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Early Access

Biological control of tomato leaf curl New Delhi virus using cucurbitaceous endophytes in bitter gourd (Momordica charantia)

DOI
https://doi.org/10.14719/pst.7162
Submitted
11 January 2025
Published
17-03-2025
Versions

Abstract

Momordica charantia L., known as bitter gourd, is a vine species classified under the Cucurbitaceae family and is extensively cultivated across Southeast Asia. The tomato leaf curl New Delhi virus (ToLCNDV), a member of the Begomovirus genus and Geminiviridae family, significantly affects bitter gourd. In this study, endophytes were isolated from different cucurbitaceous crops. The germination potential of the bacterial and actinobacterial isolates was evaluated via the roll towel method. Notably, isolate B-BGR1 demonstrated a 100% germination rate with vigor index of 5636.00 compared with the sterile water control, which presented a vigor index of 1013.00. Subsequent pot culture experiments indicated that a 2% application of B-BGR1 resulted in the lowest disease incidence, with a 78.57% reduction over the control, followed by B-BGL1, which showed a 71.43% reduction over the control. The isolate B-BGR1 was molecularly confirmed as Bacillus licheniformis through sequencing. The presence of secondary metabolites in B. licheniformis was identified via gas chromatography-mass spectrometry (GC-MS). To further explore the mechanism of action, the ToLCNDV coat protein was designed via MODELLER software, yielding a model with the highest DOPE score of -22439.755859. Molecular docking experiments revealed strong binding affinities for compounds 7,9-di-tert-butyl-1-oxaspiro(4,5)deca-6,9-dien and Mandelic acid, with values of -5.0 and -4.9 kcal/mol, respectively. This study represents the first investigation to confirm the antiviral potential of B. licheniformis through molecular docking against the ToLCNDV coat protein. These results indicate that B. licheniformis is a potential biological control agent for managing ToLCNDV in bitter gourd.

References

  1. Nagendran K, Mohankumar S, Aravintharaj R, Balaji CG, Manoranjitham SK, Singh AK, et al. The occurrence and distribution of major viruses infecting cucurbits in Tamil Nadu state, India. Crop Prot. 2017;99:10-16. https://doi.org/10.1016/j.cropro.2017.05.006
  2. India stat. Ministry of Agriculture and Farmers Welfare, Govt. of India. 2024. ON3479. https://www.indiastat.com/
  3. King AMQ, Adams MJ, Carstens EB, Lefkowitz EJ, editors. Virus taxonomy: classification and nomenclature of viruses. Ninth report of the International Committee on Taxonomy of Viruses. International Union of Microbiological Societies, Virology Division. New York: Academic Press; 2012
  4. Kiran GV, Nagaraju N, Girish TR, Ashwini BN. Molecular investigations reveal bitter gourd crop is more susceptible to tomato leaf curl New Delhi virus infection in diverse crop cultivation practices. 3 Biotech. 2021;11:1-9. https://doi.org/10.1007/s13205-021-02975-6
  5. Brown JK, Zerbini FM, Navas-Castillo J, Moriones E, Ramos-Sobrinho R, Silva JCF, et al. Revision of Begomo virus taxonomy based on pairwise sequence comparisons. Arch Virol. 2015;160:1593–619. https://doi.org/10.1007/s00705-015-2398-y
  6. Rehman M, Chakraborty P, Tanti B, Mandal B, Ghosh A. Occurrence of a new cryptic species of Bemisia tabaci (Hemiptera: Aleyrodidae): an updated record of cryptic diversity in India. Phytoparasitica. 2021;49(5):869-82. https://doi.org/10.1007/s12600-021-00909-9
  7. Beris D, Theologidis I, Skandalis N, Vassilakos N. Bacillus amyloliquefaciens strain MBI600 induces salicylic acid dependent resistance in tomato plants against tomato spotted wilt virus and potato virus Y. Sci Rep. 2018;8(1):10320. https://doi.org/10.1038/s41598-018-28677-3
  8. Gayathri M, Sharanya R, Renukadevi P, Nakkeeran S, Saranya N, Varanavasiappan S, et al. Deciphering the antiviral nature of endophytic Bacillus spp. against groundnut bud necrosis virus in cowpea and tomato. Front Microbiol. 2024;15:1410677. https://doi.org/10.3389/fmicb.2024.1410677
  9. Zehnder GW, Yao C, Murphy JF, Sikora ER, Kloepper JW. Induction of resistance in tomato against cucumber mosaic cucumo virus by plant growth-promoting rhizobacteria. Biocontrol. 2000;45:127-37. https://doi.org/10.1023/A:1009923702103
  10. Vinodkumar S, Nakkeeran S, Renukadevi P, Mohankumar S. Diversity and antiviral potential of rhizospheric and endophytic Bacillus species and phyto-antiviral principles against tobacco streak virus in cotton. Agric Ecosyst Environ. 2018;267:42-51. https://doi.org/10.1016/j.agee.2018.08.008
  11. Karthikeyan G, Barkavi G, Harish S, Varanavasiappan S. Expression of defense responsive genes in tripartite interaction of cucumber mosaic virus and plant growth promoting rhizobacteria in ridge gourd (Luffa acutangula (L.) Roxb). Physiol Mol Plant Pathol. 2024;129:102176. https://doi.org/10.1016/j.pmpp.2023.102176
  12. Hazarika SN, Saikia K, Thakur D. Characterization and selection of endophytic actinobacteria for growth and disease management of tea (Camellia sinensis L.). Front Plant Sci. 2022;13:989794. https://doi.org/10.3389/fpls.2022.989794
  13. Abdul-Baki AA, Anderson JD. Physiological and biochemical deterioration of seeds. In: Kozlowski TT, editor. Germination control, metabolism and pathology. Vol. II. New York: Academic Press; 1972. p. 283-315. https://doi.org/10.1016/B978-0-12-424303-3.50010-5
  14. Vinodkumar S, Nakkeeran S, Renukadevi P, Malathi VG. Biocontrol potentials of antimicrobial peptide producing Bacillus species: multifaceted antagonists for the management of stem rot of carnation caused by Sclerotinia sclerotiorum. Front Microbiol. 2017;8:446. https://doi.org/10.3389/fmicb.2017.00446
  15. Thiruvengadam R, Gandhi K, Vaithiyanathan S, Sankarasubramanian H, Loganathan K, Lingan R, et al. Complete genome sequence analysis of Bacillus subtilis Bbv57, a promising biocontrol agent against phytopathogens. Int J Mol Sci. 2022;23(17):9732. https://doi.org/10.3390/ijms23179732
  16. Colovos C, Yeates TO. Verification of protein structures: patterns of nonbonded atomic interactions; 1993. https://servicesn.mbi.ucla.edu/SAVES
  17. Wiederstein, Sippl. ProSA-web: interactive web service for the recognition of errors in three-dimensional structures of proteins. Nucleic Acids Res. 2007;35:W407?W410. https://prosa.services.came.sbg.ac.at/prosa.php/
  18. Tian W, Chen C, Lei X, Zhao J, Liang J. CASTp 3.0: computed atlas of surface topography of proteins. Nucleic Acids Res. 2018;46(W1):W363-67. http://sts.bioe.uic.edu/castp/index.html
  19. Kim S, Chen J, Cheng T, Gindulyte A, He J, He S, et al. PubChem 2023 update. Nucleic Acids Res. 2023 Jan 6;51(D1):D1373-80. https://pubchem.ncbi.nlm.nih.gov/
  20. Gomez KA, Gomez AA. Statistical procedures for agricultural research. 2nd ed. New York: John Wiley and Sons; 1984. p. 680.
  21. Abdelkhalek A, Al-Askar AA, Behiry SI. Bacillus licheniformis strain POT1 mediated polyphenol biosynthetic pathways genes activation and systemic resistance in potato plants against Alfalfa mosaic virus. Sci Rep. 2020;10:16120. https://doi.org/10.1038/https://doi.org/10.1038/s41598-020-72676-2
  22. Pandey N, Vaishnav R, Rajavat AS, Singh AN, Kumar S, Tripathi RM, et al. Exploring the potential of Bacillus for crop productivity and sustainable solution for combating rice false smut disease. Front Microbiol. 2024;15:1405090. https://doi.org/10.3389/fmicb.2024.1405090
  23. Gouda MR, Subramanian S. Variations in the expression of odorant binding and chemosensory proteins in the developmental stages of whitefly Bemisia tabaci Asia II-1. Sci Rep. 2024;14:15046. https://doi.org/10.1038/s41598-024-65785-9
  24. Shandeep G, Annaiyan S, Haran R, Mannu J, Somasundaram P, Shanmugam H, et al. Exploiting the nematicidal compounds from guava endo microbiome against root-knot nematodes, Meloidogyne enterolobii. Physiol Mol Plant Pathol. 2024;131:102268. https://doi.org/10.1016/j.pmpp.2024.102268
  25. Chen J, Luo X, Chen Y, Wang Y, Peng J, Xing Z. Recent research progress: Discovery of anti-plant virus agents based on natural scaffold. Front Chem. 2022;10:926202. https://doi.org/10.3389/fchem.2022.926202
  26. Xie Y, Ruan XH, Gong HY, Wang YH, Wang XB, Zhang JP, et al. Synthesis and biological activity of amide compounds containing pyrazole mandelic acid groups. J Heterocycl Chem. 2017;54(5):2644-49. https://doi.org/10.1002/jhet.2862
  27. Sangeetha B, Krishnamoorthy AS, Sharmila DJ, Renukadevi P, Malathi VG, Amirtham D. Molecular modelling of coat protein of the groundnut bud necrosis tospovirus and its binding with squalene as an antiviral agent: In vitro and in silico docking investigations. Int J Biol Macromol. 2021;189:618-34. https://doi.org/10.1016/j.ijbiomac.2021.08.143
  28. Dhanabalan S, Muthusamy K, Iruthayasamy J, Kumaresan PV, Ravikumar C, Kandasamy R, et al. Unleashing Bacillus species as versatile antagonists: Harnessing the biocontrol potentials of the plant growth-promoting rhizobacteria to combat Macrophomina phaseolina infection in Gloriosa superba. Microbiol Res. 2024;283:127678. https://doi.org/10.1016/j.micres.2024.127678

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