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Fasciola gigantica vaccine construct: an in silico approach towards identification and design of a multi-epitope subunit vaccine using calcium binding EF-hand proteins
Continuous attempts have been made to pinpoint candidate vaccine molecules and evaluate their effectiveness in order to commercialise such vaccines for the treatment of tropical fascioliasis in livestock. The pathophysiology of fascioliasis can be related to liver damage brought on by immature fluke...
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Published in: | BMC immunology 2023-01, Vol.24 (1), p.1-1, Article 1 |
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description | Continuous attempts have been made to pinpoint candidate vaccine molecules and evaluate their effectiveness in order to commercialise such vaccines for the treatment of tropical fascioliasis in livestock. The pathophysiology of fascioliasis can be related to liver damage brought on by immature flukes that migrate and feed, as well as immunological reactions to chemicals produced by the parasites and alarm signals brought on by tissue damage. Future research should, in our opinion, concentrate on the biology of invasive parasites and the resulting immune responses, particularly in the early stages of infection. The goal of the current study was to use the calcium-binding proteins from F. gigantica to create a multi-epitope subunit vaccine. The adjuvant, B-cell epitopes, CTL epitopes, and HTL epitopes that make up the vaccine construct are all connected by certain linkers. The antigenicity, allergenicity, and physiochemical properties of the vaccine construct were examined. The vaccine construct was docked with toll-like receptor 2, and simulations of the molecular dynamics of the complex's stability, interaction, and dynamics were run. After performing in silico cloning and immunosimulation, it was discovered that the construct was suitable for further investigation. New vaccination technologies and adjuvant development are advancing our food safety procedures since vaccines are seen as safe and are accepted by the user community. This research is also applicable to the F. hepatica system. |
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The pathophysiology of fascioliasis can be related to liver damage brought on by immature flukes that migrate and feed, as well as immunological reactions to chemicals produced by the parasites and alarm signals brought on by tissue damage. Future research should, in our opinion, concentrate on the biology of invasive parasites and the resulting immune responses, particularly in the early stages of infection. The goal of the current study was to use the calcium-binding proteins from F. gigantica to create a multi-epitope subunit vaccine. The adjuvant, B-cell epitopes, CTL epitopes, and HTL epitopes that make up the vaccine construct are all connected by certain linkers. The antigenicity, allergenicity, and physiochemical properties of the vaccine construct were examined. The vaccine construct was docked with toll-like receptor 2, and simulations of the molecular dynamics of the complex's stability, interaction, and dynamics were run. After performing in silico cloning and immunosimulation, it was discovered that the construct was suitable for further investigation. New vaccination technologies and adjuvant development are advancing our food safety procedures since vaccines are seen as safe and are accepted by the user community. This research is also applicable to the F. hepatica system.</description><identifier>ISSN: 1471-2172</identifier><identifier>EISSN: 1471-2172</identifier><identifier>DOI: 10.1186/s12865-022-00535-y</identifier><identifier>PMID: 36604615</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Animals ; Antigenic determinants ; Calcium ; Calcium binding EF-hand protein ; Calcium-binding proteins ; Computational Biology - methods ; Epitopes, B-Lymphocyte ; Epitopes, T-Lymphocyte ; Fasciola ; Fasciola gigantica ; Fascioliasis - prevention & control ; Fasciolosis ; Fluke infections ; Health aspects ; Immunoinformatics ; Immunological research ; Molecular Docking Simulation ; Parasite vaccines ; Prevention ; Vaccine ; Vaccines, Subunit - chemistry</subject><ispartof>BMC immunology, 2023-01, Vol.24 (1), p.1-1, Article 1</ispartof><rights>2023. The Author(s).</rights><rights>COPYRIGHT 2023 BioMed Central Ltd.</rights><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c520t-3f318b3c967ded978a093ba1d1841c1691b1138321692b45becbf3ca8d25bac03</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/PMC9813462/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813462/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,36992,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36604615$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Das, Kanhu Charan</creatorcontrib><creatorcontrib>Konhar, Ruchishree</creatorcontrib><creatorcontrib>Biswal, Devendra Kumar</creatorcontrib><title>Fasciola gigantica vaccine construct: an in silico approach towards identification and design of a multi-epitope subunit vaccine using calcium binding EF-hand proteins</title><title>BMC immunology</title><addtitle>BMC Immunol</addtitle><description>Continuous attempts have been made to pinpoint candidate vaccine molecules and evaluate their effectiveness in order to commercialise such vaccines for the treatment of tropical fascioliasis in livestock. The pathophysiology of fascioliasis can be related to liver damage brought on by immature flukes that migrate and feed, as well as immunological reactions to chemicals produced by the parasites and alarm signals brought on by tissue damage. Future research should, in our opinion, concentrate on the biology of invasive parasites and the resulting immune responses, particularly in the early stages of infection. The goal of the current study was to use the calcium-binding proteins from F. gigantica to create a multi-epitope subunit vaccine. The adjuvant, B-cell epitopes, CTL epitopes, and HTL epitopes that make up the vaccine construct are all connected by certain linkers. The antigenicity, allergenicity, and physiochemical properties of the vaccine construct were examined. The vaccine construct was docked with toll-like receptor 2, and simulations of the molecular dynamics of the complex's stability, interaction, and dynamics were run. After performing in silico cloning and immunosimulation, it was discovered that the construct was suitable for further investigation. New vaccination technologies and adjuvant development are advancing our food safety procedures since vaccines are seen as safe and are accepted by the user community. This research is also applicable to the F. hepatica system.</description><subject>Animals</subject><subject>Antigenic determinants</subject><subject>Calcium</subject><subject>Calcium binding EF-hand protein</subject><subject>Calcium-binding proteins</subject><subject>Computational Biology - methods</subject><subject>Epitopes, B-Lymphocyte</subject><subject>Epitopes, T-Lymphocyte</subject><subject>Fasciola</subject><subject>Fasciola gigantica</subject><subject>Fascioliasis - prevention & control</subject><subject>Fasciolosis</subject><subject>Fluke infections</subject><subject>Health aspects</subject><subject>Immunoinformatics</subject><subject>Immunological research</subject><subject>Molecular Docking Simulation</subject><subject>Parasite vaccines</subject><subject>Prevention</subject><subject>Vaccine</subject><subject>Vaccines, Subunit - chemistry</subject><issn>1471-2172</issn><issn>1471-2172</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNptUk1v1DAQjRCIlsIf4IAscYFDij8Sx-FQqaq6sFIlJD7O1sR2sq4SO9hOYX8RfxNvt6y6EvLB4_F7b8bjVxSvCT4nRPAPkVDB6xJTWmJcs7rcPilOSdWQkpKGPn0UnxQvYrzFmDSCiufFCeMcV5zUp8WfFURl_QhosAO4ZBWgO1DKOoOUdzGFRaWPCByyDkU7WuURzHPwoDYo-V8QdERWm8zsMzdZ7zJYI22iHRzyPQI0LWOypZlt8rNBcekWZ9OhyhKtG5CCUdllQp11ene-XpWbnU6ulIx18WXxrIcxmlcP-1nxY3X9_epzefPl0_rq8qZUNcWpZD0jomOq5Y02um0E4JZ1QDQRFVGEt6QjhAlGc0i7qu6M6nqmQGhad6AwOyvWe13t4VbOwU4QttKDlfcJHwYJIU9pNFIApbxjvWhZU5m-EqQlAEZozSvMK5G1LvZa89JNRqs8pADjkejxjbMbOfg72QrCKk6zwLsHgeB_LiYmOdmozDiCM36JkjactE3dsl3fb_fQAXJr1vU-K6odXF42jLJWYF5n1Pl_UHlpM-Wfdaa3OX9EeH9EyJhkfqcBlhjl-tvXYyzdY1XwMQbTH15KsNwZVu4NK7Nh5b1h5TaT3jye0YHyz6HsL8X26Iw</recordid><startdate>20230105</startdate><enddate>20230105</enddate><creator>Das, Kanhu Charan</creator><creator>Konhar, Ruchishree</creator><creator>Biswal, Devendra Kumar</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><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>ISR</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20230105</creationdate><title>Fasciola gigantica vaccine construct: an in silico approach towards identification and design of a multi-epitope subunit vaccine using calcium binding EF-hand proteins</title><author>Das, Kanhu Charan ; Konhar, Ruchishree ; Biswal, Devendra Kumar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c520t-3f318b3c967ded978a093ba1d1841c1691b1138321692b45becbf3ca8d25bac03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>Antigenic determinants</topic><topic>Calcium</topic><topic>Calcium binding EF-hand protein</topic><topic>Calcium-binding proteins</topic><topic>Computational Biology - methods</topic><topic>Epitopes, B-Lymphocyte</topic><topic>Epitopes, T-Lymphocyte</topic><topic>Fasciola</topic><topic>Fasciola gigantica</topic><topic>Fascioliasis - prevention & control</topic><topic>Fasciolosis</topic><topic>Fluke infections</topic><topic>Health aspects</topic><topic>Immunoinformatics</topic><topic>Immunological research</topic><topic>Molecular Docking Simulation</topic><topic>Parasite vaccines</topic><topic>Prevention</topic><topic>Vaccine</topic><topic>Vaccines, Subunit - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Das, Kanhu Charan</creatorcontrib><creatorcontrib>Konhar, Ruchishree</creatorcontrib><creatorcontrib>Biswal, Devendra Kumar</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>BMC immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Das, Kanhu Charan</au><au>Konhar, Ruchishree</au><au>Biswal, Devendra Kumar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fasciola gigantica vaccine construct: an in silico approach towards identification and design of a multi-epitope subunit vaccine using calcium binding EF-hand proteins</atitle><jtitle>BMC immunology</jtitle><addtitle>BMC Immunol</addtitle><date>2023-01-05</date><risdate>2023</risdate><volume>24</volume><issue>1</issue><spage>1</spage><epage>1</epage><pages>1-1</pages><artnum>1</artnum><issn>1471-2172</issn><eissn>1471-2172</eissn><abstract>Continuous attempts have been made to pinpoint candidate vaccine molecules and evaluate their effectiveness in order to commercialise such vaccines for the treatment of tropical fascioliasis in livestock. The pathophysiology of fascioliasis can be related to liver damage brought on by immature flukes that migrate and feed, as well as immunological reactions to chemicals produced by the parasites and alarm signals brought on by tissue damage. Future research should, in our opinion, concentrate on the biology of invasive parasites and the resulting immune responses, particularly in the early stages of infection. The goal of the current study was to use the calcium-binding proteins from F. gigantica to create a multi-epitope subunit vaccine. The adjuvant, B-cell epitopes, CTL epitopes, and HTL epitopes that make up the vaccine construct are all connected by certain linkers. The antigenicity, allergenicity, and physiochemical properties of the vaccine construct were examined. The vaccine construct was docked with toll-like receptor 2, and simulations of the molecular dynamics of the complex's stability, interaction, and dynamics were run. 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subjects | Animals Antigenic determinants Calcium Calcium binding EF-hand protein Calcium-binding proteins Computational Biology - methods Epitopes, B-Lymphocyte Epitopes, T-Lymphocyte Fasciola Fasciola gigantica Fascioliasis - prevention & control Fasciolosis Fluke infections Health aspects Immunoinformatics Immunological research Molecular Docking Simulation Parasite vaccines Prevention Vaccine Vaccines, Subunit - chemistry |
title | Fasciola gigantica vaccine construct: an in silico approach towards identification and design of a multi-epitope subunit vaccine using calcium binding EF-hand proteins |
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