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Life Cycle-Based Host Range Analysis for Tomato Spotted Wilt Virus in Korea
Plant Pathol. J. 2020;36:67-75
Published online February 1, 2020
© 2020 The Korean Society of Plant Pathology.

Eui-Joon Kil1 , Young-Jae Chung2, Hong-Soo Choi3, Sukchan Lee1* , and Chang-Seok Kim4*

1College of Biotechnology and Bioengineering, Sungkyunkwan University, Suwon 16419, Korea
2Department of Life Science and Biotechnology, Shingyeong University, Hwaseong 18274, Korea
3Crop Protection Division, National Academy of Agricultural Science, Rural Development Administration, Wanju 55365, Korea
4Highland Agriculture Research Institute, National Institute of Crop Science, Rural Development Administration, Pyeongchang 25342, Korea
Correspondence to: *Sukchan Lee
Phone) +82-31-290-7866, FAX) +82-31-290-7892
Chang-Seok Kim
Phone) +82-33-330-1935, FAX) +82-33-330-1519
Eui-Joon Kil
Sukchan Lee

Handling Editor : Ju-Yeon Yoon
Received December 5, 2019; Revised December 9, 2019; Accepted December 11, 2019.
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Tomato spotted wilt virus (TSWV) is one of the plant viruses transmitted by thrips and causes severe economic damage to various crops. From 2008 to 2011, to identify natural host species of TSWV in South Korea, weeds and crops were collected from 5 regions (Seosan, Yesan, Yeonggwang, Naju, and Suncheon) where TSWV occurred and were identified as 1,104 samples that belong to 144 species from 40 families. According to reverse transcription-polymerase chain reaction, TSWV was detected from 73 samples from 23 crop species, 5 of which belonged to family Solanaceae. Additionally, 42 weed species were confirmed as natural hosts of TSWV with three different life cycles, indicating that these weed species could play an important role as virus reservoirs during no cultivation periods of crops. This study provides up-to-date comprehensive information for TSWV natural hosts in South Korea.

Keywords : reservoir, Tomato spotted wilt virus (TSWV), Tospovirus

Tomato spotted wilt virus (TSWV) is a member of the genus Orthotospovirus in the family Tospoviridae (Maes et al., 2018). Their genome consists of three negative or ambisense, single-stranded RNA species designated as S (2.9 kb), M (4.8 kb), and L (8.9 kb) with partially complementary terminal sequences (Adkins, 2000). Their pleomorphic particles are 80–120 nm in diameter with surface projections composed of two viral glycoproteins G1 and G2 (Adkins, 2000; Pappu, 2008). The first report of the disease ‘spotted wilt of tomato’ was described by Charles Brittlebank, an Australian phytopathologist, in 1919 (Best, 1968; Brittlebank, 1919). In 1930, Samuel characterized this pathogen as a virus and named it TSWV (Samuel, 1930). According to the first report of International Committee on Taxonomy of Viruses (ICTV), TSWV was the sole member of ‘Tomato spotted wilt virus group’ (Fenner, 1976). After the early 1990s, because several similar viruses to TSWV were identified and characterized, the genus Tospovirus was created and changed to the family Tospoviridae according to the most recently proposed classification (Maes et al., 2018; Murphy et al., 1995).

TSWV-infected plants show typical symptoms such as yellowing; mottling; chlorotic, ring spots of leaves and fruits; and stunting, inducing significant crop losses. Expression of these symptoms can vary depending on strain (or isolate) of the infected TSWV, plant species, crop cultivars and growth stage of the infected plants and environmental conditions of the infected plants (Adkins, 2000; German et al., 1992; Riley et al., 2011; Scholthof et al., 2011). TSWV is transmitted by approximately 10 species of thrips including the western flower thrips (Frankliniella occidentalis) (Riley et al., 2011; Sundaraj et al., 2014). TSWV occurrences have economic importance in cultivation of many crops because of the significantly decreased crop yields of the infected plants. In addition, TSWV disease spread rapidly to new healthy plants since viruliferous western flower thrips (F. occidentalis) are difficult for population management using chemical insecticides or natural organic compounds (Adkins, 2000; Jiang et al., 2017). Mechanical transmission of TSWV is also possibly transmitted from sap of naturally infected plants (Parrella et al., 2003).

TSWV is one of the plants viruses with the largest host range (Parrella et al., 2003). Over 1,000 plant species in over 85 families including many cultivated crops such as peanut (Arachis hypogaea), pepper (Capsicum annuum), potato (Solanum tuberosum), spinach (Spinacia oleracea), tobacco (Nicotiana tabacum), and tomato (Solanum lycopersicum) are reported TSWV natural hosts (Brittlebank, 1919; Cho et al., 1987; Costa, 1941; German et al., 1992; Parrella et al., 2003; Sakimura, 1940; Sherwood et al., 2009; Smith, 1931). In addition to economic crops, various weeds are also known natural hosts of TSWV and can be act as reservoirs for viral spread to other susceptible crops (Chatzivassiliou et al., 2001; Cho et al., 1986; Parrella et al., 2003).

TSWV is one of the most important plant viruses, reported in about 100 countries on all continents (OEPP/EPPO, 1999). In South Korea, TSWV was first reported on sweet pepper (paprika) from Yesan in 2004 (Kim et al., 2004) and spread nationwide. Mainly, TSWV occurrences in Korea have been reported continuously from tomato, pepper, and potato (Yoon et al., 2017). TSWV infection was also found in soybean (Glycine max), Brugmansia suaveolens, Eustoma grandiflorum, Hoya carnosa, Humulus japonicas, and Peperomia obtusifolia in Korea (Choi et al., 2014; Kim et al., 2018; Yoon et al., 2017, 2018a, 2019). Many hot pepper farms in Korea have suffered from TSWV.

Previously, the host range investigations of TSWV in various plants including weeds were reported (Cho et al., 1986, 1987; Parrella et al., 2003). In recent years, however, report from large-scale investigations have not been issued. In this study, to update lists, we examined crop and weed hosts of TSWV in Korea.

Materials and Methods

Sample collection.

From 2008 to 2011, to investigate the influence of host plants on the spread of TSWV, samples of crops and weeds were collected. To investigate natural host plants from plants with different life cycles, plant samples were collected in the winter (November to February), spring (March to May), and summer (June to October). Sampling was conducted in five areas where occurrence of TSWV has been reported continuously (Suncheon, Naju, Yeonggwang, Seosan, and Yesan) in South Korea (Fig. 1). Sample collection points were inside and outside of non-heated greenhouses that had been used as nurseries for hot pepper seedlings, and other crop cultivating greenhouses or open fields around hot pepper cultivating greenhouses or open fields.

RNA isolation and virus diagnosis.

Total RNA was extracted from collected samples with easy-spin Total RNA Extraction Kit (Intron Biotechnology, Seongnam, Korea) according to the manufacturer’s manual. TSWV infection was confirmed by RT-PCR with AMV Reverse Transcriptase (for cDNA synthesis, Promega, Madison, WI, USA), GoTaq DNA Polymerase (for PCR, Promega), and a TSWV-specific primer set (TSWV-6F, 5′-GAGATTCTCAGAATTCCCAGT-3′; TSWV-6R, 5′-AGAGCAATCGTGTCAATTTTATTC-3′), as described in a previous study (Tables 13) (Ko et al., 2013).

Results and Discussion

Species identification of collected samples.

For 4 years, to identify natural hosts of crops and weeds that can be infected with TSWV, a total of 1,104 samples was collected from weeds (830 samples) and crops (274 samples) from five areas in Korea where TSWV has occurred (Table 1, Fig. 2). Because weeds have various life cycles (summer annual, winter annual, and perennial), it is hard to find many different kinds of weeds if sampling is conducted at a certain time only, so sample collections were done repeatedly in the different seasons. In addition, we sampled in the open fields, heated greenhouses, and non-heated greenhouses as the weed species that can be identified can vary depending on heating during winter. Collected samples were confirmed as belonging to 144 species (34 crops and 110 weeds) (Tables 13, Fig. 2).

Crop hosts.

Among crops, plants that belong to the family Solanaceae including tomato, eggplant, and sweet pepper showed high infection rates (75–100%) (Table 2). In the family Liliaceae, on the other hand, infection was observed only in shallot (Allium × proliferum). According to our observation in Yesan, shallot was cultivated in a non-heated greenhouse during winter as a perennial crop and was confirmed as an important host for propagation of western flower thrips (F. occidentalis). Thus, TSWV-infected shallot is a natural host for TSWV overwintering and propagation of the insect vector. In the family Fabaceae, three species (pea, peanut, and red bean) were confirmed as natural hosts in some places collected from an open field in Yeonggwang near many chrysanthemum cultivating greenhouses. From those farms, TSWV was also detected from chrysanthemum (19%), and large colonies of western flower thrips were observed. Based on this result, the TSWV insect vector (western flower thrips), which cannot overwinter in open fields (Brødsgaard, 1993), could directly damage the crops in the open field the next spring after overwintering in Chrysanthemum greenhouses. Tomato, eggplant (S. melongena), lettuce (Lactuca sativa), and crown daisy (Glebionis coronaria) were infected as seedling stages of the crops in nurseries with TSWV-infected hot pepper plants in Seosan.

Our results show that cooperation of thrips controls at neighboring farms is very important for effective TSWV control. In particular, the occurrence of the thrips in crops other than pepper, known as the most important host of TSWV, can be overlooked, but it is important because it can cause the spread of the thrips. In Korea, especially when farming scale is small, many kinds of crops are mixed and grown in other fields. As our results show, not only solanaceous crops but also beans, cucurbits, sesame, shallot, and curled mallow can be natural hosts of TSWV in South Korea. Since these are commonly grown crops in Korea, even if the pepper or tomato farmers manage thrips, it is very likely that viruliferous thrips including the western flower thrips (F. occidentalis) will continuously inflow from neighboring farms they are growing. This is also one of the reasons why TSWV problems continue to occur in Korea.

Weed hosts.

Table 3 shows infection rates of TSWV in weeds. Among the weeds collected in areas of TSWV occurrence (110 species), 42 species in 22 families were identified as TSWV-infected. Asteraceae, Brassicaceae, and Caryophyllaceae families had the largest numbers of infected species (6 species each). According to life cycle analyses of TSWV weed hosts, 18 species were confirmed as winter annual (42.9%), 30.9% (13 species) were summer annual, and 26.2% (11 species) were perennial (Table 3, Fig. 3). Among the weeds analyzed from numerous (>20) samples, most samples of summer annual Eclipta alba (Fig. 2G) showed TSWV infection (95.6%), and half of winter annual Stellaria media (55%) and perennial S. aquatica (54.5%) (Fig. 2C) samples were confirmed as TSWV infected. A larger number of winter annual weeds were confirmed as many of those species overwintered in heated greenhouses in TSWV occurrence areas. These results suggest that winter annual weeds play important roles in overwintering of TSWV. From our previous study on overwintering of Tomato yellow leaf curl virus (TYLCV), it has been shown that S. aquatica can act as a viral source to newly introduced insect vectors in the next cultivation after overwintering in the non-heated greenhouse (Kil et al., 2015). We did not confirm overwintering of TSWV in wintering S. aquatica plants by time-course follow-up and artificial experiments shown in the previous study on TYLCV, but it can be inferred that S. aquatica plants infected with TSWV play a similar role in overwintering and spread. S. media showed the highest infectivity among winter annual weeds, is the dominant species in greenhouses in the winter season, and had a vital role as a reservoir host for TSWV and a main host for western flower thrips. Perennial weeds including Artemisia princeps, S. aquatica, Calystegia sepium (Fig. 2F), and Phytolacca americana are common in cultivation areas in Korea, so it is likely that they can act as green bridges for TSWV.

Epidemiological aspects of TSWV infection in crops and weeds in Korea.

TSWV occurs repeatedly through complex interactions between main host plants, other crop and weed hosts, and the insect vector thrips in Korea (Fig. 4). In hot pepper cultivating farms and nurseries, TSWV occurrence is common in Korea. The western flower thrips has spread to all areas of Korea. As shown in the above results, weeds growing in a cultivation area and other crops grown in the same or neighboring greenhouses also can be infected with TSWV and weeds act as intermediate hosts. In a nursery for hot pepper seedlings in spring, TSWV infection was detected from Cetastium glomeratum, S. aquatica, S. media, Lamium amplexicaule, and Galium spurium, which are winter annual or perennial weeds. If healthy plants are moved to an open field or greenhouse for cultivation, some viruliferous insect vector can infect them, creating additional inoculum for another vector. To overcome this cycle, control of insect vectors and weeds is necessary, and selection of TSWV-resistant cultivars can reduce economic damage. However, there have been a few reports for TSWV isolates that overcome Tsw gene-mediated resistance in pepper (Boiteux and de Ávila, 1994; Jiang et al., 2017; Riley et al., 2011).

TSWV has been a long-standing problem in over 100 countries, and its host range is the largest (Cho et al., 1986, 1987; Parrella et al., 2003). In Korea, TSWV has been indigenous as a representative plant virus that continuously damages pepper cultivation, and it is damaging not only peppers but also cultivation of tomatoes, potatoes and chrysanthemums. In addition to the known hosts, new hosts are also being reported in Korea. H. japonicas, one of weeds that are easily observed in farms, was reported as TSWV-infected (Yoon et al., 2018a). Soybean (Glycine max) cultivated commonly and famous ornamental plant P. obtusifolia introduced from Taiwan and China have also been identified as TSWV recently (Yoon et al., 2018b, 2019). These reports mean that TSWV host range analyses for the commonly cultivated or newly introduced crops, and the weeds found on farms should be done continuously to update lists of TSWV hosts, which can be helpful to design strategy for effective controls. This study was conducted to investigate crop and weed hosts of TSWV from areas near hot pepper cultivating farms in Korea and 23 crop species and 42 weed species were confirmed as TSWV-infected in fields. Our updated list of natural hosts from this study can be used for TSWV control.


This study was supported by the Grant from Rural Development Administration (number PJ01011302).

Fig. 1. Korean collection locations of crop and weed samples in this study.
Fig. 2. Tomato spotted wilt virus (TSWV)-infected pepper plants and weeds collected for TSWV detection. (A) Leaf symptoms of TSWV-infected pepper plants. (B) Fruit symptoms of TSWV-infected sweet pepper plants. (C) Stellaria aquatica. (D) Amaranthus lividus. (E) Metaplexis japonica. (F) Calystegia sepium. (G) Eclipta alba. (H) Sonchus asper.
Fig. 3. Schematic diagram of Tomato spotted wilt virus (TSWV) life cycles in natural weed hosts. The three different circles indicate the three different life cycles (summer annual, winter annual, and perennial) of weed hosts introduced in this study.
Fig. 4. Schematic diagram of Tomato spotted wilt virus (TSWV) disease cycles with thrips in a nursery for seedlings and greenhouse and open field for cultivating pepper plants. H, healthy plants; I, infected plants; N, non-viruliferous thrips; and V, viruliferous thrips.

Numbers of tested crops and weeds for Tomato spotted wilt virus (TSWV) detection in this study

Family No. of tested species No. of detected species No. of tested samples
Asteraceae 29 9 300
Amaranthaceae 5 2 103
Apiaceae 2 1 13
Asclepiadaceae 1 1 4
Boraginaceae 1 0 1
Brassicaceae 9 8 80
Campanulaceae 1 1 4
Cannabaceae 1 0 3
Caprifoliaceae 1 0 1
Caryophyllaceae 6 6 104
Chenopodiaceae 4 2 46
Commelinoideae 1 1 18
Convolvulaceae 3 2 42
Crassulaceae 1 1 1
Cucurbitaceae 4 3 18
Euphorbiaceae 2 1 18
Fabaceae 12 7 36
Fagaceae 1 0 1
Lamiaceae 4 2 9
Liliaceae 6 2 38
Malvaceae 2 2 8
Meliaceae 1 0 7
Menispermaceae 1 0 1
Moraceae 3 1 10
Oleaceae 1 1 3
Oxalidaceae 3 0 4
Phytolaccaceae 1 1 60
Poaceae 8 1 56
Polygonaceae 4 1 11
Portulacaceae 1 0 4
Pteridaceae 1 0 1
Ranunculaceae 2 0 2
Rosaceae 3 0 9
Rubiaceae 2 2 16
Rutaceae 1 0 2
Scrophulariaceae 3 1 18
Solanaceae 8 6 37
Ulmaceae 1 0 3
Urticaceae 2 0 6
Vitaceae 2 0 6
144 65 1,104

Infection rate of Tomato spotted wilt virus (TSWV) in crops

Family Species No. of samples Infectivity (%)

Common name Scientific name Tested Detected
Apiaceae Carrot Daucus carota 1 0 0
Dropwort Oenanthe javanica 12 2 16.7
Asteraceae Chrysanthemum Chrysanthemum morifolium 21 4 19
Crown daisy Chrysanthemum coronarium 2 2 100
Lettuce Lactuca sativa 38 2 5.3
Brassicaceae Chinese cabbage Brassica campestris 22 17 77.3
Chinese radish Raphanus sativus 4 1 25
Campanulaceae Bellflower root Platycodon grandiflorum 1 1 100
Chenopodiaceae Spinach Spinacia oleracea 38 2 5.3
Convolvulaceae Sweet potato Ipomoea batatas 5 2 40
Cucurbitaceae Cucumber Cucumis sativus 9 3 33.3
Oriental melon Cucumis melo 1 1 100
Pumpkin Cucurbita moschata 7 0 0
Fabaceae Cassia seed Cassia tora 2 0 0
Cow pea Vigna sinensis 1 0 0
Mung bean Phaseolus radiatus 1 0 0
Pea Pisum sativum 2 2 100
Peanut Arachis hypogaea 18 5 27.8
Red bean Phaseolus angularis 4 2 50
Lamiaceae Perilla seed Perilla frutescens 2 0 0
Liliaceae Chinese Chive Allium tuberosum 5 0 0
Shallot Allium ascalonicum 24 6 25
Spring onion Allium fistulosum 5 0 0
Wild chive Allium monanthum 2 0 0
Malvaceae Curled mallow Malva verticillata 7 2 28.6
Moraceae Mulberry tree Morus alba 8 1 12.5
Pedaliacae Sesame Sesamum indicum 3 1 33.3
Ranunculaceae Peony root Paeonia lactiflora 1 0 0
Rosaceae Strawberry Fragaria ananassa 1 0 0
Solanaceae Eggplant Solanum melongena 4 3 75
Hot pepper Capsicum annuum 12 6 50
Potato Solanum tuberosum 4 1 25
Sweet pepper Capsicum annuum 6 6 100
Tomato Solanum lycopersicum 1 1 100
Total 274 73 -

Infection rate of Tomato spotted wilt virus (TSWV) in detected weeds

Family Species Life cycle No. of samples Infectivity (%)

Tested Detected
Amaranthaceae Amaranthus lividus SA 88 18 20.5
Celosia cristata SA 1 1 100
Asclepiadoideae Metaplexis japonica SA 4 1 25
Asteraceae Artemisia princeps P 50 17 34
Eclipta alba SA 45 43 95.6
Conyza canadensis WA 7 2 28.6
Hemistepta lyrata WA 14 6 42.9
Sonchus asper WA 17 11 64.7
Youngia japonica WA 12 4 33.3
Brassicaceae Brassica juncea WA 2 1 50
Cardamine fallax WA 4 2 50
Cardamine flexuosa WA 29 2 6.9
Lepidium virginicum WA 1 1 100
Rorippa indica WA 1 1 100
Rorippa palustris WA 3 1 33.3
Caryophyllaceae Cerastium glomeratum WA 8 2 25
Dianthus chinensis SA 2 2 100
Melandryum firmum SA 1 1 100
Stellaria alsine WA 2 2 100
Stellaria aquatica P 22 12 54.5
Stellaria media WA 69 33 55
Chenopodiaceae Chenopodium ficifolium SA 2 1 50
Commelinoideae Commelina communis SA 18 6 33.3
Convolvulaceae Calystegia sepium P 25 5 20
Crassulaceae Sedum sarmentosum P 1 1 100
Cucurbitaceae Trichosanthes kirilowii P 1 1 100
Euphorbiaceae Acalypha australis SA 17 1 5.9
Fabaceae Robinia pseudoacacia P 3 1 33.3
Trifolium repens P 1 1 100
Vicia amoena WA 1 1 100
Vicia hirsuta WA 1 1 100
Lamiaceae Lamium amplexicaule WA 2 2 100
Liliaceae Smilax sieboldii P 1 1 100
Malvaceae Althaea rosea SA 1 1 100
Oleaceae Forsythia koreana P 3 2 66.7
Phytolaccaceae Phytolacca americana P 60 16 26.7
Poaceae Poa annua WA 21 1 4.8
Polygonaceae Persicaria longiseta SA 5 1 20
Rubiaceae Galium spurium WA 12 8 66.7
Paederia scandens P 4 3 75
Scrophulariaceae Mazus pumilus SA 15 9 60
Solanaceae Solanum nigrum SA 6 1 16.7
Total 582 227 -

SA, summer annual; P, perennial; WA, winter annual.

  1. Adkins S. 2000. Tomato spotted wilt virus - positive steps towards negative success. Mol Plant Pathol 1: 151-157.
    Pubmed CrossRef
  2. Best RJ. 1968. Tomato spotted wilt virus. Adv Virus Res 13: 65-146.
    Pubmed CrossRef
  3. Boiteux LS, and de Ávila AC. 1994. Inheritance of a resistance specific to tomato spotted wilt tospovirus in Capsicum chinense ‘PI 159236’. Euphytica 75: 139-142.
  4. Brittlebank CC. 1919. Tomato diseases. J Agric Victoria 17: 213-235.
  5. Brødsgaard HF. 1993. Cold hardiness and tolerance to submergence in water in Frankliniella occidentalis (Thysanoptera: Thripidae). Environ Entomol 22: 647-653.
  6. Chatzivassiliou EK, Boubourakas I, Drossos E, Eleftherohorinos I, Jenser G, Peters D, and Katis NI. 2001. Weeds in greenhouses and tobacco fields are differentially infected by Tomato spotted wilt virus and infested by its vector species. Plant Dis 85: 40-46.
    Pubmed CrossRef
  7. Cho JJ, Mau RFL, Gonsalves D, and Mitchell WC. 1986. Reservoir weed hosts of tomato spotted wilt virus. Plant Dis 70: 1014-1017.
  8. Cho JJ, Mau RFL, Mitchell WC, Gonsalves D, and Yudin LS. 1987. Research Extension Series; RES-078. Host list of plants susceptible to Tomato spotted wilt virus (TSWV) . University of Hawaii, Honolulu, HI, USA. 10 pp.
  9. Choi S-K, Cho I-S, Choi G-S, and Yoon J-Y. 2014. First report of Tomato spotted wilt virus in Brugmansia suaveolens in Korea. Plant Dis 98: 1283.
    Pubmed CrossRef
  10. Costa AS. 1941. Una molestia de virus de amendoim (Arachis hypogaea L.) A mancha anular. Biologico 7: 249-251.
  11. Fenner F 1976. The classification and nomenclature of viruses. J Gen Virol 31, pp. 463-470.
  12. German TL, Ullman DE, and Moyer JW. 1992. Tospoviruses: diagnosis, molecular biology, phylogeny, and vector relationships. Annu Rev Phytopathol 30: 315-348.
    Pubmed CrossRef
  13. Jiang L, Huang Y, Sun L, Wang B, Zhu M, Li J, Huang C, Liu Y, Li F, Liu Y, Dong J, Zhang Z, and Tao X. 2017. Occurrence and diversity of Tomato spotted wilt virus isolates breaking the Tsw resistance gene of Capsicum chinense in Yunnan, southwest China. Plant Pathol 66: 980-989.
  14. Kil E-J, Byun H-S, Kim S, Cho S, Cho S, Roh K, Lee K-Y, Choi H-S, Kim C-S, and Lee S. 2015. Tomato yellow leaf curl virus can overwinter in Stellaria aquatica, a winter-hardy TYLCV-reservoir weed. Plant Dis 99: 588-592.
    Pubmed CrossRef
  15. Kim J-H, Choi G-S, Kim J-S, and Choi J-K. 2004. Characterization of Tomato spotted wilt virus from paprika in Korea. Plant Pathol J 20: 297-301.
  16. Kim M, Kim JE, Kim J, Kwak HR, Choi HS, Lee HJ, Hong SS, and Kang CS. 2018. First report of Tomato spotted wilt virus in Hoya carnosa in Korea. Plant Dis 102: 1672.
  17. Ko S-J, Kang B-R, Choi D-S, Kim D-I, Lee G-S, Kim C-S, and Choi H-S. 2013. Pattern of the occurrence of Tomato spotted wilt virus in Jeonnam province. Res Plant Dis 19: 273-280 (in Korean).
  18. Maes P, Alkhovsky SV, Bào Y, Beer M, Birkhead M, Briese T, Buchmeier MJ, Calisher CH, Charrel RN, Choi IR, Clegg CS, de la Torre JC, Delwart E, DeRisi JL, Di Bello PL, Di Serio F, Digiaro M, Dolja VV, Drosten C, Druciarek TZ, Du J, Ebihara H, Elbeaino T, Gergerich RC, Gillis AN, Gonzalez J-PJ, Haenni A-L, Hepojoki J, Hetzel U, Hồ T, Hóng N, Jain RK, Jansen van Vuren P, Jin Q, Jonson MG, Junglen S, Keller KE, Kemp A, Kipar A, Kondov NO, Koonin EV, Kormelink R, Korzyukov Y, Krupovic M, Lambert AJ, Laney AG, LeBreton M, Lukashevich IS, Marklewitz M, Markotter W, Martelli GP, Martin RR, Mielke-Ehret N, Mühlbach HP, Navarro B, Ng TFF, Nunes MRT, Palacios G, Pawęska JT, Peters CJ, Plyusnin A, Radoshitzky SR, Romanowski V, Salmenperä P, Salvato MS, Sanfaçon H, Sasaya T, Schmaljohn C, Schneider BS, Shirako Y, Siddell S, Sironen TA, Stenglein MD, Storm N, Sudini H, Tesh RB, Tzanetakis IE, Uppala M, Vapalahti O, Vasilakis N, Walker PJ, Wáng G, Wáng L, Wáng Y, Wèi T, Wiley MR, Wolf YI, Wolfe ND, Wú Z, Xú W, Yang L, Yāng Z, Yeh S-D, Zhāng YZ, Zhèng Y, Zhou X, Zhū C, Zirkel F, and Kuhn JH. 2018. Taxonomy of the family Arenaviridae and the order Bunyavirales: update 2018. Arch Virol 163: 2295-2310.
    Pubmed CrossRef
  19. Murphy FA, Fauquet CM, Bishop DHL, Ghabrial SA, Jarvis AW, Martelli GP, Mayo MA, and Summers MD. 1995. Archives of virology, supplement, Vol. 10. Virus taxonomy: classification and nomenclature of viruses. Sixth report of the International Committee on Taxonomy of Viruses . Springer-Verlag, Wien, Austria. 586 pp.
  20. Pappu HR. 2008. Tomato spotted wilt virus. In: Encyclopedia of virology, eds. by BWJ. Mahy, and MHV. Van Regenmortel , pp. 133-138. Elsevier Ltd, Oxford, UK.
  21. Parrella G, Gognalons P, Gebre-Selassiè K, Vovlas C, and Marchoux G. 2003. An update of the host range of Tomato spotted wilt virus. J Plant Pathol 85 (4 Spec): 227-264.
  22. ., OEPP/EPPO 1999. EPPO data sheets on quarantine pests. Tomato spotted wilt tospovirus. Bull OEPP/EPPO Bull 29: 465-472.
  23. Riley DG, Joseph SV, Srinivasan R, and Diffie S. 2011. Thrips vectors of tospoviruses. J Integr Pest Manag 2: I1-I10.
  24. Sakimura K. 1940. Evidence for the identity of the yellow-spot virus with the spotted-wilt virus: experiments with the vector, Thrips tabaci. Phytopathology 30: 281-299.
  25. Samuel G. 1930. Investigations on ‘spotted wilt’ of tomatoes in Australia. Commonw Aust Counc Sci Ind Res Bull 44: 8-11.
  26. Scholthof KB, Adkins S, Czosnek H, Palukaitis P, Jacquot E, Hohn T, Hohn B, Saunders K, Candresse T, Ahlquist P, Hemenway C, and Foster GD. 2011. Top 10 plant viruses in molecular plant pathology. Mol Plant Pathol 12: 938-954.
    Pubmed KoreaMed CrossRef
  27. Sherwood JL, German TL, Moyer JW, and Ullman DE, 2009 Tomato spotted wilt virus . URL [5 December 2019].
  28. Smith KM. 1931. Studies on potato virus diseases VIII. On a ringspot virus affecting solanaceous plants. Ann Appl Biol 18: 1-15.
  29. Sundaraj S, Srinivasan R, Culbreath AK, Riley DG, and Pappu HR. 2014. Host plant resistance against Tomato spotted wilt virus in peanut (Arachis hypogaea) and its impact on susceptibility to the virus, virus population genetics, and vector feeding behavior and survival. Phytopathology 104: 202-210.
    Pubmed CrossRef
  30. Yoon JY, Choi GS, and Choi SK. 2017. First report of Tomato spotted wilt virus in Eustoma grandiflorum in Korea. Plant Dis 101: 515.
  31. Yoon JY, Choi GS, Jang SW, Park SH, and Choi S-K. 2018a. First report of Tomato spotted wilt virus in Humulus japonicus in Korea. Plant Dis 102: 690.
  32. Yoon JY, Choi GS, Kwon SJ, and Cho IS. 2019. First report of Tomato spotted wilt virus infecting Peperomia obtusifolia in South Korea. Plant Dis 103: 593.
  33. Yoon YN, Jo Y, Cho WK, Choi H, Jang Y, Lee YH, Bae JY, and Lee BC. 2018b. First report of Tomato spotted wilt virus infecting soybean in Korea. Plant Dis 102: 461.

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