Agronomy Science, przyrodniczy lublin, czasopisma up, czasopisma uniwersytet przyrodniczy lublin

Diploid Triticum species as a potential source of resistance to powdery mildew

Justyna Leśniowska-Nowak

Institute of Plant Genetics, Breeding and Biotechnology, University of Life Science in Lublin
https://orcid.org/0000-0003-4910-5690

Michał Nowak

Institute of Plant Genetics, Breeding and Biotechnology, University of Life Science in Lublin
https://orcid.org/0000-0002-9166-2530

Sylwia Okoń

Institute of Plant Genetics, Breeding and Biotechnology Faculty of Agrobioengineering, University of Life Science in Lublin, Akademicka 13, 20-950 Lublin, Poland
https://orcid.org/0000-0002-5906-2017


Abstract

Powdery mildew is one of the most important fungal diseases of cereal plants. It reduces the yield and the quality of harvested grain. One of the best ways to protect crops against powdery mildew is to introduce effective resistance genes into new cultivars. In this study, diploid species of the genus Triticum were screened to identify potential sources of genetic resistance to powdery mildew.
Among the analyzed forms, 21 genotypes were identified as fully resistant to all three powdery mildew isolates used. Four of them belong to T. urartu, 12 to T. monococcum, and 4 to T. boeoticum. The tests performed showed that each of the tested species can be a source of genes determining
resistance to powdery mildew. The most resistant genotypes were identified among accessions from Lebanon and Syria. Genotypes from Türkiye showed the lowest level of resistance, which indicates that this area is not a region with high pathogen pressure.

Keywords:

resistance, powdery mildew, Triticum monococcum, Triticum boeticum, Triticum urartu

Adhikari T.B., Hansen J.M., Gurung S., Bonman J.M., 2011. Identification of new sources of resistance in winter wheat to multiple strains of Xanthomonas translucens pv. undulosa. Plant Dis. 95(5), 582–588. https://doi.org/10.1094/PDIS-10-10-0760

Ahmadi J., Pour-Aboughadareh A., Ourang S.F., Mehrabi A.A., Siddique K.H.M., 2018. Wild relatives of wheat: Aegilops–Triticum accessions disclose differential antioxidative and physiological responses to water stress. Acta Physiol. Plant. 40(5). https://doi.org/10.1007/S11738-018-2673-0

Badaeva E.D., Amosova A.V., Goncharov N.P., Macas J., Ruban A.S., Grechishnikova I.V., Zoshchuk S. A., Houben A., 2015. A set of cytogenetic markers allows the precise identification of all a-genome chromosomes in diploid and polyploid wheat. Cytogenet. Genome Res. 146(1), 71–79. https://doi.org/10.1159/000433458

Bakala H.S., Mandahal K.S., Ankita Sarao L.K., Srivastava P., 2021. Breeding wheat for biotic stress resistance: achievements, challenges and prospects. Curr. Trends Wheat Res. https://doi.org/10.5772/INTECHOPEN.97359

Brunazzi A., Scaglione D., Talini R.F., Miculan M., Magni F., Poland J., Enrico M., Brandolini A., Dell’Acqua M., 2018. Molecular diversity and landscape genomics of the crop wild relative Triticum urartu across the Fertile Crescent. Plant J. 94(4), 670–684. https://doi.org/10.1111/tpj.13888

Chen S., Hegarty J., Shen T., Hua L., Li H., Luo J., Li H., Bai S., Zhang C., Dubcovsky J., 2021. Stripe rust resistance gene Yr34 (synonym Yr48) is located within a distal translocation of Triticum monococcum chromosome 5AmL into common wheat. Theor. Appl. Genet. 134(7), 2197–2211. https://doi.org/10.1007/s00122-021-03816-z

Chhuneja P., Kaur S., Garg T., Ghai M., Kaur S., Prashar M., Bains N.S., Goel R.K., Keller B., Dhaliwal H.S., Singh K., 2008. Mapping of adult plant stripe rust resistance genes in diploid A genome wheat species and their transfer to bread wheat. Theor. Appl. Genet. 116(3), 313–324. https://doi.org/10.1007/S00122-007-0668-0

Colmer T.D., Flowers T.J., Munns R., 2006. Use of wild relatives to improve salt tolerance in wheat. J. Exp. Bot. 57(5), 1059–1078. https://doi.org/10.1093/JXB/ERJ124

Cowger C., Mehra L., Arellano C., Meyers E., Murphy P.J., 2018. Virulence differences in Blumeria graminis f. sp. tritici from the central and eastern United States. Phytopathology 108(3). https://doi.org/10.1094/PHYTO-06-17-0211-R

Dempewolf H., Baute G., Anderson, J., Kilian B., Smith Ch., Guarino L., 2017. Past and future use of wild relatives in crop breeding. Crop Sci. 57(3), 1070–1082. https://doi.org/10.2135/cropsci2016.10.0885

Dvorak J., Di Terlizzi P., Zhang H.B., Resta P., 1993. The evolution of polyploid wheats: Identification of the A genome donor species. Genome 36(1), 21–31. https://doi.org/10.1139/G93-004

Fedak G., 2015. Alien introgressions from wild Triticum species, T. monococcum, T. urartu, T. turgidum, T. dicoccum, T. dicoccoides, T. carthlicum, T. araraticum, T. timopheevii, and T. miguschovae. In: M. Molnár-Láng, C. Ceoloni, J. Doležel (eds.), Alien introgression in wheat: cytogenetics, molecular biology, and genomics. Springer, 191–219. https://doi.org/10.1007/978-3-319-23494-6_8

Fedak G., Cao W., Xue A., Savard M., Clarke J., Somers D.J., 2007. Enhancement of fusarium head blight resistance in bread wheat and durum by means of wide crosses. In: H.T. Buck, J.E. Nisi, N. Salomón (eds), Wheat production in stressed environments. Proceedings of the 7th International Wheat Conference, 27 November – 2 December 2005, Mar del Plata, Argentina, 91–95.

https://doi.org/10.1007/1-4020-5497-1_11

Feldman M., Levy A.A., 2015. Origin and evolution of wheat and related triticeae species. In: M. Molnár-Láng, C. Ceoloni, J. Doležel (eds), Alien introgression in wheat. Cytogenetics, molecular biology, and genomics Springer, 21–76. https://doi.org/10.1007/978-3-319-23494-6_2

Gao L., Zhao G., Huang D., Jia J., 2017. Candidate loci involved in domestication and improvement detected by a published 90K wheat SNP array. Sci. Rep. 7(1), 1–13. https://doi.org/10.1038/srep44530

Harlan J.R., de Wet J.M.J., 1971. Toward a rational classification of cultivated plants. Taxon 20(4), 509. https://doi.org/10.2307/1218252

He H., Ji J., Li H., Tong J., Feng Y., Wang X., Han R., Bie T., Liu C., Zhu S., 2020. Genetic diversity and evolutionary analyses reveal the powdery mildew resistance gene Pm21 undergoing diversifyingselection. Front. Genet. 11. https://doi.org/10.3389/fgene.2020.00489

He H., Liu R., Ma P., Du H., Zhang H., Wu Q., Yang L., Gong S., Liu T., Huo N., Gu Y.Q., Zhu S., 2021. Characterization of Pm68, a new powdery mildew resistance gene on chromosome 2BS of Greek durum wheat TRI 1796. Theor. Appl. Genet. 134(1), 53–62. https://doi.org/10.1007/s00122-020-03681-2

Hinterberger V., Douchkov D., Lück S., Kale S., Mascher M., Stein N., Reif J.C., Schulthess A.W., 2022. Mining for new sources of resistance to powdery mildew in genetic resources of winter wheat. Front. Plant Sci. 13, 836723. https://doi.org/10.3389/FPLS.2022.836723/BIBTEX

Hovhannisyan N.A., Dulloo M.E., Yesayan A.H., Knüpffer H., Amri A., 2011. Tracking of powdery mildew and leaf rust resistance genes in Triticum boeoticum and T. urartu, wild relatives of common wheat. Czech J. Genet. Plant Breed. 47(2), 45–57. https://doi.org/10.17221/127/2010-CJGPB

Hsam S.L.K., Peters N., Paderina E.V, Felsenstein F., Oppitz K., Zeller F.J., 1997. Genetic studies of powdery mildew resistance in common oat (Avena sativa L.) I. Cultivars and breeding lines grown in Western Europe and North America. Euphytica 96(3), 421–427. https://doi.

org/10.1023/A:1003057505151

Knox A.K., Li C., Vágújfalvi A., Galiba G., Stockinger E.J., Dubcovsky J., 2008. Identification of candidate CBF genes for the frost tolerance locus Fr-A m2 in Triticum monococcum. Plant Mol. Biol. 67(3), 277–288. https://doi.org/10.1007/s11103-008-9316-6

Mains E.B., 1934. Inheritance of resistance to powdery mildew, Erysiphe graminis tritici, in wheat. Phytopathology 24, 1257–1261.

McIntosh R.A., Dubcovsky J., Rogers W., Xia X.C., Raupp W.J., 2020. Catalogue of gene symbols for wheat: 2020 supplement. 13th International Wheat Genetics Symposium, 0711. Miller A.K., Galiba G., Dubcovsky J., 2006. A cluster of 11 CBF transcription factors is located at the frost tolerance locus Fr-Am2 in Triticum monococcum. Mol. Genet. Genom. 275(2), 193–203. https://doi.org/10.1007/s00438-005-0076-6

Nevo E., Chen G., 2010. Drought and salt tolerances in wild relatives for wheat and barley improvement. Plant Cell Environ. 33(4), 670–685. https://doi.org/10.1111/J.1365-3040.2009.02107.X

Olivera P.D., Rouse M.N., Jin Y., 2018. Identification of new sources of resistance to wheat stem rust in Aegilops spp. in the tertiary genepool of wheat. Front. Plant Sci. 871, 421105. https://doi.org/10.3389/FPLS.2018.01719/BIBTEX

Parks R., Carbone I., Murphy J.P., Marshall D., Cowger C., 2008. Virulence structure of the eastern U.S. wheat powdery mildew population. Plant Dis. 92(7), 1074–1082. https://doi.org/10.1094/PDIS-92-7-1074

Pour-Aboughadareh A., Kianersi F., Poczai P., Moradkhani H., 2021. Potential of wild relatives of wheat: ideal genetic resources for future breeding programs. Agronomy 11(8), 1656. https://doi.org/10.3390/AGRONOMY11081656

Rouse M.N., Jin Y., 2011. Stem rust resistance in a-genome diploid relatives of wheat. Plant Dis. 95(8), 941–944. https://doi.org/10.1094/PDIS-04-10-0260

Shi S., Zhao J., Pu L., Sun D., Han D., Li C., Feng X., Fan D., Hu X., 2020. Identification of new sources of resistance to crown rot and fusarium head blight in wheat. Plant Dis. 104(7), 1979–1985. https://doi.org/10.1094/PDIS-10-19-2254-RE

Singh S.P., Hurni S., Ruinelli M., Brunner S., Sanchez-Martin J., Krukowski P., Peditto D., Buchmann G., Zbinden H., Keller B., 2018. Evolutionary divergence of the rye Pm17 and Pm8 resistance genes reveals ancient diversity. Plant Mol. Biol. 98(3), 249–260. https://doi.org/10.1007/s11103-018-0780-3

Vasu K., Singh H., Chhuneja P., Singh S., Dhaliwal H.S., 2000. Molecular tagging of Karnal bunt resistance genes of Triticum monococcum L. transferred to Triticum aestivum L. Crop Improv. 27(1), 33–42.

Wang W., He H., Gao H., Xu H., Song W., Zhang X., Zhang L., Song J., Liu C., Liu K., Ma P., 2021. Characterization of the powdery mildew resistance gene in wheat breeding line KN0816 and its evaluation in marker-assisted selection. Plant Dis. 105(12), 4042–4050.

https://doi.org/10.1094/PDIS-05-21-0896-RE

Wang X., Luo G., Yang W., Li Y., Sun J., Zhan K., Liu D., Zhang A., 2017. Genetic diversity, population structure and marker-trait associations for agronomic and grain traits in wild diploid wheat Triticum urartu. BMC Plant Biol. 17(1), 112. https://doi.org/10.1186/S12870-017-1058-7

Wu J., Xu D., Fu L., Wu L., Hao W., Li J., Dong Y., Wang F., Wu Y., He Z., Si H., Ma C., Xia X., 2022. Fine mapping of a stripe rust resistance gene YrZM175 in bread wheat. Theor. Appl. Genet. 135(10), 3485–3496. https://doi.org/10.1007/s00122-022-04195-9

Yue J, Jiao J., Wang W., Jie X, Wang H., 2023. Silencing of the calcium-dependent protein kinase TaCDPK27 improves wheat resistance to powdery mildew. BMC Plant Biol. 23(1), 134. https://doi.org/10.1186/s12870-023-04140-y

Zhang W., Yu Z., Wang D., Xiao L., Su F., Mu Y., Zheng J., Li L., Yin Y., Yu T., Jin Y., Ma P., 2023. Characterization and identification of the powdery mildew resistance gene in wheat breeding line ShiCG15–009. BMC Plant Biol. 23(1), 113. https://doi.org/10.1186/s12870-023-04132-y

Zou S., Wang H., Li Y., Kong Z., Tang D., 2018. The NB-LRR gene Pm60 confers powdery mildew resistance in wheat. New Phytol. 218(1), 298–309. https://doi.org/10.1111/nph.14964

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Published
2024-04-18



Justyna Leśniowska-Nowak 
Institute of Plant Genetics, Breeding and Biotechnology, University of Life Science in Lublin https://orcid.org/0000-0003-4910-5690
Michał Nowak 
Institute of Plant Genetics, Breeding and Biotechnology, University of Life Science in Lublin https://orcid.org/0000-0002-9166-2530
Sylwia Okoń 
Institute of Plant Genetics, Breeding and Biotechnology Faculty of Agrobioengineering, University of Life Science in Lublin, Akademicka 13, 20-950 Lublin, Poland https://orcid.org/0000-0002-5906-2017



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