Evaluation of Lisianthus as an Indicator Host for Iris yellow spot virus

Iris yellow spot virus (IYSV) can severely affect onion production. IYSV is transmitted by the onion thrips, Thrips tabaci. However, information on IYSV–thrips–onion interactions is limited due to the difficulty associated with infecting onion plants experimentally. Lisianthus (Eustoma russellianum) was used as an indicator host to study mechanical transmission of IYSV, IYSV transmission by T. tabaci, IYSV distribution in the host plant, and the effect of temperature on IYSV symptom expression. Mechanical inoculation tests from IYSV-infected onion plants to noninfected lisianthus plants resulted in a mean transmission rate of 82.5 ± 6.9% (mean ± standard error), and from IYSV-infected lisianthus plants to noninfected lisianthus plants resulted in a mean transmission rate of 89.2 ± 7.1%. T. tabaci adults transmitted IYSV at a rate of 80.0 ± 8.3% from infected onion plants to noninfected lisianthus plants. To assess IYSV distribution in infected lisianthus plants, leaf sections, stems, and roots were tested by enzyme-linked immunosorbent assay (ELISA). All the plant parts tested positive for IYSV, but not on every plant assayed. Alternating night and day temperatures of 18 and 23°C, 25 and 30°C, and 30 and 37°C were evaluated for the effects on IYSV symptom expression. More severe symptoms developed on inoculated plants incubated at the 18 and 23°C or 25 and 30°C temperature regimes than at the 30 and 37°C regime, and symptoms were observed earliest on plants incubated at the 25 and 30°C temperature regime compared to the other temperature regimes.

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Screening Winter-sown Onion Entries for Iris Yellow Spot Virus Tolerance

HortScience ◽

10.21273/hortsci.44.3.627 ◽

2009 ◽

Vol 44 (3) ◽

pp. 627-632 ◽

Cited By ~ 6

Author(s):

Parminder S. Multani ◽

Christopher S. Cramer ◽

Robert L. Steiner ◽

Rebecca Creamer

Keyword(s):

Disease Progression ◽

Integrated Management ◽

Management Strategies ◽

Thrips Tabaci ◽

Iris Yellow Spot Virus ◽

Yellow Spot ◽

Enzyme Linked Immunosorbent Assay ◽

Symptom Expression ◽

Spot Virus ◽

Over Time

Identification of resistant or tolerant onion (Allium cepa L.) cultivars is crucial for the development of integrated management strategies for Iris yellow spot virus (IYSV). Exclusively vectored by onion thrips (Thrips tabaci), IYSV is a potentially devastating tospovirus of onion that has been confirmed to be present in 15 countries all over the world. In this study, 18 winter-sown onion entries were screened for IYSV symptom expression over two seasons. Over the growing season, straw-colored, necrotic lesions typical of IYSV infection were observed and rated for disease severity. Entries, NMSU 03-52-1, NMSU 04-41, NMSU 04-44-1, and ‘NuMex Jose Fernandez’, exhibited fewer symptoms than many other entries tested. ‘Caballero’, NMSU 04-57-1, NMSU 04-78-1, and ‘Cimarron’ exhibited more symptoms. Disease progression over time was rapid for entries exhibiting more symptoms and slow for entries exhibiting fewer symptoms. Enzyme-linked immunosorbent assay (ELISA) optical densities correlated poorly with the severity of disease symptoms. Trends in the disease progression over time emphasize the importance of rating IYSV symptoms late in the crop's development and to search for delayed disease progression rather than early symptom expression to determine IYSV susceptibility.

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First Report of Vidalia Onion (Allium cepa) Naturally Infected with Tomato spotted wilt virus and Iris yellow spot virus (Family Bunyaviridae, Genus Tospovirus) in Georgia

Plant Disease ◽

10.1094/pdis.2004.88.11.1285b ◽

2004 ◽

Vol 88 (11) ◽

pp. 1285-1285 ◽

Cited By ~ 19

Author(s):

S. W. Mullis ◽

D. B. Langston ◽

R. D. Gitaitis ◽

J. L. Sherwood ◽

A. C. Csinos ◽

...

Keyword(s):

Tomato Spotted Wilt Virus ◽

Thrips Tabaci ◽

Iris Yellow Spot Virus ◽

Yellow Spot ◽

Unknown Etiology ◽

Enzyme Linked Immunosorbent Assay ◽

Rt Pcr ◽

Spot Virus ◽

Tomato Spotted Wilt ◽

Wilt Virus

Vidalia onion is an important crop in Georgia's agriculture with worldwide recognition as a specialty vegetable. Vidalia onions are shortday, Granex-type sweet onions grown within a specific area of southeastern Georgia. Tomato spotted wilt virus (TSWV) has been endemic to Georgia crops for the past decade, but has gone undetected in Vidalia onions. Tobacco thrips (Frankliniella fusca) and Western flower thrips (Frankliniella occidentalis) are the primary vectors for TSWV in this region, and a number of plant species serve as reproductive reservoirs for the vector or virus. Iris yellow spot virus (IYSV), an emerging tospovirus that is potentially a devastating pathogen of onion, has been reported in many locations in the western United States (2,4). Thrips tabaci is the known vector for IYSV, but it is unknown if noncrop plants play a role in its epidemiology in Georgia. During October 2003, a small (n = 12) sampling of onions with chlorosis and dieback of unknown etiology from the Vidalia region was screened for a variety of viruses, and TSWV and IYSV infections were serologically detected. Since that time, leaf and bulb tissues from 4,424 onion samples were screened for TSWV and IYSV using double antibody sandwich-enzyme linked immunosorbent assay (DAS-ELISA) with commercial kits (Agdia Inc., Elkhart, IN). Samples were collected from 53 locations in the Vidalia region during the growing season between November 2003 and March 2004. Plants exhibiting stress, such as tip dieback, necrotic lesions, chlorosis or environmental damage were selected. Of these, 306 were positive for TSWV and 396 were positive for IYSV using positive threshold absorbance of three times the average plus two standard deviations of healthy negative onion controls. Positive serological findings of the onion tissues were verified by immunocapture-reverse transcription-polymerase chain reaction (IC-RT-PCR) for TSWV (3) and RT-PCR for IYSV (1). In both instances, a region of the viral nucleocapsid (N) gene was amplified. The PCR products were analyzed with gel electrophoresis with an ethidium bromide stain in 0.8% agarose. Eighty-six percent (n = 263) of the TSWV ELISA-positive samples exhibited the expected 774-bp product and 55 percent (n = 217) of the IYSV ELISA-positive samples exhibited the expected 962-bp product. The reduced success of the IYSV verification could be attributed to the age and deteriorated condition of the samples at the time of amplification. Thrips tabaci were obtained from onion seedbeds and cull piles within the early sampling (n = 84) and screened for TSWV by the use of an indirect-ELISA to the nonstructural (NSs) protein of TSWV. Of the thrips sampled, 25 were positive in ELISA. While the incidence of IYSV and TSWV in the Vidalia onion crop has been documented, more research is needed to illuminate their potential danger to Vidalia onions. References: (1) I. Cortês et al. Phytopathology 88:1276, 1998. (2) L. J. du Toit et al. Plant Dis. 88:222, 2004. (3) R. K. Jain et al. Plant Dis. 82:900, 1998. (4) J. W. Moyer et al. (Abstr.) Phytopathology 93(suppl.):S115, 2003.

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First Report of Onion (Allium cepa) Naturally Infected with Iris yellow spot virus in Peru

Plant Disease ◽

10.1094/pd-90-0377a ◽

2006 ◽

Vol 90 (3) ◽

pp. 377-377 ◽

Cited By ~ 8

Author(s):

S. W. Mullis ◽

R. D. Gitaitis ◽

C. Nischwitz ◽

A. S. Csinos ◽

Z. C. Rafael Mallaupoma ◽

...

Keyword(s):

The United States ◽

Thrips Tabaci ◽

Iris Yellow Spot Virus ◽

Yellow Spot ◽

N Gene ◽

Enzyme Linked Immunosorbent Assay ◽

Spot Virus ◽

First Report ◽

The Impact ◽

Das Elisa

Onions have become an important export crop for Peru during the last few years. The onions produced for export are primarily short-day onions and include Grano- or Granex-type sweet onions. The first of two growing seasons for onion in Peru occurs from February/March until September/October and the second occurs from September/October to December/January. Iris yellow spot virus (IYSV [family Bunyaviridae, genus Tospovirus]), primarily transmitted by onion thrips (Thrips tabaci), has been reported in many countries during recent years, including the United States (1,2). In South America, the virus was reported in Brazil during 1999 (3) and most recently in Chile during 2005 (4). During 2003, an investigation of necrotic lesions and dieback in onions grown near the towns of Supe and Ica, Peru led to the discovery of IYSV in this region. Of 25 samples of symptomatic plants collected from five different fields near Supe, 19 tested strongly positive and an additional three tested weakly positive for IYSV using double antibody sandwich-enzyme linked immunosorbent assay (DAS-ELISA) (Agdia Inc., Elkhart, IN). None of the samples tested positive for Tomato spotted wilt virus (TSWV). A number of onions with necrosis and dieback symptoms were also observed during 2004 and 2005. During September 2005, 25 plants with symptoms suspected to be caused by IYSV or TSWV in the Supe and Casma valleys were collected and screened for both viruses using DAS-ELISA. All plants screened were positive for IYSV. There was no serological indication of TSWV infection in these samples. The positive samples were blotted onto FTA cards (Whatman Inc., U.K.) to bind the viral RNA for preservation and processed according to the manufacturer's protocols. The presence of IYSV was verified by reverse transcription-polymerase chain reaction (RTPCR) using (5′-TCAGAAATCGAGAAACTT-3′) and (5′-TAATTATATCTATCTTTCTTGG-3′) as forward and reverse primers (1), respectively. The primers amplify the nucleocapsid (N) gene of IYSV, and the RT-PCR products from this reaction were analyzed with gel electrophoresis with an ethidium bromide stain in 0.8% agarose to verify the presence of this amplicon in the samples. Subsequent to the September 2005 sampling, 72 additional samples from regions in northern and southern Peru were analyzed in the same manner. The amplicons obtained were cloned, sequenced, and compared with known IYSV isolates for further verification. Onions have become a significant export crop for Peru, and more research is needed to determine the impact of IYSV on the Peruvian onion export crop. To our knowledge, this is the first report of IYSV in onion in Peru. References: (1) L. du Toit et al. Plant Dis. 88:222, 2004. (2) S. W. Mullis et al. Plant Dis. 88:1285, 2004. (3) L. Pozzer et al. Plant Dis. 83:345, 1999. (4) M. Rosales et al. Plant Dis. 89:1245, 2005.

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Wild Allium spp. as Natural Hosts of Iris yellow spot virus

Plant Disease ◽

10.1094/pd-90-0378a ◽

2006 ◽

Vol 90 (3) ◽

pp. 378-378 ◽

Cited By ~ 7

Author(s):

H. R. Pappu ◽

B. C. Hellier ◽

F. M. Dugan

Keyword(s):

Natural Infection ◽

The State ◽

Thrips Tabaci ◽

Iris Yellow Spot Virus ◽

Yellow Spot ◽

N Gene ◽

Enzyme Linked Immunosorbent Assay ◽

Rt Pcr ◽

Spot Virus ◽

Sequence Comparisons

The incidence of Iris yellow spot virus (IYSV) of genus Tospovirus, family Bunyaviridae in a commercial onion crop was first confirmed in Washington state during 2003 (1). First found in Adams County, IYSV has rapidly spread to all onion-producing counties in the state, affecting seed and bulb crops. The USDA-ARS Western Regional Plant Introduction Station (WRPIS) collects, maintains, and distributes various Allium (garlic and onion) accessions. As part of the regeneration process, accessions are grown under field conditions at the WRPIS farms in two locations: Pullman and Central Ferry, WA. Symptoms indicative of viral infection, now known to be caused by IYSV, first appeared in field-grown accessions in 1999. In June 2005, leaf and scape tissues were collected from WRPIS accessions of wild onions (Allium pskemense, A. vavilovii, and A. altaicum) in Central Ferry that had symptoms indicative of IYSV infection (2). IYSV infection was confirmed using enzyme-linked immunosorbent assay with a commercially available kit (Agdia Inc., Elkhart, IN). Virus infection was further verified using reverse transcription-polymerase chain reaction (RT-PCR) with primers derived from the small (S) RNA of IYSV. The primers flanked the IYSV N gene (5′-TAA AAC AAA CAT TCA AAC AA-3′ and 5′-CTC TTA AAC ACA TTT AAC AAG CAC-3′). RT-PCR gave a PCR product of expected size (≈1.2 kb). The DNA amplicon was cloned and sequenced. Nucleotide sequence comparisons with known IYSV N gene sequences showed 95 to 98% sequence identity. The prevalence of the vector, onion thrips (Thrips tabaci), combined with the widespread incidence of IYSV in seed and bulb production areas of the state may have resulted in natural infection of wild relatives of cultivated onion. The potential role of wild Allium spp. in IYSV epidemiology remains to be determined. Information on the extent of IYSV infection of onion germplasm would be useful in identifying potential sources of host plant resistance to IYSV. References: (1) L. J. du Toit et al. Plant Dis. 88:222, 2004. (2) B. Hellier et al. APSnet Image of the Week. Online publication, iw000049.asp, 2004.

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Iris yellow spot virus on Onion in New Mexico

Plant Disease ◽

10.1094/pdis.2004.88.9.1049c ◽

2004 ◽

Vol 88 (9) ◽

pp. 1049-1049 ◽

Cited By ~ 9

Author(s):

R. Creamer ◽

S. Sanogo ◽

A. Moya ◽

J. Romero ◽

R. Molina-Bravo ◽

...

Keyword(s):

United States ◽

New Mexico ◽

Thrips Tabaci ◽

Iris Yellow Spot Virus ◽

Yellow Spot ◽

Western United States ◽

Enzyme Linked Immunosorbent Assay ◽

Spot Virus ◽

Disease Symptoms ◽

On Line

Onions are an important crop for New Mexico with 7,700 acres (3,116 ha) harvested in the state in 2003 (3). In 2002, onions of several cultivars were first noticed with diamond-shaped chlorotic or bleached lesions on seed stalks or leaves, typical of those reported for Iris yellow spot virus (IYSV). A more widespread survey of breeding stocks and commercial onion fields revealed similar symptoms on thrips-infested onions in Dona Ana and Rio Arriba counties. Incidence of disease symptoms ranged from <0.5 to nearly 30%. Symptomatic leaves were assayed for the presence of IYSV using enzyme-linked immunosorbent assay (ELISA; Agdia, Elkhart, IN) and antisera acquired from Agdia. Symptomatic leaves from breeding and commercial fields tested positive for IYSV. The virus was transmitted by Thrips tabaci from symptomatic onions to three onion cvs. New Mex Mesa, New Mex Vado, and New Mex Cryspy in growth chamber tests. All three cultivars showed symptoms of IYSV and tested positive for the disease using ELISA. However, New Mex Vado and New Mex Cryspy cultivars each showed 24% infection (4 infected plants of 17 tested) compared with 59% infection (10 infected plants of 17 tested) for New Mex Mesa, suggesting that not all cultivars are equally susceptible to the virus. To our knowledge, this is the first report of IYSV in onions in New Mexico, which has also been reported in the western United States in Idaho, Oregon, Colorado, and Washington (1,2,4). References: (1) L. J. du Toit et al. Plant Dis. 88:222, 2004. (2) J. M. Hall et al. Plant Dis. 77:952, 1993. (3) National Agricultural Statistics Service, On-line publication. USDA, 2004. (4) H. F. Schwartz et al. Plant Dis. 86:560, 2002.

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Incidence and Distribution of Iris yellow spot virus on Onion in Serbia

Plant Disease ◽

10.1094/pdis-93-10-0976 ◽

2009 ◽

Vol 93 (10) ◽

pp. 976-982 ◽

Cited By ~ 16

Author(s):

Aleksandra Bulajić ◽

Ivana Djekić ◽

Jelena Jović ◽

Slobodan Krnjajić ◽

Ana Vučurović ◽

...

Keyword(s):

Iris Yellow Spot Virus ◽

Yellow Spot ◽

Onion Bulb ◽

Recent Common Ancestor ◽

Enzyme Linked Immunosorbent Assay ◽

Mechanical Transmission ◽

Vegetable Crops ◽

Spot Virus ◽

Seed Crop ◽

Onion Seed

In a survey to determine the presence and distribution of Iris yellow spot virus (IYSV) in greenhouse ornamentals and onion field crops in 14 districts of Serbia as well as on imported ornamental plants, 1,574 samples were collected and analyzed by double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA). IYSV was not detected in nearly 1,200 plant samples collected from 39 genera of ornamentals grown in greenhouses in Serbia or imported from other countries during 2005 to 2007. The virus was detected in samples from an onion seed crop in the Sirig locality (South Bačka District) that showed symptoms resembling those caused by IYSV and in samples without IYSV-like symptoms from an onion bulb crop in the Obrenovac locality (City of Belgrade District). Mechanical transmission of IYSV isolates was difficult, and only the isolate 605-SRB could infect four plant species, but not in all replications. No virus transmission could be demonstrated in 5,000 tested seeds originating from IYSV-infected onion crops. For further confirmation of IYSV, the nucleotide sequence of its nucleocapsid (NC) gene was obtained by reverse transcription–polymerase chain reaction (RT-PCR) in symptomatic onion samples as well as in symptomless leaves of Nicotiana benthamiana. Four previously developed primers were tested to determine their suitability for routine detection of Serbian IYSV isolates. Phylogenetic analysis showed clustering of isolates 605-SRB and 622-SRB from the onion seed crop and isolate 283-SRB from the onion bulb crop into two distant clades. The analysis indicated that Serbian isolates of IYSV do not share a recent common ancestor and that they represent two distinct lineages of IYSV in Serbia. Considering that onion is one of the most important and traditionally grown vegetable crops in Serbia, IYSV represents a potentially devastating pathogen in this country.

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Geographical Distribution and Survival of Iris yellow spot virus in Spiny Sowthistle, Sonchus asper, in Georgia

Plant Disease ◽

10.1094/pdis-09-11-0747-re ◽

2012 ◽

Vol 96 (8) ◽

pp. 1165-1171 ◽

Cited By ~ 10

Author(s):

C. Nischwitz ◽

R. Srinivasan ◽

S. Sundaraj ◽

S. W. Mullis ◽

B. McInnes ◽

...

Keyword(s):

Thrips Tabaci ◽

Iris Yellow Spot Virus ◽

Yellow Spot ◽

Enzyme Linked Immunosorbent Assay ◽

Onion Thrips ◽

Spot Virus ◽

Sonchus Asper ◽

Survival And Reproduction ◽

Polymerase Chain ◽

Weed Survey

Iris yellow spot virus (IYSV) has occurred in Georgia since 2003. IYSV is transmitted by onion thrips, Thrips tabaci. During a weed survey in the Vidalia onion-growing zone (VOZ), spiny sowthistle (Sonchus asper) was identified as a host for IYSV. Spiny sowthistle is widespread in Georgia, and this presented an opportunity to study the natural spread of IYSV and assess its potential role in IYSV epidemiology. From 2007 to 2009, during the spring season, 2,011 sowthistle samples were collected from various counties within and outside the VOZ. The samples were tested for IYSV infection by enzyme-linked immunosorbent assay and confirmed by reverse-transcription polymerase chain reaction and sequencing. IYSV sequences from sowthistle were 98 to 99% identical to onion IYSV sequences from onion originated from Georgia. By the third year, IYSV-infected sowthistle plants were found in 79% of the counties in the VOZ and in 61% of the sampled counties in all directions, except to the east of the VOZ. Furthermore, thrips-mediated transmission assays confirmed that T. tabaci can efficiently transmit IYSV from onion to sowthistle. Sowthistle also supported T. tabaci survival and reproduction. These findings demonstrate that sowthistle plants can serve as an IYSV inoculum source and as a thrips reservoir.

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