A recombinant canine distemper virus expressing a modified rabies virus glycoprotein induces immune responses in mice
Zhili LiJigui WangDaoli Yuan, Shuang WangJiazeng, SunBao Yi, Qiang HouYaping MaoWeiquan Liu
Abstract
Zhili LiJigui WangDaoli Yuan, Shuang WangJiazeng, SunBao Yi, Qiang HouYaping MaoWeiquan Liu
Abstract
Canine distemper virus (CDV) and rabies virus (RV) are two important pathogens of the dog. CDV, a member of the morbillivirus genus, has shown promise as an expression vector. The glycoprotein from RV is a main contributor to protective immunity and capable of eliciting the production of virus-neutralizing antibodies. In this study, we recovered an attenuated strain of canine dis- temper virus and constructed a recombinant virus, rCDV- RV-G, expressing a modified (R333Q) rabies virus glyco- protein (RV-G) of RV Flury strain LEP. RV-G expression by the recombinant viruses was confirmed. Furthermore, G was proved to be incorporated into the surface of CDV particles. While replication of the recombinant virus was slightly reduced compared with the parental CDV, it stably expressed the RV-G over ten serial passages. Inoculation of mice induced specific neutralizing antibodies against both RV-G and CDV. Therefore, the rCDV-RV-G has the po- tential as a vaccine that may be used to control rabies virus infection in dogs and other animals.
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Canine distemper virus (CDV) and rabies virus (RV) are two important pathogens of the dog. CDV, a member of the morbillivirus genus, has shown promise as an expression vector. The glycoprotein from RV is a main contributor to protective immunity and capable of eliciting the production of virus-neutralizing antibodies. In this study, we recovered an attenuated strain of canine dis- temper virus and constructed a recombinant virus, rCDV- RV-G, expressing a modified (R333Q) rabies virus glyco- protein (RV-G) of RV Flury strain LEP. RV-G expression by the recombinant viruses was confirmed. Furthermore, G was proved to be incorporated into the surface of CDV particles. While replication of the recombinant virus was slightly reduced compared with the parental CDV, it stably expressed the RV-G over ten serial passages. Inoculation of mice induced specific neutralizing antibodies against both RV-G and CDV. Therefore, the rCDV-RV-G has the po- tential as a vaccine that may be used to control rabies virus infection in dogs and other animals.
Key concepts: Canine distemper, Virology, Rabies virus, Virus, Lyssavirus, Biology, Mononegavirales, Recombinant virus