Cargando…

Expression of apoplast-targeted plant defensin MtDef4.2 confers resistance to leaf rust pathogen Puccinia triticina but does not affect mycorrhizal symbiosis in transgenic wheat

Rust fungi of the order Pucciniales are destructive pathogens of wheat worldwide. Leaf rust caused by the obligate, biotrophic basidiomycete fungus Puccinia triticina (Pt) is an economically important disease capable of causing up to 50 % yield losses. Historically, resistant wheat cultivars have be...

Descripción completa

Detalles Bibliográficos
Autores principales: Kaur, Jagdeep, Fellers, John, Adholeya, Alok, Velivelli, Siva L. S., El-Mounadi, Kaoutar, Nersesian, Natalya, Clemente, Thomas, Shah, Dilip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243879/
https://www.ncbi.nlm.nih.gov/pubmed/27582300
http://dx.doi.org/10.1007/s11248-016-9978-9
_version_ 1782496594687426560
author Kaur, Jagdeep
Fellers, John
Adholeya, Alok
Velivelli, Siva L. S.
El-Mounadi, Kaoutar
Nersesian, Natalya
Clemente, Thomas
Shah, Dilip
author_facet Kaur, Jagdeep
Fellers, John
Adholeya, Alok
Velivelli, Siva L. S.
El-Mounadi, Kaoutar
Nersesian, Natalya
Clemente, Thomas
Shah, Dilip
author_sort Kaur, Jagdeep
collection PubMed
description Rust fungi of the order Pucciniales are destructive pathogens of wheat worldwide. Leaf rust caused by the obligate, biotrophic basidiomycete fungus Puccinia triticina (Pt) is an economically important disease capable of causing up to 50 % yield losses. Historically, resistant wheat cultivars have been used to control leaf rust, but genetic resistance is ephemeral and breaks down with the emergence of new virulent Pt races. There is a need to develop alternative measures for control of leaf rust in wheat. Development of transgenic wheat expressing an antifungal defensin offers a promising approach to complement the endogenous resistance genes within the wheat germplasm for durable resistance to Pt. To that end, two different wheat genotypes, Bobwhite and Xin Chun 9 were transformed with a chimeric gene encoding an apoplast-targeted antifungal plant defensin MtDEF4.2 from Medicago truncatula. Transgenic lines from four independent events were further characterized. Homozygous transgenic wheat lines expressing MtDEF4.2 displayed resistance to Pt race MCPSS relative to the non-transgenic controls in growth chamber bioassays. Histopathological analysis suggested the presence of both pre- and posthaustorial resistance to leaf rust in these transgenic lines. MtDEF4.2 did not, however, affect the root colonization of a beneficial arbuscular mycorrhizal fungus Rhizophagus irregularis. This study demonstrates that the expression of apoplast-targeted plant defensin MtDEF4.2 can provide substantial resistance to an economically important leaf rust disease in transgenic wheat without negatively impacting its symbiotic relationship with the beneficial mycorrhizal fungus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11248-016-9978-9) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5243879
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Springer International Publishing
record_format MEDLINE/PubMed
spelling pubmed-52438792017-02-01 Expression of apoplast-targeted plant defensin MtDef4.2 confers resistance to leaf rust pathogen Puccinia triticina but does not affect mycorrhizal symbiosis in transgenic wheat Kaur, Jagdeep Fellers, John Adholeya, Alok Velivelli, Siva L. S. El-Mounadi, Kaoutar Nersesian, Natalya Clemente, Thomas Shah, Dilip Transgenic Res Original Paper Rust fungi of the order Pucciniales are destructive pathogens of wheat worldwide. Leaf rust caused by the obligate, biotrophic basidiomycete fungus Puccinia triticina (Pt) is an economically important disease capable of causing up to 50 % yield losses. Historically, resistant wheat cultivars have been used to control leaf rust, but genetic resistance is ephemeral and breaks down with the emergence of new virulent Pt races. There is a need to develop alternative measures for control of leaf rust in wheat. Development of transgenic wheat expressing an antifungal defensin offers a promising approach to complement the endogenous resistance genes within the wheat germplasm for durable resistance to Pt. To that end, two different wheat genotypes, Bobwhite and Xin Chun 9 were transformed with a chimeric gene encoding an apoplast-targeted antifungal plant defensin MtDEF4.2 from Medicago truncatula. Transgenic lines from four independent events were further characterized. Homozygous transgenic wheat lines expressing MtDEF4.2 displayed resistance to Pt race MCPSS relative to the non-transgenic controls in growth chamber bioassays. Histopathological analysis suggested the presence of both pre- and posthaustorial resistance to leaf rust in these transgenic lines. MtDEF4.2 did not, however, affect the root colonization of a beneficial arbuscular mycorrhizal fungus Rhizophagus irregularis. This study demonstrates that the expression of apoplast-targeted plant defensin MtDEF4.2 can provide substantial resistance to an economically important leaf rust disease in transgenic wheat without negatively impacting its symbiotic relationship with the beneficial mycorrhizal fungus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11248-016-9978-9) contains supplementary material, which is available to authorized users. Springer International Publishing 2016-08-31 2017 /pmc/articles/PMC5243879/ /pubmed/27582300 http://dx.doi.org/10.1007/s11248-016-9978-9 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
Kaur, Jagdeep
Fellers, John
Adholeya, Alok
Velivelli, Siva L. S.
El-Mounadi, Kaoutar
Nersesian, Natalya
Clemente, Thomas
Shah, Dilip
Expression of apoplast-targeted plant defensin MtDef4.2 confers resistance to leaf rust pathogen Puccinia triticina but does not affect mycorrhizal symbiosis in transgenic wheat
title Expression of apoplast-targeted plant defensin MtDef4.2 confers resistance to leaf rust pathogen Puccinia triticina but does not affect mycorrhizal symbiosis in transgenic wheat
title_full Expression of apoplast-targeted plant defensin MtDef4.2 confers resistance to leaf rust pathogen Puccinia triticina but does not affect mycorrhizal symbiosis in transgenic wheat
title_fullStr Expression of apoplast-targeted plant defensin MtDef4.2 confers resistance to leaf rust pathogen Puccinia triticina but does not affect mycorrhizal symbiosis in transgenic wheat
title_full_unstemmed Expression of apoplast-targeted plant defensin MtDef4.2 confers resistance to leaf rust pathogen Puccinia triticina but does not affect mycorrhizal symbiosis in transgenic wheat
title_short Expression of apoplast-targeted plant defensin MtDef4.2 confers resistance to leaf rust pathogen Puccinia triticina but does not affect mycorrhizal symbiosis in transgenic wheat
title_sort expression of apoplast-targeted plant defensin mtdef4.2 confers resistance to leaf rust pathogen puccinia triticina but does not affect mycorrhizal symbiosis in transgenic wheat
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243879/
https://www.ncbi.nlm.nih.gov/pubmed/27582300
http://dx.doi.org/10.1007/s11248-016-9978-9
work_keys_str_mv AT kaurjagdeep expressionofapoplasttargetedplantdefensinmtdef42confersresistancetoleafrustpathogenpucciniatriticinabutdoesnotaffectmycorrhizalsymbiosisintransgenicwheat
AT fellersjohn expressionofapoplasttargetedplantdefensinmtdef42confersresistancetoleafrustpathogenpucciniatriticinabutdoesnotaffectmycorrhizalsymbiosisintransgenicwheat
AT adholeyaalok expressionofapoplasttargetedplantdefensinmtdef42confersresistancetoleafrustpathogenpucciniatriticinabutdoesnotaffectmycorrhizalsymbiosisintransgenicwheat
AT velivellisivals expressionofapoplasttargetedplantdefensinmtdef42confersresistancetoleafrustpathogenpucciniatriticinabutdoesnotaffectmycorrhizalsymbiosisintransgenicwheat
AT elmounadikaoutar expressionofapoplasttargetedplantdefensinmtdef42confersresistancetoleafrustpathogenpucciniatriticinabutdoesnotaffectmycorrhizalsymbiosisintransgenicwheat
AT nersesiannatalya expressionofapoplasttargetedplantdefensinmtdef42confersresistancetoleafrustpathogenpucciniatriticinabutdoesnotaffectmycorrhizalsymbiosisintransgenicwheat
AT clementethomas expressionofapoplasttargetedplantdefensinmtdef42confersresistancetoleafrustpathogenpucciniatriticinabutdoesnotaffectmycorrhizalsymbiosisintransgenicwheat
AT shahdilip expressionofapoplasttargetedplantdefensinmtdef42confersresistancetoleafrustpathogenpucciniatriticinabutdoesnotaffectmycorrhizalsymbiosisintransgenicwheat