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Distribution of downy mildew (Bremia lactucae Regel) resistances in a genebank collection of lettuce and its wild relatives

Published online by Cambridge University Press:  21 June 2011

R. van Treuren ,
A. J. M. van der Arend  and
J. W. Schut
R. van Treuren*
Affiliation:
Centre for Genetic Resources, The Netherlands, Wageningen University and Research Centre, PO Box 16, 6700 AA Wageningen, The Netherlands
A. J. M. van der Arend
Affiliation:
Nunhems Netherlands BV, Noordlandseweg 54, 2691KM 's-Gravenzande, The Netherlands
J. W. Schut
Affiliation:
Rijk Zwaan Breeding BV, PO Box 40, 2678 ZG De Lier, The Netherlands
*
*Corresponding author. E-mail: [email protected]
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Abstract

Genebanks serve as a rich source of diversity that can be exploited for crop improvement. However, large numbers of accessions usually have to be evaluated to find material with the characters of interest, and therefore, enhanced trait information can facilitate the more efficient selection of accessions by users. In this study, we report on the distribution of resistances to 28 races of downy mildew among 1223 genebank accessions of cultivated lettuce (Lactuca sativa L.) and 14 related wild species. Due to modern plant breeding, the overall level of resistance of cultivars released after 1950 appears to have increased two- to three-fold compared with varieties from earlier periods. Although fully resistant reactions could be observed among the accessions of cultivated lettuce for each of the 28 investigated races, the resistance probability was more than two-fold higher on average for accessions from the wild gene pool. In general, species of the primary gene pool appeared less resistant than those of the secondary or tertiary gene pool. Probabilities for examined Lactuca species ranged from 0.29 for L. serriola to 1.00 for L. perennis compared with 0.19 for cultivated lettuce, with lower overall resistance probabilities observed only for L. altaica, L. dregeana and L. tenerrima. For L. serriola, the closest relative of cultivated lettuce and the wild species with the highest number of examined accessions, resistance probabilities to each of the investigated downy mildew races were relatively high for populations originating from Eastern Europe and Northern Asia.

Keywords

disease resistancedowny mildew racesgenetic resourcesgeographic distributionlettucewild gene pool
Type
Research Article
Information
Plant Genetic Resources , Volume 11 , Issue 1 , April 2013 , pp. 15 - 25
Copyright
Copyright © NIAB 2011

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References

Beharav, A, Lewinsohn, D, Lebeda, A and Nevo, E (2006) New wild Lactuca genetic resources against Bremia lactucae. Genetic Resources and Crop Evolution 53: 467–474.CrossRefGoogle Scholar
Beharav, A, Ben-David, R, Doležalová, I and Lebeda, A (2010) Eco-geographical distribution of Lactuca aculeata natural populations in northeastern Israel. Genetic Resources and Crop Evolution 57: 679–686.CrossRefGoogle Scholar
Bhullar, NK, Street, K, Mackay, M, Yahiaouia, N and Keller, B (2009) Unlocking wheat genetic resources for the molecular identification of previously undescribed functional alleles at the Pm3 resistance locus. Proceedings of the National Academy of Sciences of the USA 106: 9519–9524.Google Scholar
Bonnier, FJM, Reinink, K and Groenwold, R (1992) New sources of major gene resistance in Lactuca to Bremia lactucae. Euphytica 61: 203–211.CrossRefGoogle Scholar
CGN (2010) Centre for Genetic Resources, The Netherlands (CGN). Available atwww.cgn.wur.nl.Google Scholar
CPVO(2010) Community Plant Variety Office. Available atwww.cpvo.eu.int/documents/TP/vegetales/TP_013-4_Lettuce.pdf.Google Scholar
Crute, IR (1992a) From breeding to cloning (and back again?): a case study with lettuce downy mildew. Annual Review of Phytopathology 30: 485–506.Google Scholar
Crute, IR (1992b) The role of resistance breeding in the integrated control of downy mildew (Bremia lactucae) in protected lettuce. Euphytica 63: 95–102.Google Scholar
D'Andrea, L, Broennimann, O, Kozlowski, G, Guisan, A, Morin, X, Keller-Senften, J and Felber, F (2009) Climate change, anthropogenic disturbance and the northward range expansion of Lactuca serriola (Asteraceae). Journal of Biogeography 36: 1573–1587.Google Scholar
Engels, JMM and Visser, LA (2003) Guide to effective management of germplasm collections. IPGRI Handbook for Genebanks no. 6. Rome: International Plant Genetic Resources Institute.Google Scholar
Feráková, V (1977) The Genus Lactuca in Europe. Bratislava: Komenský University Press.Google Scholar
Guenard, M, Cadot, V, Boulineau, F and de Fontanges, H (1999) Collaboration between breeders and GEVES-SNES for the harmonization and evaluation of a disease resistance test: Bremia lactucae of the lettuce. In: Lebeda, A and Krístková, E (eds) Eucarpia Leafy Vegetables '99. Olomouc: Palacký University, pp. 177–181.Google Scholar
ILDB (2010) The International Lactuca Database. Available at http://documents.plant.wur.nl/cgn/pgr/ildb .Google Scholar
Jeuken, MJW, Pelgrom, K, Stam, P and Lindhout, P (2008) Efficient QTL detection for nonhost resistance in wild lettuce: backcross inbred lines versus F2 population. Theoretical and Applied Genetics 116: 845–857.Google Scholar
Jönsson, B, Forsberg, AS, Hägnefelt, A, Paaske, K and Svedelius, G (2005) A co-operative project to create a strategy for controlling lettuce downy mildew (Bremia lactucae) in iceberg lettuce in Scandinavia. Integrated Control in Field Vegetable Crops IOBC WPRS Bulletin 28: 145–152.Google Scholar
Koopman, WJM (2002) Zooming in on the lettuce genome: species relationships in Lactuca s.l., inferred chromosomal and molecular characters. PhD Thesis. The Netherlands: Wageningen University.Google Scholar
Krístková, E, Doležalová, I, Lebeda, A, Vinter, V and Novotná, A (2008) Description of morphological characters of lettuce (Lactuca sativa L.) genetic resources. Horticultural Science (Prague) 35: 113–129.Google Scholar
Kuang, H, van Eck, HJ, Sicard, D, Michelmore, R and Nevo, E (2008) Evolution and genetic population structure of prickly lettuce (Lactuca serriola) and its RGC2 resistance gene cluster. Genetics 178: 1547–1558.Google Scholar
Lambalk, JJM, Faber, NM, Bruijnis, AB, Conijn, PCJ, de Witte, I, Nieuwenhuis, J and de Jong, CJ (2000) Method for obtaining a plant with a lasting resistance to a pathogen. International Patent Application: PCT/NL2000/000241.Google Scholar
Lebeda, A (1989) Response of lettuce cultivars carrying the resistance gene Dm11 to isolates of Bremia lactucae from Lactuca serriola. Plant Breeding 102: 311–316.CrossRefGoogle Scholar
Lebeda, A and Zinkernagel, V (2003) Characterization of new highly virulent German isolates of Bremia lactucae and efficiency of resistance in wild Lactuca spp. germplasm. Journal of Phytopathology 151: 274–282.CrossRefGoogle Scholar
Lebeda, A, Pink, DAC and Astley, D (2002) Aspects of the interactions between wild Lactuca spp. and related genera and lettuce downy mildew (Bremia lactucae). In: Spencer-Phillips, PTN, Gisi, U and Lebeda, A (eds) Advances in Downy Mildew Research. Dordrecht: Springer, pp. 85–117.CrossRefGoogle Scholar
Lebeda, A, Doležalová, I and Astley, D (2004a) Representation of wild Lactuca spp. (Asteraceae, Lactuceae) in world genebank collections. Genetic Resources and Crop Evolution 51: 167–174.CrossRefGoogle Scholar
Lebeda, A, Doležalová, I, Feráková, V and Astley, D (2004b) Geographical distribution of wild Lactuca species (Asteraceae, Lactuceae). The Botanical Review 70: 328–356.CrossRefGoogle Scholar
Lebeda, A, Ryder, EJ, Grube, R, Doležalová, I and Krístková, E (2007) Lettuce (Asteraceae; Lactuca spp.). In: Singh, RJ (ed.) Genetic Resources, Chromosome Engineering, and Crop Improvement, Vol. 3, Vegetable Crops. Boca Raton, FL: CRC Press, pp. 377–472.Google Scholar
Lebeda, A, Kitner, M, Dziechciarková, M, Doležalová, I, Krístková, E and Lindhout, P (2009) An insight into the genetic polymorphism among European populations of Lactuca serriola assessed by AFLP. Biochemical Systematics and Ecology 37: 597–608.Google Scholar
Maisonneuve, B (2003) Lactuca virosa, a source of disease resistance genes for lettuce breeding: results and difficulties for gene introgression. In: Hintum, ThJL, van, Lebeda, A, Pink, D and Schut, JW (eds) Eucarpia Leafy Vegetables 2003. Wageningen: Centre for Genetic Resources, The Netherlands (CGN), pp. 61–67.Google Scholar
Michelmore, RW and Ochoa, OE (2009) Breeding Crisphead Lettuce. Davis, US: California Leafy Greens Research Program. The Genome Center and the Department of Plant Sciences, University of California.Google Scholar
Michelmore, RW, Truco, MJ and Ochoa, OE (2009) Breeding Leaf Lettuce. California Leafy Greens Research Program. Davis, US: The Genome Center and the Department of Plant Sciences, University of California.Google Scholar
Moreau, BMD (1994) Fungus resistant plants. European Patent Application EP94810296.Google Scholar
Mou, B (2008) Lettuce. In: Prohens, J and Nuez, F (eds) Handbook of Plant Breeding, Vegetables I, Asteraceae, Brassicaceae, Chenopodicaceae, and Cucurbitaceae. New York, NY: Springer, pp. 75–116.Google Scholar
Petrželová, I and Lebeda, A (2011) Distribution of race-specific resistance against Bremia lactucae in natural populations of Lactuca serriola. European Journal of Plant Pathology 129: 233–253.CrossRefGoogle Scholar
Reinink, K (1999) Lettuce resistance breeding. In: Lebeda, A and Krístková, E (eds) Eucarpia Leafy Vegetables '99. Olomouc: Palacký University, pp. 139–147.Google Scholar
Sicard, D, Woo, SS, Arroyo-Garcia, R, Ochoa, O, Nguyen, D, Korol, A, Nevo, E and Michelmore, R (1999) Molecular diversity at the major cluster of disease resistance genes in cultivated and wild Lactuca spp. Theoretical and Applied Genetics 99: 405–418.CrossRefGoogle ScholarPubMed
UN (2010) Composition of macro geographical (continental) regions, geographical sub-regions, and selected economic and other groupings. United Nations Statistics Division. Available athttp://unstats.un.org/unsd/methods/m49/m49regin.htm.Google Scholar
van de Wiel, CCM, Sretenović Rajičić, T, van Treuren, R, Dehmer, KJ, van der Linden, CG and van Hintum, ThJL (2010) Distribution of genetic diversity in wild European populations of prickly lettuce (Lactuca serriola): implications for plant genetic resources management. Plant Genetic Resources: Characterization and Utilization 8: 171–181.CrossRefGoogle Scholar
van de Wouw, M, Kik, C, van Hintum, ThJL, van Treuren, R and Visser, L (2010a) Genetic erosion in crops: concept, research results and challenges. Plant Genetic Resources: Characterization and Utilization 8: 1–15.CrossRefGoogle Scholar
van de Wouw, M, van Hintum, ThJL, Kik, C, van Treuren, R and Visser, L (2010b) Genetic diversity trends in twentieth century crop cultivars – a meta analysis. Theoretical and Applied Genetics 120: 1241–1252.CrossRefGoogle ScholarPubMed
van der Arend, AJM, Gautier, J, Guenard, M, Michel, H, Moreau, B, de Ruijter, J, Schut, JW and de Witte, I (2003) Identification and denomination of ‘new’ races of Bremia lactucae in Europe by IBEB until 2002. In: Hintum, ThJL, van, Lebeda, A, Pink, D and Schut, JW (eds) Eucarpia Leafy Vegetables 2003. Wageningen: Centre for Genetic Resources, The Netherlands (CGN), p. 151.Google Scholar
van der Arend, AJM, Gautier, J, Grimault, V, Kraan, P, van der Laan, R, Mazet, J, Michel, H, Schut, JW, Smilde, D and de Witte, I (2006) Identification and denomination of “new” races of Bremia lactucae in Europe by IBEB until 2006. Available athttp://www.plantum.nl/pdf/IBEB_identification_and_nomination_2006.pdf.Google Scholar
van Ettekoven, K and van der Arend, AJM (1999) Identification and denomination of ‘new’ races of Bremia lactucae. In: Lebeda, A and Krístková, E (eds) Eucarpia Leafy Vegetables '99. Olomouc: Palacký University, pp. 171–175.Google Scholar
van Treuren, R and van Hintum, ThJL (2009) Comparison of anonymous and targeted molecular markers for the estimation of genetic diversity in ex situ conserved Lactuca. Theoretical and Applied Genetics 119: 1265–1279.Google Scholar
van Treuren, R, van Hintum, ThJL and van de Wiel, CCM (2008) Marker-assisted optimization of an expert-based strategy for the acquisition of modern lettuce varieties to improve a genebank collection. Genetic Resources and Crop Evolution 55: 319–330.CrossRefGoogle Scholar
Zhang, N (2008) Genetic dissection of nonhost resistance of wild lettuce, Lactuca saligna, to downy mildew. PhD Thesis, Wageningen University, The Netherlands.Google Scholar
Zonneveld, O, de Lange, M, Briggs, W and Segura, V (2011) Plant resistant to a pathogen. International Patent Application: PCT/EP2010/059268.Google Scholar