Molecular diagnosis of phytoplasma infection in some Moldavian tomato varieties
https://doi.org/10.18619/2072-9146-2020-4-88-92
Abstract
Relevance. The use of molecular methods allows reliable and fast determination of the resistance of genotypes (varieties) to pathogens, thereby reducing possible product losses and, at the same time, maintaining its environmental safety. It is very important in conditions of increasing demand for high-quality agricultural production. Aim: Using molecular diagnosis of ʹCandidatus Phytoplasma solaniʹ to compare the degree of infection in some Moldavian tomato varieties at different stages of plant development.
Material and methods. The molecular analysis (nested-PCR) of plants of the four Moldavian tomato varieties (Elvira, Cerasus, Mary Gratefully, Desteptarea) created at the Institute of Genetics, Physiology and Plant Protection, and the wild formSolanum habrochaites, was carried out for the presence of the phytopathogen ʹCa. P. solaniʹ. Researches were made during two growing seasons.
Results. The distribution of infection between the studied varieties was different in the process of plants development. The spread of infection in the tomato field was recorded under the climatic conditions of two growing seasons: the season of 2018, which was hot but with normal rains in the middle of summer, and the season of 2019, in conditions of a very hot and dry summer. During both seasons, Cerasus variety manifested the highest resistance to ʹCa. P. solaniʹ infection. A little more than half of plants of this variety were affected by stolbur only at the end of the growing season, after harvesting most of the crop. Varieties Elvira and Desteptarea had similar levels of infection of plants with phytoplasma during two years of research. These varieties manifested a higher sensitivity to phytoplasma infection compared with Cerasus. Mary Gratefully was the genotype with the highest dependence of the sensitivity toʹCa. P. solaniʹ infection from the climatic conditions of the growing season. Plants of the wild form Solanum habrochaites demonstrated complete immunity to phytoplasma infection during the growing season. Conclusion.The Cerasus variety, as well as the wild form Solanum habrochaites, can be recommended for including in breeding programs for the creating tomato varieties or hybrids resistant to phytoplasma. Thus, molecular diagnosis may be a useful tool for the breeding resistant genotypes.
About the Authors
A. G. BahsievMoldova, Republic of
Aighiuni Gh. Bahsiev – Junior Researcher Dep. Molecular Genetics
20 Padurii St., MD-2002, Chisinau
I. A. Zamorzaeva
Moldova, Republic of
Irina A. Zamorzaeva – Doc. Sci.(Biology), Leading Researcher, Dep.molecular genetics
20 Padurii St., MD-2002, Chisinau
N. I. Mihnea
Moldova, Republic of
Nadejda I. Mikhnya – Doc. Sci. (Biology), Leading Researcher, Dep. applied genetics
20 Padurii St., MD-2002, Chisinau
References
1. Çağlar BK, Elbeaino T, Küsek M, Pehlivan D, Fidan H, Portakaldal M. Stolbur phytoplasma infections in potato and tomato plants from different locations in Turkey. J. Turk. Phytopath. 2010;39(1-3):1-8. ISSN 0378–8024 2010 [cited 2020 Apr 15]. Available from: https://www.researchgate.net/publication/264508571
2. Bertaccini A., Duduk B. Phytoplasma and phytoplasma diseases: a review of recent research. Phytopathol Mediterr [Internet]. [cited 2020 Apr 15] 2010;48(3):355–78. Available from: http://www.fupress.net/index.php/pm/article/view/3300
3. Rojas-Martínez RI. Insect vectors of phytoplasmas. Tropical biology and conservation management. [cited 2020 Apr 15]. Available from: https://www.eolss.net/Sample-Chapters/C20/E6-142-TPE-10.pdf p 46-60
4. Lee I-M., Davis R.E., Gundersen-Rindal D.E. Phytoplasma: Phytopathogenic Mollicutes. Annu Rev Microbiol [Internet]. 2000 Oct 28 [cited 2020 Apr 15]. 2000;54(1):221–55. Available from: http://www.annualreviews.org/doi/10.1146/annurev.micro.54.1.221
5. Davis R.E., Sinclair W.A. Phytoplasma identity and disease etiology. In: Phytopathology. American Phytopathological Society. 1998. P.1372–6.
6. Firrao G, Andersen M, Bertaccini A, Boudon E, Bové JM, Daire X, et al. “Candidatus Phytoplasma”, a taxon for the wall-less, non-helical prokaryotes that colonize plant phloem and insects. Int J Syst Evol Microbiol [Internet]. 2004 Jul [cited 2020 Apr 15]. 2020;54(4):1243–55. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15280299
7. Kube M. Insights in host dependency encoded within phytoplasma genomes. Bull Insectology. 2011;64:9–11. Request PDF [Internet]. [cited 2020 Apr 15]. Available from: https://www.researchgate.net/publication/228520757_Insights_in_host_dependency_encoded_within_phytoplasma_genomes
8. Dickinson M, Tuffen M, Hodgetts J. The Phytoplasmas: An Introduction. In: Methods in molecular biology (Clifton, NJ) [Internet]. 2013 [cited 2020 Apr 15]. P.1–14. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22987401
9. Bertaccini A., Duduk B., Paltrinieri S., Contaldo N. Phytoplasmas and Phytoplasma Diseases: A Severe Threat to Agriculture. Am J Plant Sci [Internet]. 2014 [cited 2020 Apr 15]; 2014;05(12):1763–88. Available from: http://www.scirp.org/journal/doi.aspx?DOI=10.4236/ajps.2014.512191
10. Manczinger L., Antal Z., Kredics L. Ecophysiology and breeding of mycoparasitic Trichoderma strains. Acta Microbiol Immunol Hung. 2002;49(1):1–14.
11. Thomas P.E., Mink G.I. Tomato hybrids with nonspecific immunity to viral and mycoplasma pathogens of potato and tomato. HortScience. 1998 Jul;33(4):764–5.
12. Gavrilescu M, Chisti Y. Biotechnology - A sustainable alternative for chemical industry. Vol. 23, Biotechnology Advances. Elsevier Inc. 2005. P.471–99.
13. Marcone C., Rao G.P. Control of phytoplasma diseases through resistant plants. In: Phytoplasmas: Plant Pathogenic Bacteria - II: Transmission and Management of Phytoplasma - Associated Diseases. Springer Singapore. 2019. P.165–84.
14. Guo Y., Cheng Z.M., Walla J.A. Rapid PCR-based Detection of Phytoplasmas from Infected Plants. HortScience. 2003 Oct;38(6):1134–6.
15. Avila C.A., Marconi T.G., Viloria Z., Kurpis J., Del Rio S.Y. Bactericera cockerelli resistance in the wild tomato Solanum habrochaites is polygenic and influenced by the presence of Candidatus Liberibacter solanacearum. Sci Rep. 2019 Dec 1;9(1):1–11.
16. Zamorzaeva I., Bahsiev A., Mihnea N. Spread of phytoplasma infection in the tomato field depending on the climatic conditions of the year. In: Материалы II Международной научной конференции «Тенденции развития агрофизики: от актуальных проблем земледелия и растениеводства к технологиям будущего». Санкт-Петербург: ФГБНУ АФИ. 2019. P.662-668. ISBN 978-5-905200-40-3. [Zamorzaeva I., Bahsiev A., Mihnea N. Spread of phytoplasma infection in the tomato field depending on the climatic conditions of the year. In: Materials of the II International Scientific Conference "Agrophysical Trends: from Actual Challenges in Arable Farming and Crop Growing towards Advanced Technologies". St. Petersburg: FSBSI AFI. 2019. P.662-668. ISBN 978-5-905200-40-3]
Review
For citations:
Bahsiev A.G., Zamorzaeva I.A., Mihnea N.I. Molecular diagnosis of phytoplasma infection in some Moldavian tomato varieties. Vegetable crops of Russia. 2020;(4):88-92. (In Russ.) https://doi.org/10.18619/2072-9146-2020-4-88-92