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dc.contributorTelangre, Rameshwaren_US
dc.contributorGhosh, Rajuen_US
dc.contributorTarafdar, Avijiten_US
dc.creatorMamta, Sharmaen_US
dc.date2015-05-25en_US
dc.date.accessioned2017-08-14T11:37:52Z
dc.date.available2017-08-14T11:37:52Z
dc.identifierhttps://mel.cgiar.org/dspace/limiteden_US
dc.identifier.citationSharma Mamta, Rameshwar Telangre, Raju Ghosh, Avijit Tarafdar. (25/5/2015). An efficient method for zoospore production, infection and real-time quantification of Phytophthora cajani causing Phytophthora blight disease in pigeonpea under elevated atmospheric CO2. BMC Plant biology, 15.en_US
dc.identifier.urihttps://hdl.handle.net/20.500.11766/7365
dc.description.abstractPhytophthora blight caused by Phytophthora cajani is an emerging disease of pigeonpea (Cajanus cajan L.) affecting the crop irrespective of cropping system, cultivar grown and soil types. Current detection and identification methods for Phytophthora species rely primarily on cultural and morphological characteristics, the assessment of which is time-consuming and not always suitable. Sensitive and reliable methods for isolation, identification, zoospore production and estimating infection severity are therefore desirable in case of Phytophthora blight of pigeonpea. RESULTS: In this study, protocols for isolation and identification of Phytophthora blight of pigeonpea were standardized. Also the method for zoospore production and in planta infection of P. cajani was developed. Quantification of fungal colonization by P. cajani using real-time PCR was further standardized. Phytophthora species infecting pigeonpea was identified based on mycological characters such as growth pattern, mycelium structure and sporangial morphology of the isolates and confirmed through molecular characterization (sequence deposited in GenBank). For Phytophthora disease development, zoospore suspension of 1 × 10(5) zoospores per ml was found optimum. Phytophthora specific real-time PCR assay was developed using specific primers based on internal transcribed spacer (ITS) 1 and 2. Use of real-time PCR allowed the quantitative estimation of fungal biomass in plant tissues. Detection sensitivities were within the range of 0.001 pg fungal DNA. A study to see the effect of elevated CO₂ on Phytophthora blight incidence was also conducted which indicated no significant difference in disease incidence, but incubation period delayed under elevated CO₂ as compared to ambient level. CONCLUSION: The zoospore infection method for Phytophthora blight of pigeonpea will facilitate the small and large scale inoculation experiments and thus devise a platform for rapid and reliable screening against Phytophthora blight disease of pigeonpea. qPCR allowed a reliable detection and quantification of P. cajani in samples with low pathogen densities. This can be useful in early warning systems prior to potential devastating outbreak of the disease.en_US
dc.formatPDFen_US
dc.languageenen_US
dc.publisherBioMed Centralen_US
dc.rightsCC-BY-NC-4.0en_US
dc.sourceBMC Plant biology;15,(2015)en_US
dc.subjectpests and diseaseen_US
dc.subjectPigeonpeaen_US
dc.titleAn efficient method for zoospore production, infection and real-time quantification of Phytophthora cajani causing Phytophthora blight disease in pigeonpea under elevated atmospheric CO2en_US
dc.typeJournal Articleen_US
cg.creator.idMamta, Sharma: 0000-0001-5745-4693en_US
cg.creator.ID-typeORCIDen_US
cg.subject.agrovocplant breedingen_US
cg.contributor.centerInternational Crops Research Institute for the Semi-Arid Tropics - ICRISATen_US
cg.contributor.crpCGIAR Research Program on Grain Legumes - GLen_US
cg.contributor.funderNot Applicableen_US
cg.date.embargo-end-date2030-12-31en_US
cg.coverage.regionGlobalen_US
cg.contactmamta.sharma@CGIAR.ORGen_US
cg.identifier.doihttps://dx.doi.org/10.1186/s12870-015-0470-0en_US
dc.identifier.statusLimited accessen_US
mel.impact-factor3.631en_US


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