Hsp70 Inhibits the Replication of Fowl Adenovirus Serotype 4 by Suppressing Viral Hexon with the Assistance of DnaJC7

Fowl adenovirus serotype 4 (FAdV-4) Infection results in serious hepatitis-hydropericardium syndrome (HHS) in broilers, which has caused great economic losses to the poultry industry; however, the specific host responses to FAdV-4 remain unknown. In this study, we identified 141 high-confidence protein-protein interactions (PPIs) between the main Viral Proteins (Hexon, Fiber 1, Fiber 2, and Penton bases) and host proteins via a liquid chromatography-tandem mass spectrometry (LC-MS/MS) assay. We found that heat shock protein 70 (HSP70), the protein with the highest score, and its cofactor DnaJ heat shock protein 40 family member C7 (DnaJC7) could negatively regulate the replication of FAdV-4. Furthermore, the nucleotide binding domain (NBD) of HSP70 and the J domain of DnaJC7 were necessary for inhibiting FAdV-4 replication. We verified that DnaJC7 as a bridge could bind to HSP70 and Hexon, assisting the indirect interaction between HSP70 and Hexon. In addition, we found that FAdV-4 Infection strongly induced the expression of Autophagy proteins and cellular HSP70 in a dose-dependent manner. Blockage of Hexon by HSP70 overexpression was significantly reduced when the Autophagy pathway was blocked by the specific inhibitor chloroquine (CQ). Our results showed that HSP70 was co-opted by DnaJC7 to interact with viral Hexon and inhibited Hexon through the Autophagy pathway, leading to a considerable restriction of FAdV-4 replication. IMPORTANCE FAdV-4, as the main cause of HHS, has quickly spread all over the world in recent years, seriously threatening the poultry industry. The aim of this study was to identify the important host proteins that have the potential to regulate the life cycle of FAdV-4. We found that HSP70 and DnaJC7 played crucial roles in regulating the amount of viral Hexon and extracellular viral titers. Moreover, we demonstrated that HSP70 interacted with viral Hexon with the assistance of DnaJC7, followed by suppressing Hexon protein through the Autophagy pathway. These results provide new insight into the role of the molecular chaperone complex Hsp70-DnaJC7 in FAdV-4 Infection and suggest a novel strategy for anti-FAdV-4 drug development by targeting the specific interactions among HSP70, DnaJC7 and Hexon.