Expression of Plasmodium falciparum Surface Antigens in Escherichia coli
The asexual blood stages of the human malarial parasite Plasmodium falciparum produce many antigens, only some of which are important for protective immunity. Most of the putative protective antigens are believed to be expressed in schizonts and merozoites, the late stages of the asexual cycle. With...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1985-04, Vol.82 (8), p.2518-2522 |
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description | The asexual blood stages of the human malarial parasite Plasmodium falciparum produce many antigens, only some of which are important for protective immunity. Most of the putative protective antigens are believed to be expressed in schizonts and merozoites, the late stages of the asexual cycle. With the aim of cloning and characterizing genes for important parasite antigens, we used late-stage P. falciparum mRNA to construct a library of cDNA sequences inserted in the Escherichia coli expression vector pUC8. Nine thousand clones from the expression library were immunologically screened in situ with serum from Aotus monkeys immune to P. falciparum, and 95 clones expressing parasite antigens were identified. Mice were immunized with lysates from 49 of the bacterial clones that reacted with Aotus sera, and the mouse sera were tested for their reactivity with parasite antigens by indirect immunofluorescence, immunoprecipitation, and immunoblotting assays. Several different P. falciparum antigens were identified by these assays. Indirect immunofluorescence studies of extracellular merozoites showed that three of these antigens appear to be located on the merozoite surface. Thus, we have identified cDNA clones to three different P. falciparum antigens that may be important in protective immunity. |
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Most of the putative protective antigens are believed to be expressed in schizonts and merozoites, the late stages of the asexual cycle. With the aim of cloning and characterizing genes for important parasite antigens, we used late-stage P. falciparum mRNA to construct a library of cDNA sequences inserted in the Escherichia coli expression vector pUC8. Nine thousand clones from the expression library were immunologically screened in situ with serum from Aotus monkeys immune to P. falciparum, and 95 clones expressing parasite antigens were identified. Mice were immunized with lysates from 49 of the bacterial clones that reacted with Aotus sera, and the mouse sera were tested for their reactivity with parasite antigens by indirect immunofluorescence, immunoprecipitation, and immunoblotting assays. Several different P. falciparum antigens were identified by these assays. Indirect immunofluorescence studies of extracellular merozoites showed that three of these antigens appear to be located on the merozoite surface. Thus, we have identified cDNA clones to three different P. falciparum antigens that may be important in protective immunity.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.82.8.2518</identifier><identifier>PMID: 3887406</identifier><identifier>CODEN: PNASA6</identifier><language>eng</language><publisher>Washington, DC: National Academy of Sciences of the United States of America</publisher><subject>Animals ; Antigens ; Antigens, Protozoan - genetics ; Antigens, Protozoan - isolation & purification ; Antigens, Surface - genetics ; Biochemistry. Physiology. Immunology. Molecular biology ; Biological and medical sciences ; Biotechnology ; Blood ; Cloning, Molecular ; Complementary DNA ; DNA - genetics ; Erythrocytes ; Escherichia coli ; Escherichia coli - genetics ; Escherichia coli - immunology ; Fundamental and applied biological sciences. Psychology ; Gels ; Genetic engineering ; Genetic technics ; Human protozoal diseases ; Infectious diseases ; Libraries ; Malaria ; Medical sciences ; Merozoites ; Methods. Procedures. Technologies ; Molecular cloning ; Parasites ; Parasitic diseases ; Parasitism ; Plasmodium falciparum ; Plasmodium falciparum - genetics ; Plasmodium falciparum - immunology ; Protozoa ; Protozoal diseases ; Schizonts ; Tropical medicine</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1985-04, Vol.82 (8), p.2518-2522</ispartof><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c516t-597e16b6c67e37a1ec5043e141074d99ca9cc2a5983788a1ad09801235809c363</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/82/8.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/25131$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/25131$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9150495$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3887406$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ardeshir, Feroza</creatorcontrib><creatorcontrib>Flint, Janette E.</creatorcontrib><creatorcontrib>Reese, Robert T.</creatorcontrib><title>Expression of Plasmodium falciparum Surface Antigens in Escherichia coli</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>The asexual blood stages of the human malarial parasite Plasmodium falciparum produce many antigens, only some of which are important for protective immunity. Most of the putative protective antigens are believed to be expressed in schizonts and merozoites, the late stages of the asexual cycle. With the aim of cloning and characterizing genes for important parasite antigens, we used late-stage P. falciparum mRNA to construct a library of cDNA sequences inserted in the Escherichia coli expression vector pUC8. Nine thousand clones from the expression library were immunologically screened in situ with serum from Aotus monkeys immune to P. falciparum, and 95 clones expressing parasite antigens were identified. Mice were immunized with lysates from 49 of the bacterial clones that reacted with Aotus sera, and the mouse sera were tested for their reactivity with parasite antigens by indirect immunofluorescence, immunoprecipitation, and immunoblotting assays. Several different P. falciparum antigens were identified by these assays. Indirect immunofluorescence studies of extracellular merozoites showed that three of these antigens appear to be located on the merozoite surface. Thus, we have identified cDNA clones to three different P. falciparum antigens that may be important in protective immunity.</description><subject>Animals</subject><subject>Antigens</subject><subject>Antigens, Protozoan - genetics</subject><subject>Antigens, Protozoan - isolation & purification</subject><subject>Antigens, Surface - genetics</subject><subject>Biochemistry. Physiology. Immunology. Molecular biology</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Blood</subject><subject>Cloning, Molecular</subject><subject>Complementary DNA</subject><subject>DNA - genetics</subject><subject>Erythrocytes</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - immunology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gels</subject><subject>Genetic engineering</subject><subject>Genetic technics</subject><subject>Human protozoal diseases</subject><subject>Infectious diseases</subject><subject>Libraries</subject><subject>Malaria</subject><subject>Medical sciences</subject><subject>Merozoites</subject><subject>Methods. Procedures. Technologies</subject><subject>Molecular cloning</subject><subject>Parasites</subject><subject>Parasitic diseases</subject><subject>Parasitism</subject><subject>Plasmodium falciparum</subject><subject>Plasmodium falciparum - genetics</subject><subject>Plasmodium falciparum - immunology</subject><subject>Protozoa</subject><subject>Protozoal diseases</subject><subject>Schizonts</subject><subject>Tropical medicine</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFrFDEYxYModa1ePQjCHKS3mSaTZJIcPJSytULBgnoOX7OZbkomGZMZqf-9WXYdVij0lMDvvS_vy0PoPcENwYKejwFyI9tGNi0n8gVaEaxI3TGFX6IVxq2oJWvZa_Qm5weMseISn6ATKqVguFuh6_XjmGzOLoYq9tWthzzEjZuHqgdv3AipXL_PqQdjq4swuXsbcuVCtc5ma5MzWweVid69Ra-KI9t3h_MU_bxa_7i8rm--ffl6eXFTG066qeZKWNLddaYTlgog1nDMqCWsLMM2ShlQxrTAlaRCSiCwwUpi0tKSWxna0VP0eT93nO8GuzE2TAm8HpMbIP3REZz-nwS31ffxt6ZKcIWL_-zgT_HXbPOkB5eN9R6CjXPWosOKiZY8KySMlpCcFWGzF5oUc062X8IQrHcd6V1HWrZa6l1HxfDxeIVFfiil8E8HDtmA7xME4_IiU6R8meJHAXfj_9HlGd3P3k_2cTp670lh4R_2_CFPMS2CwiihfwGHa7qC</recordid><startdate>19850401</startdate><enddate>19850401</enddate><creator>Ardeshir, Feroza</creator><creator>Flint, Janette E.</creator><creator>Reese, Robert T.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><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>7T5</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19850401</creationdate><title>Expression of Plasmodium falciparum Surface Antigens in Escherichia coli</title><author>Ardeshir, Feroza ; Flint, Janette E. ; Reese, Robert T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c516t-597e16b6c67e37a1ec5043e141074d99ca9cc2a5983788a1ad09801235809c363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Animals</topic><topic>Antigens</topic><topic>Antigens, Protozoan - genetics</topic><topic>Antigens, Protozoan - isolation & purification</topic><topic>Antigens, Surface - genetics</topic><topic>Biochemistry. Physiology. Immunology. Molecular biology</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Blood</topic><topic>Cloning, Molecular</topic><topic>Complementary DNA</topic><topic>DNA - genetics</topic><topic>Erythrocytes</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - immunology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gels</topic><topic>Genetic engineering</topic><topic>Genetic technics</topic><topic>Human protozoal diseases</topic><topic>Infectious diseases</topic><topic>Libraries</topic><topic>Malaria</topic><topic>Medical sciences</topic><topic>Merozoites</topic><topic>Methods. Procedures. Technologies</topic><topic>Molecular cloning</topic><topic>Parasites</topic><topic>Parasitic diseases</topic><topic>Parasitism</topic><topic>Plasmodium falciparum</topic><topic>Plasmodium falciparum - genetics</topic><topic>Plasmodium falciparum - immunology</topic><topic>Protozoa</topic><topic>Protozoal diseases</topic><topic>Schizonts</topic><topic>Tropical medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ardeshir, Feroza</creatorcontrib><creatorcontrib>Flint, Janette E.</creatorcontrib><creatorcontrib>Reese, Robert T.</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>Nucleic Acids 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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ardeshir, Feroza</au><au>Flint, Janette E.</au><au>Reese, Robert T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of Plasmodium falciparum Surface Antigens in Escherichia coli</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1985-04-01</date><risdate>1985</risdate><volume>82</volume><issue>8</issue><spage>2518</spage><epage>2522</epage><pages>2518-2522</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><coden>PNASA6</coden><abstract>The asexual blood stages of the human malarial parasite Plasmodium falciparum produce many antigens, only some of which are important for protective immunity. Most of the putative protective antigens are believed to be expressed in schizonts and merozoites, the late stages of the asexual cycle. With the aim of cloning and characterizing genes for important parasite antigens, we used late-stage P. falciparum mRNA to construct a library of cDNA sequences inserted in the Escherichia coli expression vector pUC8. Nine thousand clones from the expression library were immunologically screened in situ with serum from Aotus monkeys immune to P. falciparum, and 95 clones expressing parasite antigens were identified. Mice were immunized with lysates from 49 of the bacterial clones that reacted with Aotus sera, and the mouse sera were tested for their reactivity with parasite antigens by indirect immunofluorescence, immunoprecipitation, and immunoblotting assays. Several different P. falciparum antigens were identified by these assays. Indirect immunofluorescence studies of extracellular merozoites showed that three of these antigens appear to be located on the merozoite surface. Thus, we have identified cDNA clones to three different P. falciparum antigens that may be important in protective immunity.</abstract><cop>Washington, DC</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>3887406</pmid><doi>10.1073/pnas.82.8.2518</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antigens Antigens, Protozoan - genetics Antigens, Protozoan - isolation & purification Antigens, Surface - genetics Biochemistry. Physiology. Immunology. Molecular biology Biological and medical sciences Biotechnology Blood Cloning, Molecular Complementary DNA DNA - genetics Erythrocytes Escherichia coli Escherichia coli - genetics Escherichia coli - immunology Fundamental and applied biological sciences. Psychology Gels Genetic engineering Genetic technics Human protozoal diseases Infectious diseases Libraries Malaria Medical sciences Merozoites Methods. Procedures. Technologies Molecular cloning Parasites Parasitic diseases Parasitism Plasmodium falciparum Plasmodium falciparum - genetics Plasmodium falciparum - immunology Protozoa Protozoal diseases Schizonts Tropical medicine |
title | Expression of Plasmodium falciparum Surface Antigens in Escherichia coli |
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