Correlation of molecular markers and biological properties in Verticillium dahliae and the possible origins of some isolates

Haploid and amphihaploid Verticillium dahliae isolates were studied using PCR‐based molecular markers which: (i) discriminate the defoliating and nondefoliating pathotypes (two primer pairs INTD2f/r and INTND2f/r), and (ii) are species‐specific (primer pair 19/22). The results were compared with som...

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Veröffentlicht in:Plant pathology 2005-08, Vol.54 (4), p.549-557
Hauptverfasser: Collins, A, Mercado-Blanco, J, Jimenez-Diaz, R.M, Olivares, C, Clewes, E, Barbara, D.J
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container_issue 4
container_start_page 549
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creator Collins, A
Mercado-Blanco, J
Jimenez-Diaz, R.M
Olivares, C
Clewes, E
Barbara, D.J
description Haploid and amphihaploid Verticillium dahliae isolates were studied using PCR‐based molecular markers which: (i) discriminate the defoliating and nondefoliating pathotypes (two primer pairs INTD2f/r and INTND2f/r), and (ii) are species‐specific (primer pair 19/22). The results were compared with some known biological and other molecular properties of the isolates. Five discrete sequences of the 19/22 amplicon were found. Sequence 4 was associated with both defoliating isolates from Spain and nondefoliating isolates from Spain and USA; these pathotypes were separated by the primer pairs INTD2f/r and INTND2f/r, but the data showed that the primer espdef01 (derived from the 19/22 amplicon) cannot be used for this purpose. Amplicon sizes and sequences with primers 19/22 divided amphihaploid isolates from crucifers (thought to be interspecific hybrids) into those corresponding to the previously reported α and β groups. The β‐group isolates had either sequence 4 or 5 (these two differing by a single base). The distinct amplicon sequence 3 given by the α‐group isolates demonstrated that the V. dahliae‐like ‘parent’ of this group was molecularly unlike any haploid isolate yet studied. The overall results are discussed in relation to phytosanitary considerations and the probability of defoliating or crucifer pathotypes arising de novo within Europe, either by selection or by interspecific hybridizations.
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The results were compared with some known biological and other molecular properties of the isolates. Five discrete sequences of the 19/22 amplicon were found. Sequence 4 was associated with both defoliating isolates from Spain and nondefoliating isolates from Spain and USA; these pathotypes were separated by the primer pairs INTD2f/r and INTND2f/r, but the data showed that the primer espdef01 (derived from the 19/22 amplicon) cannot be used for this purpose. Amplicon sizes and sequences with primers 19/22 divided amphihaploid isolates from crucifers (thought to be interspecific hybrids) into those corresponding to the previously reported α and β groups. The β‐group isolates had either sequence 4 or 5 (these two differing by a single base). The distinct amplicon sequence 3 given by the α‐group isolates demonstrated that the V. dahliae‐like ‘parent’ of this group was molecularly unlike any haploid isolate yet studied. 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The results were compared with some known biological and other molecular properties of the isolates. Five discrete sequences of the 19/22 amplicon were found. Sequence 4 was associated with both defoliating isolates from Spain and nondefoliating isolates from Spain and USA; these pathotypes were separated by the primer pairs INTD2f/r and INTND2f/r, but the data showed that the primer espdef01 (derived from the 19/22 amplicon) cannot be used for this purpose. Amplicon sizes and sequences with primers 19/22 divided amphihaploid isolates from crucifers (thought to be interspecific hybrids) into those corresponding to the previously reported α and β groups. The β‐group isolates had either sequence 4 or 5 (these two differing by a single base). The distinct amplicon sequence 3 given by the α‐group isolates demonstrated that the V. dahliae‐like ‘parent’ of this group was molecularly unlike any haploid isolate yet studied. The overall results are discussed in relation to phytosanitary considerations and the probability of defoliating or crucifer pathotypes arising de novo within Europe, either by selection or by interspecific hybridizations.</description><subject>amphihaploids</subject><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungal plant pathogens</subject><subject>genetic markers</subject><subject>genetic variation</subject><subject>geographical variation</subject><subject>interspecific hybrids</subject><subject>molecular sequence data</subject><subject>nucleotide sequences</subject><subject>pathogen identification</subject><subject>pathotypes</subject><subject>Phytopathology. Animal pests. Plant and forest protection</subject><subject>plant pathogenic fungi</subject><subject>polymerase chain reaction</subject><subject>provenance</subject><subject>sequence analysis</subject><subject>vegetative compatibility</subject><subject>Verticillium dahliae</subject><subject>Verticillium wilt</subject><subject>wilt diseases</subject><issn>0032-0862</issn><issn>1365-3059</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqNUU1r3DAQFaWFbtP-hopCe7M7kmzJOvQQlvQDAg00yVVo5fFGW9naSmuaQH585WxoIafqooF5782bN4RQBjUr7-OuZkK2lYBW1xygrYHxBurbZ2T1t_GcrAAEr6CT_CV5lfMOgLVadytyv44pYbAHHycaBzrGgG4ONtHRpp-YMrVTTzc-hrj1zga6T3GP6eAxUz_R66V0PgQ_j7S3N8FbfGAcbpDuY85-E5DG5Ld-yot-jiNSn2OZiPk1eTHYkPHN439Crj6fXa6_Vuffv3xbn55XrlEtVJxbpbpNK9sGFWjminXVKhBDL_nSBIkbp3veM9YMuhGsQwdKDpx3XItenJAPR91i_teM-WBGnx2GYCeMczZMCdlppgvw3RPgLs5pKt4MZ7JjUqi2gLojyKWyYMLB7JMvad0ZBma5idmZJXqzRG-Wm5iHm5jbQn3_qG9zCXNIdnI-_-Mr4FpLUXCfjrjfPuDdf-ubi4vTpSr8t0f-YKOx21RmXP3gwAQw4KAaLv4AQo2ouA</recordid><startdate>200508</startdate><enddate>200508</enddate><creator>Collins, A</creator><creator>Mercado-Blanco, J</creator><creator>Jimenez-Diaz, R.M</creator><creator>Olivares, C</creator><creator>Clewes, E</creator><creator>Barbara, D.J</creator><general>Blackwell Science Ltd</general><general>Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>FBQ</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>200508</creationdate><title>Correlation of molecular markers and biological properties in Verticillium dahliae and the possible origins of some isolates</title><author>Collins, A ; Mercado-Blanco, J ; Jimenez-Diaz, R.M ; Olivares, C ; Clewes, E ; Barbara, D.J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4750-22a778b5654e7091c59975703fd6222a706ebc9d2d114f94318ec076f228293d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>amphihaploids</topic><topic>Biological and medical sciences</topic><topic>Fundamental and applied biological sciences. 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Plant and forest protection</topic><topic>plant pathogenic fungi</topic><topic>polymerase chain reaction</topic><topic>provenance</topic><topic>sequence analysis</topic><topic>vegetative compatibility</topic><topic>Verticillium dahliae</topic><topic>Verticillium wilt</topic><topic>wilt diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Collins, A</creatorcontrib><creatorcontrib>Mercado-Blanco, J</creatorcontrib><creatorcontrib>Jimenez-Diaz, R.M</creatorcontrib><creatorcontrib>Olivares, C</creatorcontrib><creatorcontrib>Clewes, E</creatorcontrib><creatorcontrib>Barbara, D.J</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Plant pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Collins, A</au><au>Mercado-Blanco, J</au><au>Jimenez-Diaz, R.M</au><au>Olivares, C</au><au>Clewes, E</au><au>Barbara, D.J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correlation of molecular markers and biological properties in Verticillium dahliae and the possible origins of some isolates</atitle><jtitle>Plant pathology</jtitle><date>2005-08</date><risdate>2005</risdate><volume>54</volume><issue>4</issue><spage>549</spage><epage>557</epage><pages>549-557</pages><issn>0032-0862</issn><eissn>1365-3059</eissn><coden>PLPAAD</coden><abstract>Haploid and amphihaploid Verticillium dahliae isolates were studied using PCR‐based molecular markers which: (i) discriminate the defoliating and nondefoliating pathotypes (two primer pairs INTD2f/r and INTND2f/r), and (ii) are species‐specific (primer pair 19/22). The results were compared with some known biological and other molecular properties of the isolates. Five discrete sequences of the 19/22 amplicon were found. Sequence 4 was associated with both defoliating isolates from Spain and nondefoliating isolates from Spain and USA; these pathotypes were separated by the primer pairs INTD2f/r and INTND2f/r, but the data showed that the primer espdef01 (derived from the 19/22 amplicon) cannot be used for this purpose. Amplicon sizes and sequences with primers 19/22 divided amphihaploid isolates from crucifers (thought to be interspecific hybrids) into those corresponding to the previously reported α and β groups. The β‐group isolates had either sequence 4 or 5 (these two differing by a single base). The distinct amplicon sequence 3 given by the α‐group isolates demonstrated that the V. dahliae‐like ‘parent’ of this group was molecularly unlike any haploid isolate yet studied. 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subjects amphihaploids
Biological and medical sciences
Fundamental and applied biological sciences. Psychology
Fungal plant pathogens
genetic markers
genetic variation
geographical variation
interspecific hybrids
molecular sequence data
nucleotide sequences
pathogen identification
pathotypes
Phytopathology. Animal pests. Plant and forest protection
plant pathogenic fungi
polymerase chain reaction
provenance
sequence analysis
vegetative compatibility
Verticillium dahliae
Verticillium wilt
wilt diseases
title Correlation of molecular markers and biological properties in Verticillium dahliae and the possible origins of some isolates
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