Soybean stem canker caused by diaporthe caulivora; pathogen diversity, colonization process, and plant defense activation

Mena, Eilyn - Stewart, Silvina - Montesano Quintas, Marcos Richard - Ponce de León Tadeo, Inés

Editor(es): Frenkel, O.

Resumen:

Soybean is an important crop in South America, and its production is limited by fungal diseases caused by species from the genus Diaporthe, including seed decay, pod and stem blight, and soybean stem canker (SSC). In this study, we focused on Diaporthe species isolated from soybean plants with SSC lesions in different parts of Uruguay. Diaporthe diversity was determined by sequencing the internal transcribed spacer (ITS) regions of ribosomal RNA and a partial region of the translation elongation factor 1-alpha gene (TEF1α). Phylogenetic analysis showed that the isolates belong to five defined groups of Diaporthe species, Diaporthe caulivora and Diaporthe longicolla being the most predominant species present in stem canker lesions. Due to the importance of D. caulivora as the causal agent of SSC in the region and other parts of the world, we further characterized the interaction of this pathogen with soybean. Based on genetic diversity of D. caulivora isolates evaluated with inter-sequence single repetition (ISSR), three different isolates were selected for pathogenicity assays. Differences in virulence were observed among the selected D. caulivora isolates on susceptible soybean plants. Further inspection of the infection and colonization process showed that D. caulivora hyphae are associated with trichomes in petioles, leaves, and stems, acting probably as physical adhesion sites of the hyphae. D. caulivora colonized the stem rapidly reaching the phloem and the xylem at 72 h post-inoculation (hpi), and after 96 hpi, the stem was heavily colonized. Infected soybean plants induce reinforcement of the cell walls, evidenced by incorporation of phenolic compounds. In addition, several defense genes were induced in D. caulivora–inoculated stems, including those encoding a pathogenesis-related protein-1 (PR-1), a PR-10, a β-1,3-glucanase, two chitinases, two lipoxygenases, a basic peroxidase, a defensin, a phenylalanine-ammonia lyase, and a chalcone synthase. This study provides new insights into the interaction of soybean with D. caulivora, an important pathogen causing SSC, and provides information on the activation of plant defense responses.


Detalles Bibliográficos
2020
Soybean stem canker
Diaporthe caulivora
Internal transcribed spacer (ITS)
Ribosomal RNA (rDNA)
Translation elongation factor 1-alpha gene (TEF1a)
Disease symptoms
Pathogen colonization
Cell wall
Defense genes
Inglés
Universidad de la República
COLIBRI
https://hdl.handle.net/20.500.12008/32363
Acceso abierto
Licencia Creative Commons Atribución (CC - By 4.0)
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author Mena, Eilyn
author2 Stewart, Silvina
Montesano Quintas, Marcos Richard
Ponce de León Tadeo, Inés
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author_facet Mena, Eilyn
Stewart, Silvina
Montesano Quintas, Marcos Richard
Ponce de León Tadeo, Inés
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dc.contributor.filiacion.none.fl_str_mv Mena Eilyn, IIBCE
Stewart Silvina, INIA (Uruguay)
Montesano Quintas Marcos Richard, Universidad de la República (Uruguay). Facultad de Ciencias. Centro de Investigaciones Nucleares
Ponce de León Tadeo Inés, IIBCE
dc.creator.editor.none.fl_str_mv Frenkel, O.
dc.creator.none.fl_str_mv Mena, Eilyn
Stewart, Silvina
Montesano Quintas, Marcos Richard
Ponce de León Tadeo, Inés
dc.date.accessioned.none.fl_str_mv 2022-06-24T13:52:25Z
dc.date.available.none.fl_str_mv 2022-06-24T13:52:25Z
dc.date.issued.none.fl_str_mv 2020
dc.description.abstract.none.fl_txt_mv Soybean is an important crop in South America, and its production is limited by fungal diseases caused by species from the genus Diaporthe, including seed decay, pod and stem blight, and soybean stem canker (SSC). In this study, we focused on Diaporthe species isolated from soybean plants with SSC lesions in different parts of Uruguay. Diaporthe diversity was determined by sequencing the internal transcribed spacer (ITS) regions of ribosomal RNA and a partial region of the translation elongation factor 1-alpha gene (TEF1α). Phylogenetic analysis showed that the isolates belong to five defined groups of Diaporthe species, Diaporthe caulivora and Diaporthe longicolla being the most predominant species present in stem canker lesions. Due to the importance of D. caulivora as the causal agent of SSC in the region and other parts of the world, we further characterized the interaction of this pathogen with soybean. Based on genetic diversity of D. caulivora isolates evaluated with inter-sequence single repetition (ISSR), three different isolates were selected for pathogenicity assays. Differences in virulence were observed among the selected D. caulivora isolates on susceptible soybean plants. Further inspection of the infection and colonization process showed that D. caulivora hyphae are associated with trichomes in petioles, leaves, and stems, acting probably as physical adhesion sites of the hyphae. D. caulivora colonized the stem rapidly reaching the phloem and the xylem at 72 h post-inoculation (hpi), and after 96 hpi, the stem was heavily colonized. Infected soybean plants induce reinforcement of the cell walls, evidenced by incorporation of phenolic compounds. In addition, several defense genes were induced in D. caulivora–inoculated stems, including those encoding a pathogenesis-related protein-1 (PR-1), a PR-10, a β-1,3-glucanase, two chitinases, two lipoxygenases, a basic peroxidase, a defensin, a phenylalanine-ammonia lyase, and a chalcone synthase. This study provides new insights into the interaction of soybean with D. caulivora, an important pathogen causing SSC, and provides information on the activation of plant defense responses.
dc.format.extent.es.fl_str_mv 21 h.
dc.format.mimetype.es.fl_str_mv application/pdf
dc.identifier.citation.es.fl_str_mv Mena, E, Stewart, S, Montesano Quintas, M [y otros] "Soybean stem canker caused by diaporthe caulivora; pathogen diversity, colonization process, and plant defense activation". Frontiers in Plant Science. [en línea] 2020, 10:1733. 21 h. DOI: 10.3389/fpls.2019.01733
dc.identifier.doi.none.fl_str_mv 10.3389/fpls.2019.01733
dc.identifier.issn.none.fl_str_mv 1664-462X
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/20.500.12008/32363
dc.language.iso.none.fl_str_mv en
eng
dc.publisher.es.fl_str_mv Frontiers Media
dc.relation.ispartof.es.fl_str_mv Frontiers in Plant Science, 2020, 10:1733
dc.rights.license.none.fl_str_mv Licencia Creative Commons Atribución (CC - By 4.0)
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
dc.source.none.fl_str_mv reponame:COLIBRI
instname:Universidad de la República
instacron:Universidad de la República
dc.subject.es.fl_str_mv Soybean stem canker
Diaporthe caulivora
Internal transcribed spacer (ITS)
Ribosomal RNA (rDNA)
Translation elongation factor 1-alpha gene (TEF1a)
Disease symptoms
Pathogen colonization
Cell wall
Defense genes
dc.title.none.fl_str_mv Soybean stem canker caused by diaporthe caulivora; pathogen diversity, colonization process, and plant defense activation
dc.type.es.fl_str_mv Artículo
dc.type.none.fl_str_mv info:eu-repo/semantics/article
dc.type.version.none.fl_str_mv info:eu-repo/semantics/publishedVersion
description Soybean is an important crop in South America, and its production is limited by fungal diseases caused by species from the genus Diaporthe, including seed decay, pod and stem blight, and soybean stem canker (SSC). In this study, we focused on Diaporthe species isolated from soybean plants with SSC lesions in different parts of Uruguay. Diaporthe diversity was determined by sequencing the internal transcribed spacer (ITS) regions of ribosomal RNA and a partial region of the translation elongation factor 1-alpha gene (TEF1α). Phylogenetic analysis showed that the isolates belong to five defined groups of Diaporthe species, Diaporthe caulivora and Diaporthe longicolla being the most predominant species present in stem canker lesions. Due to the importance of D. caulivora as the causal agent of SSC in the region and other parts of the world, we further characterized the interaction of this pathogen with soybean. Based on genetic diversity of D. caulivora isolates evaluated with inter-sequence single repetition (ISSR), three different isolates were selected for pathogenicity assays. Differences in virulence were observed among the selected D. caulivora isolates on susceptible soybean plants. Further inspection of the infection and colonization process showed that D. caulivora hyphae are associated with trichomes in petioles, leaves, and stems, acting probably as physical adhesion sites of the hyphae. D. caulivora colonized the stem rapidly reaching the phloem and the xylem at 72 h post-inoculation (hpi), and after 96 hpi, the stem was heavily colonized. Infected soybean plants induce reinforcement of the cell walls, evidenced by incorporation of phenolic compounds. In addition, several defense genes were induced in D. caulivora–inoculated stems, including those encoding a pathogenesis-related protein-1 (PR-1), a PR-10, a β-1,3-glucanase, two chitinases, two lipoxygenases, a basic peroxidase, a defensin, a phenylalanine-ammonia lyase, and a chalcone synthase. This study provides new insights into the interaction of soybean with D. caulivora, an important pathogen causing SSC, and provides information on the activation of plant defense responses.
eu_rights_str_mv openAccess
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identifier_str_mv Mena, E, Stewart, S, Montesano Quintas, M [y otros] "Soybean stem canker caused by diaporthe caulivora; pathogen diversity, colonization process, and plant defense activation". Frontiers in Plant Science. [en línea] 2020, 10:1733. 21 h. DOI: 10.3389/fpls.2019.01733
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10.3389/fpls.2019.01733
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repository.mail.fl_str_mv mabel.seroubian@seciu.edu.uy
repository.name.fl_str_mv COLIBRI - Universidad de la República
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rights_invalid_str_mv Licencia Creative Commons Atribución (CC - By 4.0)
spelling Mena Eilyn, IIBCEStewart Silvina, INIA (Uruguay)Montesano Quintas Marcos Richard, Universidad de la República (Uruguay). Facultad de Ciencias. Centro de Investigaciones NuclearesPonce de León Tadeo Inés, IIBCE2022-06-24T13:52:25Z2022-06-24T13:52:25Z2020Mena, E, Stewart, S, Montesano Quintas, M [y otros] "Soybean stem canker caused by diaporthe caulivora; pathogen diversity, colonization process, and plant defense activation". Frontiers in Plant Science. [en línea] 2020, 10:1733. 21 h. DOI: 10.3389/fpls.2019.017331664-462Xhttps://hdl.handle.net/20.500.12008/3236310.3389/fpls.2019.01733Soybean is an important crop in South America, and its production is limited by fungal diseases caused by species from the genus Diaporthe, including seed decay, pod and stem blight, and soybean stem canker (SSC). In this study, we focused on Diaporthe species isolated from soybean plants with SSC lesions in different parts of Uruguay. Diaporthe diversity was determined by sequencing the internal transcribed spacer (ITS) regions of ribosomal RNA and a partial region of the translation elongation factor 1-alpha gene (TEF1α). Phylogenetic analysis showed that the isolates belong to five defined groups of Diaporthe species, Diaporthe caulivora and Diaporthe longicolla being the most predominant species present in stem canker lesions. Due to the importance of D. caulivora as the causal agent of SSC in the region and other parts of the world, we further characterized the interaction of this pathogen with soybean. Based on genetic diversity of D. caulivora isolates evaluated with inter-sequence single repetition (ISSR), three different isolates were selected for pathogenicity assays. Differences in virulence were observed among the selected D. caulivora isolates on susceptible soybean plants. Further inspection of the infection and colonization process showed that D. caulivora hyphae are associated with trichomes in petioles, leaves, and stems, acting probably as physical adhesion sites of the hyphae. D. caulivora colonized the stem rapidly reaching the phloem and the xylem at 72 h post-inoculation (hpi), and after 96 hpi, the stem was heavily colonized. Infected soybean plants induce reinforcement of the cell walls, evidenced by incorporation of phenolic compounds. In addition, several defense genes were induced in D. caulivora–inoculated stems, including those encoding a pathogenesis-related protein-1 (PR-1), a PR-10, a β-1,3-glucanase, two chitinases, two lipoxygenases, a basic peroxidase, a defensin, a phenylalanine-ammonia lyase, and a chalcone synthase. This study provides new insights into the interaction of soybean with D. caulivora, an important pathogen causing SSC, and provides information on the activation of plant defense responses.Submitted by Verdun Juan Pablo (jverdun@fcien.edu.uy) on 2022-06-13T16:48:21Z No. of bitstreams: 2 license_rdf: 19875 bytes, checksum: 9fdbed07f52437945402c4e70fa4773e (MD5) 10.3389fpls.2019.01733.pdf: 10549449 bytes, checksum: e5c41eadc4ab761128ec2229b2b883cc (MD5)Approved for entry into archive by Faget Cecilia (lfaget@fcien.edu.uy) on 2022-06-24T13:44:45Z (GMT) No. of bitstreams: 2 license_rdf: 19875 bytes, checksum: 9fdbed07f52437945402c4e70fa4773e (MD5) 10.3389fpls.2019.01733.pdf: 10549449 bytes, checksum: e5c41eadc4ab761128ec2229b2b883cc (MD5)Made available in DSpace by Luna Fabiana (fabiana.luna@seciu.edu.uy) on 2022-06-24T13:52:25Z (GMT). No. of bitstreams: 2 license_rdf: 19875 bytes, checksum: 9fdbed07f52437945402c4e70fa4773e (MD5) 10.3389fpls.2019.01733.pdf: 10549449 bytes, checksum: e5c41eadc4ab761128ec2229b2b883cc (MD5) Previous issue date: 202021 h.application/pdfenengFrontiers MediaFrontiers in Plant Science, 2020, 10:1733Las obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014)info:eu-repo/semantics/openAccessLicencia Creative Commons Atribución (CC - By 4.0)Soybean stem cankerDiaporthe caulivoraInternal transcribed spacer (ITS)Ribosomal RNA (rDNA)Translation elongation factor 1-alpha gene (TEF1a)Disease symptomsPathogen colonizationCell wallDefense genesSoybean stem canker caused by diaporthe caulivora; pathogen diversity, colonization process, and plant defense activationArtículoinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionreponame:COLIBRIinstname:Universidad de la Repúblicainstacron:Universidad de la RepúblicaMena, EilynStewart, SilvinaMontesano Quintas, Marcos RichardPonce de León Tadeo, InésFrenkel, O.LICENSElicense.txtlicense.txttext/plain; charset=utf-84267http://localhost:8080/xmlui/bitstream/20.500.12008/32363/5/license.txt6429389a7df7277b72b7924fdc7d47a9MD55CC-LICENSElicense_urllicense_urltext/plain; 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- Universidad de la Repúblicafalse
spellingShingle Soybean stem canker caused by diaporthe caulivora; pathogen diversity, colonization process, and plant defense activation
Mena, Eilyn
Soybean stem canker
Diaporthe caulivora
Internal transcribed spacer (ITS)
Ribosomal RNA (rDNA)
Translation elongation factor 1-alpha gene (TEF1a)
Disease symptoms
Pathogen colonization
Cell wall
Defense genes
status_str publishedVersion
title Soybean stem canker caused by diaporthe caulivora; pathogen diversity, colonization process, and plant defense activation
title_full Soybean stem canker caused by diaporthe caulivora; pathogen diversity, colonization process, and plant defense activation
title_fullStr Soybean stem canker caused by diaporthe caulivora; pathogen diversity, colonization process, and plant defense activation
title_full_unstemmed Soybean stem canker caused by diaporthe caulivora; pathogen diversity, colonization process, and plant defense activation
title_short Soybean stem canker caused by diaporthe caulivora; pathogen diversity, colonization process, and plant defense activation
title_sort Soybean stem canker caused by diaporthe caulivora; pathogen diversity, colonization process, and plant defense activation
topic Soybean stem canker
Diaporthe caulivora
Internal transcribed spacer (ITS)
Ribosomal RNA (rDNA)
Translation elongation factor 1-alpha gene (TEF1a)
Disease symptoms
Pathogen colonization
Cell wall
Defense genes
url https://hdl.handle.net/20.500.12008/32363