Difference between revisions of "Viruses (2017) 9 (6 - 132)"

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|Author Page=Bergmann Morais Ribeiro
 
|Author Page=Bergmann Morais Ribeiro
 
|Publication date=2017
 
|Publication date=2017
|dc:title=Real-time expression analysis of selected ''[[Anticarsia gemmatalis multiple NPV (entomopathogen)|Anticarsia gemmatalis multiple nucleopolyhedrovirus]]'' gene promoters during infection of permissive, semipermissive and nonpermissive cell lines
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|dc:title=Real-time expression analysis of selected ''[[Alphabaculovirus angemmatalis (entomopathogen)|Anticarsia gemmatalis multiple nucleopolyhedrovirus]]'' gene promoters during infection of permissive, semipermissive and nonpermissive cell lines
 
|Publication journal=Viruses
 
|Publication journal=Viruses
 
|prism:volume=9 (6 - 132)
 
|prism:volume=9 (6 - 132)
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{{Beneficial record
 
{{Beneficial record
|Beneficial=Anticarsia gemmatalis multiple NPV (entomopathogen)
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|Beneficial=Alphabaculovirus angemmatalis (entomopathogen)
 
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}}

Latest revision as of 16:17, 21 August 2023

Fabricio da Silva Morgado, Daniel Mendes Pereira Ardisson-Araújo and Bergmann Morais Ribeiro (2017)
Real-time expression analysis of selected Anticarsia gemmatalis multiple nucleopolyhedrovirus gene promoters during infection of permissive, semipermissive and nonpermissive cell lines
Viruses 9 (6 - 132)
Abstract: Baculovirus infection follows a transcriptionally controlled sequence of gene expression that occurs by activation of different viral gene promoter sequences during infection. This sequence of promoter activation may be disrupted by cellular defenses against viral infection, which might interfere with viral progeny formation. In this work, the activity of the ie1, gp64, lef-1, vp39, p6.9 and polh promoters of the Anticarsia gemmatalis multiple nucleopolyhedrovirus was assessed during infection of permissive, semipermissive and nonpermissive cell lines by a novel methodology that detects reporter protein luminescence in real-time. This technique allowed us to characterize in rich detail the AgMNPV promoters in permissive cell lines and revealed differential profiles of expression in cells with limited permissivity that correlate well with limitations in viral DNA replication. Semipermissive and nonpermissive cell lines presented delays and restrictions in late and very late promoter expression. Cells undergoing apoptosis did not inhibit late gene expression; however, viral progeny formation is severely affected. This work demonstrates the application of the real-time luminescence detection methodology and how the promoter expression profile may be used to diagnose cellular permissivity to baculovirus infection.
(The abstract is excluded from the Creative Commons licence and has been copied with permission by the publisher.)
Full text of article
Database assignments for author(s): Bergmann Morais Ribeiro

Research topic(s) for pests/diseases/weeds:
biocontrol - natural enemies
Research topic(s) for beneficials or antagonists:
molecular biology - genes


Pest and/or beneficial records:

Beneficial Pest/Disease/Weed Crop/Product Country Quarant.


Alphabaculovirus angemmatalis (entomopathogen)