Dataset Information

Monitoring Seasonal Distribution of Thrips Vectors of Soybean Vein Necrosis Virus in Alabama Soybeans.

ABSTRACT: Soybean vein necrosis virus (SVNV), a new virus in the genus Orthotospovirus, has been found in all soybean-growing regions in the United States and Ontario, Canada. Soybean thrips, Neohydatothrips variabilis (Beach) (Thysanoptera: Thripidae), tobacco thrips, Frankliniella fusca (Hinds) (Thysanoptera: Thripidae), and eastern flower thrips, Frankliniella tritici (Fitch) (Thysanoptera: Thripidae) are reported vectors of this virus, but there are no reports on their distribution in Alabama. A monitoring study was conducted in 2015 and 2016 to determine thrips species composition and abundance in Alabama soybean agroecosystems. Thrips were monitored weekly by collecting them on yellow sticky traps and soybean plant parts including foliage and reproductive structures. All three reported vectors of SVNV were identified in Alabama, with N. variabilis and F. tritici as the predominant species, while F. fusca was not consistently collected from soybean plants. Four additional thrips species were collected, of which Echinothrips americanus (Morgan) (Thysanoptera: Thripidae) was commonly found on soybean at all three locations. Results presented in this study provide new information about seasonal thrips species abundance in soybean agroecosystems in Alabama, and is an important first step to understanding thrips vector species of epidemiological importance in the Southern United States.

SUBMITTER: Chitturi A

PROVIDER: S-EPMC6294239 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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Monitoring Seasonal Distribution of Thrips Vectors of Soybean Vein Necrosis Virus in Alabama Soybeans.

Chitturi Anitha A Conner Kassie K Sikora Edward J EJ Jacobson Alana L AL

Journal of economic entomology 20181201 6

Soybean vein necrosis virus (SVNV), a new virus in the genus Orthotospovirus, has been found in all soybean-growing regions in the United States and Ontario, Canada. Soybean thrips, Neohydatothrips variabilis (Beach) (Thysanoptera: Thripidae), tobacco thrips, Frankliniella fusca (Hinds) (Thysanoptera: Thripidae), and eastern flower thrips, Frankliniella tritici (Fitch) (Thysanoptera: Thripidae) are reported vectors of this virus, but there are no reports on their distribution in Alabama. A monit ...[more]

PMID: 30124887

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Project description:Soybean vein necrosis virus (SVNV) is a newly discovered species of tospovirus infecting soybean plants that is transmitted by the primary vector, soybean thrips (Neohydatothrips variabilis), and two additional secondary vectors, tobacco thrips (Frankliniella fusca) and eastern flower thrips (F. tritici). This study was undertaken to elucidate the association between virus acquisition [6, 12, 24, and 48 h acquisition access period (AAP)] and transmission efficiency [12, 24, and 48 h inoculation access period (IAP)] in the primary vector, N. variabilis, and to examine the mechanisms of vector competence by analyzing the effect of AAP (6, 12, and 24 h) on virus infection in various tissues. In addition, we examined virus infection in tissues of the two secondary vectors. We found a significant effect of virus acquisition on transmission efficiency, transmission rate post 6 and 48 h AAP was significantly lower than 12 and 24 h AAP. Our analysis did not reveal a correlation between virus transmission rate and virus RNA in corresponding N. variabilis adults. On the contrary, N. variabilis adults harboring higher accumulation of the virus (>104) resulted in lower transmission rates. Analysis of SVNV infection in the tissues revealed the presence of the virus in the foregut, midgut (region 1, 2, and 3), tubular salivary glands and principal salivary glands (PSG) of adults of all three vector species, however, the frequency of infected tissues was highest in N. variabilis followed by F. fusca and F. tritici. The frequency of SVNV infection in individual tissues specifically the salivary glands was lowest after 6 h AAP compared to 12 and 24 h AAP. This finding is in agreement with the transmission assays, where significantly lower virus transmission rate was observed post 6 h AAP. In addition, N. variabilis adults with high PSG infection (12 and 24 h AAP) were likely to have high percentage of foregut and midgut region 2 infection. Overall, results from the transmission assays and immunolabeling experiments suggest that shorter AAP results in reduced virus infection in the various tissues especially PSG, which are important determinants of vector competence in SVNV-thrips interaction.

Project description:Simple Summary Soybean vein necrosis, caused by soybean vein necrosis virus (SVNV) is an important viral disease of soybeans that can be seed borne or insect vectored. This plant viral disease affects seed qualitative parameters, including seed oil content. Increased damage is observed in late planted soybeans. The disease is widespread, and almost all soybean-growing states in USA are affected. Globally, SVNV is reported in Canada, the United States, Egypt and Pakistan. In order to manage the disease, it is important to understand the vector’s biology and the effect of SVNV on life table parameters (survival, longevity, mortality, doubling time, generation, rate of intrinsic increase) of vector soybean thrips, which can help to establish pest management predictive models. We used an age-stage two-sex life table estimation model to define the effect of SVNV on the life parameters of male and female soybean thrips. Overall, we found that SVNV infection increased viruliferous thrips survival, longevity, gross reproduction rate, life expectancy and decreased population doubling time. Overall viruliferous thrips benefit from SVNV infection and transmission due to better survival, longevity and increased fitness. Abstract Soybean vein necrosis orthotospovirus (SVNV: Tospoviridae: Orthotospovirus), the causal agent of soybean vein necrosis disease, is vectored by soybean thrips Neohydatothrips variabilis (Beach, 1896), and to a lesser extent by five other thrips species. There is increasing incidence of soybean vein necrosis (SVN) disease in all soybean growing states in the United States, Canada, Egypt and Pakistan, necessitating a study of the system’s ecology and management. We addressed the effect of SVNV on the life table parameters of the vector. We used an ‘age-stage two-sex’ life table approach, which provided detailed life stage durations of each larval instar and adults (both sexes). Our results showed that the intrinsic rate of increase (r), finite rate of increase (λ) and mortality index (qx) were higher in the infected population, while the net reproduction rate (Ro), cumulative probability of survival (lx) and gross reproduction rate (GRR) were lower in the uninfected population. Overall, in both infected and uninfected populations, the number of eggs producing haploid males via arrhenotoky ranged from 9–12 per female. Male to female ratio was female biased in the infected population. Overall, our study provided evidence that virus infection, by decreasing the population doubling time, could enhance the virus and vector populations in soybeans.

Project description:Soybean vein necrosis virus (SVNV; genus Tospovirus; Family Bunyaviridae) is a negative-sense single-stranded RNA virus that has been detected across the United States and in Ontario, Canada. In 2013, a seed lot of a commercial soybean variety (Glycine max) with a high percentage of discolored, deformed and undersized seed was obtained. A random sample of this seed was planted in a growth room under standard conditions. Germination was greater than 90% and the resulting seedlings looked normal. Four composite samples of six plants each were tested by reverse transcription polymerase chain reaction (RT-PCR) using published primers complimentary to the S genomic segment of SVNV. Two composite leaflet samples retrieved from seedlings yielded amplicons with a size and sequence predictive of SVNV. Additional testing of twelve arbitrarily selected individual plants resulted in the identification of two SVNV positive plants. Experiments were repeated by growing seedlings from the same seed lot in an isolated room inside a thrips-proof cage to further eliminate any external source of infection. Also, increased care was taken to reduce any possible PCR contamination. Three positive plants out of forty-eight were found using these measures. Published and newly designed primers for the L and M RNAs of SVNV were also used to test the extracted RNA and strengthen the diagnosis of viral infection. In experiments, by three scientists, in two different labs all three genomic RNAs of SVNV were amplified in these plant materials. RNA-seq analysis was also conducted using RNA extracted from a composite seedling sample found to be SVNV-positive and a symptomatic sample collected from the field. This analysis revealed both sense and anti-sense reads from all three gene segments in both samples. We have shown that SVNV can be transmitted in seed to seedlings from an infected seed lot at a rate of 6%. To our knowledge this is the first report of seed-transmission of a Tospovirus.

Project description:BACKGROUND: Soybeans grown in the upper Midwestern United States often suffer from iron deficiency chlorosis, which results in yield loss at the end of the season. To better understand the effect of iron availability on soybean yield, we identified genes in two near isogenic lines with changes in expression patterns when plants were grown in iron sufficient and iron deficient conditions. RESULTS: Transcriptional profiles of soybean (Glycine max, L. Merr) near isogenic lines Clark (PI548553, iron efficient) and IsoClark (PI547430, iron inefficient) grown under Fe-sufficient and Fe-limited conditions were analyzed and compared using the Affymetrix GeneChip Soybean Genome Array. There were 835 candidate genes in the Clark (PI548553) genotype and 200 candidate genes in the IsoClark (PI547430) genotype putatively involved in soybean's iron stress response. Of these candidate genes, fifty-eight genes in the Clark genotype were identified with a genetic location within known iron efficiency QTL and 21 in the IsoClark genotype. The arrays also identified 170 single feature polymorphisms (SFPs) specific to either Clark or IsoClark. A sliding window analysis of the microarray data and the 7X genome assembly coupled with an iterative model of the data showed the candidate genes are clustered in the genome. An analysis of 5' untranslated regions in the promoter of candidate genes identified 11 conserved motifs in 248 differentially expressed genes, all from the Clark genotype, representing 129 clusters identified earlier, confirming the cluster analysis results. CONCLUSION: These analyses have identified the first genes with expression patterns that are affected by iron stress and are located within QTL specific to iron deficiency stress. The genetic location and promoter motif analysis results support the hypothesis that the differentially expressed genes are co-regulated. The combined results of all analyses lead us to postulate iron inefficiency in soybean is a result of a mutation in a transcription factor(s), which controls the expression of genes required in inducing an iron stress response.

Dataset Information

Monitoring Seasonal Distribution of Thrips Vectors of Soybean Vein Necrosis Virus in Alabama Soybeans.

Publications

Monitoring Seasonal Distribution of Thrips Vectors of Soybean Vein Necrosis Virus in Alabama Soybeans.

Similar Datasets

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