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Simple and Robust in vivo and in vitro Approach for Studying Virus Assembly
Published on: March 1, 2012
Phosphatidic acid produced by phospholipase D promotes RNA replication of a plant RNA virus
Kiwamu Hyodo1, Takako Taniguchi2, Yuki Manabe3
1Laboratory of Plant Pathology, Graduate School of Agriculture, Kyoto University, Kyoto, Japan.
Abstract:
Eukaryotic positive-strand RNA [(+)RNA] viruses are intracellular obligate parasites replicate using the membrane-bound replicase complexes that contain multiple viral and host components. To replicate, (+)RNA viruses exploit host resources and modify host metabolism and membrane organization. Phospholipase D (PLD) is a phosphatidylcholine- and phosphatidylethanolamine-hydrolyzing enzyme that catalyzes the production of phosphatidic acid (PA), a lipid second messenger that modulates diverse intracellular signaling in various organisms. PA is normally present in small amounts (less than 1% of total phospholipids), but rapidly and transiently accumulates in lipid bilayers in response to different environmental cues such as biotic and abiotic stresses in plants. However, the precise functions of PLD and PA remain unknown. Here, we report the roles of PLD and PA in genomic RNA replication of a plant (+)RNA virus, Red clover necrotic mosaic virus (RCNMV). We found that RCNMV RNA replication complexes formed in Nicotiana benthamiana contained PLDα and PLDβ. Gene-silencing and pharmacological inhibition approaches showed that PLDs and PLDs-derived PA are required for viral RNA replication. Consistent with this, exogenous application of PA enhanced viral RNA replication in plant cells and plant-derived cell-free extracts. We also found that a viral auxiliary replication protein bound to PA in vitro, and that the amount of PA increased in RCNMV-infected plant leaves. Together, our findings suggest that RCNMV hijacks host PA-producing enzymes to replicate.
Insights
Red clover necrotic mosaic virus hijacks host Phospholipase D (PLD) enzymes to produce phosphatidic acid (PA), a lipid essential for viral RNA replication in plants.
Area of Science:
- Plant virology
- Molecular biology
- Biochemistry
Background:
- Positive-strand RNA [(+)RNA] viruses rely on host machinery for replication.
- Phospholipase D (PLD) enzymes produce phosphatidic acid (PA), a lipid messenger with largely unknown functions.
Purpose of the Study:
- Investigate the roles of PLD and PA in Red clover necrotic mosaic virus (RCNMV) RNA replication.
- Determine if RCNMV utilizes host PLD and PA for its life cycle.
Main Methods:
- Gene silencing and pharmacological inhibition of PLD in Nicotiana benthamiana.
- Assessing viral RNA replication levels.
- In vitro binding assays between viral protein and PA.
- Quantifying PA levels in infected plant leaves.
Main Results:
- RCNMV replication complexes contain PLDα and PLDβ.
- PLD activity and PA are necessary for RCNMV RNA replication.
- Exogenous PA application enhances viral replication.
- A viral protein binds PA, and PA levels increase upon RCNMV infection.
Conclusions:
- RCNMV exploits host PLD enzymes to generate PA.
- PA is a critical host factor for RCNMV replication.
- This study reveals a novel mechanism of viral exploitation of host lipid metabolism.
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