How plant virus hides from the host cellular degradation machinery
The main goal of obligatory viral parasites is to create the perfect environment for its multiplication. Therefore, the first step is to avoid degradation by the host cellular degradation. Tomato yellow leaf curl virus (TYLCV) is not an exception. TYLCV is a single stranded DNA begomovirus transmitted to tomato and other crops by the whitefly Bemisia tabaci. The genome of TYLCV encodes only six proteins with multiple functions. In plant cells and in the insect body, viral particles and viral proteins are considered as intruders by the host protection machinery. We have analyzed the capacity of the tomato plant and of the whitefly insect vector to degrade the six TYLCV proteins.
Ultracentrifuge fractionation of tomato and whitefly proteins indicated that the highest proteolytic activity was associated with fractions containing soluble proteins, and was much lesser in large protein aggregates; a significant decrease of TYLCV proteolysis was detected in intermediate-sized aggregates. All the six TYLCV proteins were differently targeted by the cytoplasmic and nuclear degradation machineries (proteases, ubiquitin 26S proteasome, autophagy). Therefore we hypothesized that TYLCV could confront host degradation by sheltering in small/midsized aggregates, where viral proteins are less exposed to proteolysis. Indeed, TYLCV proteins were detected specifically in such intermediate-sized aggregates at the beginning of infection in plants and during an acquisition by the whitefly vector (Fig. 1).
As infection progresses, intermediate-sized, mostly cytoplasmic protein aggregates, are converted to large nuclear inclusion bodies containing infectious virions, which function as viral factories. The appearance of large aggregates is a feature of a successful TYLCV invasion in plants. The TYLCV coat protein (CP) was shown to be prone to protease digestion and 26S proteasome degradation in viral factories. Yet, proteolysis in large aggregates could be required for the homeostasis absolutely necessary during intensive viral replication and assembly of virions. Ubiquitin and 26S subunits were shown to be associated with mammalian virus factories. The presence of the same proteasome elements in TYLCV induced large aggregates in infected tomatoes and viruliferous whiteflies points to their recruitment by virus for the regulation of correct folding, maintenance and required proteolysis of viral proteins.
The maintenance of intermediate-sized aggregates is associated with TYLCV resistance of tomato plants. The capture of viral proteins in intermediate-sized aggregates slows down the formation of new virions until the plant has grown enough to sustain the deleterious effects of the virus. This process is pronounced in resistant tomatoes, but much less effective in susceptible plants, where CP accumulates rapidly in large aggregates, favoring virus replication and pathogenesis (Fig. 2). Hence, we propose that the confrontation between TYLCV and cellular protection mechanisms occurs in intermediate-sized aggregates, especially at the early stages of plant infection. These cellular compounds play a dual and opposite role: sheltering of virus proteins from the degradation machineries in intermediate aggregates, and prevention the development of viral factories by unknown host defense mechanisms.
Whether sheltering in the specific aggregates is a common phenomenon for plant viruses or, at least, for begomoviruses with the extremely long life cycle is the subject of new investigations.
Rena Gorovits and Henryk Czosnek
Institute of Plant Sciences and Genetics in Agriculture,
Robert H. Smith Faculty of Agriculture, Food and Environment,
The Hebrew University of Jerusalem, Israel.
Tomato yellow leaf curl virus confronts host degradation by sheltering in small/midsized protein aggregates.
Gorovits R, Fridman L, Kolot M, Rotem O, Ghanim M, Shriki O, Czosnek H
Virus Res. 2016 Feb 2