Virology & Mycology

Virology & Mycology
Open Access

ISSN: 2161-0517

Review Article - (2021)Volume 10, Issue 3

Top Ten Viruses Reported on Chilly in Southeast Asia

Jitendra Kumar Kushwaha*
 
*Correspondence: Dr. Jitendra Kumar Kushwaha, Department of Botany, Deen Dayal Upadhyaya Gorakhpur University, Gorakhpur, Uttar Pradesh, India, Email:

Author info »

Abstract

Chilly is a common spice crop grown in large quantities in South Asia. India produces 75% of the total chilly crop followed by Nepal at 8% and Bangladesh at 6%, where it is grown primarily by large and small-scale farmers. It can also be found in the kitchen garden. Disease and insect pests are the most significant factors affecting the production of the chilly crop. The viral disease represents a significant threat to chilly production. Recently, 68 viruses have been reported influencing the chilly crop all over the world. Chilly Leaf Curl Virus Disease, Cucumber Mosaic Virus, Tobacco Mosaic Virus, Tomato Spotted Wilt Virus, Potato Virus Y, Alfalfa Mosaic Virus, Pepper Vein Mottle Virus, Beet Curl Top Virus, and Pepper Mild Mottle Virus are among the 68 viruses belonging to seven genera namely, Begomovirus, Cucumovirus, Tobamovirus, Tospovirus, Potyvirus, Alfamovirus and Curtovirus. In chilly cultivation, yield losses vary from 15 to 100%, depending on the virus. This review article is an analysis providing of top ten viruses reported in Chilly, including their geographic range, yield losses, symptomatology, transmission and management in South Asian Countries.

Keywords

Chilli; South-Asia; Chilly leaf curl virus; Tobacco mosaic virus; Cucumber mosaic virus; Yield loss

Introduction

Chilly belongs to the genus Capsicum, under Solanaceae family. It is an important fruit vegetable, and spice, with a frequently sharp taste and attractive appearance, so it is grown all over the world [1]. Since the introduction of the chilly crop in South Asian countries in the 16th century, the climate of the region has been favourable for its cultivation. The production of green and dry chilli across the world in 2019 was approximate 38652669 tons (FAOSTAT. 2019). India produces 1743000 tonnes of dry chilli and 81837 tonnes of green chilli. The top five chilly producing countries in South Asia in 2019 was India, Nepal, Bangladesh, Pakistan, and Iran, with a total production of 1824837, 187629, 149473, 101659, and 100232 tonnes (FAOSTAT 2019) (Table 1). Chilly is a cash crop in South Asia, it contributes to the economy in a various of ways, including as a source of income and job creation. Particularly to the rural population and foreign earners. Recognizing the importance of chilly as a cash crop in South Asia and around the world, the constraint to its production is reviewed with the goal of addressing them. High seed costs, a lack of proper and appropriate inputs, a lack of improved varieties, drought stress, low soil fertility, a lack of storage facilities, price volatility, a lack of technical knowledge at the farm level, and extreme disease are some of the major constraints. The most devastating factors in the production of chilly crop are viral diseases, which cause serious economic losses to chilli cultivators. In this review we are reporting a wide range of viral diseases which affects the chilli crop in all South Asian countries, including India.

Plant miRNA targeted Effect on plant Referene
Arabidopsis miR394 Tolerant to drought [48]
miR165/166 Tolerant to drought [75]
miR393 Sensitive to salinity [24]
miR396 Sensitive to salinity [23]
miR417 Sensitive to salt and ABA [31]
miR156 Tolerant to heat stress [58]
miR173 Tolerant to heat stress [38]
miR402 Tolerant to drought, salt and cold stress 33
Rice miR159 Tolerant to drought [93]
miR166 Tolerant to drought [84]
miR319 Increased cold tolerance [76]
miR156 Reduced cold tolerance [13]
  Tomato miR169 Tolerant to drought [88]

Table 1: Total chilli (Area harvested/Yield/Production) in South-Asian countries (Source of Data: FAOSTAT, 2019).

Literature Review

This is a retrospective and descriptive study based on the medical records of patients seen in dermatology consultations over the period from January 1, 2010 to December 31, 2020 (10 years). Included were patients of all ages and both sexes in whom a positive diagnosis of onychomycosis was made, based on clinical and mycological examinations. Only complete patient files were retained. Data was collected on the basis of a technical sheet including the study variables: the socio-demographic data of the patients, clinical and mycological (Table 2).

Plant miRNA targeted Resistant to virus Reference
Arabidopsis thaliana     AthMIR159a Cucumber Mosaic Virus (CMV) [17]
  Turnip Mosaic Virus (TuMV) [35]
Turnip Yellow Mosaic Virus (TYMV) [49]
Nicotiana tabacum AthMIR159a Cucumber Mosaic Virus (CMV) [17]
Potato Virus X (PVX) [1]
Potato Virus Y (PVY) [1]
AthMIR167b Potato Virus X (PVX) [1]
AthMIR171a Cucumber Mosaic Virus (CMV) [54]
AthMIR319a Potato Virus Y (PVY) [57]
Tobacco Etch Virus (TEV) [57]
Solanum lycopersicum AthMIR159a Cucumber Mosaic Virus (CMV) [87]
AthMIR319a Tomato leaf curl New Delhi Virus (ToLCNDV) [66]
AthMIR390a Tomato Spotted Wilt Virus (TSWV) [9]
SlyMIR159a Tomato Leaf Curl New Delhi Virus (ToLCNDV) [66]
Oryza sativa OsaMIR528 Rice Black Streaked Dwarf Virus (RBSDV) + Rice Stripe Virus (RSV) [60]
Triticum aestivum OsaMIR395 Wheat Streak Mosaic Virus [20]
Zea mays ZmaMIR159a Rice Black Streaked Dwarf Virus (RBSDV) [74]

Table 2: Details of top ten viruses reported in chilly in South-Asian countries.

Chilly Leaf Curl Virus (ChiLCVD)

Chilly Leaf Curl Virus (ChiLCVD) is a member of the genus Begomovirus and family Geminiviridae. They are primarily found in the tropical and subtropical regions of the globe. Geminiviruses are recognized as one of the most destructive plant viruses in the world, causing a major threat to global food security [2,3]. South Asian countries, such as India, have also been listed [4,5]. It is also reported in Nepal and Pakistan, Bangladesh [6].

Yield loss: Yield losses caused by some geminiviruses have been estimated to be as high as 88-100% [7].

Symptoms: ChiLCVD symptoms include abaxial and adaxial curling of the leaves, puckering, and blistering of interveinous areas, thickening and swelling of the vein, and stunted growth [8,9]. Transmission of Leaf curl virus is reported by M. persicae, A. nasturtii, A. craccivora. Bemisia tabaci and Bemisia gossypiperda [10].

Resistant variety: The best resistant varieties reported are Pusa Jawala and Phule Jyoti.

Cucumber Mosaic Virus (CMV)

Cucumber Mosaic Virus (CMV) belongs to the genus Cucumovirus and family Bromoviridae. It occurs globally, mainly in temperate, tropic and sub-tropic regions of the world [11]. It has been found in India, Nepal, Sri Lanka, Bhutan, Pakistan, and Iran, and is one of the most widespread viruses in South-Asia [12,13]. CMV has affected over 1000 species in over 100 families, causing major economic losses in a variety of ornamental, horticultural, and vegetable crops. CMV disease incidence ranges from 46 to 47% in young plant stages [14].

Yield loss: CMV causes yield losses ranging from 20 to 100% and 10 to 20% even during harvesting time [15].

Symptoms: The Symptoms includes yellow moulting, distorted leaves, and stunted growth [16,17]. Mild mosaic and dull-coloured leaves, mottling, shoe-string, fern leaf, vein banding, vein clearing, leaf deformation, and stunted growth and decreased fruit size are the most common symptoms of naturally affected chilly plants [18].

Resistant variety: CMV-resistant pepper genotypes have been reported. For example, genotype CA23 (Noakhali) is resistant to CMV in both natural and inoculated conditions, whereas genotype CA12 (Comilla-2) is moderately resistant [21].

Tobacco Mosaic Virus (TMV)

The Tobacco Mosaic Virus (TMV) is the first virus to be discovered. It belongs to the genus Tobamovirus and family Virgaviridae [22]. The virus was reported to infect the Chilly crop in India, Bangladesh, Pakistan, Nepal, Iran, Srilanka, and Bhutan [23,24].

Yield loss: The heavy yield losses due to this virus have been worldwide reported in tobacco, tomato, and pepper. The yield losses of up to 90% have been recorded in bell pepper because of TMV infection [25].

Symptoms: Infected pepper plants are usually stunted, deformed, with raised bumps and mottled areas in the leaves, as well as dark and light green areas [26]. Other symptoms include leaf mosaic, leaf curling, and stunted growth Fruit that has been infected shrinks dramatically in size and ripens unevenly [23,27].

Transmission: TMV is a seed-borne disease in chilly disease transmitted primarily by plant-to-seed communication, mechanical means such as hand, cutting tool, and other tools, but not by insect-vectors. TMV infects at least 125 different crop types, including tobacco, tomato, chilly, and cucumber [27].

Resistant variety: Pant C-1, Arka Harika, and Hisar Vijay are some of the TMV resistant varieties (Source: seednet.gov.in).

Tomato Spotted Wilt Virus (TSWV)

Tomato Spotted Wilt Virus (TSWV) is member of the genus Tospovirus and family Bunyauitidae. It occurs globally and mainly in temperate, tropic, and sub-tropic regions of the world [28,29]. Chilli has been identified to be infected by this virus in India, Pakistan, Nepal, Bangladesh, and Iran [24]. It can also be found in Asia and Europe [30].

Yield loss: TSWV reduced yield from 45% to 95% and in some cases up to 100%.

Symptoms: Mostly, infected chilly plant shows necrotic lesion or chlorotic spots, bronzing, curling, and wilting of leaves and necrotic streaks on the stem [31].

Transmission: Viruses are spread between plants in a variety of ways, including vegetative propagation, mechanical transmission by sap, seed, pollen, insects, mites, nematodes, dodder, and fungi. Thrips (Frankliniella occidentalis) transmit it [32]. Capsicum annum is a susceptible variety toward TSWV.

Resistant variety: TSWV resistant varieties include Capsicum chinense PI15225 and PI159236 [33].

Potato Virus Y (PVY)

Potato Virus Y (PVY) is a member of the genus potyvirus and family Potyviridae [34]. PVY is most common in crops of the Solanaceae family, such as potato and chilli, and has a higher prevalence in pepper.

Yield loss: PVY Virus diseases resulted in yield losses ranging from 60 to 100%, and these were regarded as major constraints to the crop's economic production [35].

Symptoms: The symptom appeared in the naturally infected chilly plant were developed mild yellowing, vein clearing, vein banding, mottling, mosaic, and interveinal chlorosis in leaves and stunted hight.

Transmission: PVY is naturally transmitted by numerous species of aphid [36].

Resistant variety: PVY-resistant cultivars include Capsicum amaranticolor and Capsicum quinoa

Alfalfa Mosaic Virus (AMV)

Alfalfa Mosaic Virus (AMV), which belongs to the genus Alfamovirus and family Bromoviridae [37]. It infects over 400 plant species worldwide, including several vegetable and woody crops [38]. Although AMV is found all over the world, but in South Asia, it is most common in India, Iran, Bangladesh, and Pakistan [39]. In chilly fields, disease incidence ranged from 80 to 100%.

Symptoms: Common symptoms associated with AMV on pepper are blotchy white and bright yellow mosaic on its leaves [40]. Plants that are infected with the virus at a young stage display stunted growth with misshapen and blotchy fruits.

Transmission: AMV is the only one of these viruses that can be spread through pollen grains and seeds [41]. AMV has a broad host range and is spread by aphid species such as the Pea Aphid (Acyrthosiphon pisum) through mechanical and non-persistent transmission [42].

Resistant variety: As a result, resistant varieties such as Pusa Sadabahar, Arka Meghana, and Pusa Jawala must be used (Source: seednet.gov.in).

Pepper Veinal Mottle Virus (PVMV)

PVMV (Pepper Veinal Mottle Virus) belongs to the genus Potyvirus and the family Potyviridae. It is distributed worldwide [43].

Yield loss: PVMV causes yield losses ranging from 55 to 65% and disease incidents up to 100% in Nepal and other South Asian countries [44].

Symptoms: On infected chilly plants, PVMV causes curling, vein banding, mosaic, mottle, ringspot, leaf yellowing, blistering deformation, and plant stunting [45].

Transmission: PVMV is transmitted with aphid, the disease is usually transmitted by six species of aphids including (Aphid creccivora, A. spiraecola, A. febae, A. gossypii, Myzus persicae and Rhapalosiphum maidis). But Myzus persicae and A. gossypii are most probably transmission vectors [46].

Resistant variety: The majority of chilly cultivars are susceptible to PVMV, except for NHV1-D96 and NHV1-E96, which are highly tolerant to PVMV infection [44].

Beet Curly Top Virus (BCTV)

Beet Curl Top Virus (BCTV) is a member of the Curtovirus genus and the Geminiviridae family. It is a virus that causes significant loss to the chilly, tomato, and sugar beet crops all over the world [47]. It is widely distributed throughout the Middle East and Africa, as well as in South Asian countries such as Iran, Pakistan, Nepal, and India [48].

Yield Loss: In the late 1900s, BCTV caused yield losses of up to 80% in southern New Mexico, as well as Iron, Pakistan, Nepal, and India in South Asia [48].

Symptoms: BCTV-infected chilly plant with curling, yellowing, mosaic spot, and leaf rolling, severe interveinal chlorosis, and internode shortening resulting in stunted height.

Transmission: Circulifer tenellus and C. haematoceps naturally transmit Beet Curl Top Viruses in a circulative persistent manner with a diverse host range of plants including beet, tomato, and chilly [49].

Resistant variety: BCTV resistant varieties include Pusa Jawala and Pant C-1 (Source: seednet.gov.in).

Pepper Mild Mottle Virus (PMMoV)

Pepper Mild Mottle Virus (PMMoV) is a single-stranded RNA virus that belongs to genus Tobamovirus and family Virgaviridae [50]. PMMoV is often distributing worldwide. It is found in South Asian countries such as India, Iran, Pakistan, Sri Lanka, and Bangladesh [51].

Yield loss: When a young plant becomes infected with this viral disease, it causes significant yield losses as well as significant damage to the quality of the fruits. Disease incidence ranges from 20 to 80%, with yield losses ranging from 50 to 100% [52].

Symptoms: Various symptoms have been associated with PMMoV disease elsewhere and include mottling, mosaic, chlorosis, stunted growth, mottling, puckering, malformed leaves, small and deformed fruits, [53].

Transmission: PMMoV is highly infectious, and it is spread in the fields by seed and soil, rather than insects [54]. PMMoV can survive on infected debris and in soil. It serves as primary inoculum for consequent crops [55]. Capsicum spp. is the virus's primary host, but studies have shown that it can infect up to 24 Solanaceae species as well as other Chenopodiaceae, Cucurbitaceae, Labiatae, and Plantaginaceae species.

Resistant variety: The susceptible variety is Kashi Shurkh (CCH-2) while the resistant varieties are Phule Jyoti, Pant C-1, and Pusa Jawala (Source: seednet.gov.in).

Tomato Mosaic Virus (ToMV)

Tomato Mosaic Virus (ToMV) is belongs to genus Tobamovirus and the family Virgaviridae. Genetic material is a positive, single-stranded RNA virus present with Road-shaped virion. ToMV has a worldwide distribution . In South Asian countries, it is found in India, Pakistan, Iran, Bangladesh, and Sri Lanka [56-59].

Yield loss: According to a survey conducted in two districts of Coimbatore, Tamil Nadu, India during March 2016 [60], disease incidence ranges from 15 to 20%, and it can cause yield loss ranging from 20 to 90% .

Symptoms: ToMV symptoms resemble those of TMV in most cases, with mosaic mottling, crinkling, curling of leaves, and stunted growth on pepper plants infected with ToMV [61,62]. It has been identified as infecting over 150 economically important crop species, including vegetables and ornamental flowers [37]. It is more common on tomato and pepper than TMV.

Transmission: Contact is the most common mode of transmission, but it can also be transmitted mechanically or by seed [25,63].

Resistant variety: Azad Mirch-1 is tolerant to (ToMV) but not resistant to it. Pant C-1 was thus used as a resistant cultivar (Source: seednet. gov.in)

Discussion

We have listed all the top ten viruses of chilly in a table form which include their names, Genus, Family, symptoms, mode of transmission, Genotype, Country and references (Table 2). There are many other viruses reported in South-east Asia. Some of them are Chilly Veinal Mottle Virus (ChiVMV) and Tomato Yellow Leaf Curl Virus reported from Bangladesh, Tomato Leaf Curl Karnataka Virus (ToLCKV) and Tomato Leaf Curl New Delhi Virus (ToLCNDV) are reported in India [18,40]. Potato Virus X (PVX) and Tobacco Itch Virus (TIV) are reported in Sri-lanka as well as India [35]. The virus diseases in Chilly is a prevalent feature new species and strains of viruses are frequently being discovered, causing damage to the cultivar.

Conclusion

In this review we have discussed top 10 viruses that infect chilly crop in South Asian countries, it has been noticed that Chilly Leaf Curl Virus Disease (ChiLCVD), Potato Virus Y (PVY), and Cucumber Mosaic Virus (CMV) are most harmful and widespread. In our survey we found that India Pakistan, Bangladesh, and Iran have significant research work done while no virus-related work on chilly has been reported in Afghanistan and Maldives. Knowledge of different types of viruses infecting chilly crop may provide us basis to develop resistant varieties. Although many research works have been conducted on virus infecting chilly but still there are gaps to be filled in term of management of viruses.

Acknowledgement

We are thankful to Prof. Pooja Singh Head, Department of Botany, DDU Gorakhpur University for her valuable suggession and support.

References

  1. Mehta I. Chillies-The Prime Spice-A History. IOSR J Humanit Soc Sci (IOSR-JHSS). 2017;22(7);32-36.
  2. Brown JK, Zerbini FM, Navas-Castillo J, Moriones E, Ramos-Sobrinho R, Silva JC, et al. Revision of begomovirus taxonomy based on pairwise sequence comparisons. Arch Virol. 2015;160(6):1593-619
  3. Fauquet CM, Stanley J. Geminivirus classification and nomenclature: Progress and problems. Ann Appl Biol. 2003;142(2):165-189.
  4. Thakur H, Jindal SK, Sharma A, Dhaliwal MS. Chilli leaf curl virus disease: a serious threat for chilli cultivation.J Plant Dis Prot. 2018;125(3):239-249.
  5. Kumar A, Sinha V, Khan Z, Sarin NB, Singh S,  Tiwari A. A new monopartite begomovirus associated with betasatellite molecule causing leaf curl disease of chilli in India. Int J Adv Res. 2016;4(4):636-641.
  6. Senanayake DMJB, Dhammika WAR,Dassanayake P JK, Navoditha AMA, Kumari KASI. Detection of chilli leaf curl Srilanka virus in chilli plants showing different virus like symptoms and in alternative weed hosts. Ann Srilanka Agric.2015;17:76-79.
  7. Zehra SB, Ahmad A, Sharma A, Sofi S, Lateef A, Bashir Z,et al.Chilli leaf curl virus an emerging threat to chilli in India. Int J Pure App Biosci.2017;5(5):404-414.
  8. Mishra MD, Raychaudhuri SP, Ashrafi J. Virus causing leaf curl of chilli (Capsicum annuum L.) Indian. J Microbiol. 1963;3(2):73-76.
  9. Kumar RV, Singh AK, Chakraborty S. A new monopartite begomovirus species, chilli leaf curl Vellanad virus, and associated betasatellites infecting chilli in the Vellanad region of Kerala, India. New Dis Rep. 2012;20.
  10. Tahir M, Haider M S, Iqbal J, Briddon RW. Association of a distinct begomovirus and a betasatellite with leaf curls symptoms in Pedilanthus tithymaloides. J Phytopathol. 2009; 157(3):188-193.
  11. Arogundade O, Balogun OS, Kareem KT. Occurrence and distribution of pepper veinal mottle virus and cucumber mosaic virus in pepper in Ibadan, Nigeria. Virol J. 2012; 9(1):1-4
  12. Venkatesh HL, Kavyashri VV, Padmaja AS, Nagaraju N, Ramesh S. Biological confirmation of resistance from segregating populations of Gherkin (Cucumis anguria L.) against cucumber mosaic virus (CMV). J Appl Nat Sci. 2019;11(1):199-204.
  13. Rahman MS, Akanda M, Mian IH, Bhuiyan K,Hossain M.  Study the effect of Cucumber Mosaic Virus (CMV) on different growth stages of chili. Ann Bangladesh Agric. 2015;19:65-73.
  14. Ashfaq M, Ahmad A. First report of Tomato spotted wilt virus in hot pepper in Pakistan. Plant Pathol. 2017; 99(1):291.
  15. Green SK, Kim JS. Characteristics and control of viruses infecting peppers: a literature review. Asian Vegetable Research and Development Center;1991; 18:60.
  16. Azizan NH, Abidin ZA, Phang IC. Study of cucumber mosaic virus gene expression in capsicum annuum. Sci Herit J. 2017;1(2):29-31.
  17. Rai GS.Aetiology and integrated management of Phytophthora wilt of chilli (Capsicum annuum L.) in Bhutan. 2021.
  18. Rashid MH, Khalequzzaman KM, Alam MS, Uddin SA, Green SK. Screening of different sweet pepper lines against cucumber mosaic virus and chili veinal mottle virus. Int J Sustain Crop Prod. 2007;2(3): 1-4.
  19. Ashfaq M, Iqbal S, Mukhtar T, Shah H. Screening for resistance to cucumber mosaic cucumovirus in chilli pepper. J Anim Plant Sci. 2014; 24(3):791-795.
  20. Ali A, Kobayashi M. Seed transmission of Cucumber mosaic virus in pepper. J Virol Methods. 2010; 163(2):234-237.
  21. Rahman MS, Akanda M, Mian IH, Bhuiyan K, Hossain M. New sources of resistance to cucumber mosaic virus in Capsicum annuum. J Crop Sci Biotechnol. 2016;19(3):249-258.
  22. Scholthof KBG. Tobacco mosaic virus: the beginning of plant virology. APSnet Features. 2008.
  23. Alishiri A, Rakhshandehroo F, Zamanizadeh HR, Palukaitis P. Prevalence of tobacco mosaic virus in Iran and evolutionary analyses of the coat protein gene. Plant Pathol J. 2013; 29(3):260-273.
  24. Akhter MS, Akanda AM, Kobayashi K, Jain RK, Mandal B. Plant virus diseases and their management in Bangladesh. J Crop Prot.2019; 118:57-65.
  25. Chitra TR, Prakash HS, Albrechtsen SE, Shetty HS, Mathur SB. Indexing of leaf and seed samples of tomato and bell pepper for tobamoviruses Indian. Phytopathol. 2002; 55(1):84-86.
  26. Pazarlar S,Gumus M,Oztekin GB.The effects of tobacco mosaic virus infection on growth and physiological parameters in some pepper varieties (Capsicum annuum L.). Not Bot Horti Agrobo.2013;41(2):427-433.
  27. Kumar S,Udaya Shankar AC,Nayaka SC,Lund OS,Prakash HS.Detection of Tobacco mosaic virus and Tomato mosaic virus in pepper and tomato by multiplex RT–PCR. Lett Appl Microbiol. (2011);53(3):359-363.
  28. Norris DO. The strain complex and symptom variability of tomato spotted wilt virus.Research Publications Repository.1946.
  29. Rudolph C, Schreier PH, Uhrig JF. Peptide-mediated broad-spectrum plant resistance to tospoviruses. Proceedings of the  Natl Acad Sci. 2003;100(8):4429-4434.
  30. Cho JD, Kim JS, Kim JY, Kim JH, Lee SH, Choi GS, et al. Occurrence and symptoms of tomato spotted wilt virus on vegetables in Korea (I). Plant Dis. 2005; 11(2):213-216.
  31. Agrios GN. Plant pathology 5th Edition: Elsevier Academic Press. 2005; 79-103.
  32. Wijkamp I, van Lent J, Kormelink R, Goldbach R, Peters D. Multiplication of tomato spotted wilt virus in its insect vector, frankliniella occidentalis.J GEN VIROL.1993;74(3):341-349.
  33. Black LL, Hobbs HA, Gatti Jr JM. Tomato spotted wilt virus resistance in capsicum chinense PI 152225 and 159236. Plant Dis.1991; 75(8):863.
  34. Hollings M, Brunt AA. Potyvirus group. CMI/AAB descriptions of plant viruses.1981;245(7).
  35. Green SK. Pepper virus research in taiwan and other Asian countries. InSymposium on plant virus and virus-like diseases.1993; 213-243.
  36. Radcliffe EB, Ragsdale DW. Aphid-transmitted potato viruses: the importance of understanding vector biology. Am J Potato Res. 2002;79(5):353-386.
  37. Waweru B, Kilalo D, Miano D, Kimenju JW, Rukundo P.Diversity and economic importance of viral diseases of pepper (Capsicum spp.) in Eastern Africa.J Appl Hortic. 2019;21(1):70-76.
  38. Parrella G, Lanave C, Marchoux G, Finetti-Sialer MM,Di Franco A, Gallitelli D.Evidence for two distinct subgroups of Alfalfa mosaic virus AMV from France and Italy and their relationship with other AMV strains.Arch Virol. 2000;145(12):2659-2667.
  39. Damiri N. Mixed viral infection and growth stage on Chilli (Capsicum annuum L.) production. Pertanika J. Trop. Agric. Sci. 2014; 37(2):275-83.
  40. Kenyon L, Kumar S, Tsai WS, Hughes JDA. Virus diseases of peppers (Capsicum spp.) and their control.Adv Virus Res. 2014;90:297-354.
  41. Garran J, Gibbs A. Studies on alfalfa mosaic virus and alfalfa aphids Aust. J Agric Res. 1982; 33(4):657-664.
  42. Moury B, Palloix A, Caranta C, Gognalons P, Souche S, Selassie KG, et al. Serological, molecular, and pathotype diversity of pepper veinal mottle virus and chili veinal mottle virus. Phytopathology. 2005;95(3):227-232.
  43. Fajinmi AA, Odebode CA, Fajinmi OB. The effect of agro-ecological zones on the incidence and distribution of aphid vectors of pepper veinal mottle virus, on cultivated pepper (Capsicum annuum L.) in Nigeria. J Cent Eur Agric. 2011;12(3).
  44. Tsai WS, Abdourhamane IK, Kenyon L. First report of pepper veinal mottle virus associated with mosaic and mottle diseases of tomato and pepper in mali. Plant Dis. 2010;94(3): 378-378.
  45. Alegbejo MD, Abo ME. Ecology, epidemiology and control of pepper veinal mottle virus (PVMV), genus Potyvirus, in west Africa. J Sustain Agric. 2002;20(2):5-16.
  46. Wintermantel WM, Mosqueda NF, Cortez AA, Anchieta AG. Beet curly top virus revisited: factors contributing to re-emergence in California. In 1st Joint IIRBASSBT Congress. 2003;295-302.
  47. Eini O, Sahraei GE, Behjatnia SA. Molecular characterization and construction of an infectious clone of a pepper isolate of beet curly top Iran virus. Mol Biol Res Commun. 2016;5(2):101-103.
  48. Yazdi HB, Heydarnejad J, Massumi H. Genome characterization and genetic diversity of beet curly top Iran virus: A geminivirus with a novel nonanucleotide.Virus genes. 2008;36(3):539-545.
  49. Yoon JY, Ahn HI, Kim M, Tsuda S, Ryu KH. Pepper mild mottle virus pathogenicity determinants and cross protection effect of attenuated mutants in pepper. Virus research. 2006; 118(1-2):23-30.
  50. Ahmad A, Tiberini A, Ashfaq M, Tomassoli L. First report of pepper mild mottle virus infecting chilli pepper in Pakistan. New Dis Rep. 2015;32(1):31.
  51. Martínez-Ochoa N, Langston DB,Mullis SW,Flanders JT.First report of pepper mild mottle virus in Jalapeno pepper in Georgia. Plant Health Prog.2003;4(1):26.
  52. Güldür ME, Çağlar BK. Outbreaks of pepper mild mottle virus in greenhouses in Sanliurfa, Turkey. J Plant Pathol. 2006;88(3):339-342.
  53. Rialch N, Sharma V, Sharma A, Sharm PN. Characterization and complete nucleotide sequencing of Pepper mild mottle virus infecting bell pepper in India. Phytoparasitica. 2015;43(3):327-337.
  54. Lamb EM, Adkins S, Shuler KD ,Roberts PD. Pepper mild mottle virus.IFAS Ext.2001;808.
  55. King A M, Adams MJ, Carstens EB, Lefkowitz EJ.Virus taxonomy. Ninth report of the International Committee on Taxonomy of Viruses.2012;486-487.
  56. Hu Q, Jiang T, Xue C, Zhou X. Characterization and complete nucleotide sequence of two isolates of tomato mosaic virus. Phytopathology. 2012; 160(3):115-119.
  57. Jamuna S, Rajendran L, Haokip BD, Nagendran K, Karthikeyan G, Manoranjitham SK. First report of natural infection of solanum nigrum with tomato mosaic virus in India. Plant Dis. 2018;102(5): 1044-1044.
  58. Farshad R. Phylogenetic analysis and genetic structure of new isolates of tomato mosaic virus in Iran. J Plant Prot Res. 2018;58(1):25-35.
  59. Ullah N, Ali A, Ahmad M, Fahim M,Din N,Ahmad F.  Evaluation of tomato genotypes against tomato mosaic virus (ToMV) and its effect on yield contributing parameters. Pak J Bot. 2017;49(4):1585-1592.
  60. Broadbent L. Epidemiology and control of tomato mosaic virus. Annu Rev Phytopathol. 1976; 14(1):75-96.
  61. Imran M, Khan MA, Fiaz M, Azeem M, Mustafa M. Influence of environmental conditions on tomato mosaic virus disease development under natural condition Pakistan. J Phytopathol. 2013;25(2):117-122.
  62. Kenyon L, Kumar S, Tsai WS, Hughes JDA. Virus diseases of peppers (Capsicum spp.) and their control. Adv Virus Res. 2014;90:97-354.

Author Info

Jitendra Kumar Kushwaha*
 
Department of Botany, Deen Dayal Upadhyaya Gorakhpur University, Gorakhpur, Uttar Pradesh, India
 

Citation: Kushwaha JK, Rai AK, Srivastava D (2021) Top Ten Viruses Reported on Chilly in Southeast Asia. Virol Mycol. 10:209.

Received: 23-Jun-2021 Accepted: 07-Jul-2021 Published: 14-Jul-2021 , DOI: 10.35248/2161-0517.21.10.209

Copyright: © Kushwaha JK, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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