Protective immunity against Eimeria tenella infection in chickens following oral immunization with Bacillus subtilis expressing Eimeria tenella 3-1E protein
The current experiment was conducted to construct recombinant Bacillus subtilis WB600 expressing Eimeria tenella 3-1E protein to investigate the oral immunization protective effects against E. tenella. The merozoite surface antigen 3-1E gene of E. tenella was introduced into the pBS-H1 expression ve...
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Veröffentlicht in: | Parasitology research (1987) 2015-09, Vol.114 (9), p.3229-3236 |
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description | The current experiment was conducted to construct recombinant Bacillus subtilis WB600 expressing Eimeria tenella 3-1E protein to investigate the oral immunization protective effects against E. tenella. The merozoite surface antigen 3-1E gene of E. tenella was introduced into the pBS-H1 expression vector with a novel signal peptide sequence. After the electro-transformation, the expression of objective protein in B. subtilis WB600 was detected by Western blot. The results showed that the recombinant B. subtilis strain with the ability of high-level secretion of 3-1E was constructed successfully. Seven-day-old broiler chickens were orally vaccinated with B. subtilis WB600 harboring 3-1E (B.S-pBS-H1-3-1E) or B. subtilis WB600 with empty plasmid (B.S-pBS-H1) 10 days prior to challenge with sporulated E. tenella oocysts. The results showed the recombinant B. subtilis strain with the ability of high-level secretion of 3-1E was constructed successfully. Vaccination with B.S-pBS-H1-3-1E strain significantly increased the anti-coccidial index and reduced cecal lesion scores compared with the positive control group (chickens were challenged with sporulated E. tenella oocysts without oral administration of B.S-pBS-H1-3-1E strain) and B.S-pBS-H1 group. Ceca mucosal sIgA, secretion, and IL-2, IL-12, IFN-γ, and IL-10 level after challenge were greater in the B.S-pBS-H1-3-1E group than in the positive control group. Taken together, these results indicated that B. subtilis WB600 harboring 3-1E protein induces protective immunity against E. tenella. |
doi_str_mv | 10.1007/s00436-015-4539-3 |
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The merozoite surface antigen 3-1E gene of E. tenella was introduced into the pBS-H1 expression vector with a novel signal peptide sequence. After the electro-transformation, the expression of objective protein in B. subtilis WB600 was detected by Western blot. The results showed that the recombinant B. subtilis strain with the ability of high-level secretion of 3-1E was constructed successfully. Seven-day-old broiler chickens were orally vaccinated with B. subtilis WB600 harboring 3-1E (B.S-pBS-H1-3-1E) or B. subtilis WB600 with empty plasmid (B.S-pBS-H1) 10 days prior to challenge with sporulated E. tenella oocysts. The results showed the recombinant B. subtilis strain with the ability of high-level secretion of 3-1E was constructed successfully. Vaccination with B.S-pBS-H1-3-1E strain significantly increased the anti-coccidial index and reduced cecal lesion scores compared with the positive control group (chickens were challenged with sporulated E. tenella oocysts without oral administration of B.S-pBS-H1-3-1E strain) and B.S-pBS-H1 group. Ceca mucosal sIgA, secretion, and IL-2, IL-12, IFN-γ, and IL-10 level after challenge were greater in the B.S-pBS-H1-3-1E group than in the positive control group. Taken together, these results indicated that B. subtilis WB600 harboring 3-1E protein induces protective immunity against E. tenella.</description><identifier>ISSN: 0932-0113</identifier><identifier>EISSN: 1432-1955</identifier><identifier>DOI: 10.1007/s00436-015-4539-3</identifier><identifier>PMID: 25994313</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Animals ; Apicomplexa ; Bacillus subtilis ; Bacillus subtilis - genetics ; Bacterial proteins ; Bacterial Vaccines - immunology ; Biomedical and Life Sciences ; Biomedicine ; Chickens ; Chickens - immunology ; Coccidiosis - prevention & control ; Coccidiosis - veterinary ; Eimeria tenella ; Eimeria tenella - metabolism ; Health aspects ; Host-parasite relationships ; Immunology ; Interleukin-12 - genetics ; Interleukin-2 ; Medical Microbiology ; Microbiology ; Original Paper ; Poultry Diseases - prevention & control ; Prevention ; Protozoan Proteins - immunology ; Recombinant Proteins - genetics ; Recombinant Proteins - metabolism ; Vaccination - methods</subject><ispartof>Parasitology research (1987), 2015-09, Vol.114 (9), p.3229-3236</ispartof><rights>Springer-Verlag Berlin Heidelberg 2015</rights><rights>COPYRIGHT 2015 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c501t-2a62668da7309727544fa2f6b025aa1903b61a59c61496c30a4e219c27acae43</citedby><cites>FETCH-LOGICAL-c501t-2a62668da7309727544fa2f6b025aa1903b61a59c61496c30a4e219c27acae43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00436-015-4539-3$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00436-015-4539-3$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25994313$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lin, Zhiwei</creatorcontrib><creatorcontrib>Shi, Yanyun</creatorcontrib><creatorcontrib>Deng, Bin</creatorcontrib><creatorcontrib>Mao, Xiangfei</creatorcontrib><creatorcontrib>Yu, Dongyou</creatorcontrib><creatorcontrib>Li, Weifen</creatorcontrib><title>Protective immunity against Eimeria tenella infection in chickens following oral immunization with Bacillus subtilis expressing Eimeria tenella 3-1E protein</title><title>Parasitology research (1987)</title><addtitle>Parasitol Res</addtitle><addtitle>Parasitol Res</addtitle><description>The current experiment was conducted to construct recombinant Bacillus subtilis WB600 expressing Eimeria tenella 3-1E protein to investigate the oral immunization protective effects against E. tenella. The merozoite surface antigen 3-1E gene of E. tenella was introduced into the pBS-H1 expression vector with a novel signal peptide sequence. After the electro-transformation, the expression of objective protein in B. subtilis WB600 was detected by Western blot. The results showed that the recombinant B. subtilis strain with the ability of high-level secretion of 3-1E was constructed successfully. Seven-day-old broiler chickens were orally vaccinated with B. subtilis WB600 harboring 3-1E (B.S-pBS-H1-3-1E) or B. subtilis WB600 with empty plasmid (B.S-pBS-H1) 10 days prior to challenge with sporulated E. tenella oocysts. The results showed the recombinant B. subtilis strain with the ability of high-level secretion of 3-1E was constructed successfully. Vaccination with B.S-pBS-H1-3-1E strain significantly increased the anti-coccidial index and reduced cecal lesion scores compared with the positive control group (chickens were challenged with sporulated E. tenella oocysts without oral administration of B.S-pBS-H1-3-1E strain) and B.S-pBS-H1 group. Ceca mucosal sIgA, secretion, and IL-2, IL-12, IFN-γ, and IL-10 level after challenge were greater in the B.S-pBS-H1-3-1E group than in the positive control group. Taken together, these results indicated that B. subtilis WB600 harboring 3-1E protein induces protective immunity against E. tenella.</description><subject>Animals</subject><subject>Apicomplexa</subject><subject>Bacillus subtilis</subject><subject>Bacillus subtilis - genetics</subject><subject>Bacterial proteins</subject><subject>Bacterial Vaccines - immunology</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Chickens</subject><subject>Chickens - immunology</subject><subject>Coccidiosis - prevention & control</subject><subject>Coccidiosis - veterinary</subject><subject>Eimeria tenella</subject><subject>Eimeria tenella - metabolism</subject><subject>Health aspects</subject><subject>Host-parasite relationships</subject><subject>Immunology</subject><subject>Interleukin-12 - genetics</subject><subject>Interleukin-2</subject><subject>Medical Microbiology</subject><subject>Microbiology</subject><subject>Original Paper</subject><subject>Poultry Diseases - prevention & control</subject><subject>Prevention</subject><subject>Protozoan Proteins - immunology</subject><subject>Recombinant Proteins - genetics</subject><subject>Recombinant Proteins - metabolism</subject><subject>Vaccination - methods</subject><issn>0932-0113</issn><issn>1432-1955</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkt1u1DAQhSMEokvhAbgBS9xwk-LxX9aXbbX8SJVAolxbs14ndUnsxU4o5Vl4WByyIIEQQr7wyP7OzOjoVNVjoCdAafMiUyq4qinIWkiua36nWoHgrAYt5d1qRXWpKQA_qh7kfE0pNEqI-9URk1oLDnxVfXuX4ujs6D874odhCn68JdihD3kkGz-45JGMLri-R-JDO6MxlIrYK28_upBJG_s-3vjQkZiwP3T5ij-4Gz9ekTO0vu-nTPK0HX3vM3Ff9snlPGv-nMFr2JD9vJQPD6t7LfbZPTrcx9Xly83l-ev64u2rN-enF7WVFMaaoWJKrXfYcKob1kghWmSt2lImEUFTvlWAUlsFQivLKQrHQFvWoEUn-HH1fGlbxn6aXB7N4LOdtwkuTtlAA43QTfHuP1Aqi818zQr6bEE77J0p1sUxoZ1xcyqYVEDXShfq5C9UOTs3eBuDa315_00Ai8CmmHNyrdknP2C6NUDNnAqzpMKUVJg5FYYXzZPD1tN2cLtfip8xKABbgFy-QueSuY5TCsXzf3Z9uohajAa75LP58J5RUMWA4jNX_DuN0Mwg</recordid><startdate>20150901</startdate><enddate>20150901</enddate><creator>Lin, Zhiwei</creator><creator>Shi, Yanyun</creator><creator>Deng, Bin</creator><creator>Mao, Xiangfei</creator><creator>Yu, Dongyou</creator><creator>Li, Weifen</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><scope>FBQ</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>7X8</scope><scope>7T5</scope><scope>H94</scope><scope>M7N</scope></search><sort><creationdate>20150901</creationdate><title>Protective immunity against Eimeria tenella infection in chickens following oral immunization with Bacillus subtilis expressing Eimeria tenella 3-1E protein</title><author>Lin, Zhiwei ; Shi, Yanyun ; Deng, Bin ; Mao, Xiangfei ; Yu, Dongyou ; Li, Weifen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c501t-2a62668da7309727544fa2f6b025aa1903b61a59c61496c30a4e219c27acae43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Apicomplexa</topic><topic>Bacillus subtilis</topic><topic>Bacillus subtilis - genetics</topic><topic>Bacterial proteins</topic><topic>Bacterial Vaccines - immunology</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Chickens</topic><topic>Chickens - immunology</topic><topic>Coccidiosis - prevention & control</topic><topic>Coccidiosis - veterinary</topic><topic>Eimeria tenella</topic><topic>Eimeria tenella - metabolism</topic><topic>Health aspects</topic><topic>Host-parasite relationships</topic><topic>Immunology</topic><topic>Interleukin-12 - genetics</topic><topic>Interleukin-2</topic><topic>Medical Microbiology</topic><topic>Microbiology</topic><topic>Original Paper</topic><topic>Poultry Diseases - prevention & control</topic><topic>Prevention</topic><topic>Protozoan Proteins - immunology</topic><topic>Recombinant Proteins - genetics</topic><topic>Recombinant Proteins - metabolism</topic><topic>Vaccination - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Zhiwei</creatorcontrib><creatorcontrib>Shi, Yanyun</creatorcontrib><creatorcontrib>Deng, Bin</creatorcontrib><creatorcontrib>Mao, Xiangfei</creatorcontrib><creatorcontrib>Yu, Dongyou</creatorcontrib><creatorcontrib>Li, Weifen</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Parasitology research (1987)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Zhiwei</au><au>Shi, Yanyun</au><au>Deng, Bin</au><au>Mao, Xiangfei</au><au>Yu, Dongyou</au><au>Li, Weifen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protective immunity against Eimeria tenella infection in chickens following oral immunization with Bacillus subtilis expressing Eimeria tenella 3-1E protein</atitle><jtitle>Parasitology research (1987)</jtitle><stitle>Parasitol Res</stitle><addtitle>Parasitol Res</addtitle><date>2015-09-01</date><risdate>2015</risdate><volume>114</volume><issue>9</issue><spage>3229</spage><epage>3236</epage><pages>3229-3236</pages><issn>0932-0113</issn><eissn>1432-1955</eissn><abstract>The current experiment was conducted to construct recombinant Bacillus subtilis WB600 expressing Eimeria tenella 3-1E protein to investigate the oral immunization protective effects against E. tenella. The merozoite surface antigen 3-1E gene of E. tenella was introduced into the pBS-H1 expression vector with a novel signal peptide sequence. After the electro-transformation, the expression of objective protein in B. subtilis WB600 was detected by Western blot. The results showed that the recombinant B. subtilis strain with the ability of high-level secretion of 3-1E was constructed successfully. Seven-day-old broiler chickens were orally vaccinated with B. subtilis WB600 harboring 3-1E (B.S-pBS-H1-3-1E) or B. subtilis WB600 with empty plasmid (B.S-pBS-H1) 10 days prior to challenge with sporulated E. tenella oocysts. The results showed the recombinant B. subtilis strain with the ability of high-level secretion of 3-1E was constructed successfully. Vaccination with B.S-pBS-H1-3-1E strain significantly increased the anti-coccidial index and reduced cecal lesion scores compared with the positive control group (chickens were challenged with sporulated E. tenella oocysts without oral administration of B.S-pBS-H1-3-1E strain) and B.S-pBS-H1 group. Ceca mucosal sIgA, secretion, and IL-2, IL-12, IFN-γ, and IL-10 level after challenge were greater in the B.S-pBS-H1-3-1E group than in the positive control group. Taken together, these results indicated that B. subtilis WB600 harboring 3-1E protein induces protective immunity against E. tenella.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>25994313</pmid><doi>10.1007/s00436-015-4539-3</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Apicomplexa Bacillus subtilis Bacillus subtilis - genetics Bacterial proteins Bacterial Vaccines - immunology Biomedical and Life Sciences Biomedicine Chickens Chickens - immunology Coccidiosis - prevention & control Coccidiosis - veterinary Eimeria tenella Eimeria tenella - metabolism Health aspects Host-parasite relationships Immunology Interleukin-12 - genetics Interleukin-2 Medical Microbiology Microbiology Original Paper Poultry Diseases - prevention & control Prevention Protozoan Proteins - immunology Recombinant Proteins - genetics Recombinant Proteins - metabolism Vaccination - methods |
title | Protective immunity against Eimeria tenella infection in chickens following oral immunization with Bacillus subtilis expressing Eimeria tenella 3-1E protein |
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