Stacking three late blight resistance genes from wild species directly into African highland potato varieties confers complete field resistance to local blight races

Considered responsible for one million deaths in Ireland and widespread famine in the European continent during the 1840s, late blight, caused by Phytophthora infestans, remains the most devastating disease of potato (Solanum tuberosum L.) with about 15%–30% annual yield loss in sub‐Saharan Africa,...

Descripción completa

Detalles Bibliográficos
Autores principales: Ghislain, M., Byarugaba, A.A., Magembe, E., Njoroge, A.W., Rivera, C., Roman, M.L., Tovar, J.C., Gamboa, S., Forbes, G., Kreuze, Jan F., Barekye, A., Kiggundu, A.
Formato: Journal Article
Lenguaje:Inglés
Publicado: Wiley 2018
Materias:
Acceso en línea:https://hdl.handle.net/10568/99120
_version_ 1855519033897517056
author Ghislain, M.
Byarugaba, A.A.
Magembe, E.
Njoroge, A.W.
Rivera, C.
Roman, M.L.
Tovar, J.C.
Gamboa, S.
Forbes, G.
Kreuze, Jan F.
Barekye, A.
Kiggundu, A.
author_browse Barekye, A.
Byarugaba, A.A.
Forbes, G.
Gamboa, S.
Ghislain, M.
Kiggundu, A.
Kreuze, Jan F.
Magembe, E.
Njoroge, A.W.
Rivera, C.
Roman, M.L.
Tovar, J.C.
author_facet Ghislain, M.
Byarugaba, A.A.
Magembe, E.
Njoroge, A.W.
Rivera, C.
Roman, M.L.
Tovar, J.C.
Gamboa, S.
Forbes, G.
Kreuze, Jan F.
Barekye, A.
Kiggundu, A.
author_sort Ghislain, M.
collection Repository of Agricultural Research Outputs (CGSpace)
description Considered responsible for one million deaths in Ireland and widespread famine in the European continent during the 1840s, late blight, caused by Phytophthora infestans, remains the most devastating disease of potato (Solanum tuberosum L.) with about 15%–30% annual yield loss in sub‐Saharan Africa, affecting mainly smallholder farmers. We show here that the transfer of three resistance (R) genes from wild relatives [RB, Rpi‐blb2 from Solanum bulbocastanum and Rpi‐vnt1.1 from S. venturii] into potato provided complete resistance in the field over several seasons. We observed that the stacking of the three R genes produced a high frequency of transgenic events with resistance to late blight. In the field, 13 resistant transgenic events with the 3R‐gene stack from the potato varieties ‘Desiree’ and ‘Victoria’ grew normally without showing pathogen damage and without any fungicide spray, whereas their non‐transgenic equivalent varieties were rapidly killed. Characteristics of the local pathogen population suggest that the resistance to late blight may be long‐lasting because it has low diversity, and essentially consists of the single lineage, 2_A1, which expresses the cognate avirulence effector genes. Yields of two transgenic events from ‘Desiree’ and ‘Victoria’ grown without fungicide to reflect small‐scale farm holders were estimated to be 29 and 45 t/ha respectively. This represents a three to four‐fold increase over the national average. Thus, these late blight resistant potato varieties, which are the farmers’ preferred varieties, could be rapidly adopted and bring significant income to smallholder farmers in sub‐Saharan Africa
format Journal Article
id CGSpace99120
institution CGIAR Consortium
language Inglés
publishDate 2018
publishDateRange 2018
publishDateSort 2018
publisher Wiley
publisherStr Wiley
record_format dspace
spelling CGSpace991202025-11-29T05:22:13Z Stacking three late blight resistance genes from wild species directly into African highland potato varieties confers complete field resistance to local blight races Ghislain, M. Byarugaba, A.A. Magembe, E. Njoroge, A.W. Rivera, C. Roman, M.L. Tovar, J.C. Gamboa, S. Forbes, G. Kreuze, Jan F. Barekye, A. Kiggundu, A. potatoes phytophthora infestans varieties resistance varieties biotechnology Considered responsible for one million deaths in Ireland and widespread famine in the European continent during the 1840s, late blight, caused by Phytophthora infestans, remains the most devastating disease of potato (Solanum tuberosum L.) with about 15%–30% annual yield loss in sub‐Saharan Africa, affecting mainly smallholder farmers. We show here that the transfer of three resistance (R) genes from wild relatives [RB, Rpi‐blb2 from Solanum bulbocastanum and Rpi‐vnt1.1 from S. venturii] into potato provided complete resistance in the field over several seasons. We observed that the stacking of the three R genes produced a high frequency of transgenic events with resistance to late blight. In the field, 13 resistant transgenic events with the 3R‐gene stack from the potato varieties ‘Desiree’ and ‘Victoria’ grew normally without showing pathogen damage and without any fungicide spray, whereas their non‐transgenic equivalent varieties were rapidly killed. Characteristics of the local pathogen population suggest that the resistance to late blight may be long‐lasting because it has low diversity, and essentially consists of the single lineage, 2_A1, which expresses the cognate avirulence effector genes. Yields of two transgenic events from ‘Desiree’ and ‘Victoria’ grown without fungicide to reflect small‐scale farm holders were estimated to be 29 and 45 t/ha respectively. This represents a three to four‐fold increase over the national average. Thus, these late blight resistant potato varieties, which are the farmers’ preferred varieties, could be rapidly adopted and bring significant income to smallholder farmers in sub‐Saharan Africa 2018-11-22 2019-01-21T14:08:26Z 2019-01-21T14:08:26Z Journal Article https://hdl.handle.net/10568/99120 en Open Access Wiley Ghislain, M.; Byarugaba, A.A.; Magembe, E.; Njoroge, A.W.; Rivera, C.; Roman, M.L.; Tovar, J.C.; Gamboa, S.; Forbes, G.; Kreuze, J.F.; Barekye, A.; Kiggundu, A. 2018. Stacking three late blight resistance genes from wild species directly into African highland potato varieties confers complete field resistance to local blight races. Plant Biotechnology Journal. ISSN 1467-7652. 17. pp. 1119-1129.
spellingShingle potatoes
phytophthora infestans
varieties
resistance varieties
biotechnology
Ghislain, M.
Byarugaba, A.A.
Magembe, E.
Njoroge, A.W.
Rivera, C.
Roman, M.L.
Tovar, J.C.
Gamboa, S.
Forbes, G.
Kreuze, Jan F.
Barekye, A.
Kiggundu, A.
Stacking three late blight resistance genes from wild species directly into African highland potato varieties confers complete field resistance to local blight races
title Stacking three late blight resistance genes from wild species directly into African highland potato varieties confers complete field resistance to local blight races
title_full Stacking three late blight resistance genes from wild species directly into African highland potato varieties confers complete field resistance to local blight races
title_fullStr Stacking three late blight resistance genes from wild species directly into African highland potato varieties confers complete field resistance to local blight races
title_full_unstemmed Stacking three late blight resistance genes from wild species directly into African highland potato varieties confers complete field resistance to local blight races
title_short Stacking three late blight resistance genes from wild species directly into African highland potato varieties confers complete field resistance to local blight races
title_sort stacking three late blight resistance genes from wild species directly into african highland potato varieties confers complete field resistance to local blight races
topic potatoes
phytophthora infestans
varieties
resistance varieties
biotechnology
url https://hdl.handle.net/10568/99120
work_keys_str_mv AT ghislainm stackingthreelateblightresistancegenesfromwildspeciesdirectlyintoafricanhighlandpotatovarietiesconferscompletefieldresistancetolocalblightraces
AT byarugabaaa stackingthreelateblightresistancegenesfromwildspeciesdirectlyintoafricanhighlandpotatovarietiesconferscompletefieldresistancetolocalblightraces
AT magembee stackingthreelateblightresistancegenesfromwildspeciesdirectlyintoafricanhighlandpotatovarietiesconferscompletefieldresistancetolocalblightraces
AT njorogeaw stackingthreelateblightresistancegenesfromwildspeciesdirectlyintoafricanhighlandpotatovarietiesconferscompletefieldresistancetolocalblightraces
AT riverac stackingthreelateblightresistancegenesfromwildspeciesdirectlyintoafricanhighlandpotatovarietiesconferscompletefieldresistancetolocalblightraces
AT romanml stackingthreelateblightresistancegenesfromwildspeciesdirectlyintoafricanhighlandpotatovarietiesconferscompletefieldresistancetolocalblightraces
AT tovarjc stackingthreelateblightresistancegenesfromwildspeciesdirectlyintoafricanhighlandpotatovarietiesconferscompletefieldresistancetolocalblightraces
AT gamboas stackingthreelateblightresistancegenesfromwildspeciesdirectlyintoafricanhighlandpotatovarietiesconferscompletefieldresistancetolocalblightraces
AT forbesg stackingthreelateblightresistancegenesfromwildspeciesdirectlyintoafricanhighlandpotatovarietiesconferscompletefieldresistancetolocalblightraces
AT kreuzejanf stackingthreelateblightresistancegenesfromwildspeciesdirectlyintoafricanhighlandpotatovarietiesconferscompletefieldresistancetolocalblightraces
AT barekyea stackingthreelateblightresistancegenesfromwildspeciesdirectlyintoafricanhighlandpotatovarietiesconferscompletefieldresistancetolocalblightraces
AT kiggundua stackingthreelateblightresistancegenesfromwildspeciesdirectlyintoafricanhighlandpotatovarietiesconferscompletefieldresistancetolocalblightraces