Induction of antigen-specific immune responses in mice by recombinant baculovirus expressing premembrane and envelope proteins of West Nile virus

<p>Abstract</p> <p>Background</p> <p>West Nile Virus (WNV) is an emerging arthropod-born flavivirus with increasing distribution worldwide that is responsible for a large proportion of viral encephalitis in humans and horses. Given that there are no effective antiviral...

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Main Authors: Zhu Bibo, Ye Jing, Lu Ping, Jiang Rong, Yang Xiaohong, Fu Zhen F, Chen Huanchun, Cao Shengbo
Format: Article
Language:English
Published: BMC 2012-07-01
Series:Virology Journal
Subjects:
Online Access:http://www.virologyj.com/content/9/1/132
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spelling doaj-77e45c265f8c40acbca01a77047dfa762020-11-24T22:56:53ZengBMCVirology Journal1743-422X2012-07-019113210.1186/1743-422X-9-132Induction of antigen-specific immune responses in mice by recombinant baculovirus expressing premembrane and envelope proteins of West Nile virusZhu BiboYe JingLu PingJiang RongYang XiaohongFu Zhen FChen HuanchunCao Shengbo<p>Abstract</p> <p>Background</p> <p>West Nile Virus (WNV) is an emerging arthropod-born flavivirus with increasing distribution worldwide that is responsible for a large proportion of viral encephalitis in humans and horses. Given that there are no effective antiviral drugs available for treatment of the disease, efforts have been directed to develop vaccines to prevent WNV infection. Recently baculovirus has emerged as a novel and attractive gene delivery vehicle for mammalian cells.</p> <p>Results</p> <p>In the present study, recombinant baculoviruses expressing WNV premembrane (prM) and envelope (E) proteins under the cytomegalovirus (CMV) promoter with or without vesicular stomatitis virus glycoprotein (VSV/G) were constructed. The recombinant baculoviruses designated Bac-G-prM/E and Bac-prM/E, efficiently express E protein in mammalian cells. Intramuscular injection of the two recombinant baculoviruses (at doses of 10<sup>8</sup> or 10<sup>9</sup> PFU/mouse) induced the production of WNV-specific antibodies, neutralizing antibodies as well as gamma interferon (IFN-γ) in a dose-dependent pattern. Interestingly, the recombinant baculovirus Bac-G-prM/E was found to be a more efficient immunogen than Bac-prM/E to elicit a robust immune response upon intramuscular injection. In addition, inoculation of baculovirus resulted in the secretion of inflammatory cytokines, such as TNF-α, IL-2 and IL-6.</p> <p>Conclusions</p> <p>These recombinant baculoviruses are capable of eliciting robust humoral and cellular immune responses in mice, and may be considered as novel vaccine candidates for West Nile Virus.</p> http://www.virologyj.com/content/9/1/132West Nile virusRcombinant baculovirusPremembrane/Envelope proteinImmune responses
collection DOAJ
language English
format Article
sources DOAJ
author Zhu Bibo
Ye Jing
Lu Ping
Jiang Rong
Yang Xiaohong
Fu Zhen F
Chen Huanchun
Cao Shengbo
spellingShingle Zhu Bibo
Ye Jing
Lu Ping
Jiang Rong
Yang Xiaohong
Fu Zhen F
Chen Huanchun
Cao Shengbo
Induction of antigen-specific immune responses in mice by recombinant baculovirus expressing premembrane and envelope proteins of West Nile virus
Virology Journal
West Nile virus
Rcombinant baculovirus
Premembrane/Envelope protein
Immune responses
author_facet Zhu Bibo
Ye Jing
Lu Ping
Jiang Rong
Yang Xiaohong
Fu Zhen F
Chen Huanchun
Cao Shengbo
author_sort Zhu Bibo
title Induction of antigen-specific immune responses in mice by recombinant baculovirus expressing premembrane and envelope proteins of West Nile virus
title_short Induction of antigen-specific immune responses in mice by recombinant baculovirus expressing premembrane and envelope proteins of West Nile virus
title_full Induction of antigen-specific immune responses in mice by recombinant baculovirus expressing premembrane and envelope proteins of West Nile virus
title_fullStr Induction of antigen-specific immune responses in mice by recombinant baculovirus expressing premembrane and envelope proteins of West Nile virus
title_full_unstemmed Induction of antigen-specific immune responses in mice by recombinant baculovirus expressing premembrane and envelope proteins of West Nile virus
title_sort induction of antigen-specific immune responses in mice by recombinant baculovirus expressing premembrane and envelope proteins of west nile virus
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2012-07-01
description <p>Abstract</p> <p>Background</p> <p>West Nile Virus (WNV) is an emerging arthropod-born flavivirus with increasing distribution worldwide that is responsible for a large proportion of viral encephalitis in humans and horses. Given that there are no effective antiviral drugs available for treatment of the disease, efforts have been directed to develop vaccines to prevent WNV infection. Recently baculovirus has emerged as a novel and attractive gene delivery vehicle for mammalian cells.</p> <p>Results</p> <p>In the present study, recombinant baculoviruses expressing WNV premembrane (prM) and envelope (E) proteins under the cytomegalovirus (CMV) promoter with or without vesicular stomatitis virus glycoprotein (VSV/G) were constructed. The recombinant baculoviruses designated Bac-G-prM/E and Bac-prM/E, efficiently express E protein in mammalian cells. Intramuscular injection of the two recombinant baculoviruses (at doses of 10<sup>8</sup> or 10<sup>9</sup> PFU/mouse) induced the production of WNV-specific antibodies, neutralizing antibodies as well as gamma interferon (IFN-γ) in a dose-dependent pattern. Interestingly, the recombinant baculovirus Bac-G-prM/E was found to be a more efficient immunogen than Bac-prM/E to elicit a robust immune response upon intramuscular injection. In addition, inoculation of baculovirus resulted in the secretion of inflammatory cytokines, such as TNF-α, IL-2 and IL-6.</p> <p>Conclusions</p> <p>These recombinant baculoviruses are capable of eliciting robust humoral and cellular immune responses in mice, and may be considered as novel vaccine candidates for West Nile Virus.</p>
topic West Nile virus
Rcombinant baculovirus
Premembrane/Envelope protein
Immune responses
url http://www.virologyj.com/content/9/1/132
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