Hybridization in larch-alternating Melampsora epitea (M. larici-epitea)
Crossing and selfing experiments were carried out with six field collections and five isolates belonging to three formae speciales, larici-epitea typica (LET), larici-daphnoides (LD), and larici-retusae (LR), of willow rust, Melampsora epitea. European larch (Larix decidua) was inoculated with basid...
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description | Crossing and selfing experiments were carried out with six field collections and five isolates belonging to three formae speciales,
larici-epitea typica (LET), larici-daphnoides (LD), and larici-retusae (LR), of willow rust, Melampsora epitea. European larch (Larix decidua)
was inoculated with basidiospores produced on overwintered telial leaves and the resulting spermagonial lesions on larch needles
subsequently paired in vitro. In two crosses between LR and LD involving a total of 439 lesion pairs, only two cultures obtained
were identified as hybrids. These two cultures were non-pathogenic to the maternal host Salix burjatica cv. Korso and weakly
pathogenic to the paternal host S. daphnoides cv. Meikle. No identifiable hybrids were obtained from 56 lesion pairs between LET
and LD. In a cross between LET as receptor and LD as donor, one-third of the lesions formed aecia. In the reciprocal combination,
however, less than 1% developed aecia. All F1 cultures between LET and LR were weakly pathogenic to the parental hosts
S. viminalis cv. Mullatin and S. burjatica cv. Korso. When three of the F1 cultures were used to produce telia, only one developed
mature teliospores. Subsequent selfing experiments showed that this culture was predominantly self-sterile, with only 1% of lesions
producing aecia. In selfing and crossing two pathotypes within the same f. spp., 20–40% of needles produced aecia and the rate of
aecial formation was similar in both directions. The results obtained suggest that M. epitea is heterothallic and the sexual
compatibility is controlled by a pair of alleles at a locus. It is concluded that the three f. spp. are genetically different populations and
ecologically fit new pathotypes cannot arise easily as a result of hybridization between them. Within a f. sp., however, many
pathotypes exist or will occur due to exchange of genes for virulence during the sexual life-cycle. |
doi_str_mv | 10.1017/S0953756299008655 |
format | Article |
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larici-epitea typica (LET), larici-daphnoides (LD), and larici-retusae (LR), of willow rust, Melampsora epitea. European larch (Larix decidua)
was inoculated with basidiospores produced on overwintered telial leaves and the resulting spermagonial lesions on larch needles
subsequently paired in vitro. In two crosses between LR and LD involving a total of 439 lesion pairs, only two cultures obtained
were identified as hybrids. These two cultures were non-pathogenic to the maternal host Salix burjatica cv. Korso and weakly
pathogenic to the paternal host S. daphnoides cv. Meikle. No identifiable hybrids were obtained from 56 lesion pairs between LET
and LD. In a cross between LET as receptor and LD as donor, one-third of the lesions formed aecia. In the reciprocal combination,
however, less than 1% developed aecia. All F1 cultures between LET and LR were weakly pathogenic to the parental hosts
S. viminalis cv. Mullatin and S. burjatica cv. Korso. When three of the F1 cultures were used to produce telia, only one developed
mature teliospores. Subsequent selfing experiments showed that this culture was predominantly self-sterile, with only 1% of lesions
producing aecia. In selfing and crossing two pathotypes within the same f. spp., 20–40% of needles produced aecia and the rate of
aecial formation was similar in both directions. The results obtained suggest that M. epitea is heterothallic and the sexual
compatibility is controlled by a pair of alleles at a locus. It is concluded that the three f. spp. are genetically different populations and
ecologically fit new pathotypes cannot arise easily as a result of hybridization between them. Within a f. sp., however, many
pathotypes exist or will occur due to exchange of genes for virulence during the sexual life-cycle.</description><identifier>ISSN: 0953-7562</identifier><identifier>EISSN: 1469-8102</identifier><identifier>DOI: 10.1017/S0953756299008655</identifier><language>eng</language><publisher>Oxford: Cambridge University Press</publisher><subject>alleles ; basidiospores ; Biological and medical sciences ; biological development ; compatibility ; conifer needles ; crossing ; experimental infections ; Fundamental and applied biological sciences. Psychology ; fungal diseases of plants ; Fungal plant pathogens ; growth ; host plants ; hybridization ; Larix decidua ; leaf spotting ; leaves ; lesions ; life cycle (organisms) ; loci ; Melampsora ; Melampsora epitea ; pathogenicity ; pathotypes ; Phytopathology. Animal pests. Plant and forest protection ; plant diseases and disorders ; rust diseases ; Salix ; self compatibility ; sexual reproduction ; Variation, races, biotypes, parasitic specialization, genetics ; virulence</subject><ispartof>Mycological research, 1999, Vol.103 (11), p.1440-1446</ispartof><rights>The British Mycological Society 1999</rights><rights>1999 British Mycological Society</rights><rights>2000 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c518t-5fdf05fa060bcacd548174033b7cef2676579a10b1608e32dfe53e6c6a584a963</citedby><cites>FETCH-LOGICAL-c518t-5fdf05fa060bcacd548174033b7cef2676579a10b1608e32dfe53e6c6a584a963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1184886$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>PEI, M. H.</creatorcontrib><creatorcontrib>ROYLE, D. J.</creatorcontrib><creatorcontrib>HUNTER, T.</creatorcontrib><title>Hybridization in larch-alternating Melampsora epitea (M. larici-epitea)</title><title>Mycological research</title><addtitle>Mycol. Res</addtitle><description>Crossing and selfing experiments were carried out with six field collections and five isolates belonging to three formae speciales,
larici-epitea typica (LET), larici-daphnoides (LD), and larici-retusae (LR), of willow rust, Melampsora epitea. European larch (Larix decidua)
was inoculated with basidiospores produced on overwintered telial leaves and the resulting spermagonial lesions on larch needles
subsequently paired in vitro. In two crosses between LR and LD involving a total of 439 lesion pairs, only two cultures obtained
were identified as hybrids. These two cultures were non-pathogenic to the maternal host Salix burjatica cv. Korso and weakly
pathogenic to the paternal host S. daphnoides cv. Meikle. No identifiable hybrids were obtained from 56 lesion pairs between LET
and LD. In a cross between LET as receptor and LD as donor, one-third of the lesions formed aecia. In the reciprocal combination,
however, less than 1% developed aecia. All F1 cultures between LET and LR were weakly pathogenic to the parental hosts
S. viminalis cv. Mullatin and S. burjatica cv. Korso. When three of the F1 cultures were used to produce telia, only one developed
mature teliospores. Subsequent selfing experiments showed that this culture was predominantly self-sterile, with only 1% of lesions
producing aecia. In selfing and crossing two pathotypes within the same f. spp., 20–40% of needles produced aecia and the rate of
aecial formation was similar in both directions. The results obtained suggest that M. epitea is heterothallic and the sexual
compatibility is controlled by a pair of alleles at a locus. It is concluded that the three f. spp. are genetically different populations and
ecologically fit new pathotypes cannot arise easily as a result of hybridization between them. Within a f. sp., however, many
pathotypes exist or will occur due to exchange of genes for virulence during the sexual life-cycle.</description><subject>alleles</subject><subject>basidiospores</subject><subject>Biological and medical sciences</subject><subject>biological development</subject><subject>compatibility</subject><subject>conifer needles</subject><subject>crossing</subject><subject>experimental infections</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>fungal diseases of plants</subject><subject>Fungal plant pathogens</subject><subject>growth</subject><subject>host plants</subject><subject>hybridization</subject><subject>Larix decidua</subject><subject>leaf spotting</subject><subject>leaves</subject><subject>lesions</subject><subject>life cycle (organisms)</subject><subject>loci</subject><subject>Melampsora</subject><subject>Melampsora epitea</subject><subject>pathogenicity</subject><subject>pathotypes</subject><subject>Phytopathology. Animal pests. Plant and forest protection</subject><subject>plant diseases and disorders</subject><subject>rust diseases</subject><subject>Salix</subject><subject>self compatibility</subject><subject>sexual reproduction</subject><subject>Variation, races, biotypes, parasitic specialization, genetics</subject><subject>virulence</subject><issn>0953-7562</issn><issn>1469-8102</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNp9kU9L5EAQxZtFYUfdD7CnzUFED3Gr0-lOB08i_oMRD67npqZTPduSScbujDB-ejtkwIPgqaDq9x6PV4z95nDOgVd_n6CWopKqqGsAraT8wWa8VHWuORR7bDae8_H-kx3E-ALABedixm7vtovgG_-Og--7zHdZi8H-z7EdKHRp2S2zB2pxtY59wIzWfiDMTh_OR85bn0-bsyO277CN9Gs3D9nzzfW_q7t8_nh7f3U5z63kesilaxxIh6BgYdE2stS8KkGIRWXJFapSsqqRw4Ir0CSKxpEUpKxCqUuslThkJ5PvOvSvG4qDWfloqW2xo34TTXIrZVFBAvkE2tDHGMiZdfArDFvDwYyVmS-VJc3xzhyjxdYF7KyPn0KuS63HDH8mzGFvcBkS8vxUpEahqMvkVSfiYiIoVfHmKZhoPXWWGh_IDqbp_bcxxC46rsbnLMm89Jv0jTZ-o_oAx8eViA</recordid><startdate>1999</startdate><enddate>1999</enddate><creator>PEI, M. H.</creator><creator>ROYLE, D. J.</creator><creator>HUNTER, T.</creator><general>Cambridge University Press</general><general>Elsevier Ltd</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>M7N</scope></search><sort><creationdate>1999</creationdate><title>Hybridization in larch-alternating Melampsora epitea (M. larici-epitea)</title><author>PEI, M. H. ; ROYLE, D. J. ; HUNTER, T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c518t-5fdf05fa060bcacd548174033b7cef2676579a10b1608e32dfe53e6c6a584a963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>alleles</topic><topic>basidiospores</topic><topic>Biological and medical sciences</topic><topic>biological development</topic><topic>compatibility</topic><topic>conifer needles</topic><topic>crossing</topic><topic>experimental infections</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>fungal diseases of plants</topic><topic>Fungal plant pathogens</topic><topic>growth</topic><topic>host plants</topic><topic>hybridization</topic><topic>Larix decidua</topic><topic>leaf spotting</topic><topic>leaves</topic><topic>lesions</topic><topic>life cycle (organisms)</topic><topic>loci</topic><topic>Melampsora</topic><topic>Melampsora epitea</topic><topic>pathogenicity</topic><topic>pathotypes</topic><topic>Phytopathology. Animal pests. Plant and forest protection</topic><topic>plant diseases and disorders</topic><topic>rust diseases</topic><topic>Salix</topic><topic>self compatibility</topic><topic>sexual reproduction</topic><topic>Variation, races, biotypes, parasitic specialization, genetics</topic><topic>virulence</topic><toplevel>online_resources</toplevel><creatorcontrib>PEI, M. H.</creatorcontrib><creatorcontrib>ROYLE, D. J.</creatorcontrib><creatorcontrib>HUNTER, T.</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Mycological research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PEI, M. H.</au><au>ROYLE, D. J.</au><au>HUNTER, T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hybridization in larch-alternating Melampsora epitea (M. larici-epitea)</atitle><jtitle>Mycological research</jtitle><addtitle>Mycol. Res</addtitle><date>1999</date><risdate>1999</risdate><volume>103</volume><issue>11</issue><spage>1440</spage><epage>1446</epage><pages>1440-1446</pages><issn>0953-7562</issn><eissn>1469-8102</eissn><abstract>Crossing and selfing experiments were carried out with six field collections and five isolates belonging to three formae speciales,
larici-epitea typica (LET), larici-daphnoides (LD), and larici-retusae (LR), of willow rust, Melampsora epitea. European larch (Larix decidua)
was inoculated with basidiospores produced on overwintered telial leaves and the resulting spermagonial lesions on larch needles
subsequently paired in vitro. In two crosses between LR and LD involving a total of 439 lesion pairs, only two cultures obtained
were identified as hybrids. These two cultures were non-pathogenic to the maternal host Salix burjatica cv. Korso and weakly
pathogenic to the paternal host S. daphnoides cv. Meikle. No identifiable hybrids were obtained from 56 lesion pairs between LET
and LD. In a cross between LET as receptor and LD as donor, one-third of the lesions formed aecia. In the reciprocal combination,
however, less than 1% developed aecia. All F1 cultures between LET and LR were weakly pathogenic to the parental hosts
S. viminalis cv. Mullatin and S. burjatica cv. Korso. When three of the F1 cultures were used to produce telia, only one developed
mature teliospores. Subsequent selfing experiments showed that this culture was predominantly self-sterile, with only 1% of lesions
producing aecia. In selfing and crossing two pathotypes within the same f. spp., 20–40% of needles produced aecia and the rate of
aecial formation was similar in both directions. The results obtained suggest that M. epitea is heterothallic and the sexual
compatibility is controlled by a pair of alleles at a locus. It is concluded that the three f. spp. are genetically different populations and
ecologically fit new pathotypes cannot arise easily as a result of hybridization between them. Within a f. sp., however, many
pathotypes exist or will occur due to exchange of genes for virulence during the sexual life-cycle.</abstract><cop>Oxford</cop><pub>Cambridge University Press</pub><doi>10.1017/S0953756299008655</doi><tpages>7</tpages></addata></record> |
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source | Alma/SFX Local Collection |
subjects | alleles basidiospores Biological and medical sciences biological development compatibility conifer needles crossing experimental infections Fundamental and applied biological sciences. Psychology fungal diseases of plants Fungal plant pathogens growth host plants hybridization Larix decidua leaf spotting leaves lesions life cycle (organisms) loci Melampsora Melampsora epitea pathogenicity pathotypes Phytopathology. Animal pests. Plant and forest protection plant diseases and disorders rust diseases Salix self compatibility sexual reproduction Variation, races, biotypes, parasitic specialization, genetics virulence |
title | Hybridization in larch-alternating Melampsora epitea (M. larici-epitea) |
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