Viruses (e.g. Human immunodeficiency virus, Human simplex virus and Prototype foamy virus) are obligate intracellular parasites and therefore depend on the cellular machinery for cellular trafficking. Bovine foamy vir...Viruses (e.g. Human immunodeficiency virus, Human simplex virus and Prototype foamy virus) are obligate intracellular parasites and therefore depend on the cellular machinery for cellular trafficking. Bovine foamy virus (BFV) is a member of the Spumaretrovirinae subfamily of Retroviruses, however, details of its cellular trafficking remain unknown. In this study, we cloned the BFV gag gene into prokaryotic expression vector pET28a and purified the denaturalized Gag protein. The protein was used to immunize BALB/c mouse to produce antiserum, which could specifically recognize the BFV Gag protein in BFV-infected cells through western blot assay. Additionally, these results demonstrated that both the optimal and suboptimal cleavage of Gag protein occur in BFV-infected cells. Subsequently, the Gag antiserum was used to investigate subcellular localization of BFV. In immunofluorescence microscopy assays, colocalization microtubules (MTs) and assembling viral particles were clearly observed, which implied that BFV may transport along cellular MTs in host cells. Furthermore, MTs-depolymerizing assay indicated MTs were required for the efficient replication of BFV. In conclusion, our study suggests that BFV has evolved the mechanism to hijack the cellular cytoskeleton for its replication.展开更多
Vaccines are used in integrated control strategies to guard poultry against H5N1 high-pathogenicity avian influenza （AI）. This study was to evaluate the efficacy of AI vaccine against AI in poultry. About 400 serum ...Vaccines are used in integrated control strategies to guard poultry against H5N1 high-pathogenicity avian influenza （AI）. This study was to evaluate the efficacy of AI vaccine against AI in poultry. About 400 serum samples were collected from the selected 130 farms located at Rajshahi region, Bangladesh. The study was carried out from January, 2013 to January, 2015. The AI vaccine titres were compared in different breed of layer, environmental temperature, feed and egg production. Result showed that the value of titres （mean ± SD） in Hyline brown, Hyline white, Bovans white and Novogen white were 6.71 ± 0.05, 6.67 ± 0.06, 6.79 ± 0.03 and 6.43 ± 0.04, respectively. The highest serum antibody titres were 6.61 ± 0.24 against AI antibody in 〉 26 ℃ environment temperature. The highest and lowest serum antibody value of AI against feed brand （nutrient） were 7.75 ± 0.08 and 5.58 ± 0.22 for Aftab and Quality brand feed, respectively.展开更多
基金The Key Project of the Ministry of Education of China (108028)National Natural Science Foundation of China (3090068)Grant from State Key Laboratory for Infectious Diseases Prevention and Control, SKL (2008SKLID310)
文摘Viruses (e.g. Human immunodeficiency virus, Human simplex virus and Prototype foamy virus) are obligate intracellular parasites and therefore depend on the cellular machinery for cellular trafficking. Bovine foamy virus (BFV) is a member of the Spumaretrovirinae subfamily of Retroviruses, however, details of its cellular trafficking remain unknown. In this study, we cloned the BFV gag gene into prokaryotic expression vector pET28a and purified the denaturalized Gag protein. The protein was used to immunize BALB/c mouse to produce antiserum, which could specifically recognize the BFV Gag protein in BFV-infected cells through western blot assay. Additionally, these results demonstrated that both the optimal and suboptimal cleavage of Gag protein occur in BFV-infected cells. Subsequently, the Gag antiserum was used to investigate subcellular localization of BFV. In immunofluorescence microscopy assays, colocalization microtubules (MTs) and assembling viral particles were clearly observed, which implied that BFV may transport along cellular MTs in host cells. Furthermore, MTs-depolymerizing assay indicated MTs were required for the efficient replication of BFV. In conclusion, our study suggests that BFV has evolved the mechanism to hijack the cellular cytoskeleton for its replication.
文摘Vaccines are used in integrated control strategies to guard poultry against H5N1 high-pathogenicity avian influenza （AI）. This study was to evaluate the efficacy of AI vaccine against AI in poultry. About 400 serum samples were collected from the selected 130 farms located at Rajshahi region, Bangladesh. The study was carried out from January, 2013 to January, 2015. The AI vaccine titres were compared in different breed of layer, environmental temperature, feed and egg production. Result showed that the value of titres （mean ± SD） in Hyline brown, Hyline white, Bovans white and Novogen white were 6.71 ± 0.05, 6.67 ± 0.06, 6.79 ± 0.03 and 6.43 ± 0.04, respectively. The highest serum antibody titres were 6.61 ± 0.24 against AI antibody in 〉 26 ℃ environment temperature. The highest and lowest serum antibody value of AI against feed brand （nutrient） were 7.75 ± 0.08 and 5.58 ± 0.22 for Aftab and Quality brand feed, respectively.
