Genomic Sequence of Spodoptera frugiperda Ascovirus 1a , an Enveloped, Double-Stranded DNA Insect Virus That Manipulates Apoptosis for Viral Reproduction

Author:

Bideshi Dennis K.1,Demattei Marie-Véronique2,Rouleux-Bonnin Florence2,Stasiak Karine2,Tan Yeping1,Bigot Sylvie2,Bigot Yves2,Federici Brian A.13

Affiliation:

1. Department of Entomology, University of California, Riverside, California 92521

2. Unit of Eukaryotic Parasite Genetics, FRE CNRS 2969, University François Rabelais of Tours, Tours, France

3. Interdepartmental Graduate Programs in Genetics, Microbiology, and Cell, Molecular, and Developmental Biology, University of California, Riverside, California 92521

Abstract

ABSTRACT Ascoviruses (family Ascoviridae ) are double-stranded DNA viruses with circular genomes that attack lepidopterans, where they produce large, enveloped virions, 150 by 400 nm, and cause a chronic, fatal disease with a cytopathology resembling that of apoptosis. After infection, host cell DNA is degraded, the nucleus fragments, and the cell then cleaves into large virion-containing vesicles. These vesicles and virions circulate in the hemolymph, where they are acquired by parasitic wasps during oviposition and subsequently transmitted to new hosts. To develop a better understanding of ascovirus biology, we sequenced the genome of the type species Spodoptera frugiperda ascovirus 1a (SfAV-1a). The genome consisted of 156,922 bp, with a G+C ratio of 49.2%, and contained 123 putative open reading frames coding for a variety of enzymes and virion structural proteins, of which tentative functions were assigned to 44. Among the most interesting enzymes, due to their potential role in apoptosis and viral vesicle formation, were a caspase, a cathepsin B, several kinases, E3 ubiquitin ligases, and especially several enzymes involved in lipid metabolism, including a fatty acid elongase, a sphingomyelinase, a phosphate acyltransferase, and a patatin-like phospholipase. Comparison of SfAV-1a proteins with those of other viruses showed that 10% were orthologs of Chilo iridescent virus proteins, the highest correspondence with any virus, providing further evidence that ascoviruses evolved from a lepidopteran iridovirus. The SfAV-1a genome sequence will facilitate the determination of how ascoviruses manipulate apoptosis to generate the novel virion-containing vesicles characteristic of these viruses and enable study of their origin and evolution.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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