Abstract:The Autographa californica nucleopolyhedrovirus (AcMNPV) contains three apoptosis suppressor genes: p35, iap1 and iap2. AcMNPV P35 functions as a pancaspase inhibitor, but the function of IAP1 and IAP2 has not been entirely resolved. In this paper, we analyze the function of IAP1 and IAP2 in detail. AcMNPV with p35-deletion inhibited the apoptosis of BTI-Tn-5B1-4 (Tn-Hi5) cells induced by a Helicoverpa armigera single nucleocapsid NPV (HearNPV) infection and rescued the replication of HearNPV and BV production… Show more
“…Similarly, HycuNPV IAP-1 and -2 [36], as well as HearNPV IAP-2 [37] were also reported to lack anti-apoptotic activity. In contrast, both AcMNPV IAP-1 and IAP-2 were reported to be able to inhibit apoptosis induced by HearNPV in the T. ni cell line Tn-Hi5, which is resistant to most apoptotic signals [43]. EppoNPV IAP-2 was reported to block apoptosis in SF-21 cells, while IAP-1 from this virus delayed apoptosis [38].…”
Section: Which Viral Iaps Can Inhibit Apoptosis?mentioning
“…Similarly, HycuNPV IAP-1 and -2 [36], as well as HearNPV IAP-2 [37] were also reported to lack anti-apoptotic activity. In contrast, both AcMNPV IAP-1 and IAP-2 were reported to be able to inhibit apoptosis induced by HearNPV in the T. ni cell line Tn-Hi5, which is resistant to most apoptotic signals [43]. EppoNPV IAP-2 was reported to block apoptosis in SF-21 cells, while IAP-1 from this virus delayed apoptosis [38].…”
Section: Which Viral Iaps Can Inhibit Apoptosis?mentioning
“…One pathway regulates the process of viral DNA replication, since IE2 and PE38 act as stimulators for the DNA replication (Kool et al, 1994). Another one is associated with a host insect cell apoptosis, because IAP2 acts as an inhibitor of apoptosis (Zeng et al, 2009). Although much effort is paid to these processes, their mechanisms remain elusive.…”
Ubiquitin (UB) is a conserved protein that regulates a number of processes in eukaryotic cells. Nearly all lepidopteran baculoviruses encode UB homologs showing a partial sequence identity with human UB (Hu-UB). In this study, the sequence, predicted 3D-structure and subcellular localization of UB homologs encoded by two different nucleopolyhedroviruses of Bombyx mori (BmNPV) and Helicoverpa armigera (HaNPV) were compared. UBs of BmNPV and HaNPV (Bm-UB, Ha-UB, respectively) shared only 73% of sequence identity of the different aa in relation to Hu-UB being localized in non-conserved parts, namely in two heterogeneous regions of aa 15-32 and aa 53-60. Interestingly, Bm-UB and Ha-UB share the same seven lysines except for an additional Lys54 in Bm-UB. However, in spite of the sequence heterogeneity, Bm-UB and Ha-UB have a similar predicted 3D-structure. A difference in their subcellular localization during virus growth in insect cell lines was found in the late stage of formation of occlusion-derived virus (ODV). In particular Bm-UB was localized mainly and evenly in the nucleus, while Ha-UB on the nuclear membrane. These data suggest that (i) UBs, besides being engaged in various cellular processes, have a role in specific processes of virus growth, and (ii) Bm-UB and Ha-UB may show certain different activities associated with the virus growth.
“…The cell line TUAT-SpLi221 (SpLi-221) is derived from the tobacco cutworm ( S. litura )15. The BTI-Tn-5B1-4 (Hi5) cell strain is derived from the cabbage looper ( T. ni )1536. These cells were maintained at 27 °C in TNM-FH medium (Invitrogen Life Technologies) supplemented with 10% fetal bovine serum (FBS), penicillin (100 μg/ml), and streptomycin (30 μg/ml).…”
As baculoviruses usually have a narrow insecticidal spectrum, knowing the mechanisms by which they control the host-range is prerequisite for improvement of their applications as pesticides. In this study, from supernatant of culture cells transfected with DNAs of an Autographa californica multiple nucleopolyhedrovirus (AcMNPV) mutant lacking the antiapoptotic gene p35 (vAc∆P35) and a cosmid representing a fragment of Spodoptera exigua nucleopolyhedrovirus (SeMNPV), a viral strain was plaque-purified and named vAcRev. vAcRev had a broader host range than either vAc∆P35 or SeMNPV parental virus, being able to infect not only the permissive hosts of its parental viruses but also a nonpermissive host (Spodoptera litura). Genome sequencing indicated that vAcRev comprises a mixture of two viruses with different circular dsDNA genomes. One virus contains a genome similar to vAc∆P35, while in the other viral genome, a 24.4 kbp-fragment containing 10 essential genesis replaced with a 4 kbp-fragment containing three SeMNPV genes including a truncated Se-iap3 gene. RNA interference and ectopic expression assays found that Se-iap3 is responsible for the host range expansion of vAcRev, suggesting that Se-iap3 inhibits the progression of apoptosis initiated by viral infection and promotes viral propagation in hosts both permissive and non-permissive for AcMNPV and SeMNPV.
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