2008
DOI: 10.1080/03235400600940855
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Detection of pigeonpea sterility mosaic virus, the causal agent of sterility mosaic disease of pigeonpea in viruliferous mite vector by DAS-ELISA and DIBA

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Cited by 10 publications
(10 citation statements)
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“…Polyclonal antibodies to PPSMV particle preparations are effective in detecting PPSMV in plant tissues by the double antibody sandwich enzyme‐linked immunosorbent assay (DAS‐ELISA) using enzyme‐labelled (alkaline phosphatase) immunogammaglobulin (Kumar et al ., , ). Serological diagnostic methods, such as DAS‐ELISA and dot‐immunobinding assay (DIBA), have been developed to detect the presence of PPSMV from the viruliferous vector using whole mite extract as an antigen (Latha and Doraiswamy, ). Both DAS‐ELISA and DIBA are sensitive for virus detection in vector mites; however, detection is possible only in groups of 10 or more mites.…”
Section: Virus Diagnosticsmentioning
confidence: 97%
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“…Polyclonal antibodies to PPSMV particle preparations are effective in detecting PPSMV in plant tissues by the double antibody sandwich enzyme‐linked immunosorbent assay (DAS‐ELISA) using enzyme‐labelled (alkaline phosphatase) immunogammaglobulin (Kumar et al ., , ). Serological diagnostic methods, such as DAS‐ELISA and dot‐immunobinding assay (DIBA), have been developed to detect the presence of PPSMV from the viruliferous vector using whole mite extract as an antigen (Latha and Doraiswamy, ). Both DAS‐ELISA and DIBA are sensitive for virus detection in vector mites; however, detection is possible only in groups of 10 or more mites.…”
Section: Virus Diagnosticsmentioning
confidence: 97%
“…in tomato and aubergine, A. mangiferae (Sayed) in mango, and Eriophyes cernuus (Massee) in ber (Singh and Raghuraman, ). Several A. cajani populations were collected from various SMD endemic locations in India, Nepal and Myanmar, and were subjected to PCR‐restriction fragment length polymorphism (RFLP) and sequencing for the ITS regions of rDNA (Kumar et al ., ; Latha and Doraiswamy, ). No significant variation was found in either the ITS regions of rDNA or the morphological features of the eriophyid mites.…”
Section: Virus Transmissionmentioning
confidence: 97%
“…Spreading of virus-infected seeds in virus-free areas infested by A. tosichella could easily start a new infection by means of the mite. In contrast, PPSMV is transmitted only by A. cajani on pigeon pea and not by plant sap, seed or dodder (Latha and Doraiswamy, 2008; Maurya et al, 2017) sustaining the management of the virus disease by means of resistant varieties (Pallavi and Ramappa, 2014). The effectiveness of A. tosichella in transmitting viruses to the wheat can be influenced by the mite population composition and origin, and it might be related to the genetic mite lineage (Schiffer et al, 2009; Navia et al, 2013b; McMechan et al, 2014; Skoracka et al, 2018).…”
Section: Eriophyoids As Vectors Of Plant Virusesmentioning
confidence: 99%
“…The effects of the virus infected plants on the biology of the Eriophyidae are poorly known even though a strict co-evolution of the pathosystem may have produced advantages to mites. Aceria tosichella and A. cajani increase their fecundity rate and density, respectively, on WSMV and PPSMV infected and susceptible plant genotypes (Reddy and Nene, 1980; Kulkarni et al, 2002; Jones et al, 2004; Siriwetwiwat, 2006; Latha and Doraiswamy, 2008; Murugan et al, 2011; Skoracka et al, 2018). Field populations of P. fructiphilus were up to 17 times denser on rose rosette disease-symptomatic multiflora rose than on symptomless ones and the virus transmission was more efficient only when the mite was feeding on rapidly growing plant organs, which are more susceptible to the mite and more receptive for virus infection (Epstein and Hill, 1999).…”
Section: Eriophyoids As Vectors Of Plant Virusesmentioning
confidence: 99%
“…The puri ication procedure for minimizing the effects of components by extraction of infected leaves in buffers containing chelating and reducing agents, high concentrations of nonionic detergent, and the precipitation. Puri ication was achieved by quasi-equilibrium zoning centrifugation Sucrose and CsCl gradients [29]. In order to detect the presence of PPSMV from their virulent vector using whole mite extract as an antigen, serological diagnostic techniques such as DAS-ELISA (double antibody sandwich ELISA) and DIBA (dot immunobinding assay) were developed.…”
Section: Etiology and Virus Transmissionmentioning
confidence: 99%