scholarly journals Evaluation of Soybean for Resistance to Neohyadatothrips variabilis (Thysanoptera: Thripidae) Noninfected and Infected With Soybean Vein Necrosis Virus

2019 ◽  
Vol 113 (2) ◽  
pp. 949-955 ◽  
Author(s):  
D Lagos-Kutz ◽  
M L Pawlowski ◽  
J Haudenshield ◽  
J Han ◽  
L L Domier ◽  
...  

Abstract Soybean vein necrosis virus (SVNV) was first identified in Arkansas and Tennessee in 2008 and is now known to be widespread in the United States and Canada. Multiple species of thrips transmit this and other tospoviruses with Neohydatothrips variabilis (Beach) (soybean thrips) cited as the most efficient vector for SVNV. In this study, 18 soybean, Glycine max (L.) Merr., genotypes were evaluated in four experiments by infesting plants with noninfected and SVNV-infected thrips using choice and no-choice assays. In both choice experiments with noninfected and SVNV-infected thrips, the lowest number of immature soybean thrips occurred on plant introductions (PIs) 229358 and 604464 while cultivars Williams 82 and Williamsfield Illini 3590N supported higher counts of mature thrips. The counts between the two assays (noninfected and SVNV-infected thrips) were positively correlated. In both no-choice experiments with noninfected and SVNV-infected thrips, counts of thrips did not differ by soybean genotypes. Further studies are needed to characterize the inheritance and mechanisms involved in the resistance found in the choice assay.

Plant Disease ◽  
2013 ◽  
Vol 97 (12) ◽  
pp. 1664-1664 ◽  
Author(s):  
A. Ali ◽  
O. A. Abdalla

Soybean vein necrosis virus (SVNV) causes a new emerging disease of soybean that has been recorded in more than 10 states (1,2,3,4) of the United States, but so far no information is available about its presence in soybean crops of Oklahoma. Surveys of commercial soybean fields were conducted for soybean viruses during summer of 2012. A total of 327 samples were randomly collected from soybean fields in 11 counties. Symptoms typical of SVNV infections including leaf chlorosis and leaf-vein necrosis were observed on some soybean plants in the field (4). All soybean leaf samples were tested against SVNV polyclonal antisera obtained from AC Diagnostics, Inc. (Fayetteville, AR) by dot-immunobinding assay (DIBA) (1). Fifty-three samples reacted positively with SVNV antisera. Total RNA was extracted from three DIBA-positive samples collected from soybean plants in Choctaw County and tested by reverse transcription (RT)-PCR using SVNV-specific primers (forward primer 5′-ATGTTCTCTCTATAATAGCCA and reverse primer 5′-ACCCATAACAATTGATCAAGA-3′) that were designed from the available sequence in the GenBank (Accession No. GU722317.1) to amplify a fragment from RNA1. A band of the expected size of 344 bp was observed on a 1% agarose gel in all three samples. The PCR products were purified using QIAquick PCR Purification Kit (QIAGEN, Valencia, CA), cloned (pGEM-T Easy Vector, Promega, Madison, WI) and sequenced in both directions. The consensus sequence of the 344-bp fragment was 99% identical with the corresponding region of RNA 1 of SVNV isolate ‘Milan_TN’ (Accession No. GU722317.1). These results confirmed the presence of SVNV in soybean fields, which are mostly located in Criage, Choctaw, Hughes, LeFlore, Mayes, Muskogee, McCurtain, Okmulgee, Ottawa, Rogers, and Sequoyah counties of Oklahoma. None of the samples collected from north central or western parts of the state were positive against SVNV. To our knowledge, this is the first report of SVNV in soybean crops in Oklahoma. Soybean is one of the major oil seed crops cultivated on approximately 200,000 hectares annually in Oklahoma and the presence of SVNV could pose a potential threat to the production of soybean in the future. References: (1) J. L. Jacobs and M. I. Chilvers. Plant Dis. 97:1387, 2013. (2) J. Han et al. Plant Dis. 97:693, 2013. (3) D. L. Smith et al. Plant Dis. 97:693, 2013. (4) J. Zhou et al. Virus Genes 43:289, 2011.


2018 ◽  
Vol 19 (2) ◽  
pp. 176-181 ◽  
Author(s):  
Melissa D. Irizarry ◽  
Manjula G. Elmore ◽  
Jean C. Batzer ◽  
Steven A. Whitham ◽  
Daren S. Mueller

Soybean vein necrosis virus (SVNV), a tospovirus and one of the most widespread soybean viruses in North America, is primarily transmitted by soybean thrips (Neohydatothrips variabilis). Although soybean is not considered the primary plant host for SVNV, there is a dearth of knowledge about alternative host plants for SVNV. We therefore investigated whether commonly present specialty and cover crops in Iowa can serve as alternative hosts for SVNV. Seventeen cover crops and seven specialty crops were tested using mechanical and thrips inoculations. Clear symptoms of SVNV and systemic infection in buckwheat and clear local infection with possible systemic infection on melon were shown. Additionally, we compared soybean thrips feeding on 18 cover crops and determined that they preferred alfalfa, buckwheat, crimson clover, and red clover. Our results suggested that alternative host crops may harbor SVNV and be a possible source of inoculum for soybean.


2013 ◽  
Vol 103 (9) ◽  
pp. 966-971 ◽  
Author(s):  
Jing Zhou ◽  
Ioannis E. Tzanetakis

Soybean vein necrosis-associated virus has been linked to an emerging soybean disease in the United States and Canada. Virus distribution and population structure in major growing areas were evaluated. Data were employed to design and develop sensitive detection protocols, able to detect all virus isolates available in databases. The host range for the virus was assessed and several species were found to sustain virus replication, including ivyleaf morning glory, a common weed species in soybean-growing areas in the United States. Koch's postulates were fulfilled using soybean thrips and transmission efficiency was determined. This article provides significant insight into the biology of the most widespread soybean virus in the United States.


Plant Disease ◽  
2013 ◽  
Vol 97 (10) ◽  
pp. 1387-1387 ◽  
Author(s):  
J. L. Jacobs ◽  
M. I. Chilvers

Soybean vein necrosis virus (SVNV) is associated with an emerging disease in soybean producing regions of the United States. Soybean leaves with necrotic vein symptoms were initially noted in 2008 or 2009 in fields across Arkansas, Kansas, Missouri, Illinois, Mississippi, Tennessee, and Kentucky and SVNV was determined to be the causal agent (2). In 2012, widespread reports of SVNV were made across most soybean (Glycine max) producing states including the recent confirmation of SVNV in Iowa and Wisconsin (1). Foliar symptoms similar to those reported for SVNV were observed at approximately 1 to 10% incidence in soybean fields across Michigan in late August and September of 2012, including fields located in Cass, Ingham, Midland, Saginaw, and Van Buren counties. Symptoms included chlorosis and necrosis which initiated on the veins with subsequent spread across the leaf. An initial sample collected from the East Lansing Agricultural Research Station was confirmed to have SVNV with a polyclonal antibody using double antibody sandwich (DAS)-ELISA at AC Diagnostics, Inc. (Fayetteville, AR) and with reverse transcription PCR by Ioannis Tzanetakis, University of Arkansas, Fayetteville. Additional samples from five fields were subsequently collected from Cass, Ingham, and Van Buren counties. Duplicate leaf tissue samples were tested with DAS-ELISA using the SVNV test kit (AC Diagnostics). All symptomatic leaf samples exhibited a strong positive reaction based on the optical density reading at 405 nm. Absorbance reading that exceeded the healthy soybean tissue by a standard deviation of +3× were considered positive. Total RNA was also extracted from each sample using the RNeasy Plant Mini Kit (Qiagen, Germantown, MD). Complementary DNA (cDNA) was generated using virus-specific LdetR and SdetR primers (2) with the High Capacity RT cDNA kit (Life Technologies; Carlsbad, CA). The cDNA was used as template for PCR with the SVNV-specific primers that amplify regions of the L (LdetF/LdetR) and the S (SdetF/SdetR) RNAs (1). Amplification products of the expected 297 and 861 bp size, respectively, were detected in all symptomatic samples while no amplification products were generated from healthy soybean plant tissues grown under greenhouse conditions. Significantly, this is the first documentation and confirmation of the widespread prevalence of SVNV across the state of Michigan in 2012. References: (1) D. L. Smith et al. Plant Dis. http://dx.doi.org/10.1094/PDIS-11-12-1096-PDN . (2) J. Zhou et al. Virus Genes 43:289, 2011.


Plant Disease ◽  
2003 ◽  
Vol 87 (2) ◽  
pp. 154-158 ◽  
Author(s):  
T. D. Vuong ◽  
G. L. Hartman

Sclerotinia stem rot of soybean is one of the major soybean diseases in the north central region of the United States. One disease management option is to plant cultivars that have resistance. Some sources of partial resistance have been identified, but information pertaining to the nature of resistance is limited. The objective of this study was to determine if the expression of resistance is dictated by shoots of resistant plants and if this can be altered by using resistant and susceptible soybean genotypes grafted in different shoot and rootstock combinations of self-, single-, or double-shoot grafts. After successful grafts were made, several experiments were conducted using different inoculation techniques and soybean genotypes. In one experiment, cotyledons were inoculated with a plug of fungal mycelium, plants were incubated in a mist chamber for 23 h, and plant survival was recorded over time. Based on seven grafting combinations of cross- and self-grafted plants using two soybean cultivars, grafts with NKS19-90 (partially resistant) as shoots had greater (P ≤ 0.05) plant survival at 3, 4, and 5 days after inoculation than the other graft combinations. In another experiment, a total of 17 graft combinations were generated using resistant plant introductions and two susceptible cultivars. Resistant self-grafts of the plant introductions had greater (P ≤ 0.05) plant survival (mean = 75%) than self-grafts of the susceptible cultivars (mean = 15%) at 5 days after inoculation. Inter-genotypic grafts with resistant shoots had greater (P ≤ 0.05) plant survival (mean = 65%) than those in reciprocal combinations (mean = 8%) 5 days after inoculation. A cut stem inoculation method was used to test graft combinations of one resistant and two susceptible cultivars. Grafts with susceptible shoots of cvs. Williams 82 and Asgrow 2242 had greater (P < 0.05) lesion lengths (mean = 13.2 cm) than shoots of NKS19-90 (mean = 9.2 cm) regardless of the rootstock 15 days after inoculation. In a double-graft experiment, shoots of both NKS19-90 and Williams 82 were grafted to either NKS19-90 or Williams 82 rootstocks. Regardless of the rootstock, the shoots of Williams 82 died while shoots of NKS19-90 survived. For all the experiments, resistance was greater when the grafted shoot came from a resistant source on a susceptible rootstock compared with the reciprocal combination regardless of the type of grafting technique or inoculation method.


Viruses ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 1376
Author(s):  
Thanuja Thekke-Veetil ◽  
Doris Lagos-Kutz ◽  
Nancy K. McCoppin ◽  
Glen L. Hartman ◽  
Hye-Kyoung Ju ◽  
...  

Soybean thrips (Neohydatothrips variabilis) are one of the most efficient vectors of soybean vein necrosis virus, which can cause severe necrotic symptoms in sensitive soybean plants. To determine which other viruses are associated with soybean thrips, the metatranscriptome of soybean thrips, collected by the Midwest Suction Trap Network during 2018, was analyzed. Contigs assembled from the data revealed a remarkable diversity of virus-like sequences. Of the 181 virus-like sequences identified, 155 were novel and associated primarily with taxa of arthropod-infecting viruses, but sequences similar to plant and fungus-infecting viruses were also identified. The novel viruses were predicted to have positive-sense RNA, negative-stranded RNA, double-stranded RNA, and single-stranded DNA genomes. The assembled sequences included 100 contigs that represented at least 95% coverage of a virus genome or genome segment. Sequences represented 12 previously described arthropod viruses including eight viruses reported from Hubei Province in China, and 12 plant virus sequences of which six have been previously described. The presence of diverse populations of plant viruses within soybean thrips suggests they feed on and acquire viruses from multiple host plant species that could be transmitted to soybean. Assessment of the virome of soybean thrips provides, for the first time, information on the diversity of viruses present in thrips.


Plant Disease ◽  
2018 ◽  
Vol 102 (8) ◽  
pp. 1674-1674 ◽  
Author(s):  
J. Zhou ◽  
N. Aboughanem-Sabanadzovic ◽  
S. Sabanadzovic ◽  
I. E. Tzanetakis

2018 ◽  
Vol 19 (1) ◽  
pp. 76-81 ◽  
Author(s):  
Edward J. Sikora ◽  
Kassie N. Conner ◽  
Alana L. Jacobson

Soybean vein necrosis virus (SVNV) was first reported in the United States during 2008 and has since rapidly spread to all major soybean-producing regions of North America. In 2013, a 4-year study was initiated to determine the distribution and incidence of the virus in Alabama soybean fields and potential weed hosts in the state. The weed host survey focused on populations of morning glory growing adjacent to maturing soybeans fields, along with additional commonly occurring weed species found in Alabama. SVNV was detected throughout Alabama (27 of 28 counties tested) and was most common in the northern region of the state. The average incidence of SVNV in fields in northern Alabama increased from 31.8% in 2013 to 82.6% in 2016. Average incidence of the virus in central Alabama soybean fields ranged from 5.1 to 14.8%, and southern Alabama fields ranged from 0 to 8.8% over the 3-year period. Only one population of morning glory tested positive for SVNV during the 3-year survey of this potential weed host. None of the 15 additional weed species screened tested positive for SVNV. This study has demonstrated that SVNV is found in Alabama soybean fields throughout the state and that soybeans grown in northern Alabama are at greater risk for infection.


Plant Disease ◽  
2012 ◽  
Vol 96 (1) ◽  
pp. 75-81 ◽  
Author(s):  
M. Twizeyimana ◽  
G. L. Hartman

The introduction of Phakopsora pachyrhizi, the cause of soybean rust, into the United States is a classic case of a pathogen introduction that became established in a new geographical region overwintering on a perennial host (kudzu, Pueraria lobata). The objective of our study was to classify the pathogenic variation of P. pachyrhizi isolates collected in the United States, and to determine the spatial and temporal associations. In total, 72 isolates of P. pachyrhizi collected from infected kudzu and soybean leaves in the United States were purified, then established and increased on detached soybean leaves. These isolates were tested for virulence and aggressiveness on a differential set of soybean genotypes that included six genotypes with known resistance genes (Rpp), one resistant genotype without any known characterized resistance gene, and a susceptible genotype. Three pathotypes were identified among the 72 U.S. P. pachyrhizi isolates based on the virulence of these isolates on the genotypes in the differential set. Six aggressiveness groups were established based on sporulating-uredinia production recorded for each isolate on each soybean genotype. All three pathotypes and all six aggressiveness groups were found in isolates collected from the southern region and from both hosts (kudzu or soybean) in 2008. Shannon's index based on the number of pathotypes indicated that isolates from the South region were more diverse (H = 0.83) compared with the isolates collected in other regions. This study establishes a baseline of pathogenic variation of P. pachyrhizi in the United States that can be further compared with variation reported in other regions of the world and in future studies that monitor P. pachyrhizi virulence in association to deployment of rust resistance genes.


Plant Disease ◽  
2009 ◽  
Vol 93 (8) ◽  
pp. 797-803 ◽  
Author(s):  
Renuka N. Attanayake ◽  
Dean A. Glawe ◽  
Frank M. Dugan ◽  
Weidong Chen

The taxonomy of the powdery mildew fungus infecting lentil in the Pacific Northwest (PNW) of the United States was investigated on the basis of morphology and rDNA internal transcribed spacer (ITS) sequences. Anamorphic characters were in close agreement with descriptions of Erysiphe trifolii. However, teleomorphs formed chasmothecial appendages with highly branched apices, whereas E. trifolii has been described as producing flexuous or sometimes loosely branched appendages. Branched appendages have been described in Erysiphe diffusa, a fungus reported from species of Lens, Glycine, and Sophora, raising the possibility that the PNW fungus could be E. diffusa. Examination of morphological characters of an authentic specimen of E. trifolii from Austria determined that it included chasmothecial appendages resembling those seen in PNW specimens. Furthermore, ITS sequences from five powdery mildew samples collected from lentils in PNW greenhouses and fields from 2006 to 2008 were identical to one another, and exhibited higher similarity to sequences of E. trifolii (99%) than to those of any other Erysiphe spp. available in GenBank. Parsimony analysis grouped the lentil powdery mildew into a clade with Erysiphe baeumleri, E. trifolii, and E. trifolii–like Oidium sp., but indicated a more distant relationship to E. diffusa. In greenhouse inoculation studies, the lentil powdery mildew fungus did not infect soybean genotypes known to be susceptible to E. diffusa. The pathogenicity of E. trifolii on lentil was confirmed using modified Koch's postulates. This is the first report of E. trifolii infecting lentil. E. diffusa and E. trifolii have different host ranges, so the discovery of E. trifolii on lentil has implications both for determining species of powdery mildews on cool-season grain legumes, and in disease management.


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