Comparative experiments reveal challenges in using viral vectors for gene expression modulation in rice, suggesting a need for novel approaches.
Virus‐enabled reverse genetics (VERG) is a powerful tool for transient gene expression modulation in plants, particularly where stable transformation is challenging. However, the efficacy of VERG varies across species. In this study, we tested two commonly used viral vectors, barley stripe mosaic virus (BSMV) and foxtail mosaic virus (FoMV), for their ability to induce virus‐induced gene silencing (VIGS) and virus‐mediated overexpression (VOX) in rice ( Oryza sativa ). While both vectors successfully altered gene expression in wheat ( Triticum aestivum ), they failed to do so in six rice cultivars from different subspecies and subgroups, despite rigorous optimization of inoculation methods and environmental conditions. The BSMV vector carrying a portion of phytoene desaturase ( PDS ) in antisense did not induce the expected photobleaching phenotype, and FoMV‐driven GFP expression was absent in rice. These findings contrast with previous reports of successful VERG in other monocots and suggest that intrinsic mechanisms exist in rice that inhibit or reduce the efficacy of VIGS and VOX with these protocols and vectors. Our results highlight the species‐specific limitations of VERG and underscore the need for alternative viral systems or novel vector designs for functional genomics research in rice. By sharing our unsuccessful attempts, we aim to prevent redundant efforts and encourage further exploration of VERG in Oryza species.
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Turra et al. (2025) studied this question.
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