Construction and immunogenicity of recombinant Mycobacterium bovis BCG expressing GP5 and M protein of porcine reproductive respiratory syndrome virus

Mycobacterium bovis BCG was used to express a truncated form of GP5 (lacking the first 30 NH 2-terminal residues) and M protein of porcine reproductive and respiratory syndrome virus (PRRSV). The PRRSV proteins were expressed in BCG under control of the mycobacterial hsp60 gene promoter either in th...

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Veröffentlicht in:Vaccine 2002-11, Vol.21 (1), p.21-29
Hauptverfasser: Bastos, Reginaldo G, Dellagostin, Odir A, Barletta, Raúl G, Doster, Allan R, Nelson, Eric, Osorio, Fernando A
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container_end_page 29
container_issue 1
container_start_page 21
container_title Vaccine
container_volume 21
creator Bastos, Reginaldo G
Dellagostin, Odir A
Barletta, Raúl G
Doster, Allan R
Nelson, Eric
Osorio, Fernando A
description Mycobacterium bovis BCG was used to express a truncated form of GP5 (lacking the first 30 NH 2-terminal residues) and M protein of porcine reproductive and respiratory syndrome virus (PRRSV). The PRRSV proteins were expressed in BCG under control of the mycobacterial hsp60 gene promoter either in the mycobacterial cytoplasm (BCGGP5cyt and BCGMcyt) or as MT19-fusion proteins on the mycobacterial surface (BCGGP5surf and BCGMsurf). Mice inoculated with BCGGP5surf and BCGMsurf developed antibodies against the viral proteins at 30 days post-inoculation (dpi) as detected by ELISA and Western blot. By 60 dpi, the animals developed titer of neutralizing antibodies of 8. A PRRSV-specific gamma interferon response was also detected in splenocytes of recombinant BCG-inoculated mice at 60 and 90 dpi. These results indicate that BCG was able to express antigens of PRRSV and elicit an immune response against the viral proteins in mice.
doi_str_mv 10.1016/S0264-410X(02)00443-7
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The PRRSV proteins were expressed in BCG under control of the mycobacterial hsp60 gene promoter either in the mycobacterial cytoplasm (BCGGP5cyt and BCGMcyt) or as MT19-fusion proteins on the mycobacterial surface (BCGGP5surf and BCGMsurf). Mice inoculated with BCGGP5surf and BCGMsurf developed antibodies against the viral proteins at 30 days post-inoculation (dpi) as detected by ELISA and Western blot. By 60 dpi, the animals developed titer of neutralizing antibodies of 8. A PRRSV-specific gamma interferon response was also detected in splenocytes of recombinant BCG-inoculated mice at 60 and 90 dpi. 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Psychology</topic><topic>gamma -Interferon</topic><topic>Gene Expression</topic><topic>Genetic Vectors</topic><topic>glycoprotein gp35</topic><topic>glycoprotein gp5</topic><topic>GP5 and M PRRSV protein</topic><topic>HSP60 gene</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Microbiology</topic><topic>movement protein</topic><topic>Mycobacterium bovis</topic><topic>Mycobacterium bovis - genetics</topic><topic>Peptides - chemical synthesis</topic><topic>Peptides - chemistry</topic><topic>Peptides - immunology</topic><topic>Porcine respiratory and reproductive syndrome virus</topic><topic>Porcine respiratory and reproductive syndrome virus - chemistry</topic><topic>Porcine respiratory and reproductive syndrome virus - genetics</topic><topic>Porcine respiratory and reproductive syndrome virus - isolation &amp; purification</topic><topic>PRRSV</topic><topic>Recombinant BCG</topic><topic>Recombinant Proteins - immunology</topic><topic>Swine</topic><topic>Vaccination</topic><topic>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies</topic><topic>Vaccines, DNA - immunology</topic><topic>Viral Envelope Proteins - genetics</topic><topic>Viral Envelope Proteins - immunology</topic><topic>Viral Matrix Proteins - genetics</topic><topic>Viral Matrix Proteins - immunology</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bastos, Reginaldo G</creatorcontrib><creatorcontrib>Dellagostin, Odir A</creatorcontrib><creatorcontrib>Barletta, Raúl G</creatorcontrib><creatorcontrib>Doster, Allan R</creatorcontrib><creatorcontrib>Nelson, Eric</creatorcontrib><creatorcontrib>Osorio, Fernando A</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Vaccine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bastos, Reginaldo G</au><au>Dellagostin, Odir A</au><au>Barletta, Raúl G</au><au>Doster, Allan R</au><au>Nelson, Eric</au><au>Osorio, Fernando A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Construction and immunogenicity of recombinant Mycobacterium bovis BCG expressing GP5 and M protein of porcine reproductive respiratory syndrome virus</atitle><jtitle>Vaccine</jtitle><addtitle>Vaccine</addtitle><date>2002-11-22</date><risdate>2002</risdate><volume>21</volume><issue>1</issue><spage>21</spage><epage>29</epage><pages>21-29</pages><issn>0264-410X</issn><eissn>1873-2518</eissn><coden>VACCDE</coden><abstract>Mycobacterium bovis BCG was used to express a truncated form of GP5 (lacking the first 30 NH 2-terminal residues) and M protein of porcine reproductive and respiratory syndrome virus (PRRSV). The PRRSV proteins were expressed in BCG under control of the mycobacterial hsp60 gene promoter either in the mycobacterial cytoplasm (BCGGP5cyt and BCGMcyt) or as MT19-fusion proteins on the mycobacterial surface (BCGGP5surf and BCGMsurf). Mice inoculated with BCGGP5surf and BCGMsurf developed antibodies against the viral proteins at 30 days post-inoculation (dpi) as detected by ELISA and Western blot. By 60 dpi, the animals developed titer of neutralizing antibodies of 8. A PRRSV-specific gamma interferon response was also detected in splenocytes of recombinant BCG-inoculated mice at 60 and 90 dpi. These results indicate that BCG was able to express antigens of PRRSV and elicit an immune response against the viral proteins in mice.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>12443659</pmid><doi>10.1016/S0264-410X(02)00443-7</doi><tpages>9</tpages></addata></record>
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subjects Animals
Antibodies, Viral - immunology
Biological and medical sciences
Blotting, Western
Cloning, Molecular
double prime M protein
Enzyme-Linked Immunosorbent Assay
Fundamental and applied biological sciences. Psychology
gamma -Interferon
Gene Expression
Genetic Vectors
glycoprotein gp35
glycoprotein gp5
GP5 and M PRRSV protein
HSP60 gene
Mice
Mice, Inbred BALB C
Microbiology
movement protein
Mycobacterium bovis
Mycobacterium bovis - genetics
Peptides - chemical synthesis
Peptides - chemistry
Peptides - immunology
Porcine respiratory and reproductive syndrome virus
Porcine respiratory and reproductive syndrome virus - chemistry
Porcine respiratory and reproductive syndrome virus - genetics
Porcine respiratory and reproductive syndrome virus - isolation & purification
PRRSV
Recombinant BCG
Recombinant Proteins - immunology
Swine
Vaccination
Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies
Vaccines, DNA - immunology
Viral Envelope Proteins - genetics
Viral Envelope Proteins - immunology
Viral Matrix Proteins - genetics
Viral Matrix Proteins - immunology
Virology
title Construction and immunogenicity of recombinant Mycobacterium bovis BCG expressing GP5 and M protein of porcine reproductive respiratory syndrome virus
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