Author: Barrado-Gil, LucÃa; del Puerto, Ana; Galindo, Inmaculada; Cuesta-Geijo, Miguel Ãngel; GarcÃa-Dorival, Isabel; de Motes, Carlos Maluquer; Alonso, Covadonga
                    Title: African Swine Fever Virus Ubiquitin-Conjugating Enzyme Is an Immunomodulator Targeting NF-κB Activation  Cord-id: lass9uo5  Document date: 2021_6_17
                    ID: lass9uo5
                    
                    Snippet: African swine fever virus (ASFV) is an acute and persistent swine virus with a high economic burden that encodes multiple genes to evade host immune response. In this work, we have revealed that early viral protein UBCv1, the only known conjugating enzyme encoded by a virus, modulates innate immune and inflammatory signaling. Transient overexpression of UBCv1 impaired activation of NF-κB and AP-1 transcription factors induced by several agonists of these pathways. In contrast, activation of IRF
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: African swine fever virus (ASFV) is an acute and persistent swine virus with a high economic burden that encodes multiple genes to evade host immune response. In this work, we have revealed that early viral protein UBCv1, the only known conjugating enzyme encoded by a virus, modulates innate immune and inflammatory signaling. Transient overexpression of UBCv1 impaired activation of NF-κB and AP-1 transcription factors induced by several agonists of these pathways. In contrast, activation of IRF3 and ISRE signaling upon stimulation with TRIFΔRIP, cGAS/STING or RIG-I-CARD remained unaltered. Experiments aimed at mapping UBCv1 inhibitory activity indicated that this viral protein acts upstream or at the level step of IKKβ. In agreement with this, UBCv1 was able to block p65 nuclear translocation upon cytokine stimulation, a key event in NF-ĸB signaling. Additionally, A549 stably transduced for UBCv1 showed a significant decrease in the levels of NF-ĸB dependent genes. Interestingly, despite the well-defined capacity of UBCv1 to conjugate ubiquitin chains, a mutant disabled for ubiquitylation activity retained similar immunomodulatory activity as the wild-type enzyme, suggesting that the two functions are segregated. Altogether these data suggest that ASFV UBCv1 manipulates the innate immune response targeting the NF-κB and AP-1 pathways and opens new questions about the multifunctionality of this enzyme.
 
  Search related documents: 
                                Co phrase  search for related documents- adaptor protein and madison promega: 1
- luciferase activity and madison promega: 1, 2, 3, 4, 5, 6
- luciferase reporter and madison promega: 1, 2, 3, 4
- luciferase transfection and madison promega: 1, 2, 3, 4, 5
- luciferase transfection control and madison promega: 1, 2
 
                                Co phrase  search for related documents, hyperlinks ordered by date