect trees by efficiently transmitting CHV-1 by hyphal anastomosis between fungal isolates of the same VCG and converting virulent to hypovirulent cankers. The hypovirulent effect was positively correlated with the virus concentration, tested by four different reverse-transcription PCRs, two end-point and two real-time methods, one of which represents a newly developed real-time PCR for the detection and quantification of CHV-1. MDPI 2022-11-29 /pmc/articles/PMC9785502/ /pubmed/36560682 http://dx.doi.org/10.3390/v14122678 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Romon-Ochoa, Pedro
Forster, Jack
Chitty, Ruth
Gorton, Caroline
Lewis, Alex
Eacock, Amy
Kupper, Quirin
Rigling, Daniel
Pérez-Sierra, Ana
Canker Development and Biocontrol Potential of CHV-1 Infected English Isolates of Cryphonectria parasitica Is Dependent on the Virus Concentration and the Compatibility of the Fungal Inoculums
title Canker Development and Biocontrol Potential of CHV-1 Infected English Isolates of Cryphonectria parasitica Is Dependent on the Virus Concentration and the Compatibility of the Fungal Inoculums
title_full Canker Development and Biocontrol Potential of CHV-1 Infected English Isolates of Cryphonectria parasitica Is Dependent on the Virus Concentration and the Compatibility of the Fungal Inoculums
title_fullStr Canker Development and Biocontrol Potential of CHV-1 Infected English Isolates of Cryphonectria parasitica Is Dependent on the Virus Concentration and the Compatibility of the Fungal Inoculums
title_full_unstemmed Canker Development and Biocontrol Potential of CHV-1 Infected English Isolates of Cryphonectria parasitica Is Dependent on the Virus Concentration and the Compatibility of the Fungal Inoculums
title_short Canker Development and Biocontrol Potential of CHV-1 Infected English Isolates of Cryphonectria parasitica Is Dependent on the Virus Concentration and the Compatibility of the Fungal Inoculums
title_sort canker development and biocontrol potential of chv-1 infected english isolates of cryphonectria parasitica is dependent on the virus concentration and the compatibility of the fungal inoculums
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9785502/
https://www.ncbi.nlm.nih.gov/pubmed/36560682
http://dx.doi.org/10.3390/v14122678
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