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Type :article
Subject :S Agriculture
ISSN :0973-6263
Main Author :Abu Kassim Faizah
Additional Authors :Hasbullah Nor Azlina
Thaer Sarah
Al-Obaidi Jameel R
Title :Characterisation of virus-related red tip disease in pineapple (Ananas comosus)
Place of Production :Tanjong Malim
Publisher :Fakulti Teknikal dan Vokasional
Year of Publication :2021
Corporate Name :Universiti Pendidikan Sultan Idris

Abstract : Universiti Pendidikan Sultan Idris
Pineapple (Ananas comosus) is one of the tropical fruits that is cultivated in Malaysia for export as well as domestic use. Unfortunately, the production is heavily affected by the red tip disease which was detected in the southern part of Malaysia 3 decades ago. Despite the identification of this disease, causal agent receives less attention from researchers. Nevertheless, symptoms associated with this infection and the mode of transference inside the plantations indicate viral-like disease. RNA extracted from the pineapple infected leaves introduced to Nicotiana tabacum cv. Coker by kneading the plant leaves to extract fresh sap. Yellowish necrosis was detected three weeks after artificial inoculation. The staining of the fresh diseased sample and inoculated Nicotiana tabacum cv. Coker showed the existence of round particles with an average diameter of 94.25nm under the transmission electron microscope. SDS-PAGE analysis revealed proteins bands similar to those of tospovirus at 25, 55 and 128 kDa. Further protein identification and validation suggested for molecular confirmation of the disease causative agent.

References

1. Altendorf S., Global prospects for major tropical fruits: shortterm outlook, challenges and opportunities in a vibrant global marketplace, Food outlook: biannual report on global food markets, FAO Trade and Markets Division, Rome (2017)

2. Alwabli A.S., Khattab E.A.H. and Farag A.G., Biological, Serological and Molecular Characterization of Papper MildMottle Virus Isolated from Weast Region of Kingdom of Saudi Arabia, Research Journal of Infectious Diseases, 5, 1 (2017)

3. Badillo-Vargas I.E., Chen Y., Martin K.M., Rotenberg D. and Whitfield A.E., Discovery of Novel Thrips Vector Proteins That Bind to the Viral Attachment Protein of the Plant Bunyavirus Tomato Spotted Wilt Virus, J Virol., 93, e00699-19 (2019)

4. Balasundram S., Abu Kassim F., Vadamalai G. and Hanif A., Estimation of red tip disease severity in pineapple using a noncontact sensor approach, Agricultural Sciences, 04, 206-8 (2013)

5. Berniak H., Characterization of a New Tomato Spotted Wilt Virus Isolates Found in Hippeastrum hybridum (Hort.) Plants in Poland, Journal of Horticultural Research, 24, 5-12 (2016)

6. Brewer H.C., Hird D.L., Bailey A.M., Seal S.E. and Foster G.D., A guide to the contained use of plant virus infectious clones, Plant Biotechnol J., 16, 832-43 (2018)

7. Çaglayan K. et al, Identification and characterization of a novel Robigovirus species from sweet cherry in turkey, Pathogens, 8, 57 (2019)

8. Chen G., Su Q., Shi X., Pan H., Jiao X. and Zhang Y., Persistently Transmitted Viruses Restrict the Transmission of Other Viruses by Affecting Their Vectors, Front Physiol., 9, 1-11 (2018)

9. Chitturi A., Conner K., Sikora E.J. and Jacobson A.L., Monitoring Seasonal Distribution of Thrips Vectors of Soybean Vein Necrosis Virus in Alabama Soybeans, J Econ Entomol., 111, 2562-9 (2018)

10. De Ronde D., Lohuis D. and Kormelink R., Identification and characterization of a new class of Tomato spotted wilt virus isolates that break Tsw-based resistance in a temperaturedependent manner, Plant Pathol., 68, 60-71 (2019)

11. Delic D. et al, Molecular identification of Tomato spotted wilt virus on pepper and tobacco in Republic of Srpska (Bosnia and Herzegovina), Eur J Plant Pathol., 150, 785-9 (2018)

12. Dijkstra J. and De Jager C., Practical plant virology: protocols and exercises, Springer Science & Business Media (2012)

13. Eyvazi A., Dizadji A., Rastgou M. and Habibi M.K., Bioassay and phylogeny of five Iranian isolates of Cucumber mosaic virus from different hosts based on CP gene sequence, Plant Prot Sci., 51, 200-7 (2015)

14. Fang Y. and Ramasamy R.P., Current and prospective methods for plant disease detection, Biosensors, 5, 537-61 (2015)

15. FAOSTAT, Food and agriculture organization corporate statistical database, Rome, Italy: The Food and Agriculture Organization (FAO) (2019)

16. Gelderblom H.R. and Madeley D., Rapid Viral Diagnosis of Orthopoxviruses by Electron Microscopy: Optional or a Must?, Viruses, 10, 142 (2018)

17. Golnaraghi A., Shahraeen N. and Nguyen H.D., Characterization and Genetic Structure of a Tospovirus Causing Chlorotic Ring Spots and Chlorosis Disease on Peanut; Comparison with Iranian and Polish Populations of Tomato yellow fruit ring virus, Plant Dis., 102, 1509-19 (2018)

18. Gronenborn B. et al, Analysis of DNAs associated with coconut foliar decay disease implicates a unique single-stranded DNA virus representing a new taxon, Scientific Reports, 8, 1-14 (2018)

19. Holkar S.K., Kumar R., Yogita M., Katiyar A., Jain R.K. and Mandal B., Diagnostic assays for two closely related tospovirus species, Watermelon bud necrosis virus and Groundnut bud necrosis virus and identification of new natural hosts, J Plant Biochem Biotechnol., 26, 43-51 (2017)

20. Hommel A., Global Market Update: Pineapple, Market Analysis, Tridge (2020)

21. Hong J.S. and Ju H.J., The Plant Cellular Systems for Plant Virus Movement, Plant Pathol J., 33, 213-28 (2017)

22. Huang C. et al, Non-Structural Protein NSm of Tomato Spotted Wilt Virus Is an Avirulence Factor Recognized by Resistance Genes of Tobacco and Tomato via Different Elicitor Active Sites, Viruses, 10, 660 (2018)

23. Hull R., Mathews’ plant virology, Academic Press, London, UK[Google Scholar] (2014)

24. Ishibashi K., Matsumoto-Yokoyama E. and Ishikawa M., A Tomato Spotted Wilt Virus S RNA-based Replicon System in Yeas, Scientific Reports, 7, 12647 (2017)

25. Jeong J.J., Ju H.J. and Noh J., A review of detection methods for the plant viruses, Research in Plant Disease, 20, 173-81 (2014)

26. Jezewska M., Trzmiel K. and Zarzynska-Nowak A., Detection of infectious Brome mosaic virus in irrigation ditches and draining strands in Poland, Eur J Plant Pathol., 153, 285-92 (2019)

27. Karavina C. and Gubba A., An african perspective on tospoviruses, J Plant Pathol., 99, 5-16 (2017)

28. Kikkert M., Van Lent J., Storms M., Bodegom P., Kormelink R. and Goldbach R., Tomato Spotted Wilt Virus Particle Morphogenesis in Plant Cells, J Virol., 73, 2288-97 (1999)

29. Komoda K., Ishibashi K., Kawamura-Nagaya K. and Ishikawa M., Possible involvement of eEF1A in Tomato spotted wilt virus RNA synthesis, Virology, 468-470, 81-7 (2014)

30. Legrand P., Biological assays for plant viruses and other grafttransmissible pathogens diagnoses: a review, EPPO Bulletin, 45, 240-51 (2015)

31. Li J. et al, Structure and Function Analysis of Nucleocapsid Protein of Tomato Spotted Wilt Virus Interacting with RNA Using Homology Modeling*, J Biol Chem., 290, 3950-61 (2015)

32. Lokesh B., Rashmi P.R., Amruta B.S., Srisathiyanarayanan D., Murthy M.R.N. and Savithri H.S., NSs Encoded by Groundnut Bud Necrosis Virus Is a Bifunctional Enzyme, PLos One, 5, e9757 (2010)

33. Maliogka V.I. et al, Recent advances on detection and characterization of fruit tree viruses using high-throughput sequencing technologies, Viruses, 10, 436 (2018)

34. Mandal B., Jain R., Krishnareddy M., Krishna Kumar N., Ravi K. and Pappu H., Emerging problems of tospoviruses (Bunyaviridae) and their management in the Indian subcontinent, Plant Dis., 96, 468-79 (2012)

35. Mandal B., Pappu H.R. and Culbreath A.K., Factors Affecting Mechanical Transmission of Tomato spotted wilt virus to Peanut (Arachis hypogaea), Plant Dis., 85, 1259-63 (2001)

36. Margaria P. et al, The NSs protein of tomato spotted wilt virus is required for persistent infection and transmission by Frankliniella occidentalis, J Virol., 88, 5788-802 (2014)

37. Mauck K.E., De Moraes C.M. and Mescher M.C., Evidence of Local Adaptation in Plant Virus Effects on Host–Vector Interactions, Integr Comp Biol., 54, 193-209 (2014)

38. McGovern R.J. and Elmer W.H., Handbook of Florists' Crops Diseases, Springer (2018)

39. Mitter N., Koundal V., Williams S. and Pappu H., Differential Expression of Tomato Spotted Wilt Virus-Derived Viral Small RNAs in Infected Commercial and Experimental Host Plants, PLos One, 8, e76276 (2013)

40. Mohd-Yusuf Y. et al, Standardized bioassays: An improved method for studying Fusarium oxysporum f. sp. cubense race 4 (FocR4) pathogen stress response in Musa acuminata cv.'Berangan' (2019)

41. Montero-Astúa M. et al, Disruption of vector transmission by a plant-expressed viral glycoprotein, Mol Plant-Microbe Interact., 27, 296-304 (2014)

42. Navarro J.A., Sanchez-Navarro J.A. and Pallas V., Chapter One - Key checkpoints in the movement of plant viruses through the host, In Kielian M., Mettenleiter T.C. and Roossinck M.J., eds., Adv Virus Res., Academic Press, 1-64 (2019)

43. Niu Y., Wang D., Cui L., Wang B., Pang X. and Yu P., Monoclonal antibody-based colloid gold immunochromatographic strip for the rapid detection of Tomato zonate spot tospovirus, Virol J., 15, 15 (2018)

44. Olmos A. et al, High-throughput sequencing technologies for plant pest diagnosis: challenges and opportunities, EPPO Bulletin, 48, 219-24 (2018)

45. Popov V.L., Tesh R.B., Weaver S.C. and Vasilakis N., Electron microscopy in discovery of novel and emerging viruses from the collection of the world reference center for emerging viruses and Arboviruses (WRCEVA), Viruses, 11, 477 (2019)

46. Roenhorst J.W., Botermans M. and Verhoeven J.T.J., Quality control in bioassays used in screening for plant viruses, EPPO Bulletin, 43, 244-9 (2013)

47. Scarff C.A., Fuller M.J., Thompson R.F. and Iadanza M.G., Variations on negative stain electron microscopy methods: tools for tackling challenging systems, Journal of Visualized Experiments, 2018, e57199 (2018)

48. Sharma A. and Kulshrestha S., Molecular characterization of tospoviruses associated with ringspot disease in bell pepper from different districts of Himachal Pradesh, VirusDisease, 27, 188-92 (2016)

49. Singh P., Indi S.S. and Savithri H.S., Groundnut Bud Necrosis Virus Encoded NSm Associates with Membranes via Its CTerminal Domain, PLos One, 9, e99370 (2014)

50. Sivaprasad Y., Garrido P., Mendez K., Pachacama S., Garrido A. and Ramos L., First report of tomato spotted wilt virus infecting Chrysanthemum in Ecuador, J Plant Pathol., 100, 113- (2018)

51. Van Knippenberg I., Goldbach R. and Kormelink R., Purified Tomato spotted wilt virus Particles Support Both Genome Replication and Transcription in Vitro, Virology, 303, 278-86 (2002)

52. Verhoeven J.T.J. and Roenhorst J.W., Herbaceous test plants for the detection of quarantine viruses of potato*, EPPO Bulletin, 30, 463-7 (2000)

53. Vijayan V., López-González S., Sánchez F., Ponz F. and Pagán I., Virulence evolution of a sterilizing plant virus: Tuning multiplication and resource exploitation, Virus Evolution, 3, 1-11 (2017)

54. Yoon J.Y., Choi G.S., Kwon S.J. and Cho I.S., First Report of Tomato spotted wilt virus Infecting Peperomia obtusifolia in South Korea, Plant Dis., 103, 593 (2019)

55. Zhang Z., Zheng K., Dong J., Fang Q., Hong J. and Wang X., Clustering and cellular distribution characteristics of virus particles of Tomato spotted wilt virus and Tomato zonate spot virus in different plant hosts, Virol J., 13, 11 (2016).


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