Research article

Structure and evolution of a proviral locus of Glyptapanteles indiensis bracovirus

Christopher A Desjardins^1,5 , Dawn E Gundersen-Rindal² , Jessica B Hostetler¹ , Luke J Tallon¹ , Roger W Fuester³ , Michael C Schatz^1,4 , Monica J Pedroni² , Douglas W Fadrosh¹ , Brian J Haas¹ , Bradley S Toms¹ , Dan Chen¹ and Vishvanath Nene¹

¹The Institute for Genomic Research, a division of J. Craig Venter Institute, Rockville, Maryland, USA

²USDA-ARS Insect Biocontrol Laboratory, Beltsville, Maryland, USA

³USDA-ARS Beneficial Insect Introductions Research Laboratory, Newark, Delaware, USA

⁴Center for Bioinformatics and Computational Biology, University of Maryland, College Park, Maryland, USA

⁵Department of Biology, University of Rochester, Rochester, New York, USA

author email corresponding author email

BMC Microbiology 2007, 7:61doi:10.1186/1471-2180-7-61

Published:	26 June 2007

Abstract

Background

Bracoviruses (BVs), a group of double-stranded DNA viruses with segmented genomes, are mutualistic endosymbionts of parasitoid wasps. Virus particles are replication deficient and are produced only by female wasps from proviral sequences integrated into the wasp genome. Virus particles are injected along with eggs into caterpillar hosts, where viral gene expression facilitates parasitoid survival and therefore perpetuation of proviral DNA. Here we describe a 223 kbp region of Glyptapanteles indiensis genomic DNA which contains a part of the G. indiensis bracovirus (GiBV) proviral genome.

Results

Eighteen of ~24 GiBV viral segment sequences are encoded by 7 non-overlapping sets of BAC clones, revealing that some proviral segment sequences are separated by long stretches of intervening DNA. Two overlapping BACs, which contain a locus of 8 tandemly arrayed proviral segments flanked on either side by ~35 kbp of non-packaged DNA, were sequenced and annotated. Structural and compositional analyses of this cluster revealed it exhibits a G+C and nucleotide composition distinct from the flanking DNA. By analyzing sequence polymorphisms in the 8 GiBV viral segment sequences, we found evidence for widespread selection acting on both protein-coding and non-coding DNA. Comparative analysis of viral and proviral segment sequences revealed a sequence motif involved in the excision of proviral genome segments which is highly conserved in two other bracoviruses.

Conclusion

Contrary to current concepts of bracovirus proviral genome organization our results demonstrate that some but not all GiBV proviral segment sequences exist in a tandem array. Unexpectedly, non-coding DNA in the 8 proviral genome segments which typically occupies ~70% of BV viral genomes is under selection pressure suggesting it serves some function(s). We hypothesize that selection acting on GiBV proviral sequences maintains the genetic island-like nature of the cluster of proviral genome segments described herein. In contrast to large differences in the predicted gene composition of BV genomes, sequences that appear to mediate processes of viral segment formation, such as proviral segment excision and circularization, appear to be highly conserved, supporting the hypothesis of a single origin for BVs.