Cereal chlorotic mottle virus — a rhabdovirus of Gramineae in Australia transmitted by Nesoclutha pallida (Evans)

1979 ◽  
Vol 30 (3) ◽  
pp. 433 ◽  
Author(s):  
RS Greber

An undescribed rhabdovirus was found in eight species of Gramineae at locations extending over 1000 km of the tropical and subtropical Australian east coast. The incidence in maize was usually low but sometimes reached 50% in susceptible hybrids. Cereal chlorotic mottle virus (CCMV) was shown experimentally to infect Avena sativa L., Digitaria ciliaris (Retz.) Koeler, Dinebra retroflexa (Fahl.) Panz., Echinochloa colona (L.) Link., Eleusine coracana (L.) Gaertn., Eleusine indica (L.) Gaertn., Hordeum vulgare L., Triticum aestivum L. and Zea mays L. Symptoms in all hosts began as chlorotic striations, but were often reduced to a fine chlorotic mottle in subsequent growth. After a 3-day acquisition, 50% of individuals of the cicadellid Nesoclutha pallida (Evans) transmitted CCMV in consecutive test feeds with only occasional failures, but some insects then failed to transmit for up to 30 days before death. The time between acquisition and first transmission was 11–24 days and the time for symptom development in the plant was 11–21 days. The virus was acquired and transmitted by both nymphs and adults and by males and females. Transmission continued through the moult to adult. In negative stain the particles were bullet-shaped, 214 by 75 nm, with a net-like surface pattern and core width of 28 nm. There were c. 48 helix cross-striations and 52 surface projections around the full perimeter of bacilliform particles when viewed after brief fixing with glutaraldehyde before staining.

2009 ◽  
Vol 157 (5) ◽  
pp. 325-328 ◽  
Author(s):  
Fabián Giolitti ◽  
Nicolás Bejerman ◽  
Sergio Lenardon

2011 ◽  
Vol 1317 ◽  
Author(s):  
Yuanzheng Wu ◽  
Hetong Yang ◽  
Hyun-Jae Shin

Abstract:Cowpea chlorotic mottle virus (CCMV) has been a model system for virus studies for over 40 years and now is considered to be a perfect candidate as nanoplatform for applications in materials science and medicine. The ability of CCMV to self assemblein vitrointo virus-like particles (VLPs) or capsids makes an ideal reaction vessel for nanomaterial synthesis and entrapment. Here we report expression of codon optimized CCMV coat protein inPichia pastorisand production of self assembled CCMV VLPs by large-scale fermentation. CCMV coat protein gene (573 bp) was synthesized according to codon preference ofP. pastorisand cloned into pPICZA vector. The recombinant plasmid pPICZA-CP was transformed intoP. pastorisGS115 by electroporation. The resulting yeast colonies were screened by PCR and analyzed for protein expression by SDS-PAGE. After large-scale fermentation CCMV coat protein yields reached 4.8 g L−1. The CCMV VLPs were purified by modified PEG precipitation followed by cesium chloride density gradient ultracentrifugation, and then analyzed by size exclusion fast performance liquid chromatography (FPLC), UV spectrometry and transmission electron microscopy. Myoglobin was used as a model protein to be encapsulated in CCMV VLPs. The fluorescence spectroscopy showed that inclusion of myoglobin had occurred. The results indicated the production of CCMV capsids byP. pastorisfermentation now available for utilization in pharmacology or nanotechnology fields.


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