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Potential Inoculum Sources of Phaeomoniellachlamydospora in South African Grapevine Nurseries

Petri disease of grapevine is primarily caused by Phaeomoniella chlamydospora. This pathogen affects mostly young grapevines, but is also implicated in esca disease of older grapevines. Little is known about the disease cycle of this fungus. Infected propagation material was identified as a major me...

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Autores principales: Retief, E., McLeod, A., Fourie, P. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088137/
https://www.ncbi.nlm.nih.gov/pubmed/32214676
http://dx.doi.org/10.1007/s10658-006-9025-4
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author Retief, E.
McLeod, A.
Fourie, P. H.
author_facet Retief, E.
McLeod, A.
Fourie, P. H.
author_sort Retief, E.
collection PubMed
description Petri disease of grapevine is primarily caused by Phaeomoniella chlamydospora. This pathogen affects mostly young grapevines, but is also implicated in esca disease of older grapevines. Little is known about the disease cycle of this fungus. Infected propagation material was identified as a major means of dissemination of the pathogen. Recently, the pathogen was also detected from soil in South Africa and airborne conidia have been found in vineyards. The aim of this study was to use a molecular detection technique to test different samples collected from nurseries in South Africa at different nursery stages for the presence of P. chlamydospora. A one-tube nested-PCR technique was optimised for detecting P. chlamydospora in DNA extracted from soil, water, callusing medium and grapevine wood. The one-tube nested-PCR was sensitive enough to detect as little as 1 fg of P. chlamydospora genomic DNA from water and 10 fg from wood, callusing medium and soil. PCR analyses of the different nursery samples revealed the presence of several putative 360 bp P. chlamydospora specific bands. Subsequent sequence analyses and/or restriction enzyme digestions of all 360 bp PCR bands confirmed that all bands were P. chlamydospora specific, except for five bands obtained from callusing media and one from water. Phaeomoniella chlamydospora was positively detected in 25% of rootstock cane sections collected from mother blocks, 42% of rootstock cuttings and 16% of scion cuttings collected during grafting, 40% of water samples collected after pre-storage hydration, 67% of water samples collected during grafting, 8% of callusing medium samples and 17% of soil samples collected from mother blocks. These media can therefore be considered as possible inoculum sources of the pathogen during the nursery stages.
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spelling pubmed-70881372020-03-23 Potential Inoculum Sources of Phaeomoniellachlamydospora in South African Grapevine Nurseries Retief, E. McLeod, A. Fourie, P. H. Eur J Plant Pathol Article Petri disease of grapevine is primarily caused by Phaeomoniella chlamydospora. This pathogen affects mostly young grapevines, but is also implicated in esca disease of older grapevines. Little is known about the disease cycle of this fungus. Infected propagation material was identified as a major means of dissemination of the pathogen. Recently, the pathogen was also detected from soil in South Africa and airborne conidia have been found in vineyards. The aim of this study was to use a molecular detection technique to test different samples collected from nurseries in South Africa at different nursery stages for the presence of P. chlamydospora. A one-tube nested-PCR technique was optimised for detecting P. chlamydospora in DNA extracted from soil, water, callusing medium and grapevine wood. The one-tube nested-PCR was sensitive enough to detect as little as 1 fg of P. chlamydospora genomic DNA from water and 10 fg from wood, callusing medium and soil. PCR analyses of the different nursery samples revealed the presence of several putative 360 bp P. chlamydospora specific bands. Subsequent sequence analyses and/or restriction enzyme digestions of all 360 bp PCR bands confirmed that all bands were P. chlamydospora specific, except for five bands obtained from callusing media and one from water. Phaeomoniella chlamydospora was positively detected in 25% of rootstock cane sections collected from mother blocks, 42% of rootstock cuttings and 16% of scion cuttings collected during grafting, 40% of water samples collected after pre-storage hydration, 67% of water samples collected during grafting, 8% of callusing medium samples and 17% of soil samples collected from mother blocks. These media can therefore be considered as possible inoculum sources of the pathogen during the nursery stages. Springer Netherlands 2006-06-07 2006 /pmc/articles/PMC7088137/ /pubmed/32214676 http://dx.doi.org/10.1007/s10658-006-9025-4 Text en © Springer Science+Business Media, Inc. 2006 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Retief, E.
McLeod, A.
Fourie, P. H.
Potential Inoculum Sources of Phaeomoniellachlamydospora in South African Grapevine Nurseries
title Potential Inoculum Sources of Phaeomoniellachlamydospora in South African Grapevine Nurseries
title_full Potential Inoculum Sources of Phaeomoniellachlamydospora in South African Grapevine Nurseries
title_fullStr Potential Inoculum Sources of Phaeomoniellachlamydospora in South African Grapevine Nurseries
title_full_unstemmed Potential Inoculum Sources of Phaeomoniellachlamydospora in South African Grapevine Nurseries
title_short Potential Inoculum Sources of Phaeomoniellachlamydospora in South African Grapevine Nurseries
title_sort potential inoculum sources of phaeomoniellachlamydospora in south african grapevine nurseries
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088137/
https://www.ncbi.nlm.nih.gov/pubmed/32214676
http://dx.doi.org/10.1007/s10658-006-9025-4
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