2018
DOI: 10.1016/j.pmpp.2018.05.010
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Characterization of Cucumber mosaic virus infecting snake gourd and bottle gourd in India

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Cited by 14 publications
(11 citation statements)
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“…For tospovirus, the reaction mixture contains total RNA, random primer and nuclease free water up to 12.5 µl were incubated at 65 °C for 5 min followed by 5× reaction buffer, 10 mM dNTP mix, RNase inhibitor and reverse transcriptase were added and incubated for 1 h at 42 °C 47 . The presence of CMV was confirmed through RT-PCR with CMV coat protein gene specific primer (RsCMV-F and RsCMV-R) with a cyclic condition of 94 °C for 2 min followed by 94 °C for 30 s of denaturation, 59 °C for 30 s of annealing, 72 °C for 60 s with final extension of 72 °C for 10 min 48 . The tospovirus was confirmed through RT-PCR using tospovirus universal primer (gL3637 and gL4435C) corresponding to L segment (RdRp) with the cycling condition of 94 °C for 5 min followed by 35 cycles of 94 °C for 30 s, 56 °C for 1 min and 72 °C for 1 min with 72 °C for 10 min of final extension 44 , 49 .…”
Section: Methodsmentioning
confidence: 99%
“…For tospovirus, the reaction mixture contains total RNA, random primer and nuclease free water up to 12.5 µl were incubated at 65 °C for 5 min followed by 5× reaction buffer, 10 mM dNTP mix, RNase inhibitor and reverse transcriptase were added and incubated for 1 h at 42 °C 47 . The presence of CMV was confirmed through RT-PCR with CMV coat protein gene specific primer (RsCMV-F and RsCMV-R) with a cyclic condition of 94 °C for 2 min followed by 94 °C for 30 s of denaturation, 59 °C for 30 s of annealing, 72 °C for 60 s with final extension of 72 °C for 10 min 48 . The tospovirus was confirmed through RT-PCR using tospovirus universal primer (gL3637 and gL4435C) corresponding to L segment (RdRp) with the cycling condition of 94 °C for 5 min followed by 35 cycles of 94 °C for 30 s, 56 °C for 1 min and 72 °C for 1 min with 72 °C for 10 min of final extension 44 , 49 .…”
Section: Methodsmentioning
confidence: 99%
“…Similarly Nagendran et al (2018) reported the presence of CMV in the virus infected samples of cucurbitaceous crops viz., bottle gourd and snake gourd in areas of Tamil Nadu and found that the virus isolates were found in close resemblance with subgroup of IB. Pratap et al (2008) categorized the subgroup of CMV strains based on the coat protein sequence analysis infecting tomato in India.…”
Section: Characteristic Symptoms Ofmentioning
confidence: 96%
“…Subgroup I was divided into IA and IB based on phylogenetic analysis of coat protein gene. CMV subgroups IA and II are present worldwide, while subgroup IB is originated from Asia (Nagendran et al, 2018). The molecular analysis and determination of the phy logenetic status of viruses is one of the most important steps towards the elucidation of the virus epidemiology and is necessary for the control of plant viral diseases, by introducing appropriate varieties for cultivation by farm ers.…”
Section: Introductionmentioning
confidence: 99%
“…CMV has been categorized into subgroup I and II based on serology, host range and peptide mapping. Further, subgroup I is divided into subgroup IA and IB based on 5′ non-coding region of RNA3 and sequence similarity (Roossinck 2001;Revathy and Bhat 2017;Nagendran et al 2018). Subgroup IA and II have worldwide distribution whereas subgroup IB found in Asian countries and comparatively, subgroup I strains are more virulent than subgroup II strains.…”
Section: Introductionmentioning
confidence: 99%