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Plant viruses are a group of intracellular pathogens that persistently threaten global food security. Significant advances in plant virology have been achieved by Chinese scientists over the last 20 years, including basic research and technologies for preventing and controlling plant viral diseases. Here, we review these milestones and advances, including the identification of new crop‐infecting viruses, dissection of pathogenic mechanisms of multiple viruses, examination of multilayered interactions among viruses, their host plants, and virus‐transmitting arthropod vectors, and in‐depth interrogation of plant‐encoded resistance and susceptibility determinants. Notably, various plant virus‐based vectors have also been successfully developed for gene function studies and target gene expression in plants. We also recommend future plant virology studies in China. [ABSTRACT FROM AUTHOR]

Summary: Phase separation has emerged as a fundamental principle for organizing viral and cellular membraneless organelles. Although these subcellular compartments have been recognized for decades, their biogenesis and mechanisms of regulation are poorly understood.Here, we investigate the formation of membraneless inclusion bodies (IBs) induced during the infection of a plant rhabdovirus, tomato yellow mottle‐associated virus (TYMaV). We generated recombinant TYMaV encoding a fluorescently labeled IB constituent protein and employed live‐cell imaging to characterize the intracellular dynamics and maturation of viral IBs in infected Nicotiana benthamiana cells.We show that TYMaV IBs are phase‐separated biomolecular condensates and that viral nucleoprotein and phosphoprotein are minimally required for IB formation in vivo and in vitro. TYMaV IBs move along the microfilaments, likely through the anchoring of viral phosphoprotein to myosin XIs. Furthermore, pharmacological disruption of microfilaments or inhibition of myosin XI functions suppresses IB motility, resulting in arrested IB growth and inefficient virus replication.Our study establishes phase separation as a process driving the formation of liquid viral factories and emphasizes the role of the cytoskeletal system in regulating the dynamics of condensate maturation. [ABSTRACT FROM AUTHOR]

Soil mercury (Hg) contamination has long been a problem that threatens the environment and organisms. Thus, exploring the migration and transformation of Hg from soil to vegetable is vital. In this study, different Hg solutions were employed in greenhouse experiments. The Hg contents in soil and vegetable samples were determined by inductively coupled plasma – mass spectrometry. The results showed that the Hg accumulation depended on its concentration and form. A greater accumulation of inorganic Hg was observed in the roots (2.2–27.4 mg/kg) than in the aerial parts (0.6–6.0 mg/kg). A similar trend was also found in the methyl mercury (MeHg) and ethyl mercury (EtHg) irrigated groups. The MeHg contents were 0.7–8.0 μg/kg in roots and 0.1–3.7 μg/kg in aerial parts. The EtHg concentrations were 0.5–3.3 μg/kg in roots and 0.3–1.1 μg/kg in aerial parts. The translocation factors of inorganic Hg and organic Hg for both vegetables in most treatments were less than 0.5, which suggested that Hg primarily accumulated in the roots. The biological concentration factors of inorganic Hg were less than 0.4, and those for MeHg and EtHg were between 0.4 and 0.95, which indicated that the vegetables were more likely to absorb organic Hg from the soil. The methylation of inorganic Hg occurred in the roots. The potential hazards of Hg on food safety and human health must be considered in regions with serious Hg pollution. [ABSTRACT FROM AUTHOR]

The clustered regularly interspersed short palindromic repeats (CRISPR)/Cas systems have become the most widely adopted genome editing platform owing to their unprecedented simplicity, efficiency, and versatility. Typically, the genome editing enzyme is expressed in plant cells from an integrated transgene delivered by either Agrobacterium-mediated or biolistic transformation. Recently, plant virus vectors have emerged as promising tools for the in planta delivery of CRISPR/Cas reagent. Here, we provide a protocol for CRISPR/Cas9-mediated genome editing in the model tobacco plant Nicotiana benthamiana using a recombinant negative-stranded RNA rhabdovirus vector. The method is based on infection of N. benthamiana with a Sonchus yellow net virus (SYNV)-based vector that carries the Cas9 and guide RNA expression cassettes to target specific genome loci for mutagenesis. With this method, mutant plants free of foreign DNA can be obtained within 4-5 months., (© 2023. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.)

Productive viral infection entails highly regulated and sequential protein-protein interactions between viral factors and between virus and host factors. Deciphering such interactions is of paramount importance for a better understanding of virus infection cycles and the development of new strategies for virus prevention and control. In this protocol, we describe a split-luciferase complementation (SLC ) assay for the detection of protein-protein interaction in Nicotiana benthamiana leaves following agroinfiltration-mediated transient protein expression. In this assay, the firefly luciferase protein is divided into two halves, each expressed as a fusion to a prey or bait protein, respectively. Interaction of the two candidate proteins brings the two otherwise nonfunctional halves into close proximity to restore the luciferase activity, which catalyzes the substrate D-luciferin to emit luminescence. The SLC assay allows for noninvasive, quantitative measurement of dynamic protein interactions in living cells within their native cellular compartments., (© 2022. Springer Science+Business Media, LLC, part of Springer Nature.)