Skip to main navigation menu Skip to main content Skip to site footer

Research Articles

Vol. 12 No. 3 (2025)

Identification and genomic characterization of a novel tomato leaf curl virus infecting Alternanthera ficoidea in Tamil Nadu, India

DOI
https://doi.org/10.14719/pst.8724
Submitted
7 April 2025
Published
14-07-2025 — Updated on 29-07-2025
Versions

Abstract

Begomoviruses are single-stranded DNA viruses that cause significant yield losses in economically important crops and are transmitted mainly by the whitefly, Bemisia tabaci. Weeds frequently serve as alternate reservoirs for viruses when major crop hosts are not available, thereby promoting virus persistence and spread. During a survey in 2024 in tomato-growing regions of Coimbatore, Tamil Nadu, Alternanthera ficoidea plants exhibiting yellow-green mosaic and yellow vein mosaic symptoms were observed. PCR amplification using begomovirus specific primers PARIv772/PALIc1960 confirmed the presence of begomoviruses in all symptomatic samples, whereas healthy plants showed no amplification. The remaining sequence of the DNA-A genome was amplified using primer pairs GKToLCV-F/GKToLCV-R and PAL1v1978/PAR1c715. BLASTn analysis of the consensus sequence (2764 bp) revealed a 95.12 % nucleotide identity with tomato leaf curl Kerala virus (ToLCKeV) isolate OQ128343. Subsequent investigation of the ToLCKeV isolate found in this study (GenBank accession no: PQ901324) showed significant genetic variation and recombination, with the potential recombination parents being tomato leaf curl Sri Lanka virus (PP935251) and tomato leaf curl New Delhi virus (MK883715). This study provides the first report of ToLCKeV infecting A. ficoidea, suggesting its role as an alternative host and potential reservoir during off seasons, contributing to the persistence and spread of this virus. These findings underscore the importance of weed management in integrated approaches to manage leaf curl diseases caused by begomoviruses.

References

  1. 1. Singla RK, Dhir V, Madaan R, Kumar D, Singh Bola S, Bansal M, et al. The Genus Alternanthera: Phytochemical and ethnopharmacological perspectives. Front Pharmacol. 2022;13:769111. https://doi.org/10.3389/fphar.2022.769111
  2. 2. Patil RB, and Basavaraj AK. Phytoconstituents, pigments, gas chromatography mass spectrometry analysis, and allelopathy effect of Alternanthera ficoidea (L.) P. Beauv. Asian J Pharm Clin Res. 2017;10(2):103–8. https://doi.org/10.9790/3008-1305041823
  3. 3. Pandey S, Pal AK, Sahu AN, Nandi MK. A phytopharmacological review on Alternanthera ficoidea. Int J Pharm Res. 2019;11(3):20-5. https://doi.org/10.31838/ijpr/2019.11.03.008
  4. 4. Shehzad A, Qayyum A, Rehman R, Nadeem F, Raffi M. A review of bioactivity guided medicinal uses and therapeutic potentials of noxious weed (Alternanthera sessilis). Int J Chem Biochem Sci. 2018;14:95-103.
  5. 5. Rajendran SS, Sukardha M, Pradeepa D, Preethika D, Ramesh V, Sanjay R. Isolation and purification of lutein from Alternanthera ficoidea. Asian J Res Biol Pharm Sci. 2022;9(4):147-52. https://doi.org/10.36673/AJRBPS.2022.v09.i04.A20
  6. 6. Malathi VG, Renukadevi P, Chakraborty S, Biswas KK, Roy A, Sivalingam PN, Venkataravanappa V, Mandal B. Begomoviruses and their satellites occurring in India: distribution, diversity and pathogenesis. A century of plant virology in India. 2017:75-177.
  7. 7. Seal SE, van den Bosch F, Jeger MJ. Factors influencing begomovirus evolution and their increasing global significance: implications for sustainable control. Crit Rev Plant Sci. 2006;25:23–46. https://doi.org/10.1080/07352680500365257
  8. 8. Sattar MN, Khurshid M, El-Beltagi HS, Iqbal Z. Identification and estimation of sequence variation dynamics of Tomato leaf curl Palampur virus and betasatellite complex infecting a new weed host. BiotechnolBiotechnol Equip 2022;36:609–19.
  9. 9. Venkataravanappa V, Lakshminarayana Reddy C, Shankarappa K, Krishna Reddy M. Association of Tomato leaf curl New Delhi virus, betasatellite, and alphasatellite with mosaic disease of spine gourd (Momordica dioicaRoxb. Willd) in India. Iran J Biotechnol. 2019;17:17–29. https://doi.org/10.21859/ijb.2134
  10. 10. Mugerwa H, Colvin J, Alicai T, Omongo CA, Kabaalu R, Visendi P, et al. Genetic diversity of whitefly (Bemisia spp.) on crop and uncultivated plants in Uganda: implications for the control of this devastating pest species complex in Africa. J Pest Sci. 2021;94(4):1307-30. https://doi.org/10.1007/s10340-021-01355-6
  11. 11. Chetan SJ, Prameela HA, Rangaswamy KT. Transmission characteristics and vector-virus relationship of yellow vein mosaic virus on Alternanthera (Alternanthera sessilis Linn.) DC. Mysore J Agric Sci.2012; 46(4):800-4.
  12. 12. Marabi RS, Das SB, Tripathi N, Wada T, Noda H. Identification of begomoviruses from legume crop and weed plants and viruliferous status of the whitefly Bemisia tabaci in Central India. Curr Sci. 2021;120(7):1240–6. https://doi.org/10.18520/cs/v120/i7/1233-1240
  13. 13. Turaki AA, Ahmad B, Magaji UF, et al. Optimised cetyltrimethylammonium bromide (CTAB) DNA extraction method of plant leaf with high polysaccharide and polyphenolic compounds for downstream reliable molecular analyses. Afr J Biotechnol. 2017;16:1354–65. https://doi.org/10.5897/AJB2017.15942
  14. 14. Rojas MR, Gilbertson RL, Russell DR, Maxwell DP. Use of degenerate primers in the polymerase chain reaction to detect whitefly transmitted geminiviruses. Plant Dis. 1993;77:340–7.
  15. 15. Nagendran K, Kumar SM, Manoranjitham SK, Karthikeyan G. Molecular detection and characterization of Tomato leaf curl New Delhi virus causing mosaic disease on bitter gourd in Tamil Nadu, India. Trends Biosci2014;7:3925–31.
  16. 16. Muhire BM, Varsani A, Martin DP. SDT: a virus classification tool based on pairwise sequence alignment and identity calculation PloS one. 2014;9:e108277. https://doi.org/10.1371/journal.pone.0108277
  17. 17. Tamura K, Stecher G, Kumar S. MEGA11: Molecular Evolutionary Genetics Analysis Version 11. Mol Biol Evol. 2021;38:3022–7. https://doi.org/10.1093/molbev/msab120
  18. 18. Letunic I, Bork P. Interactive Tree of Life (iTOL) v5: An online tool for phylogenetic tree display and annotation. Nucleic Acids Res. 2021;49:W293–W296. https://doi.org/10.1093/nar/gkab301
  19. 19. Librado P, Rozas J. DnaSP v5: A software for comprehensive analysis of DNA polymorphism data. Bioinformatics. 2009;25:1451–2. https://doi.org/10.1093/bioinformatics/btp187
  20. 20. Martin DP, Murrell B, Golden M, et al. RDP4: Detection and analysis of recombination patterns in virus genomes. Virus Evol. 2015;1(1):vev003. https://doi.org/10.1093/ve/vev003
  21. 21. Brown JK, Zerbini FM, Navas-Castillo J, et al. Revision of Begomovirus taxonomy based on pairwise sequence comparisons. Arch. Virol. 2015;160:1593–619. https://doi.org/10.1007/s00705-015-2398-y
  22. 22. Salati R, Nahkla MK, Rojas MR, Guzman P, Jaquez J, Maxwell D, Gilbertson RL. Tomato yellow leaf curl virus in the Dominican Republic: characterization of an infectious clone, virus monitoring in whiteflies, and identification of reservoir hosts. Phytopathology. 2002;92:487–96.
  23. 23. Prajapat R, Marwal A, Gaur RK. Begomovirus associated with alternative host weeds: a critical appraisal. Arch Phytopathol Plant Prot. 2014;47(2):157–70. https://doi.org/doi.org/10.1080/03235408.2013.805497
  24. 24. Ansari NA, Tewari JP. Hitherto unrecorded weed reservoirs of Tomato leaf curl virus (TLCV) in Eastern UP and its role in epidemiology of the disease. J Living World. 2005;12:22–6.
  25. 25. Khan MS, Tiwari AK, Ji SH, Chun SC. First report of a Croton yellow vein mosaic virus (CYVMV) associated with tomato leaf curl disease in India. J Phytopathol. 2015;163(9):777–9. https://doi.org/doi.org/10.1111/jph.12319
  26. 26. Lager P, Sharma J, Kumar Y. First report of a begomovirus and associated betasatellite causing yellow vein mosaic disease of Celosia cristata. New Dis Rep. 2023;48(1):e12211. https://doi.org/10.1002/ndr2.12211
  27. 27. Sinha S, Samad A. First report of a begomovirus infecting Ocimum kilimandscharicum in India. New Dis Rep. 2023;47(1):e12157. https://doi.org/10.1002/ndr2.12157
  28. 28. Marwal A, Sahu A, Prajapat R, Choudhary DK, Gaur RK. First report of association of a begomovirus with the leaf curl disease of a common weed, Datura inoxia. Indian J Virol. 2012;23:83–4. https://doi.org/10.1007/s13337-012-0064-5
  29. 29. Kumar S, Srivastava A, Jaidi M, Chauhan PS, Raj SK. Molecular characterization of a begomovirus, α-satellite, and β-satellite associated with leaf curl disease of Parthenium hysterophorus in India. Plant Dis. 2016;100(11):2299–305. https://doi.org/10.1094/pdis-09-15-0982-re
  30. 30. Lefeuvre P, Martin DP, Hoareau M, et al. Begomovirus "melting pot" in the south-west Indian Ocean islands: molecular diversity and evolution through recombination. J Gen Virol. 2007;88:3458–68. https://doi.org/10.1099/vir.0.83252-0
  31. 31. Avedi EK, Adediji AO, Kilalo DC, Olubayo FM, Macharia I, Ateka EM, et al. Metagenomic analyses and genetic diversity of Tomato leaf curl Arusha virus affecting tomato plants in Kenya. Virol J. 2021;18:1–5. https://doi.org/10.1186/s12985-020-01466-z
  32. 32. da Silva SJC, Castillo-Urquiza GP, Hora Júnior BT, et al. High genetic variability and recombination in a begomovirus population infecting the ubiquitous weed Cleome affinis in northeastern Brazil. Arch Virol. 2011;156:2205–13. https://doi.org/10.1007/s00705-011-1119-4
  33. 33. Roshan P, Kulshreshtha A, Hallan V. Global weed-infecting geminiviruses. In: Kumar R. (eds) Geminiviruses. Springer, Cham. 2019:103–121. https://doi.org/10.1007/978-3-030-18248-9_6
  34. 34. Naveed H, Islam W, Jafir M, Andoh V, Chen L, Chen K. A review of interactions between plants and whitefly-transmitted begomoviruses. Plants (Basel). 2023;12(21):3677. https://doi.org/10.3390/plants12213677

Downloads

Download data is not yet available.