2020
DOI: 10.1016/j.jviromet.2019.113750
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DsRNA-mediated protection against two isolates of Papaya ringspot virus through topical application of dsRNA in papaya

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Cited by 35 publications
(17 citation statements)
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“…We chose the CP coding region for ToMV, and for experiments with PVY. Actually, the cp gene has been the preferred to induce viral resistance by dsRNA topical application 14,15,21,[23][24][25][26] . Pooggin 39 proposed that the viral genomic regions that do not generate a large quantity of siRNA molecules in virus-infected plants are more promising targets for protection than viral siRNA hotspot regions.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…We chose the CP coding region for ToMV, and for experiments with PVY. Actually, the cp gene has been the preferred to induce viral resistance by dsRNA topical application 14,15,21,[23][24][25][26] . Pooggin 39 proposed that the viral genomic regions that do not generate a large quantity of siRNA molecules in virus-infected plants are more promising targets for protection than viral siRNA hotspot regions.…”
Section: Discussionmentioning
confidence: 99%
“…The dsRNA of the cp gene was selected for the further experiments with ToMV in tomato plants as it induced a slightly lower average number of lesions in both hypersensitive hosts ( Supplementary Fig. S1), and because it is commonly used in RNAi-based resistance reports 14,15,21,[23][24][25][26] . Protection against ToMV infection by dsRNA topical application.…”
Section: Inhibition Of Tomv-related Local Lesions Development In Hypementioning
confidence: 99%
“…Specifically, BCMV could be regulated when targeting CP and Nuclear Inclusion b (NIb) genes by application of dsRNA [11]. On the other hand, CP and Helper component-proteinase (HC-pro) genes were selected as target genes to control papaya ringspot virus so that dsRNAs conferred high resistance to plant against viral infection [19].…”
Section: Introductionmentioning
confidence: 99%
“…Several studies reported that foliar applications of dsRNAs induce plant resistance against target viruses ( Tenllado and Diaz‐Ruiz, 2001 ; Carbonell et al., 2008 ; Konakalla et al., 2016 ; Kaldis et al., 2018 ; Worrall et al., 2019 ; Vadlamudi et al., 2020 ). The effects of exogenously applied dsRNAs on conferring resistance against viruses have been reported in various host species, including tomato, tobacco, maize, papaya, cowpea, cucumber, watermelon, and squash against different viruses such as tobacco etch virus (TEV), tobacco mosaic virus (TMV), alfalfa mosaic virus (AMV), pepper mild mottle virus (PMMoV), potyvirus, bean common mosaic virus (BCMV), papaya ringspot virus (PRSV), and zucchini yellow mosaic virus (ZYMV) (reviewed in Dubrovina and Kiselev, 2019 ).…”
Section: The Possible Fate Of Dsrnas Into the Plant Cellmentioning
confidence: 99%
“…From these perspectives, exogenously applied dsRNAs to induce gene silencing have been perceived as another alternative to the genetic transformation that could provide similar benefits, without risking ecological stability and societal acceptance ( Dubrovina and Kiselev, 2019 ; Dalakouras et al., 2020 ). Indeed, several studies have reported that induction of RNAi mechanism by exogenous dsRNAs, short interfering RNAs (siRNAs), or hairpin RNAs (hpRNAs) has the potential to protect plants against plant pathogenic viruses ( Tenllado and Diaz‐Ruiz, 2001 ; Carbonell et al., 2008 ; Yin et al., 2009 ; Gan et al., 2010 ; Konakalla et al., 2016 ; Vadlamudi et al, 2020 ), fungi ( Koch et al., 2016 ; Wang et al., 2016 ; Wang et al., 2017 ), insects ( Baum et al., 2007 ; Li et al., 2013 ; Ghosh et al., 2017 ; Luo et al., 2017 ), mites, and nematodes (reviewed in Dubrovina and Kiselev, 2019 ; Dalakouras et al., 2020 ), which could eventually reduce the ecological footprints caused by chemical pesticides. However, it should be noted that most of the studies on the efficacy of exogenously applied dsRNAs were carried out under set experimental conditions, e.g., using detached leaves, targeting of transgenes, co-inoculation of dsRNAs with target viruses, etc, and have rarely been implemented under open-field conditions where several factors can largely affect their stability, uptake, and overall applicability.…”
Section: Introductionmentioning
confidence: 99%