scholarly journals Proteotoxic stress induced by Autographa californica nucleopolyhedrovirus infection of Spodoptera frugiperda Sf9 cells

Virology ◽  
2013 ◽  
Vol 436 (1) ◽  
pp. 49-58 ◽  
Author(s):  
Yulia V. Lyupina ◽  
Svetlana B. Abaturova ◽  
Pavel A. Erokhov ◽  
Olga V. Orlova ◽  
Svetlana N. Beljelarskaya ◽  
...  
2020 ◽  
Vol 72 (2) ◽  
pp. 315-325
Author(s):  
Wenqiang Wei ◽  
Zichao Hu ◽  
Yuting Jia ◽  
TingXuan Gu ◽  
Wei Zhao ◽  
...  

2014 ◽  
Vol 192 ◽  
pp. 1-5 ◽  
Author(s):  
Yulia V. Lyupina ◽  
Olga V. Orlova ◽  
Svetlana B. Abaturova ◽  
Svetlana N. Beljelarskaya ◽  
Andrey N. Lavrov ◽  
...  

2005 ◽  
Vol 79 (15) ◽  
pp. 10077-10082 ◽  
Author(s):  
Lu Liqun ◽  
Hadassah Rivkin ◽  
Nor Chejanovsky

ABSTRACT The role of the Autographa californica multiple nucleopolyhedrovirus (AcMNPV) immediate-early protein IE0 in the baculoviral infection is not clear. In this study, we constructed the recombinant virus vAcΔie0 null for ie0 expression by targeted mutagenesis replacing exon0 with the cat gene. We found that vAcΔie0 replicated efficiently in Spodoptera littoralis SL2 cells, which are poorly permissive for AcMNPV. In contrast, in Spodoptera frugiperda SF9 cells, which are fully permissive for AcMNPV, vAcΔie0 DNA replication and budded virus production were delayed. These results and recently published data (X. Dai et al., J. Virol. 78:9633-9644, 2004) indicate that ie0 is not essential for AcMNPV replication but enhances it in permissive SF9 cells.


1999 ◽  
Vol 73 (2) ◽  
pp. 1278-1285 ◽  
Author(s):  
Quansheng Du ◽  
Dana Lehavi ◽  
Ouriel Faktor ◽  
Yipeng Qi ◽  
Nor Chejanovsky

ABSTRACT Spodoptera frugiperda SF9 cells infected with mutants of the Autographa californica nucleopolyhedrovirus (AcMNPV) which lack a functional p35 gene undergo apoptosis, aborting the viral infection. The Spodoptera littoralis nucleopolyhedrovirus (SlNPV) was able to suppress apoptosis triggered by vΔP35K/pol+, an AcMNPVp35 null mutant. To identify the putative apoptotic suppressor gene of SlNPV, overlapping cosmid clones representing the entire SlNPV genome were individually cotransfected along with genomic DNA of vΔP35K/pol+. Using this complementation assay, we isolated a SlNPV DNA fragment that was able to rescue the vΔP35K/pol+ infection in SF9 cells. By further subcloning and rescue, we identified a novel SlNPV gene, Slp49. TheSlp49 sequence predicted a 49-kDa polypeptide with about 48.8% identity to the AcMNPV apoptotic suppressor P35. SLP49 displays a potential recognition site, TVTDG, for cleavage by death caspases. Recombinant AcMNPVs deficient inp35 bearing the Slp49 gene did not induce apoptosis and showed successful productive infections in SF9 cells, indicating that Slp49 is a functional homologue ofp35. A 1.5-kbp Slp49-specific transcript was identified in SF9 cells infected with SlNPV or with vAc496, a vΔP35K/pol+-recombinant bearing Slp49. The discovery of Slp49 contributes to the identification of important functional motifs conserved in p35-like apoptotic suppressors and to the future isolation of p35-like genes from other baculoviruses.


2006 ◽  
Vol 87 (3) ◽  
pp. 531-536 ◽  
Author(s):  
Barbara J. Kelly ◽  
Linda A. King ◽  
Robert D. Possee ◽  
Susan D. J. Chapple

Spodoptera frugiperda cells infected with Autographa californica nucleopolyhedrovirus (AcMNPV) lacking a functional anti-apoptotic p35 protein undergo apoptosis. However, such mutants replicate normally in Trichoplusia ni (TN-368) cells. An AcMNPV plaque isolate (AcdefrT) was identified during propagation of a virus deficient in p35 in TN-368 cells. This virus exhibited enhanced budded-particle formation in TN-368 cells, but was partially defective for polyhedra production in the same cells. Virus replication in AcdefrT-infected TN-368 cells was accompanied by extensive plasma-membrane blebbing and caspase activation late in infection, both features of apoptosis. Rescue of the p35 locus of AcdefrT continued to result in a reduction in polyhedra and increase in budded virus production in TN-368 cells, but no plasma-membrane blebbing was observed. The mutation was mapped to the FP-25 gene locus. This gene mutation combined with the non-functional p35 was found to be responsible for the cell-blebbing effect observed in AcdefrT-infected TN-368 cells.


2020 ◽  
Author(s):  
Tiejun Zhao ◽  
Riqiang Deng ◽  
Mengqiu Chen ◽  
Xunzhang Wang

Abstract Autographa californica multiple Nucleopolyhedrovirus (AcMNPV) is the archetypal species of the alphabaculovirus. Sf9 are the ovarian cells of their host—Spodoptera frugiperda. In this study, a total of 3,463 pieces of time-series differentially expressed RNA are identified, including 1,200 mRNA and 2,263 lncRNA, with high-throughput sequencing technology using samples collected from Sf9 cells at different time points after AcMNPV infection. The result could provide a reference for the further study of the interaction and regulatory mechanism between the virus and the host.


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