Loading…
Characterization of novel di-, tri-, and tetranucleotide microsatellite primers suitable for genotyping various plant pathogenic fungi with special emphasis on Fusaria and Mycospherella graminicola
The goals of this investigation were to identify and evaluate the use of polymorphic microsatellite marker (PMM) analysis for molecular typing of seventeen plant pathogenic fungi. Primers for di-, tri-, and tetranucleotide loci were designed directly from the recently published genomic sequence of M...
Saved in:
Published in: | International journal of molecular sciences 2012-03, Vol.13 (3), p.2951-2964 |
---|---|
Main Authors: | , , , , |
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-c444t-7a51b6e5f2095be8569df151393453164e42960563ac5f3ef9f850e72fd7c5153 |
---|---|
cites | cdi_FETCH-LOGICAL-c444t-7a51b6e5f2095be8569df151393453164e42960563ac5f3ef9f850e72fd7c5153 |
container_end_page | 2964 |
container_issue | 3 |
container_start_page | 2951 |
container_title | International journal of molecular sciences |
container_volume | 13 |
creator | Bahkali, Ali H Abd-Elsalam, Kamel A Guo, Jian-Rong Khiyami, Mohamed A Verreet, Joseph-Alexander |
description | The goals of this investigation were to identify and evaluate the use of polymorphic microsatellite marker (PMM) analysis for molecular typing of seventeen plant pathogenic fungi. Primers for di-, tri-, and tetranucleotide loci were designed directly from the recently published genomic sequence of Mycospherlla graminicola and Fusarium graminearum. A total of 20 new microsatellite primers as easy-to-score markers were developed. Microsatellite primer PCR (MP-PCR) yielded highly reproducible and complex genomic fingerprints, with several bands ranging in size from 200 to 3000 bp. Of the 20 primers tested, only (TAGG)4, (TCC)5 and (CA)7T produced a high number of polymorphic bands from either F. graminearum or F. culmorum. (ATG)5 led to successful amplifications in M. graminicola isolates collected from Germany. Percentage of polymorphic bands among Fusarium species ranged from 9 to 100%. Cluster analysis of banding patterns of the isolates corresponded well to the established species delineations based on morphology and other methods of phylogenetic analysis. The current research demonstrates that the newly designed microsatellite primers are reliable, sensitive and technically simple tools for assaying genetic variability in plant pathogenic fungi. |
doi_str_mv | 10.3390/ijms13032951 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3317696</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3308573581</sourcerecordid><originalsourceid>FETCH-LOGICAL-c444t-7a51b6e5f2095be8569df151393453164e42960563ac5f3ef9f850e72fd7c5153</originalsourceid><addsrcrecordid>eNp9kk9v1DAQxSMEomXhxhlZ4gCHBvwnTtYXJLRqAamIC5yjWWe88Sqxg-0sWr4f36sOLdXCgYttyT-_eW88RfGc0TdCKPrW7sfIBBVcSfagOGcV5yWldfPw5HxWPIlxTykXXKrHxRnn1VoxIc-LX5seAuiEwf6EZL0j3hDnDziQzpYXJIVlBdeRhCmAm_WAPtkOyWh18BESDoNNSKZgRwyRxNkm2A5IjA9kh86n42TdjhwgWD9HMg3gEpkg9T7fWk3M7HaW_LCpJ3FCbWEgOE49RBtJtnM1x_wSflv4fNQ-Tj2GXBPILsBos4If4GnxyMAQ8dndviq-XV1-3Xwsr798-LR5f13qqqpS2YBk2xql4VTJLa5lrTrDJBNKVFKwusKKq5rKWoCWRqBRZi0pNtx0jZZMilXx7lZ3mrcjdhpd7snQLtkhHFsPtv37xtm-3flDKwRralVngVd3AsF_nzGmdrRRL3Ec5u60Si1klQ2titf_JRnjkgtZNeuMvvwH3fs5uNyIlkle0xyMLaUvbqnl22JAc2-b0XaZpPZ0kjL-4jTqPfxndMQNYqrJsA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1526016416</pqid></control><display><type>article</type><title>Characterization of novel di-, tri-, and tetranucleotide microsatellite primers suitable for genotyping various plant pathogenic fungi with special emphasis on Fusaria and Mycospherella graminicola</title><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Bahkali, Ali H ; Abd-Elsalam, Kamel A ; Guo, Jian-Rong ; Khiyami, Mohamed A ; Verreet, Joseph-Alexander</creator><creatorcontrib>Bahkali, Ali H ; Abd-Elsalam, Kamel A ; Guo, Jian-Rong ; Khiyami, Mohamed A ; Verreet, Joseph-Alexander</creatorcontrib><description>The goals of this investigation were to identify and evaluate the use of polymorphic microsatellite marker (PMM) analysis for molecular typing of seventeen plant pathogenic fungi. Primers for di-, tri-, and tetranucleotide loci were designed directly from the recently published genomic sequence of Mycospherlla graminicola and Fusarium graminearum. A total of 20 new microsatellite primers as easy-to-score markers were developed. Microsatellite primer PCR (MP-PCR) yielded highly reproducible and complex genomic fingerprints, with several bands ranging in size from 200 to 3000 bp. Of the 20 primers tested, only (TAGG)4, (TCC)5 and (CA)7T produced a high number of polymorphic bands from either F. graminearum or F. culmorum. (ATG)5 led to successful amplifications in M. graminicola isolates collected from Germany. Percentage of polymorphic bands among Fusarium species ranged from 9 to 100%. Cluster analysis of banding patterns of the isolates corresponded well to the established species delineations based on morphology and other methods of phylogenetic analysis. The current research demonstrates that the newly designed microsatellite primers are reliable, sensitive and technically simple tools for assaying genetic variability in plant pathogenic fungi.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms13032951</identifier><identifier>PMID: 22489135</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Ascomycota - genetics ; Ascomycota - isolation & purification ; Ascomycota - pathogenicity ; Banding ; DNA Fingerprinting ; DNA Primers - genetics ; DNA, Fungal - genetics ; Fungi ; Fusarium - genetics ; Fusarium - isolation & purification ; Fusarium - pathogenicity ; Fusarium graminearum ; Genetic diversity ; Genetic markers ; Genomes ; genomics ; Genotype ; Genotyping ; Microsatellite Repeats ; Microsatellites ; Pathogens ; Phylogeny ; Plant Diseases - microbiology ; Plants - microbiology ; Polymerase chain reaction ; Polymorphism ; Polymorphism, Genetic ; Primers</subject><ispartof>International journal of molecular sciences, 2012-03, Vol.13 (3), p.2951-2964</ispartof><rights>Copyright MDPI AG 2012</rights><rights>2012 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c444t-7a51b6e5f2095be8569df151393453164e42960563ac5f3ef9f850e72fd7c5153</citedby><cites>FETCH-LOGICAL-c444t-7a51b6e5f2095be8569df151393453164e42960563ac5f3ef9f850e72fd7c5153</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1526016416/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1526016416?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25730,27900,27901,36988,36989,44565,53765,53767,75095</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22489135$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bahkali, Ali H</creatorcontrib><creatorcontrib>Abd-Elsalam, Kamel A</creatorcontrib><creatorcontrib>Guo, Jian-Rong</creatorcontrib><creatorcontrib>Khiyami, Mohamed A</creatorcontrib><creatorcontrib>Verreet, Joseph-Alexander</creatorcontrib><title>Characterization of novel di-, tri-, and tetranucleotide microsatellite primers suitable for genotyping various plant pathogenic fungi with special emphasis on Fusaria and Mycospherella graminicola</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>The goals of this investigation were to identify and evaluate the use of polymorphic microsatellite marker (PMM) analysis for molecular typing of seventeen plant pathogenic fungi. Primers for di-, tri-, and tetranucleotide loci were designed directly from the recently published genomic sequence of Mycospherlla graminicola and Fusarium graminearum. A total of 20 new microsatellite primers as easy-to-score markers were developed. Microsatellite primer PCR (MP-PCR) yielded highly reproducible and complex genomic fingerprints, with several bands ranging in size from 200 to 3000 bp. Of the 20 primers tested, only (TAGG)4, (TCC)5 and (CA)7T produced a high number of polymorphic bands from either F. graminearum or F. culmorum. (ATG)5 led to successful amplifications in M. graminicola isolates collected from Germany. Percentage of polymorphic bands among Fusarium species ranged from 9 to 100%. Cluster analysis of banding patterns of the isolates corresponded well to the established species delineations based on morphology and other methods of phylogenetic analysis. The current research demonstrates that the newly designed microsatellite primers are reliable, sensitive and technically simple tools for assaying genetic variability in plant pathogenic fungi.</description><subject>Ascomycota - genetics</subject><subject>Ascomycota - isolation & purification</subject><subject>Ascomycota - pathogenicity</subject><subject>Banding</subject><subject>DNA Fingerprinting</subject><subject>DNA Primers - genetics</subject><subject>DNA, Fungal - genetics</subject><subject>Fungi</subject><subject>Fusarium - genetics</subject><subject>Fusarium - isolation & purification</subject><subject>Fusarium - pathogenicity</subject><subject>Fusarium graminearum</subject><subject>Genetic diversity</subject><subject>Genetic markers</subject><subject>Genomes</subject><subject>genomics</subject><subject>Genotype</subject><subject>Genotyping</subject><subject>Microsatellite Repeats</subject><subject>Microsatellites</subject><subject>Pathogens</subject><subject>Phylogeny</subject><subject>Plant Diseases - microbiology</subject><subject>Plants - microbiology</subject><subject>Polymerase chain reaction</subject><subject>Polymorphism</subject><subject>Polymorphism, Genetic</subject><subject>Primers</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp9kk9v1DAQxSMEomXhxhlZ4gCHBvwnTtYXJLRqAamIC5yjWWe88Sqxg-0sWr4f36sOLdXCgYttyT-_eW88RfGc0TdCKPrW7sfIBBVcSfagOGcV5yWldfPw5HxWPIlxTykXXKrHxRnn1VoxIc-LX5seAuiEwf6EZL0j3hDnDziQzpYXJIVlBdeRhCmAm_WAPtkOyWh18BESDoNNSKZgRwyRxNkm2A5IjA9kh86n42TdjhwgWD9HMg3gEpkg9T7fWk3M7HaW_LCpJ3FCbWEgOE49RBtJtnM1x_wSflv4fNQ-Tj2GXBPILsBos4If4GnxyMAQ8dndviq-XV1-3Xwsr798-LR5f13qqqpS2YBk2xql4VTJLa5lrTrDJBNKVFKwusKKq5rKWoCWRqBRZi0pNtx0jZZMilXx7lZ3mrcjdhpd7snQLtkhHFsPtv37xtm-3flDKwRralVngVd3AsF_nzGmdrRRL3Ec5u60Si1klQ2titf_JRnjkgtZNeuMvvwH3fs5uNyIlkle0xyMLaUvbqnl22JAc2-b0XaZpPZ0kjL-4jTqPfxndMQNYqrJsA</recordid><startdate>20120301</startdate><enddate>20120301</enddate><creator>Bahkali, Ali H</creator><creator>Abd-Elsalam, Kamel A</creator><creator>Guo, Jian-Rong</creator><creator>Khiyami, Mohamed A</creator><creator>Verreet, Joseph-Alexander</creator><general>MDPI AG</general><general>Molecular Diversity Preservation International (MDPI)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20120301</creationdate><title>Characterization of novel di-, tri-, and tetranucleotide microsatellite primers suitable for genotyping various plant pathogenic fungi with special emphasis on Fusaria and Mycospherella graminicola</title><author>Bahkali, Ali H ; Abd-Elsalam, Kamel A ; Guo, Jian-Rong ; Khiyami, Mohamed A ; Verreet, Joseph-Alexander</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c444t-7a51b6e5f2095be8569df151393453164e42960563ac5f3ef9f850e72fd7c5153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Ascomycota - genetics</topic><topic>Ascomycota - isolation & purification</topic><topic>Ascomycota - pathogenicity</topic><topic>Banding</topic><topic>DNA Fingerprinting</topic><topic>DNA Primers - genetics</topic><topic>DNA, Fungal - genetics</topic><topic>Fungi</topic><topic>Fusarium - genetics</topic><topic>Fusarium - isolation & purification</topic><topic>Fusarium - pathogenicity</topic><topic>Fusarium graminearum</topic><topic>Genetic diversity</topic><topic>Genetic markers</topic><topic>Genomes</topic><topic>genomics</topic><topic>Genotype</topic><topic>Genotyping</topic><topic>Microsatellite Repeats</topic><topic>Microsatellites</topic><topic>Pathogens</topic><topic>Phylogeny</topic><topic>Plant Diseases - microbiology</topic><topic>Plants - microbiology</topic><topic>Polymerase chain reaction</topic><topic>Polymorphism</topic><topic>Polymorphism, Genetic</topic><topic>Primers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bahkali, Ali H</creatorcontrib><creatorcontrib>Abd-Elsalam, Kamel A</creatorcontrib><creatorcontrib>Guo, Jian-Rong</creatorcontrib><creatorcontrib>Khiyami, Mohamed A</creatorcontrib><creatorcontrib>Verreet, Joseph-Alexander</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bahkali, Ali H</au><au>Abd-Elsalam, Kamel A</au><au>Guo, Jian-Rong</au><au>Khiyami, Mohamed A</au><au>Verreet, Joseph-Alexander</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of novel di-, tri-, and tetranucleotide microsatellite primers suitable for genotyping various plant pathogenic fungi with special emphasis on Fusaria and Mycospherella graminicola</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2012-03-01</date><risdate>2012</risdate><volume>13</volume><issue>3</issue><spage>2951</spage><epage>2964</epage><pages>2951-2964</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>The goals of this investigation were to identify and evaluate the use of polymorphic microsatellite marker (PMM) analysis for molecular typing of seventeen plant pathogenic fungi. Primers for di-, tri-, and tetranucleotide loci were designed directly from the recently published genomic sequence of Mycospherlla graminicola and Fusarium graminearum. A total of 20 new microsatellite primers as easy-to-score markers were developed. Microsatellite primer PCR (MP-PCR) yielded highly reproducible and complex genomic fingerprints, with several bands ranging in size from 200 to 3000 bp. Of the 20 primers tested, only (TAGG)4, (TCC)5 and (CA)7T produced a high number of polymorphic bands from either F. graminearum or F. culmorum. (ATG)5 led to successful amplifications in M. graminicola isolates collected from Germany. Percentage of polymorphic bands among Fusarium species ranged from 9 to 100%. Cluster analysis of banding patterns of the isolates corresponded well to the established species delineations based on morphology and other methods of phylogenetic analysis. The current research demonstrates that the newly designed microsatellite primers are reliable, sensitive and technically simple tools for assaying genetic variability in plant pathogenic fungi.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>22489135</pmid><doi>10.3390/ijms13032951</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1422-0067 |
ispartof | International journal of molecular sciences, 2012-03, Vol.13 (3), p.2951-2964 |
issn | 1422-0067 1661-6596 1422-0067 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3317696 |
source | Publicly Available Content Database; PubMed Central |
subjects | Ascomycota - genetics Ascomycota - isolation & purification Ascomycota - pathogenicity Banding DNA Fingerprinting DNA Primers - genetics DNA, Fungal - genetics Fungi Fusarium - genetics Fusarium - isolation & purification Fusarium - pathogenicity Fusarium graminearum Genetic diversity Genetic markers Genomes genomics Genotype Genotyping Microsatellite Repeats Microsatellites Pathogens Phylogeny Plant Diseases - microbiology Plants - microbiology Polymerase chain reaction Polymorphism Polymorphism, Genetic Primers |
title | Characterization of novel di-, tri-, and tetranucleotide microsatellite primers suitable for genotyping various plant pathogenic fungi with special emphasis on Fusaria and Mycospherella graminicola |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-24T18%3A20%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Characterization%20of%20novel%20di-,%20tri-,%20and%20tetranucleotide%20microsatellite%20primers%20suitable%20for%20genotyping%20various%20plant%20pathogenic%20fungi%20with%20special%20emphasis%20on%20Fusaria%20and%20Mycospherella%20graminicola&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Bahkali,%20Ali%20H&rft.date=2012-03-01&rft.volume=13&rft.issue=3&rft.spage=2951&rft.epage=2964&rft.pages=2951-2964&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms13032951&rft_dat=%3Cproquest_pubme%3E3308573581%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c444t-7a51b6e5f2095be8569df151393453164e42960563ac5f3ef9f850e72fd7c5153%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1526016416&rft_id=info:pmid/22489135&rfr_iscdi=true |