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Book of Abstracts <strong>First</strong> <strong>Legume</strong> <strong>Society</strong> <strong>Conference</strong> 2013: A <strong>Legume</strong> Odyssey Novi Sad, Serbia, 9-11 May 2013<br />

_________________________________________________________________________________________<br />

Analysis of eIF4E gene sconfering resistance to Pea seed-borne mosaic virus (PSbMV)<br />

and other potyviruses in pea<br />

Petr Smýkal 1 , Eva Konečná 2 , Pavel Hanáček 2 , Gregoire Aubert 3 , Dana Šafářová 4 , Milan Navrátil 4<br />

1<br />

Department of Botany, Faculty of Science, Palacký University, Olomouc, Czech Republic<br />

2<br />

Mendel University, Department of Plant Biology, Faculty of Agronomy Brno, Czech Republic<br />

3<br />

Unité Mixte de Recherches en Génétique et Ecophysiologie des Légumineuses à Graines, INRA-UMRLEG,<br />

Dijon, France<br />

4<br />

Department of Cell Biology and Genetics, Faculty of Science, Palacký University,Olomouc, Czech Republic<br />

Pea seed-borne mosaic virus (PSbMV) belongs among the most frequent viral pathogens causing<br />

severe losses in field pea and other legumes. These losses might be prevented by growth of<br />

resistant varieties. Resistance to the common P1 strain of PSbMV isconferred by a single<br />

recessive gene (eIF4E), localized on LG VI (sbm-1 locus), while to lentil L1 strainis localized on<br />

LGII atsbm-2locus. Gene-specific single nucleotide polymorphism and co-dominant amplicon<br />

length polymorphism markers were developed. From the comparison of genotype verses<br />

phenotype for selection of resistance/susceptibility in F 2 plants, t<strong>here</strong> was a 26% discrepancy<br />

between the PCR and ELISA-based assays with potentially susceptible heterozygote plants<br />

missed. We used qRT-PCR to analyze expression of both resistant and sensitive eIF4E alleles in<br />

heterozygotes, sensitive and resistant homozygotes after PSbMV infection, together with<br />

evaluation of viral concentration. The novel eIF4E alleles were detected in wider pea germplasm<br />

and TILLING mutants and these were virologically tested. We have analyzed eIF4E allelic<br />

variation in over 2000 accesions within geographical context. Furthemore, analysis of second sbm-<br />

2 locus with eIF4E iso and eIF4G genes as candidate targets, will be presented. It can be expected<br />

that information gain in this study might be extended to other legume species, particularly to<br />

economically important species of tribus Fabeae or even to subfamily Papilionoideae such as<br />

chickpea, lentil, faba bean or soybean w<strong>here</strong> Potyviruses cause problems.<br />

Acknowledgements:<br />

The work was supported by NAZV QI91A229 project.<br />

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