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

Research Articles

Vol. 13 No. 3 (2026)

Citrus tristeza virus resistance and graft compatibility of indigenous Citrus rootstocks for Khasi mandarin

DOI
https://doi.org/10.14719/pst.13535
Submitted
5 January 2026
Published
13-07-2026 — Updated on 29-09-2026
Versions

Abstract

Khasi mandarin (Citrus reticulata Blanco) is a unique mandarin ecotype of Northeast India, playing a vital role in the socio-economic advancement of the people in this region. However, there is a rapid decline in the production and productivity of Khasi mandarin particularly in Meghalaya, primarily due to Citrus tristeza virus (CTV), which leads to an overall decline in production. The CTV is one of the major reasons leading to the overall decline in production and fruit quality. The use of resistant or tolerant Citrus species as rootstocks is one such strategy to combat the spread of disease thereby increasing the overall production. With this idea, exploration of locally available Citrus species as potential rootstocks was conducted at the College of Post Graduate Studies in Agricultural Sciences (CPGSAS), Umiam, Meghalaya during, 2024–25. Seven locally available Citrus species viz. Indian wild orange/Memang Narang (Citrus indica Tanaka), Pomelo/Soh-bah (Citrus maxima (Burm.) Merr.), Khasi papeda/Soh-Shyrkhoit (Citrus latipes Hook.f. & Thomson), Melanesian papeda/Soh-kwit (Citrus macroptera Montrouz.), Rough Lemon/Soh-myndong (Citrus jambhiri Lush.), Sweet orange/ Soh-niangriang (Citrus sinensis (L.) Osbeck) were screened for resistance against CTV by using reverse transcription-polymerase chain reaction (RT-PCR). It was observed that CTV relative band intensity in C. jambhiri (Soh-myndong) and C. maxima (Soh-bah) was found to decrease by 4.5-fold and 6.67-fold from 45 days to 90 days of CTV inoculation respectively, indicating that both species are resistant or tolerant to CTV. Further, graft compatibility of Khasi Mandarin using these resistant rootstocks were studied. Graft success rate of the cleft method was found to be 80 % in rough lemon and 72 % in pomelo. Similarly, graft success rate of T-budding method showed 75 % in rough lemon and 70 % in pomelo. Furthermore, CTV relative band intensity in the grafted plants reduced by 3-fold in rough lemon as rootstock and 5.71-fold in pomelo as rootstock, from 45 days to 90 days after CTV inoculation, with a significant decrease at 0.1 % level of significance, suggesting that both rough lemon and pomelo can be used as a rootstock for production of CTV resistant/tolerant quality panting materials.

References

  1. 1. Biswas KK, Tarafdar A, Sharma SK, Singh JK, Dwivedi S, Biswas K, et al. Current status of Citrus tristeza virus incidence and its spatial distribution in citrus growing geographical zones of India. Indian J Agric Sci. 2014;84:184–9. https://doi.org/10.56093/ijas.v84i2.38028
  2. 2. Bar-Joseph M. On the trail of the longest plant RNA virus: Citrus tristeza virus. Viruses. 2025;17(4):508. https://doi.org/10.3390/v17040508
  3. 3. Barzegar A, Rahimian H, Hashemi Sohi H. Comparison of the minor coat protein gene sequences of aphid-transmissible and nontransmissible isolates of Citrus tristeza virus. J Gen Plant Pathol. 2010;76(2):143–51. https://doi.org/10.1007/s10327-009-0216-7
  4. 4. Marroquín C, Olmos A, Gorris MT, Bertolini E, Martínez MC, Carbonell EA, et al. Estimation of the number of aphids carrying Citrus tristeza virus that visit adult citrus trees. Virus Res. 2004;100(1):101–8. https://doi.org/10.1016/j.virusres.2003.12.018
  5. 5. Flores R, Ruiz-Ruiz S, Soler N, Sánchez-Navarro J, Fagoaga C, López C, et al. Citrus tristeza virus p23: a unique protein mediating key virus-host interactions. Front Microbiol. 2013;4:98. https://doi.org/10.3389/fmicb.2013.00098
  6. 6. Ghosh DK, Aglave B, Baranwal VK. Simultaneous detection of one RNA and one DNA virus from naturally infected citrus plants using duplex PCR technique. Curr Sci. 2008;94:1314–8.
  7. 7. Ray BK, Deka PC. Numerical taxonomic study of different mandarin oranges using morphological characters. Indian J Genet Plant Breed. 2000.
  8. 8. Hazarika TK. Citrus genetic diversity of north-east India, their distribution, ecogeography and ecobiology. Genet Resour. 2012;59(6):1267–80. https://doi.org/10.1007/s10722-012-9846-2
  9. 9. APEDA. Indian production of mandarin [Internet]. 2025 [cited 2025 Jul 29].
  10. 10. Zhou Y, Zhou CY, Liu KH, Liu YQ, Wang XF. Influence of the quantity and variability of citrus tristeza virus on transmissibility by single Toxoptera citricida. J Plant Pathol. 2011;93(1):97–103.
  11. 11. Biswas KK. Molecular characterization of Citrus tristeza virus isolates from the Northeastern Himalayan region of India. Arch Virol. 2010;155(6):959–63. https://doi.org/10.1007/s00705-010-0602-7
  12. 12. Patel RK, Babu KD, Singh A, Yadav DS, De LC. Soft wood grafting in Mandarin (C. reticulata Blanco): a novel vegetative propagation technique. Int J Fruit Sci. 2010;10(1):54–64. https://doi.org/10.1080/15538361003676793
  13. 13. Brunt AA. Plant viruses online: descriptions and lists from the VIDE database. University of Idaho; 1996.
  14. 14. Yokomi RK, Lastra R, Stoetzel MB, Damsteegt VD, Lee RF, Garnsey SM, et al. Establishment of the brown citrus aphid (Homoptera: Aphididae) in Central America and the Caribbean Basin and transmission of citrus tristeza virus. J Econ Entomol. 1994;87(4):1078–85. https://doi.org/10.1093/jee/87.4.1078
  15. 15. Sun Y, Yokomi RK, Folimonova SY. Citrus tristeza virus: a century-long challenge for the world's citrus industries. Ann Appl Biol. 2024;185(3):304–22. https://doi.org/10.1111/aab.12939
  16. 16. Liu J, Li L, Zhao H, Zhou Y, Wang H, Li Z, et al. Titer variation of citrus tristeza virus in aphids at different acquisition access periods and its association with transmission efficiency. Plant Dis. 2019;103(5):874–9. https://doi.org/10.1094/PDIS-05-18-0811-RE
  17. 17. Singh AK, Meetei NT, Singh BK, Mandal N. Khasi mandarin: its importance, problems and prospects of cultivation in North-eastern Himalayan region. IJAEB. 2016;9(4):573. https://doi.org/10.5958/2230-732X.2016.00076.0
  18. 18. Ghosh A, Das A, Meena R, Baranwal VK. Evidence for resistance to Citrus tristeza virus in pomelo (Citrus maxima Merr.) grown in Darjeeling and Sikkim hills of India. Phytoparasitica. 2014;42(4):503–8. https://doi.org/10.1007/s12600-014-0387-4
  19. 19. Kavous Ayazpour KA, Kamaruzaman Sijam KS, Ganesan Vadamalai GV, Hawa Jaafar HJ. Status of Citrus tristeza virus (CTV) in Peninsular Malaysia. Afr J Microbiol Res. 2011;5:838–43. https://doi.org/10.5897/AJMR10.862
  20. 20. Fagoaga C, López C, Moreno P, Navarro L, Flores R, Peña L. Viral-like symptoms induced by the ectopic expression of the p23 gene of Citrus tristeza virus are citrus specific and do not correlate with the pathogenicity of the virus strain. MPMI. 2005;18(5):435–45. https://doi.org/10.1094/MPMI-18-0435
  21. 21. Altaf N, Khan AR, Ali L, Bhatti IA. Propagation of rough lemon (Citrus jambhiri Lush.) through in vitro culture and adventitious rooting in cuttings. EJEAFChe. 2008;7:3326–33.
  22. 22. Abobatta WF. Why do Citrus need rootstocks? Adv Agri Tech Plant Sciences. 2019;2(2):180041.
  23. 23. Hartmann HT, Kester DE, Davies FT, Geneve RL. Plant propagation: principles and practices. 8th ed. New Delhi: Prentice Hall of India Pvt Ltd; 1997. p. 770.
  24. 24. Ghimire BK, Kim SH, Yu CY, Chung IM. Biochemical and physiological changes during early adventitious root formation in Chrysanthemum indicum Linné cuttings. Plants. 2022;11(11):1440. https://doi.org/10.3390/plants11111440
  25. 25. Dubey AK, Mishra M, Yadav DS. Softwood grafting in Khasi mandarin (Citrus reticulata Blanco). Ind J Hort Sci. 2004;61:263–4.
  26. 26. Deshmukh NA, Patel RK, Krishnappa R, Verma BC, Rymbai H, Assumi SR, et al. Influence of rootstock age and propagation methods on scion physiology and root morphology of Khasi mandarin (Citrus reticulata). Indian J Agric Sci. 2017;87(2):203–9. https://doi.org/10.56093/ijas.v87i2.67569
  27. 27. Dubey AK, Mishra M, Yadav DS. Studies on new technique for Khasi mandarin (Citrus reticulata Blanco). Indian J Citriculture. 2002;1(1):103–7.
  28. 28. Singh J, Yadav A, Bhatnagar P, Arya CK, Jain MC, Sharma MK, et al. Budding performance of Nagpur mandarin on different rootstocks under Hadoti region of Rajasthan. Indian J Hortic. 2012;69(1):20–6. https://doi.org/10.5958/0974-0112.2017.00008.1
  29. 29. Cline JA, Hunter DM, Bonn WG, Bijl M. Resistance of the Vineland series of apple rootstocks to fire blight caused by Erwinia amylovora. J Am Pomol Soc. 2001;55(4):218. https://doi.org/10.71318/apom.2001.55.4.218
  30. 30. Shalaby TA, Taha NA, Rakha MT, El-Beltagi HS, Shehata WF, Ramadan KM, et al. Can grafting manage Fusarium wilt disease of cucumber and increase productivity under heat stress? Plants. 2022;11(9):1147. https://doi.org/10.3390/plants11091147
  31. 31. Laino P, Russo MP, Guardo M, Reforgiato‐Recupero G, Valè G, Cattivelli L, et al. Rootstock-scion interaction affecting citrus response to CTV infection: a proteomic view. Physiol Plant. 2016;156(4):444–67. https://doi.org/10.1111/ppl.12395
  32. 32. Bogoescu M, Doltu M, Sora D. Prevention and control of soilborne diseases and nematodes in eggplants crop by grafting plants combined with soil fumigation. In: VIII International Symposium on Chemical and Non-Chemical Soil and Substrate Disinfestation; 2014. p. 331–6. https://doi.org/10.17660/ActaHortic.2014.1044.43
  33. 33. Polat E, Geboloğlu N. Evaluation of grafting onto different rootstocks on yield and disease incidence of eggplant (Solanum melongena L.) under Verticillium and Fusarium wilt stress. TURJAF. 2025;13(6):1555–61. https://doi.org/10.24925/turjaf.v13i6.1555-1561.7680
  34. 34. Marè C, Aprile A, Roncaglia E, Tocci E, Corino LG, De Bellis L, et al. Rootstock and soil induce transcriptome modulation of phenylpropanoid pathway in grape leaves. J Plant Interact. 2013;8(4):334–49. https://doi.org/10.1080/17429145.2012.754958
  35. 35. Zhang M, Zhang H, Tan J, Huang S, Chen X, Jiang D, et al. Transcriptome analysis of eggplant root in response to root-knot nematode infection. Pathogens. 2021;10(4):470. https://doi.org/10.3390/pathogens10040470

Downloads

Download data is not yet available.