Plant-Based Vaccine: Mice Immunized with Chloroplast-Derived Anthrax Protective Antigen Survive Anthrax Lethal Toxin Challenge
The currently available human vaccine for anthrax, derived from the culture supernatant of Bacillus anthracis, contains the protective antigen (PA) and traces of the lethal and edema factors, which may contribute to adverse side effects associated with this vaccine. Therefore, an effective expressio...
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description | The currently available human vaccine for anthrax, derived from the culture supernatant of Bacillus anthracis, contains the protective antigen (PA) and traces of the lethal and edema factors, which may contribute to adverse side effects associated with this vaccine. Therefore, an effective expression system that can provide a clean, safe, and efficacious vaccine is required. In an effort to produce anthrax vaccine in large quantities and free of extraneous bacterial contaminants, PA was expressed in transgenic tobacco chloroplasts by inserting the pagA gene into the chloroplast genome. Chloroplast integration of the pagA gene was confirmed by PCR and Southern analysis. Mature leaves grown under continuous illumination contained PA as up to 14.2% of the total soluble protein. Cytotoxicity measurements in macrophage lysis assays showed that chloroplast-derived PA was equal in potency to PA produced in B. anthracis. Subcutaneous immunization of mice with partially purified chloroplast-derived or B. anthracis-derived PA with adjuvant yielded immunoglobulin G titers up to 1:320,000, and both groups of mice survived (100%) challenge with lethal doses of toxin. An average yield of about 150 mg of PA per plant should produce 360 million doses of a purified vaccine free of bacterial toxins edema factor and lethal factor from 1 acre of land. Such high expression levels without using fermenters and the immunoprotection offered by the chloroplast-derived PA should facilitate development of a cleaner and safer anthrax vaccine at a lower production cost. These results demonstrate the immunogenic and immunoprotective properties of plant-derived anthrax vaccine antigen. |
doi_str_mv | 10.1128/IAI.73.12.8266-8274.2005 |
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Therefore, an effective expression system that can provide a clean, safe, and efficacious vaccine is required. In an effort to produce anthrax vaccine in large quantities and free of extraneous bacterial contaminants, PA was expressed in transgenic tobacco chloroplasts by inserting the pagA gene into the chloroplast genome. Chloroplast integration of the pagA gene was confirmed by PCR and Southern analysis. Mature leaves grown under continuous illumination contained PA as up to 14.2% of the total soluble protein. Cytotoxicity measurements in macrophage lysis assays showed that chloroplast-derived PA was equal in potency to PA produced in B. anthracis. Subcutaneous immunization of mice with partially purified chloroplast-derived or B. anthracis-derived PA with adjuvant yielded immunoglobulin G titers up to 1:320,000, and both groups of mice survived (100%) challenge with lethal doses of toxin. An average yield of about 150 mg of PA per plant should produce 360 million doses of a purified vaccine free of bacterial toxins edema factor and lethal factor from 1 acre of land. Such high expression levels without using fermenters and the immunoprotection offered by the chloroplast-derived PA should facilitate development of a cleaner and safer anthrax vaccine at a lower production cost. These results demonstrate the immunogenic and immunoprotective properties of plant-derived anthrax vaccine antigen.</description><identifier>ISSN: 0019-9567</identifier><identifier>EISSN: 1098-5522</identifier><identifier>DOI: 10.1128/IAI.73.12.8266-8274.2005</identifier><identifier>PMID: 16299323</identifier><identifier>CODEN: INFIBR</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Animals ; Anthrax - prevention & control ; Anthrax Vaccines - administration & dosage ; Anthrax Vaccines - genetics ; Anthrax Vaccines - immunology ; Antigens, Bacterial - biosynthesis ; Antigens, Bacterial - genetics ; Antigens, Bacterial - immunology ; Applied microbiology ; Bacillus anthracis ; Bacterial Toxins - biosynthesis ; Bacterial Toxins - genetics ; Bacterial Toxins - immunology ; Biological and medical sciences ; Blotting, Southern ; Chloroplasts - genetics ; Chloroplasts - metabolism ; Fundamental and applied biological sciences. Psychology ; Immune Sera - immunology ; Immunization ; Immunoblotting ; Immunoglobulin G - blood ; Macrophages - drug effects ; Mice ; Mice, Inbred BALB C ; Microbial Immunity and Vaccines ; Microbiology ; Nicotiana - genetics ; Nicotiana - metabolism ; Plant Leaves - genetics ; Plant Leaves - metabolism ; Plants, Genetically Modified - genetics ; Plants, Genetically Modified - metabolism ; Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</subject><ispartof>Infection and Immunity, 2005-12, Vol.73 (12), p.8266-8274</ispartof><rights>2006 INIST-CNRS</rights><rights>Copyright © 2005, American Society for Microbiology 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c585t-a5279729a04f15dacc08435727f9b57ec4a199dd358acd8358d66b503db644533</citedby><cites>FETCH-LOGICAL-c585t-a5279729a04f15dacc08435727f9b57ec4a199dd358acd8358d66b503db644533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1307059/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1307059/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,728,781,785,886,3189,3190,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17290932$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16299323$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koya, Vijay</creatorcontrib><creatorcontrib>Moayeri, Mahtab</creatorcontrib><creatorcontrib>Leppla, Stephen H</creatorcontrib><creatorcontrib>Daniell, Henry</creatorcontrib><title>Plant-Based Vaccine: Mice Immunized with Chloroplast-Derived Anthrax Protective Antigen Survive Anthrax Lethal Toxin Challenge</title><title>Infection and Immunity</title><addtitle>Infect Immun</addtitle><description>The currently available human vaccine for anthrax, derived from the culture supernatant of Bacillus anthracis, contains the protective antigen (PA) and traces of the lethal and edema factors, which may contribute to adverse side effects associated with this vaccine. Therefore, an effective expression system that can provide a clean, safe, and efficacious vaccine is required. In an effort to produce anthrax vaccine in large quantities and free of extraneous bacterial contaminants, PA was expressed in transgenic tobacco chloroplasts by inserting the pagA gene into the chloroplast genome. Chloroplast integration of the pagA gene was confirmed by PCR and Southern analysis. Mature leaves grown under continuous illumination contained PA as up to 14.2% of the total soluble protein. Cytotoxicity measurements in macrophage lysis assays showed that chloroplast-derived PA was equal in potency to PA produced in B. anthracis. Subcutaneous immunization of mice with partially purified chloroplast-derived or B. anthracis-derived PA with adjuvant yielded immunoglobulin G titers up to 1:320,000, and both groups of mice survived (100%) challenge with lethal doses of toxin. An average yield of about 150 mg of PA per plant should produce 360 million doses of a purified vaccine free of bacterial toxins edema factor and lethal factor from 1 acre of land. Such high expression levels without using fermenters and the immunoprotection offered by the chloroplast-derived PA should facilitate development of a cleaner and safer anthrax vaccine at a lower production cost. These results demonstrate the immunogenic and immunoprotective properties of plant-derived anthrax vaccine antigen.</description><subject>Animals</subject><subject>Anthrax - prevention & control</subject><subject>Anthrax Vaccines - administration & dosage</subject><subject>Anthrax Vaccines - genetics</subject><subject>Anthrax Vaccines - immunology</subject><subject>Antigens, Bacterial - biosynthesis</subject><subject>Antigens, Bacterial - genetics</subject><subject>Antigens, Bacterial - immunology</subject><subject>Applied microbiology</subject><subject>Bacillus anthracis</subject><subject>Bacterial Toxins - biosynthesis</subject><subject>Bacterial Toxins - genetics</subject><subject>Bacterial Toxins - immunology</subject><subject>Biological and medical sciences</subject><subject>Blotting, Southern</subject><subject>Chloroplasts - genetics</subject><subject>Chloroplasts - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Immune Sera - immunology</subject><subject>Immunization</subject><subject>Immunoblotting</subject><subject>Immunoglobulin G - blood</subject><subject>Macrophages - drug effects</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Microbial Immunity and Vaccines</subject><subject>Microbiology</subject><subject>Nicotiana - genetics</subject><subject>Nicotiana - metabolism</subject><subject>Plant Leaves - genetics</subject><subject>Plant Leaves - metabolism</subject><subject>Plants, Genetically Modified - genetics</subject><subject>Plants, Genetically Modified - metabolism</subject><subject>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</subject><issn>0019-9567</issn><issn>1098-5522</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1vEzEQhi0EomngL8AKCW4b_Lm2OVQKKR-RgqjUlqs18XqzRvsR7E1aOPDb8ZKIwInTaGaeeT2eF6GM4BkhVL1ezpczyWaEzhQtilxRyWcUY_EATQjWKheC0odogjHRuRaFPEPnMX5NKedcPUZnpKBaM8om6OdVA92Qv4XoyuwLWOs79yb75K3Llm276_yPVL_zQ50t6qYP_baBOOSXLvh9asy7oQ5wn12FfnB2SLWx5Deuy653YX_MfyMrN9TQZDf9ve-SFjSN6zbuCXpUQRPd02Ocotv3724WH_PV5w_LxXyVW6HEkIOgUkuqAfOKiDKtiRVnQlJZ6bWQznIgWpclEwpsqVIoi2ItMCvXBeeCsSm6OOhud-vWldZ1Q4DGbINvIXw3PXjzb6fztdn0e0MYlljoJPDqKBD6bzsXB9P6aF2Truf6XTSFUoQTKv4LEs2kTmgC1QG0oY8xuOrPNgSb0WWTXDaSGULN6LIZXTajy2n02d-_OQ0ebU3AyyMA0UJTBeisjycunRKP4BS9OHC139R3PjgDsTU-XeP0boKeH6AKegObkIRurylOlyGYE8II-wV4ncbP</recordid><startdate>20051201</startdate><enddate>20051201</enddate><creator>Koya, Vijay</creator><creator>Moayeri, Mahtab</creator><creator>Leppla, Stephen H</creator><creator>Daniell, Henry</creator><general>American Society for Microbiology</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T5</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20051201</creationdate><title>Plant-Based Vaccine: Mice Immunized with Chloroplast-Derived Anthrax Protective Antigen Survive Anthrax Lethal Toxin Challenge</title><author>Koya, Vijay ; Moayeri, Mahtab ; Leppla, Stephen H ; Daniell, Henry</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c585t-a5279729a04f15dacc08435727f9b57ec4a199dd358acd8358d66b503db644533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Anthrax - prevention & control</topic><topic>Anthrax Vaccines - administration & dosage</topic><topic>Anthrax Vaccines - genetics</topic><topic>Anthrax Vaccines - immunology</topic><topic>Antigens, Bacterial - biosynthesis</topic><topic>Antigens, Bacterial - genetics</topic><topic>Antigens, Bacterial - immunology</topic><topic>Applied microbiology</topic><topic>Bacillus anthracis</topic><topic>Bacterial Toxins - biosynthesis</topic><topic>Bacterial Toxins - genetics</topic><topic>Bacterial Toxins - immunology</topic><topic>Biological and medical sciences</topic><topic>Blotting, Southern</topic><topic>Chloroplasts - genetics</topic><topic>Chloroplasts - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Immune Sera - immunology</topic><topic>Immunization</topic><topic>Immunoblotting</topic><topic>Immunoglobulin G - blood</topic><topic>Macrophages - drug effects</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Microbial Immunity and Vaccines</topic><topic>Microbiology</topic><topic>Nicotiana - genetics</topic><topic>Nicotiana - metabolism</topic><topic>Plant Leaves - genetics</topic><topic>Plant Leaves - metabolism</topic><topic>Plants, Genetically Modified - genetics</topic><topic>Plants, Genetically Modified - metabolism</topic><topic>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koya, Vijay</creatorcontrib><creatorcontrib>Moayeri, Mahtab</creatorcontrib><creatorcontrib>Leppla, Stephen H</creatorcontrib><creatorcontrib>Daniell, Henry</creatorcontrib><collection>AGRIS</collection><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>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Infection and Immunity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koya, Vijay</au><au>Moayeri, Mahtab</au><au>Leppla, Stephen H</au><au>Daniell, Henry</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plant-Based Vaccine: Mice Immunized with Chloroplast-Derived Anthrax Protective Antigen Survive Anthrax Lethal Toxin Challenge</atitle><jtitle>Infection and Immunity</jtitle><addtitle>Infect Immun</addtitle><date>2005-12-01</date><risdate>2005</risdate><volume>73</volume><issue>12</issue><spage>8266</spage><epage>8274</epage><pages>8266-8274</pages><issn>0019-9567</issn><eissn>1098-5522</eissn><coden>INFIBR</coden><abstract>The currently available human vaccine for anthrax, derived from the culture supernatant of Bacillus anthracis, contains the protective antigen (PA) and traces of the lethal and edema factors, which may contribute to adverse side effects associated with this vaccine. Therefore, an effective expression system that can provide a clean, safe, and efficacious vaccine is required. In an effort to produce anthrax vaccine in large quantities and free of extraneous bacterial contaminants, PA was expressed in transgenic tobacco chloroplasts by inserting the pagA gene into the chloroplast genome. Chloroplast integration of the pagA gene was confirmed by PCR and Southern analysis. Mature leaves grown under continuous illumination contained PA as up to 14.2% of the total soluble protein. Cytotoxicity measurements in macrophage lysis assays showed that chloroplast-derived PA was equal in potency to PA produced in B. anthracis. Subcutaneous immunization of mice with partially purified chloroplast-derived or B. anthracis-derived PA with adjuvant yielded immunoglobulin G titers up to 1:320,000, and both groups of mice survived (100%) challenge with lethal doses of toxin. An average yield of about 150 mg of PA per plant should produce 360 million doses of a purified vaccine free of bacterial toxins edema factor and lethal factor from 1 acre of land. Such high expression levels without using fermenters and the immunoprotection offered by the chloroplast-derived PA should facilitate development of a cleaner and safer anthrax vaccine at a lower production cost. These results demonstrate the immunogenic and immunoprotective properties of plant-derived anthrax vaccine antigen.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>16299323</pmid><doi>10.1128/IAI.73.12.8266-8274.2005</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Anthrax - prevention & control Anthrax Vaccines - administration & dosage Anthrax Vaccines - genetics Anthrax Vaccines - immunology Antigens, Bacterial - biosynthesis Antigens, Bacterial - genetics Antigens, Bacterial - immunology Applied microbiology Bacillus anthracis Bacterial Toxins - biosynthesis Bacterial Toxins - genetics Bacterial Toxins - immunology Biological and medical sciences Blotting, Southern Chloroplasts - genetics Chloroplasts - metabolism Fundamental and applied biological sciences. Psychology Immune Sera - immunology Immunization Immunoblotting Immunoglobulin G - blood Macrophages - drug effects Mice Mice, Inbred BALB C Microbial Immunity and Vaccines Microbiology Nicotiana - genetics Nicotiana - metabolism Plant Leaves - genetics Plant Leaves - metabolism Plants, Genetically Modified - genetics Plants, Genetically Modified - metabolism Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) |
title | Plant-Based Vaccine: Mice Immunized with Chloroplast-Derived Anthrax Protective Antigen Survive Anthrax Lethal Toxin Challenge |
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