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Solanum nigrum L. is a potato spindle tuber viroid reservoir

https://doi.org/10.30901/2227-8834-2022-3-194-203

Abstract

Background. Among the weeds of the Solanaceae family, a potential viroid infection reservoir, black nightshade (Solanum nigrum L.), is ubiquitous in Russia.

Materials and methods. Molecular diagnostics of the viroid was performed using RT-PCR with the P3/P4 primers specific for PSTVd and 6Pospi F/R specific for the Pospiviroidae family of viroids. The amplification products were cloned and sequenced, and the nucleotide sequences were deposited in the GenBank database.

Results. RT-PCR showed that 80–100% of plants were infected with PSTVd. The cDNA amplicons of two plants from Nizhny Novgorod (Sn1 and Sn2) and one plant from Tula Province (Sn3) were cloned (3 clones each) and sequenced. An analysis of the nucleotide variability in the clones revealed significant genetic differences between the PSTVd strains, independent of the geographical origin. Mutations U120C and U192C, compared with the reference strain VP35 (LC523658), were found in all 9 clones. The Sn1 isolate was close to the “potato” VP35 isolate and differed from it only by three mutations. The Sn2 isolate was represented by three identical clones and differed from VP35 by nine mutations, while Sn3 had 22 mutations in the region of 49–310 nucleotide positions in total for three clones. After artificial infection of healthy S. nigrum plants in a greenhouse, the presence of PSTVd in infected plants was confirmed and it was proved that the viroid was transmitted by seeds to plants of the next generation.

Conclusion. For the first time in externally healthy plants of S. nigrum, widely distributed in the potato fields of Russia (Nizhny Novgorod and Tula Province), the potato spindle tuber viroid, PSTVd, was detected. It was proved that the viroid was preserved in the seeds of S. nigrum and transmitted to their progeny. Genetic heterogeneity of PSTVd strains from S. nigrum plants was found. Two mutations, U120C and U192C, were common for all tested clones of PSTVd strains.

About the Authors

N. V. Mironenko
All­-Russian Research Institute of Plant Protection
Russian Federation

Nina V. Mironenko - Dr. Sci. (Biology), Leading Researcher, All-Russian Research Institute of Plant Protection.

3 Podbelskogo Hwy., Pushkin, St. Petersburg 196608.



A. V. Khiutti
All­-Russian Research Institute of Plant Protection
Russian Federation

Alexander V. Khiutti - Cand. Sci. (Biology), Senior Researcher, All-Russian Research Institute of Plant Protection.

3 Podbelskogo Hwy., Pushkin, St. Petersburg 196608.



E. I. Kyrova
All­-Russian Research Institute of Plant Protection
Russian Federation

Elena I. Kyrova - Postgraduate Student, Associate Researcher, All-Russian Research Institute of Plant Protection.

3 Podbelskogo Hwy., Pushkin, St. Petersburg 196608.



N. M. Lashina
All­-Russian Research Institute of Plant Protection
Russian Federation

Nina M. Lashina - Cand. Sci. (Biology), Senior Researcher, All-Russian Research Institute of Plant Protection.

3 Podbelskogo Hwy., Pushkin, St. Petersburg 196608.



O. S. Afanasenko
All­-Russian Research Institute of Plant Protection
Russian Federation

Olga S. Afanasenko - Dr. Sci. (Biology), Professor of the RAS, Leading Researcher, All-Russian Research Institute of Plant Protection.

3 Podbelskogo Hwy., Pushkin, St. Petersburg 196608.



References

1. Adkar-Purushothama C.R., Bolduc F., Bru P., Perreault J.P. Insights into potato spindle tuber viroid quasi-species from infection to disease. Frontiers in Microbiology. 2020;11:1235. DOI: 10.3389/fmicb.2020.01235

2. Behjatnia A., Dry I., Krake L., Condé B.D., Connelly M.I., Randles J. et al. New potato spindle tuber viroid and tomato leaf curl geminivirus strains from a wild Solanum sp. Phytopathology. 1996;86:880-886. DOI: 10.1094/Phyto-86-880

3. Kastalyeva T.B., Mozhaeva K.A., Pisetskaya N.F., Romanova S.A., Trofimets L.N. The potato spindle tuber viroid and bringing potato into a healthy state (Viroid veretenovidnosti klubney i ozdorovleniye kartofelya). Vestnik of the Russian Agricultural Science. 1992;(3):22-24. [in Russian]

4. Keese P., Symons R.H. Domains in viroids: evidence of intermolecular RNA rearrangements and their contribution to viroid evolution. Proceedings of the National Academy of Sciences of the United States of America. 1985;82(14):4582-4586. DOI: 10.1073/pnas.82.14.4582

5. Kumar S., Stecher G., Li M., Knyaz C., Tamura K. MEGA X: molecular evolutionary genetics analysis across computing platforms. Molecular Biology and Evolution. 2018;35(6):1547-1549. DOI: 10.1093/molbev/msy096

6. Ma Y., Marais A., Lefebvre M., Faure C., Candresse T. Metagenomic analysis of virome cross-talk between cultivated Solanum lycopersicum and wild Solanum nigrum. Virology. 2020;540:38-44. DOI: 10.1016/j.virol.2019.11.009

7. Mackie A.E.; Barbetti M.J.; Rodoni B., McKirdy S., Jones R.A.C. Effects of a potato spindle tuber viroid tomato strain on the symptoms, biomass, and yields of classical indicator and currently grown potato and tomato cultivars. Plant Disease. 2019;103(12):3009-3017. DOI: 10.1094/PDIS-02-19-0312-RE

8. Mackie A.E., Rodoni B.C., Barbetti M.J., McKirdy S.J., Jones R.A.C. Potato spindle tuber viroid: alternative host reservoirs and strain found in a remote subtropical irrigation area. European Journal of Plant Pathology. 2016;145:433-446. DOI: 10.1007/s10658-016-0857-2

9. Matsushita Y. Chrysanthemum stunt viroid. Japan Agricultural Research Quarterly. 2013;47(3):237-247. DOI: 10.6090/jarq.47.237

10. Matsushita Y., Penmetcha K.K.R. In vitro transcribed Chrysanthemum stunt viroid (CSVd) RNA is infectious to chrysanthemum and other plants. Phytopathology. 2009;99(1):58-66. DOI: 10.1094/PHYTO-99-1-0058

11. Matsushita Y., Yanagisawa H., Khiutti A., Mironenko N., Ohto Y., Afanasenko O. Genetic diversity and pathogenicity of potato spindle tuber viroid and chrysanthemum stunt viroid isolates in Russia. European Journal of Plant Pathology. 2021;161(3):529-542. DOI: 10.1007/s10658-021-02339-z

12. Matsushita Y., Yanagisawa H., Sano T. Vertical and horizontal transmission of pospiviroids. Viruses. 2018;10(12):706. DOI: 10.3390/v10120706

13. Notredame C.; Higgins D.G.; Heringa J. (2000). T-Coffee: A novel method for fast and accurate multiple sequence alignment. Journal of Molecular Biology. 2020;302(1):205-217. DOI: 10.1006/jmbi.2000.4042.

14. Owens R.A., Girsova N.V., Kromina K.A., Lee I.M., Mozhaeva K.A., Kastalyeva T. Russian isolates of potato spindle tuber viroid exhibit low sequence diversity. Plant Disease. 2009;93(7):752-759. DOI: 10.1094/PDIS-93-7-0752

15. Owens R.A., Steger G., Hu Y., Fels A., Hammond R.W., Riesner D. RNA structural features responsible for potato spindle tuber viroid pathogenicity. Virology. 1996;222(1):144-158. DOI: 10.1006/viro.1996.0405

16. Owens R.A., Verhoeven J.Th.J. Potato spindle tuber viroid. In: A. Hadidi, R. Flores, J. Randles, P. Palukaitis (eds). Viroids and Satellites. London; Academic Press; 2017. p.149-158. DOI: 10.1016/B978-0-12-801498-1.00014-0

17. Romanova S.A., Volkov Y., Kakareka N., Pleshakova T.I., Koslovskaya Z.N. Potato disease caused by combined infection with potato spindle tuber viroid and potato virus Y necrotic strain. Russian Agricultural Sciences. 2007;33(3):162-165. DOI: 10.3103/S1068367407030081

18. Qi Y., Ding B. Inhibition of cell growth and shoot development by a specific nucleotide sequence in a noncoding viroid RNA. The Plant Cell. 2003;15(6):1360-1374. DOI: 10.1105/tpc.011585

19. Sano T., Candresse T., Hammond R.W., Diener T.O., Owens R.A. Identification of multiple structural domains regulating viroid pathogenicity. Proceedings of the National Academy of Sciences of the United States of America. 1992;89(21):10104-10108. DOI: 10.1073/pnas.89.21.10104

20. Schmitz A., Riesner D. Correlation between bending of the VM region and the pathogenicity of different potato spindle tuber viroid strains. RNA. 1998;4(10):1295-1303. DOI: 10.1017/s1355838298980815

21. Singh R.P. Experimental host range of the potato spindle tuber ‘virus’. American Potato Journal. 1973;50(4):111-123. DOI: 10.1007/BF02857207

22. Singh R.P., Boucher A., Somerville T.H. Detection of potato spindle tuber viroid in the pollen and various parts of potato plant pollinated with viroid-infected pollen. Plant Disease. 1992;76:951-953. DOI: 10.1094/PD-76-0951

23. Syller J., Marczewski W., Pawłowicz J. Transmission by aphids of potato spindle tuber viroid encapsidated by potato leafroll luteovirus particles. European Journal of Plant Pathology. 1997;103:285-289. DOI: 10.1023/A:1008648822190

24. Verhoeven J.T.J., Roenhorst J.W. High stability of original predominant pospiviroid genotypes upon mechanical inoculation from ornamentals to potato and tomato. Archives of Virology. 2010;155(2):269-274. DOI: 10.1007/s00705-009-0572-9

25. Yanagisawa H., Shiki Y., Matsushita Y., Ooishi M., Takaue N., Tsuda S. Development of a comprehensive detection and identification molecular based system for eight pospiviroids. European Journal of Plant Pathology. 2017;149(1):11-23. DOI: 10.1007/s10658-017-1157-1


Review

For citations:


Mironenko N.V., Khiutti A.V., Kyrova E.I., Lashina N.M., Afanasenko O.S. Solanum nigrum L. is a potato spindle tuber viroid reservoir. Proceedings on applied botany, genetics and breeding. 2022;183(3):194-203. (In Russ.) https://doi.org/10.30901/2227-8834-2022-3-194-203

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ISSN 2227-8834 (Print)
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