Elevated Carbon Dioxide Levels Decreases Cucumber Mosaic Virus Accumulation in Correlation with Greater Accumulation of rgs-CaM, an Inhibitor of a Viral Suppressor of RNAi

Plant viruses cause a range of plant diseases symptoms that are often responsible for significant crop production losses and the severity and spread of the symptoms may be affected by climate change. While the increase in anthropogenic activities has caused a critical problem of increased CO2 levels in the atmosphere, these elevated CO2 levels have been reported to reduce virus disease severity in some plant species. In such instances, it is not clear if the plant defense mechanisms are being enhanced or virus-mediated mechanisms to overcome plant resistance are being defeated. Additionally, a few studies have been attempted in this area to determine if reduced disease is the norm or the exception under enhanced CO2 levels. In the present study, the effects of elevated CO2 levels (750 ppm vs. 390 ppm) on RNAi-mediated resistance of Nicotiana tabacum against the cucumber mosaic virus (CMV), and the activity of viral suppressor of RNAi (VSR) 2b protein of CMV were evaluated. On the one hand, our results showed that elevated CO2 decreased the transcription of dicer-like protein 2 (DCL2), DCL4, and argonaut 1 (AGO1) genes with functions related to RNAi-mediated resistance when infected by CMV, which is contradictory with the decreased CMV copy numbers under elevated CO2. On the other hand, we found that elevated CO2 increased the calcium concentration and expression of the calcium-binding protein rgs-CaM in tobacco plants when infected by CMV, which directly weakened the function of 2b protein, the VSR of CMV, and therefore decreased the infection efficiency of the virus and suppressed the severity of CMV in tobacco plants under elevated CO2. This study provides molecular insights into the ecological implications underlying the development of prevention strategies against plant virus infection in the context of climate change.

Constrained Peptides Mimic a Viral Suppressor of RNA Silencing

The structure-based design of constrained alpha-helical peptides derived from the viral suppressor of RNA silencing TAV2b is described. We observe that the introduction of two inter-side chain crosslinks provides peptides with increased alpha-helicity and protease stability. One of these modified peptides (B3) shows high affinity for different double-stranded RNA structures including a palindromic siRNA as well as microRNA-21 and its precursor pre-miR-21. Notably, B3 binding to pre-miR-21 inhibits Dicer processing in a biochemical assay. As a further characteristic this peptide also exhibits cellular entry. <br>

Constrained Peptides Mimic a Viral Suppressor of RNA Silencing

The structure-based design of constrained alpha-helical peptides derived from the viral suppressor of RNA silencing TAV2b is described. We observe that the introduction of two inter-side chain crosslinks provides peptides with increased alpha-helicity and protease stability. One of these modified peptides (B3) shows high affinity for different double-stranded RNA structures including a palindromic siRNA as well as microRNA-21 and its precursor pre-miR-21. Notably, B3 binding to pre-miR-21 inhibits Dicer processing in a biochemical assay. As a further characteristic this peptide also exhibits cellular entry. <br>

Investigation of the Effects of P1 on Hc-Pro-Mediated Gene Silencing Suppression Through Genetics and Omics Approaches

Background: Viral suppressor negatively controls posttranscriptional gene silencing (PTGS) byinhibiting microRNA (miRNA) and short-interfering RNA (siRNA)regulation in plants. The first identified viral suppressor-P1/HC-Pro is afusion protein. Upon infecting plants, theP1 protein itself gets released from HC-Pro bythe self-cleaving activity of P1. P1 has an unknown function in enhancing HC-Pro-mediated PTGS suppression.We performed proteomics to identifyP1-interacting proteins and observedwhole gene correlationsin P1/HC-Pro-mediated PTGS suppression through transcriptomic studied comparative networks.Results: First, we demonstrated that P1 enhances HC-Pro function and that the mechanism might workthrough the P1 binding to VERNALIZATION INDEPENDENCE 3/ SUPERKILLER8 (VIP3/SKI8),a subunit of the exosome, to interferewith the 5'-fragment of the PTGS-cleaved RNA degradation product.Second,specifically the AGO1 wasposttranslationaldegraded in transgenic Arabidopsis expressing P1/HC-Pro of turnip mosaic virus (TuMV) (P1/HCTu plant).Third, transcriptomic comparative networkshighlighted critical genes inPTGS, including miRNA targets,calcium signaling, hormone (JA, ET, and ABA) signaling, and defense response.Conclusion: Through thesetransgenic and omics approaches, we revealed an overall perspective and new findings in our understandingof the mechanism of P1/HC-Pro-mediated PTGS suppression. Many of the criticalgenes that weresignificantlyimpacted in the omics profiles will be further investigated by CRISPR-knockoutor gain-of-function to understand PTGS in plant better.