2015•Unpublished venueRequires access

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

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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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What this paper is about

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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Available 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.

Key concepts: Canine distemper, Virology, Rabies virus, Virus, Lyssavirus, Biology, Mononegavirales, Recombinant virus

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