| Literature DB >> 35170309 |
Zahra Rashidijahanabad1,2, Meagan Kelly3, Mohammad Kamruzzaman4, Firdausi Qadri4, Taufiqur R Bhuiyan4, Hunter McFall-Boegeman1,2, Di Wu5, Grzegorz Piszczek5, Peng Xu6, Edward T Ryan3,7,8, Xuefei Huang1,2,9.
Abstract
Vibrio cholerae, a noninvasive mucosal pathogen, is endemic in more than 50 countries. Oral cholera vaccines, based on killed whole-cell strains of Vibrio cholerae, can provide significant protection in adults and children for 2-5 years. However, they have relatively limited direct protection in young children. To overcome current challenges, in this study, a potential conjugate vaccine was developed by linking O-specific polysaccharide (OSP) antigen purified from V. cholerae O1 El Tor Inaba strain PIC018 with Qβ virus-like particles efficiently via squarate chemistry. The Qβ-OSP conjugate was characterized with mass photometry (MP) on the whole particle level. Pertinent immunologic display of OSP was confirmed by immunoreactivity of the conjugate with convalescent phase samples from humans with cholera. Mouse immunization with the Qβ-OSP conjugate showed that the construct generated prominent and long-lasting IgG antibody responses against OSP, and the resulting antibodies could recognize the native lipopolysaccharide from Vibrio cholerae O1 Inaba. This was the first time that Qβ was conjugated with a bacterial polysaccharide for vaccine development, broadening the scope of this powerful carrier.Entities:
Keywords: O-specific polysaccharide; Vibrio cholera; bacteriophage Qβ; mass photometry; vaccine
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Year: 2022 PMID: 35170309 PMCID: PMC9119010 DOI: 10.1021/acsinfecdis.1c00585
Source DB: PubMed Journal: ACS Infect Dis ISSN: 2373-8227 Impact factor: 5.578