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Glycoconjugation of Shigella flexneri type 2a O-polysaccharide with CRM197 as a potential vaccine candidate for shigellosis
Shigellosis, a diarrheal disorder caused by an entero-invasive bacterium Shigella, is a major concern among children often leading to mortality. As most of these strains have developed universal antibiotic resistance, the development of a vaccine is crucial in combating the infection. The O-specific...
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Published in: | Biologicals 2021-07, Vol.72, p.1-9 |
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description | Shigellosis, a diarrheal disorder caused by an entero-invasive bacterium Shigella, is a major concern among children often leading to mortality. As most of these strains have developed universal antibiotic resistance, the development of a vaccine is crucial in combating the infection. The O-specific polysaccharide (O-PSs) from S. flexneri type 2a is considered to be the major disease-causing antigen in shigellosis. Therefore, the O-PSs conjugated with carrier proteins, can serve as a potential high molecular weight vaccine candidate. Accordingly, in the present study, O-PS extracted from S. flexneri 2a is conjugated with Cross-Reactive Material (CRM197), a non-toxic mutant of diphtheria toxin. We derivatized CRM197 and O-PS separately with adipic acid dihydrazide (ADH) and reacted with their counterparts to probe the conjugation efficacy. Among the two strategies, the CRM197-ADH treated with O-PS has yielded a stable glycoconjugate of 311 kDa. The conjugation efficiency has been probed by estimating the free protein, free O-PS and O-PS:CRM197 ratio using slot-blot, size exclusion and high-performance anion exchange chromatography techniques. The conjugate exhibited enhanced shelf-life of three months. The cytotoxicity studies with Vero/MRC-5 cells have confirmed the non-toxicity of the conjugate, which makes the glycoconjugate a potential vaccine candidate for shigellosis.
•CRM197-S. flexneri O-PS conjugate as a potential vaccine candidate for shigellosis.•ADH was used to separately activate CRM197 and O-PS for efficient conjugation.•ADH-CRM197 + O-PS conjugate yielded a high molecular weight immunogen (>300 kDa).•The glycoconjugate exhibited sustained shelf-life of over three months. |
doi_str_mv | 10.1016/j.biologicals.2021.07.001 |
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•CRM197-S. flexneri O-PS conjugate as a potential vaccine candidate for shigellosis.•ADH was used to separately activate CRM197 and O-PS for efficient conjugation.•ADH-CRM197 + O-PS conjugate yielded a high molecular weight immunogen (>300 kDa).•The glycoconjugate exhibited sustained shelf-life of over three months.</description><identifier>ISSN: 1045-1056</identifier><identifier>EISSN: 1095-8320</identifier><identifier>DOI: 10.1016/j.biologicals.2021.07.001</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Adipic acid dihydrazide ; CRM197 ; Glycoconjugate ; O-specific polysaccharide ; Shigellosis</subject><ispartof>Biologicals, 2021-07, Vol.72, p.1-9</ispartof><rights>2021 International Alliance for Biological Standardization</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c354t-399d4c2cc2f379269d0ca2c454e587b50b1c364ea705e3875901a3a504a3c6c43</citedby><cites>FETCH-LOGICAL-c354t-399d4c2cc2f379269d0ca2c454e587b50b1c364ea705e3875901a3a504a3c6c43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Narayana, P.V.S.L.S.S.</creatorcontrib><creatorcontrib>Dutta, Jayati Ray</creatorcontrib><title>Glycoconjugation of Shigella flexneri type 2a O-polysaccharide with CRM197 as a potential vaccine candidate for shigellosis</title><title>Biologicals</title><description>Shigellosis, a diarrheal disorder caused by an entero-invasive bacterium Shigella, is a major concern among children often leading to mortality. As most of these strains have developed universal antibiotic resistance, the development of a vaccine is crucial in combating the infection. The O-specific polysaccharide (O-PSs) from S. flexneri type 2a is considered to be the major disease-causing antigen in shigellosis. Therefore, the O-PSs conjugated with carrier proteins, can serve as a potential high molecular weight vaccine candidate. Accordingly, in the present study, O-PS extracted from S. flexneri 2a is conjugated with Cross-Reactive Material (CRM197), a non-toxic mutant of diphtheria toxin. We derivatized CRM197 and O-PS separately with adipic acid dihydrazide (ADH) and reacted with their counterparts to probe the conjugation efficacy. Among the two strategies, the CRM197-ADH treated with O-PS has yielded a stable glycoconjugate of 311 kDa. The conjugation efficiency has been probed by estimating the free protein, free O-PS and O-PS:CRM197 ratio using slot-blot, size exclusion and high-performance anion exchange chromatography techniques. The conjugate exhibited enhanced shelf-life of three months. The cytotoxicity studies with Vero/MRC-5 cells have confirmed the non-toxicity of the conjugate, which makes the glycoconjugate a potential vaccine candidate for shigellosis.
•CRM197-S. flexneri O-PS conjugate as a potential vaccine candidate for shigellosis.•ADH was used to separately activate CRM197 and O-PS for efficient conjugation.•ADH-CRM197 + O-PS conjugate yielded a high molecular weight immunogen (>300 kDa).•The glycoconjugate exhibited sustained shelf-life of over three months.</description><subject>Adipic acid dihydrazide</subject><subject>CRM197</subject><subject>Glycoconjugate</subject><subject>O-specific polysaccharide</subject><subject>Shigellosis</subject><issn>1045-1056</issn><issn>1095-8320</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqNkE1P20AQhq2qlUpp_8P2xsVm9suOj1UEtBIIiY_zajIeJxsZr9ndUCL-fB2FQ4-cZg7P-2rmKYqfEioJsj7fVisfhrD2hEOqFChZQVMByE_FiYTWlgut4PNhN7aUYOuvxbeUtjMgTWNOirerYU-BwrjdrTH7MIrQi_uNX_MwoOgHfh05epH3EwuF4racwrBPSLTB6DsWf33eiOXdjWwbgUmgmELmMXscxMtM-ZEF4dj5DjOLPkSRjt0h-fS9-NLPV_OP93laPF5ePCx_l9e3V3-Wv65L0tbkUrdtZ0gRqV43rarbDggVGWvYLpqVhZUkXRvGBizrRWNbkKjRgkFNNRl9Wpwde6cYnnecsnvyiQ4Pjhx2ySlrodYw25nR9ohSDClF7t0U_RPGvZPgDsLd1v0n3B2EO2jc7HPOLo9Znn958RxdIs8jcecjU3Zd8B9o-Qcix5Ba</recordid><startdate>202107</startdate><enddate>202107</enddate><creator>Narayana, P.V.S.L.S.S.</creator><creator>Dutta, Jayati Ray</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202107</creationdate><title>Glycoconjugation of Shigella flexneri type 2a O-polysaccharide with CRM197 as a potential vaccine candidate for shigellosis</title><author>Narayana, P.V.S.L.S.S. ; Dutta, Jayati Ray</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c354t-399d4c2cc2f379269d0ca2c454e587b50b1c364ea705e3875901a3a504a3c6c43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adipic acid dihydrazide</topic><topic>CRM197</topic><topic>Glycoconjugate</topic><topic>O-specific polysaccharide</topic><topic>Shigellosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Narayana, P.V.S.L.S.S.</creatorcontrib><creatorcontrib>Dutta, Jayati Ray</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biologicals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Narayana, P.V.S.L.S.S.</au><au>Dutta, Jayati Ray</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glycoconjugation of Shigella flexneri type 2a O-polysaccharide with CRM197 as a potential vaccine candidate for shigellosis</atitle><jtitle>Biologicals</jtitle><date>2021-07</date><risdate>2021</risdate><volume>72</volume><spage>1</spage><epage>9</epage><pages>1-9</pages><issn>1045-1056</issn><eissn>1095-8320</eissn><abstract>Shigellosis, a diarrheal disorder caused by an entero-invasive bacterium Shigella, is a major concern among children often leading to mortality. As most of these strains have developed universal antibiotic resistance, the development of a vaccine is crucial in combating the infection. The O-specific polysaccharide (O-PSs) from S. flexneri type 2a is considered to be the major disease-causing antigen in shigellosis. Therefore, the O-PSs conjugated with carrier proteins, can serve as a potential high molecular weight vaccine candidate. Accordingly, in the present study, O-PS extracted from S. flexneri 2a is conjugated with Cross-Reactive Material (CRM197), a non-toxic mutant of diphtheria toxin. We derivatized CRM197 and O-PS separately with adipic acid dihydrazide (ADH) and reacted with their counterparts to probe the conjugation efficacy. Among the two strategies, the CRM197-ADH treated with O-PS has yielded a stable glycoconjugate of 311 kDa. The conjugation efficiency has been probed by estimating the free protein, free O-PS and O-PS:CRM197 ratio using slot-blot, size exclusion and high-performance anion exchange chromatography techniques. The conjugate exhibited enhanced shelf-life of three months. The cytotoxicity studies with Vero/MRC-5 cells have confirmed the non-toxicity of the conjugate, which makes the glycoconjugate a potential vaccine candidate for shigellosis.
•CRM197-S. flexneri O-PS conjugate as a potential vaccine candidate for shigellosis.•ADH was used to separately activate CRM197 and O-PS for efficient conjugation.•ADH-CRM197 + O-PS conjugate yielded a high molecular weight immunogen (>300 kDa).•The glycoconjugate exhibited sustained shelf-life of over three months.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.biologicals.2021.07.001</doi><tpages>9</tpages></addata></record> |
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subjects | Adipic acid dihydrazide CRM197 Glycoconjugate O-specific polysaccharide Shigellosis |
title | Glycoconjugation of Shigella flexneri type 2a O-polysaccharide with CRM197 as a potential vaccine candidate for shigellosis |
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