Molecular characterization of genes in the GP41 region of baculoviruses and phylogenetic analysis based upon GP41 and polyhedrin genes

Citation
Jc. Liu et Je. Maruniak, Molecular characterization of genes in the GP41 region of baculoviruses and phylogenetic analysis based upon GP41 and polyhedrin genes, VIRUS RES, 64(2), 1999, pp. 187-196
Citations number
37
Categorie Soggetti
Microbiology
Journal title
VIRUS RESEARCH
ISSN journal
01681702 → ACNP
Volume
64
Issue
2
Year of publication
1999
Pages
187 - 196
Database
ISI
SICI code
0168-1702(199911)64:2<187:MCOGIT>2.0.ZU;2-V
Abstract
A newly sequenced Anticarsia gemmatalis multiple nucleopolyhedrovirus (AgMN PV) gp41 gene was used to reconstruct the phylogeny for gp41 by comparison with Autographa californica MNPV, Bombyx mori MNPV, Helicoverpa tea single nucleopolyhedrovirus (SNPV), Lymantria dispar MNPV, Orgyia pseudotsugata MN PV and Spodoptera frugiperda MNPV. The 3.5 kb fragment of the AgMNPV gp41 r egion not only contained the gp41 gene but also three other open reading fr ames that had significant homology with the very late factor (vlf-l) of bac uloviruses, AcMNPV ORF78, AcMNPV ORF79, and one partial open reading frame homologous to AcMNPV ORF81. The reconstructed phylogenetic tree of baculovi rus gp41 genes compared with the polyhedrin gene tree produced similar topo logies. Two other phylogenetic trees were reconstructed based on either com bined gp41 and polyhedrin nucleotide sequences (total evidence) or combined evolutionary histories of both genes (strict consensus tree). The former h ad an identical tree topology as the gp41 gene tree alone, and the latter l ost resolution in the branch of AcMNPV and BmMNPV. Mutation rate analysis s howed the gp41 gene had a higher nucleotide substitution rate than the poly hedrin gene, implying that the polyhedrin gene may have a different selecti on constraint than the gp41 gene. Both genes have nonsynonymous/synonymous substitution values close to 0.1, similar to other DNA viruses. (C) 1999 Pu blished by Elsevier Science B.V. All rights reserved.