Loading…

Early detection of Ascochyta blight (Ascochyta rabiei) of chickpea by traditional PCR

Ascochyta blight is the major disease affecting chickpea (Cicer arietinum) around the world. Since the first report of Ascochyta rabiei's isolation in Argentina in 2012, the pathogen has caused severe economic losses in crop production; so, the detection and rapid identification of the pathogen...

Full description

Saved in:
Bibliographic Details
Published in:Crop protection 2021-05, Vol.143, p.105463, Article 105463
Main Authors: Valetti, Lucio, Cazón, Luis Ignacio, Crociara, Clara, Pastor, Silvina
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c352t-ddf38ce1899d4c44faf86ce073221781297da2428fb3eb788a0e8701d3fedc73
cites cdi_FETCH-LOGICAL-c352t-ddf38ce1899d4c44faf86ce073221781297da2428fb3eb788a0e8701d3fedc73
container_end_page
container_issue
container_start_page 105463
container_title Crop protection
container_volume 143
creator Valetti, Lucio
Cazón, Luis Ignacio
Crociara, Clara
Pastor, Silvina
description Ascochyta blight is the major disease affecting chickpea (Cicer arietinum) around the world. Since the first report of Ascochyta rabiei's isolation in Argentina in 2012, the pathogen has caused severe economic losses in crop production; so, the detection and rapid identification of the pathogen in early stages is key for the management of the disease. In this work, a traditional PCR procedure for detection of A. rabiei directly from plant tissues has been described based on beta-tubulin gene. The TP-6/TP-9 specific primers designed, amplified only a single PCR band of 770 bp from A. rabiei. The specificity of the primers was checked using 12 isolates of A. rabiei and DNA from 10 other different fungi including common pathogens of chickpea as Alternaria alternata, Botrytis cinerea, Sclerotinia sclerotiorum and Phoma medicaginis that cause similar symptoms. The detection sensitivity with primers was 2 × 104 ng μl−1 genomic DNA. In inoculated plant material, PCR amplification gave a band of the expected size and no amplification was observed when DNA was from healthy and uninoculated plants. The results suggested that the assay detected the pathogen more rapidly and accurately than standard isolation methods. The PCR-based method developed here can simplify both plant disease diagnosis, and pathogen monitoring in an early phase, as well as aid in effective management practices that avoid the disease advance and minimize losses. •A rapid, sensitive, and effective molecular method to detect A. rabiei in early stages of the disease was developed.•A. rabiei specific primers were designed from beta-tubulin gene.•Field samples with incipient symptoms of Ascochyta bligth of 50 sites were monitored using the molecular method developed.
doi_str_mv 10.1016/j.cropro.2020.105463
format article
fullrecord <record><control><sourceid>elsevier_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1016_j_cropro_2020_105463</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0261219420303963</els_id><sourcerecordid>S0261219420303963</sourcerecordid><originalsourceid>FETCH-LOGICAL-c352t-ddf38ce1899d4c44faf86ce073221781297da2428fb3eb788a0e8701d3fedc73</originalsourceid><addsrcrecordid>eNp9kEtLxDAUhYMoOI7-AxdZ6qI1r2nSjTAM4wMGFBnXIU1ubMY6LUkR-u9tqeDO1YXDOYdzP4SuKckpocXdIbex7WKbM8ImaSUKfoIWVEmeFSURp2hBWEEzRktxji5SOhBCGOdsgd63JjYDdtCD7UN7xK3H62RbWw-9wVUTPuoe3_wp0VQBwu1ks3Wwnx2MrgH30bgw5U2DXzdvl-jMmybB1e9dov3Ddr95ynYvj8-b9S6zfMX6zDnPlQWqytIJK4Q3XhUWiOSMUakoK6UzTDDlKw6VVMoQUJJQxz04K_kSibl2fD-lCF53MXyZOGhK9ERGH_RMRk9k9ExmjN3PMRinfQeIOtkARwsuxJGCdm34v-AHeGBuwQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Early detection of Ascochyta blight (Ascochyta rabiei) of chickpea by traditional PCR</title><source>Elsevier</source><creator>Valetti, Lucio ; Cazón, Luis Ignacio ; Crociara, Clara ; Pastor, Silvina</creator><creatorcontrib>Valetti, Lucio ; Cazón, Luis Ignacio ; Crociara, Clara ; Pastor, Silvina</creatorcontrib><description>Ascochyta blight is the major disease affecting chickpea (Cicer arietinum) around the world. Since the first report of Ascochyta rabiei's isolation in Argentina in 2012, the pathogen has caused severe economic losses in crop production; so, the detection and rapid identification of the pathogen in early stages is key for the management of the disease. In this work, a traditional PCR procedure for detection of A. rabiei directly from plant tissues has been described based on beta-tubulin gene. The TP-6/TP-9 specific primers designed, amplified only a single PCR band of 770 bp from A. rabiei. The specificity of the primers was checked using 12 isolates of A. rabiei and DNA from 10 other different fungi including common pathogens of chickpea as Alternaria alternata, Botrytis cinerea, Sclerotinia sclerotiorum and Phoma medicaginis that cause similar symptoms. The detection sensitivity with primers was 2 × 104 ng μl−1 genomic DNA. In inoculated plant material, PCR amplification gave a band of the expected size and no amplification was observed when DNA was from healthy and uninoculated plants. The results suggested that the assay detected the pathogen more rapidly and accurately than standard isolation methods. The PCR-based method developed here can simplify both plant disease diagnosis, and pathogen monitoring in an early phase, as well as aid in effective management practices that avoid the disease advance and minimize losses. •A rapid, sensitive, and effective molecular method to detect A. rabiei in early stages of the disease was developed.•A. rabiei specific primers were designed from beta-tubulin gene.•Field samples with incipient symptoms of Ascochyta bligth of 50 sites were monitored using the molecular method developed.</description><identifier>ISSN: 0261-2194</identifier><identifier>EISSN: 1873-6904</identifier><identifier>DOI: 10.1016/j.cropro.2020.105463</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Ascochyta blight ; Ascochyta rabiei ; Chickpea ; Molecular diagnostic</subject><ispartof>Crop protection, 2021-05, Vol.143, p.105463, Article 105463</ispartof><rights>2020 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-ddf38ce1899d4c44faf86ce073221781297da2428fb3eb788a0e8701d3fedc73</citedby><cites>FETCH-LOGICAL-c352t-ddf38ce1899d4c44faf86ce073221781297da2428fb3eb788a0e8701d3fedc73</cites><orcidid>0000-0002-8600-8673</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Valetti, Lucio</creatorcontrib><creatorcontrib>Cazón, Luis Ignacio</creatorcontrib><creatorcontrib>Crociara, Clara</creatorcontrib><creatorcontrib>Pastor, Silvina</creatorcontrib><title>Early detection of Ascochyta blight (Ascochyta rabiei) of chickpea by traditional PCR</title><title>Crop protection</title><description>Ascochyta blight is the major disease affecting chickpea (Cicer arietinum) around the world. Since the first report of Ascochyta rabiei's isolation in Argentina in 2012, the pathogen has caused severe economic losses in crop production; so, the detection and rapid identification of the pathogen in early stages is key for the management of the disease. In this work, a traditional PCR procedure for detection of A. rabiei directly from plant tissues has been described based on beta-tubulin gene. The TP-6/TP-9 specific primers designed, amplified only a single PCR band of 770 bp from A. rabiei. The specificity of the primers was checked using 12 isolates of A. rabiei and DNA from 10 other different fungi including common pathogens of chickpea as Alternaria alternata, Botrytis cinerea, Sclerotinia sclerotiorum and Phoma medicaginis that cause similar symptoms. The detection sensitivity with primers was 2 × 104 ng μl−1 genomic DNA. In inoculated plant material, PCR amplification gave a band of the expected size and no amplification was observed when DNA was from healthy and uninoculated plants. The results suggested that the assay detected the pathogen more rapidly and accurately than standard isolation methods. The PCR-based method developed here can simplify both plant disease diagnosis, and pathogen monitoring in an early phase, as well as aid in effective management practices that avoid the disease advance and minimize losses. •A rapid, sensitive, and effective molecular method to detect A. rabiei in early stages of the disease was developed.•A. rabiei specific primers were designed from beta-tubulin gene.•Field samples with incipient symptoms of Ascochyta bligth of 50 sites were monitored using the molecular method developed.</description><subject>Ascochyta blight</subject><subject>Ascochyta rabiei</subject><subject>Chickpea</subject><subject>Molecular diagnostic</subject><issn>0261-2194</issn><issn>1873-6904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kEtLxDAUhYMoOI7-AxdZ6qI1r2nSjTAM4wMGFBnXIU1ubMY6LUkR-u9tqeDO1YXDOYdzP4SuKckpocXdIbex7WKbM8ImaSUKfoIWVEmeFSURp2hBWEEzRktxji5SOhBCGOdsgd63JjYDdtCD7UN7xK3H62RbWw-9wVUTPuoe3_wp0VQBwu1ks3Wwnx2MrgH30bgw5U2DXzdvl-jMmybB1e9dov3Ddr95ynYvj8-b9S6zfMX6zDnPlQWqytIJK4Q3XhUWiOSMUakoK6UzTDDlKw6VVMoQUJJQxz04K_kSibl2fD-lCF53MXyZOGhK9ERGH_RMRk9k9ExmjN3PMRinfQeIOtkARwsuxJGCdm34v-AHeGBuwQ</recordid><startdate>202105</startdate><enddate>202105</enddate><creator>Valetti, Lucio</creator><creator>Cazón, Luis Ignacio</creator><creator>Crociara, Clara</creator><creator>Pastor, Silvina</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-8600-8673</orcidid></search><sort><creationdate>202105</creationdate><title>Early detection of Ascochyta blight (Ascochyta rabiei) of chickpea by traditional PCR</title><author>Valetti, Lucio ; Cazón, Luis Ignacio ; Crociara, Clara ; Pastor, Silvina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-ddf38ce1899d4c44faf86ce073221781297da2428fb3eb788a0e8701d3fedc73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Ascochyta blight</topic><topic>Ascochyta rabiei</topic><topic>Chickpea</topic><topic>Molecular diagnostic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Valetti, Lucio</creatorcontrib><creatorcontrib>Cazón, Luis Ignacio</creatorcontrib><creatorcontrib>Crociara, Clara</creatorcontrib><creatorcontrib>Pastor, Silvina</creatorcontrib><collection>CrossRef</collection><jtitle>Crop protection</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Valetti, Lucio</au><au>Cazón, Luis Ignacio</au><au>Crociara, Clara</au><au>Pastor, Silvina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Early detection of Ascochyta blight (Ascochyta rabiei) of chickpea by traditional PCR</atitle><jtitle>Crop protection</jtitle><date>2021-05</date><risdate>2021</risdate><volume>143</volume><spage>105463</spage><pages>105463-</pages><artnum>105463</artnum><issn>0261-2194</issn><eissn>1873-6904</eissn><abstract>Ascochyta blight is the major disease affecting chickpea (Cicer arietinum) around the world. Since the first report of Ascochyta rabiei's isolation in Argentina in 2012, the pathogen has caused severe economic losses in crop production; so, the detection and rapid identification of the pathogen in early stages is key for the management of the disease. In this work, a traditional PCR procedure for detection of A. rabiei directly from plant tissues has been described based on beta-tubulin gene. The TP-6/TP-9 specific primers designed, amplified only a single PCR band of 770 bp from A. rabiei. The specificity of the primers was checked using 12 isolates of A. rabiei and DNA from 10 other different fungi including common pathogens of chickpea as Alternaria alternata, Botrytis cinerea, Sclerotinia sclerotiorum and Phoma medicaginis that cause similar symptoms. The detection sensitivity with primers was 2 × 104 ng μl−1 genomic DNA. In inoculated plant material, PCR amplification gave a band of the expected size and no amplification was observed when DNA was from healthy and uninoculated plants. The results suggested that the assay detected the pathogen more rapidly and accurately than standard isolation methods. The PCR-based method developed here can simplify both plant disease diagnosis, and pathogen monitoring in an early phase, as well as aid in effective management practices that avoid the disease advance and minimize losses. •A rapid, sensitive, and effective molecular method to detect A. rabiei in early stages of the disease was developed.•A. rabiei specific primers were designed from beta-tubulin gene.•Field samples with incipient symptoms of Ascochyta bligth of 50 sites were monitored using the molecular method developed.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.cropro.2020.105463</doi><orcidid>https://orcid.org/0000-0002-8600-8673</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0261-2194
ispartof Crop protection, 2021-05, Vol.143, p.105463, Article 105463
issn 0261-2194
1873-6904
language eng
recordid cdi_crossref_primary_10_1016_j_cropro_2020_105463
source Elsevier
subjects Ascochyta blight
Ascochyta rabiei
Chickpea
Molecular diagnostic
title Early detection of Ascochyta blight (Ascochyta rabiei) of chickpea by traditional PCR
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T17%3A38%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Early%20detection%20of%20Ascochyta%20blight%20(Ascochyta%20rabiei)%20of%20chickpea%20by%20traditional%20PCR&rft.jtitle=Crop%20protection&rft.au=Valetti,%20Lucio&rft.date=2021-05&rft.volume=143&rft.spage=105463&rft.pages=105463-&rft.artnum=105463&rft.issn=0261-2194&rft.eissn=1873-6904&rft_id=info:doi/10.1016/j.cropro.2020.105463&rft_dat=%3Celsevier_cross%3ES0261219420303963%3C/elsevier_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c352t-ddf38ce1899d4c44faf86ce073221781297da2428fb3eb788a0e8701d3fedc73%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true