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J Gen Virol 87 (2006), 3233-3250; DOI 10.1099/vir.0.82161-0

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© 2006 Society for General Microbiology

Genome of the most widely used viral biopesticide: Anticarsia gemmatalis multiple nucleopolyhedrovirus

Juliana Velasco de Castro Oliveira1, José Luiz Caldas Wolff2, Alejandra Garcia-Maruniak3, Bergmann Morais Ribeiro4, Maria Elita Batista de Castro5, Marlinda Lobo de Souza5, Flavio Moscardi6, James Edward Maruniak3 and Paolo Marinho de Andrade Zanotto1

1 Laboratório de Evolução Molecular e Bionformática, Departamento de Microbiologia, Instituto de Ciências Biomédicas, Universidade de São Paulo, SP, Brazil
2 Laboratório de Virologia Molecular, Núcleo Integrado de Biotecnologia, Universidade de Mogi das Cruzes, Mogi das Cruzes, SP, Brazil
3 Entomology and Nematology Department, PO Box 110620, University of Florida, Gainesville, FL 32611-0620, USA
4 Departamento de Biologia Celular, Universidade de Brasília, Brasília, DF, Brazil
5 Embrapa Recursos Genéticos e Biotecnologia-Núcleo Temático de Controle Biológico (NTCB), Brasília, DF, Brazil
6 EMBRAPA-CNPSo, Londrina, PR, Brazil

Correspondence
Paolo Marinho de Andrade Zanotto
pzanotto{at}usp.br

The genome of Anticarsia gemmatalis multiple nucleopolyhedrovirus isolate 2D (AgMNPV-2D), which is the most extensively used virus pesticide in the world, was completely sequenced and shown to have 132 239 bp (G+C content 44.5 mol%) and to be capable of encoding 152 non-overlapping open reading frames (ORFs). Three ORFs were unique to AgMNPV-2D, one of which (ag31) had similarity to eukaryotic poly(ADP-ribose) polymerases. The lack of chiA and v-cath may explain some of the success and growth of the AgMNPV biological control programme, as it may explain the high recovery of polyhedra sequestered inside dead larvae in the field, which are collected and used for further application as biological pesticides in soybean fields. The genome organization was similar to that of the Choristoneura fumiferana defective MNPV (CfDefNPV). Most of the variation between the two genomes took place near highly repetitive regions, which were also closely associated with bro-coding regions. The separation of the NPVs into groups I and II was supported by: (i) a phenogram of the complete genomes of 28 baculovirus and Heliothis zea virus 1, (ii) the most parsimonious reconstruction of gene content along the phenograms and (iii) comparisons of genomic features. Moreover, these data also reinforced the notion that group I of the NPVs can be split further into the AgMNPV lineage (AgMNPV, CfDefNPV, Epiphyas postvittana NPV, Orgyia pseudotsugata MNPV and C. fumiferana MNPV), sharing eight defining genes, and the Autographa californica MNPV (AcMNPV) lineage (AcMNPV, Rachiplusia ou NPV and Bombyx mori NPV), sharing nine defining genes.

The GenBank/EMBL/DDBJ accession number for the sequence determined in this work is DQ813662.




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