J Gen Virol Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Originally published as JGV in Press, 10.1099/vir.0.009035-0 on March 4, 2009 J Gen Virol 90 (2009), 1499-1504; DOI 10.1099/vir.0.009035-0

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
vir.0.009035-0v1
90/6/1499    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Google Scholar
Right arrow Articles by Yu, I.-L.
Right arrow Articles by Lung, O.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yu, I.-L.
Right arrow Articles by Lung, O.
Agricola
Right arrow Articles by Yu, I.-L.
Right arrow Articles by Lung, O.

Short Communication

Autographa californica multiple nucleopolyhedrovirus ORF 23 null mutant produces occlusion-derived virions with fewer nucleocapsids

Ian-Ling Yu1,{dagger}, Doug Bray1, Ying-Chu Lin2 and Oliver Lung1,{ddagger}

1 Department of Biological Sciences, University of Lethbridge, Lethbridge, AB T1K 3M4, Canada
2 Faculty of Dentistry, Kaohsiung Medical University, Kaohsiung, Taiwan, ROC

Correspondence
Oliver Lung
oliver.lung{at}inspection.gc.ca

Two envelope fusion protein gene homologues have been identified in the baculovirus Autographa californica multiple nucleopolyhedrovirus (AcMNPV). AcMNPV GP64 protein is fusogenic and essential for propagation and pathogenicity. The F homologue (Ac23) is not essential, is fusion-incompetent in standard assays, but contributes to faster host death. Here, we show that occlusion bodies (OBs) from Ac23null mutants and control viruses do not differ significantly in size and the number of occlusion-derived virions (ODVs) contained; however, Ac23null OBs had a much higher percentage of ODVs with a single nucleocapsid (44.6 %) than the near-isogenic control (11.3 %). Infection of Sf9 cells with Ac23–green fluorescent protein (gfp)-expressing recombinant viruses showed Ac23–gfp fluorescence overlapping perinuclear DAPI staining at later times, a pattern not observed with GP64. These results suggest that F proteins have evolved functions beyond envelope fusion and play a different role from that of GP64 in viruses that contain both proteins.

{dagger}Present address: Canadian Centre for Behavioural Neuroscience, University of Lethbridge, AB T1K 3M4, Canada.

{ddagger}Present address: Lethbridge Laboratory, Canadian Food Inspection Agency, PO Box 640, Lethbridge, AB T1J 3Z4, Canada.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2009 by the Society for General Microbiology.