Agronomy Science, przyrodniczy lublin, czasopisma up, czasopisma uniwersytet przyrodniczy lublin
Przejdź do głównego menu Przejdź do sekcji głównej Przejdź do stopki
Agronomy Science Baner text

Tom 78 Nr 4 (2023)

Artykuły

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

DOI: https://doi.org/10.24326/as.2023.5282
Przesłane: 6 października 2023
Opublikowane: 18-04-2024

Abstrakt

Mączniak prawdziwy jest jedną z najważniejszych chorób grzybowych roślin zbożowych. Powoduje obniżenie plonu i jakości zbieranego ziarna. Jednym z najlepszych sposobów
ochrony roślin przed mączniakiem jest wprowadzenie do odmian uprawnych efektywnych genów odporności. W niniejszej pracy przeprowadzono screening diploidalnych gatunków z rodzaju Triticum pod kątem identyfikacji potencjalnych źródeł genetycznej odporności na mączniaka. Spośród analizowanych form zidentyfikowano 21 genotypów, które wykazywały pełną odporność na wszystkie 3 zastosowane izolaty mączniaka. Cztery z nich należą do gatunku T. urartu, 12 do T. monococcum i 4 do T. boeoticum. Badania przedstawione w niniejszej pracy wykazały, że każdy z badanych gatunków może być źródłem genów odporności na mączniaka prawdziwego. Ponadto najbardziej odporne genotypy zidentyfikowano wśród form z Libanu i Syrii. Najniższy poziom odporności wykazały
genotypy z Turcji, co wskazuje, że obszar ten nie jest regionem o dużej presji tego patogena.

Bibliografia

  1. 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 DOI: https://doi.org/10.1094/PDIS-10-10-0760
  2. 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 DOI: https://doi.org/10.1007/s11738-018-2673-0
  3. 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 DOI: https://doi.org/10.1159/000433458
  4. 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 DOI: https://doi.org/10.5772/intechopen.97359
  5. 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 DOI: https://doi.org/10.1111/tpj.13888
  6. 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 DOI: https://doi.org/10.1007/s00122-021-03816-z
  7. 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 DOI: https://doi.org/10.1007/s00122-007-0668-0
  8. 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 DOI: https://doi.org/10.1093/jxb/erj124
  9. 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 DOI: https://doi.org/10.1094/PHYTO-06-17-0211-R
  10. 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 DOI: https://doi.org/10.2135/cropsci2016.10.0885
  11. 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 DOI: https://doi.org/10.1139/g93-004
  12. 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 DOI: https://doi.org/10.1007/978-3-319-23494-6_8
  13. 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.
  14. https://doi.org/10.1007/1-4020-5497-1_11 DOI: https://doi.org/10.1007/1-4020-5497-1_11
  15. 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 DOI: https://doi.org/10.1007/978-3-319-23494-6_2
  16. 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 DOI: https://doi.org/10.1038/srep44530
  17. 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 DOI: https://doi.org/10.2307/1218252
  18. 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 DOI: https://doi.org/10.3389/fgene.2020.00489
  19. 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 DOI: https://doi.org/10.1007/s00122-020-03681-2
  20. 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 DOI: https://doi.org/10.3389/fpls.2022.836723
  21. 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 DOI: https://doi.org/10.17221/127/2010-CJGPB
  22. 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. DOI: https://doi.org/10.1023/A:1003057505151
  23. org/10.1023/A:1003057505151
  24. 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 DOI: https://doi.org/10.1007/s11103-008-9316-6
  25. Mains E.B., 1934. Inheritance of resistance to powdery mildew, Erysiphe graminis tritici, in wheat. Phytopathology 24, 1257–1261.
  26. 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 DOI: https://doi.org/10.1007/s00438-005-0076-6
  27. 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 DOI: https://doi.org/10.1111/j.1365-3040.2009.02107.x
  28. 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 DOI: https://doi.org/10.3389/fpls.2018.01719
  29. 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 DOI: https://doi.org/10.1094/PDIS-92-7-1074
  30. 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 DOI: https://doi.org/10.3390/agronomy11081656
  31. 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 DOI: https://doi.org/10.1094/PDIS-04-10-0260
  32. 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 DOI: https://doi.org/10.1094/PDIS-10-19-2254-RE
  33. 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 DOI: https://doi.org/10.1007/s11103-018-0780-3
  34. 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.
  35. 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.
  36. https://doi.org/10.1094/PDIS-05-21-0896-RE DOI: https://doi.org/10.1094/PDIS-05-21-0896-RE
  37. 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 DOI: https://doi.org/10.1186/s12870-017-1058-7
  38. 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 DOI: https://doi.org/10.1007/s00122-022-04195-9
  39. 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 DOI: https://doi.org/10.1186/s12870-023-04140-y
  40. 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 DOI: https://doi.org/10.1186/s12870-023-04132-y
  41. 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 DOI: https://doi.org/10.1111/nph.14964

Downloads

Download data is not yet available.

Inne teksty tego samego autora

1 2 > >> 

Podobne artykuły

<< < 2 3 4 5 6 7 8 9 > >> 

Możesz również Rozpocznij zaawansowane wyszukiwanie podobieństw dla tego artykułu.