Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/53330
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dc.contributor.authorOgunniyi, A.-
dc.contributor.authorPaton, J.-
dc.contributor.authorKirby, A.-
dc.contributor.authorMcCullers, J.-
dc.contributor.authorCook, J.-
dc.contributor.authorHyodo, M.-
dc.contributor.authorHayakawa, Y.-
dc.contributor.authorKaraolis, D.-
dc.date.issued2008-
dc.identifier.citationVaccine, 2008; 26(36):4676-4685-
dc.identifier.issn0264-410X-
dc.identifier.issn1873-2518-
dc.identifier.urihttp://hdl.handle.net/2440/53330-
dc.descriptionCopyright © 2008 Elsevier Ltd All rights reserved.-
dc.description.abstractCyclic diguanylate (c-di-GMP) is a unique bacterial intracellular signaling molecule capable of stimulating enhanced protective innate immunity against various bacterial infections. The effects of intranasal pretreatment with c-di-GMP, or intraperitoneal coadministration of c-di-GMP with the pneumolysin toxoid (PdB) or pneumococcal surface protein A (PspA) before pneumococcal challenge, were investigated in mice. We found that c-di-GMP had no significant direct short-term effect on the growth rate of Streptococcus pneumoniae either in vitro or in vivo. However, intranasal pretreatment of mice with c-di-GMP resulted in a significant decrease in bacterial load in lungs and blood after serotypes 2 and 3 challenge, and a significant decrease in lung titers after serotype 4 challenge. Potential cellular mediators of these enhanced protective responses were identified in lungs and draining lymph nodes. Intraperitoneal coadministration of c-di-GMP with PdB or PspA before challenge resulted in significantly higher antigen-specific antibody titers and increased survival of mice, compared to that obtained with alum adjuvant. These findings demonstrate that local or systemic c-di-GMP administration stimulates innate and adaptive immunity against invasive pneumococcal disease. We propose that c-di-GMP can be used as an effective broad spectrum immunomodulator and vaccine adjuvant to prevent infectious diseases.-
dc.description.statementofresponsibilityAbiodun D. Ogunniyi, James C. Paton, Alun C. Kirby, Jonathan A. McCullers, Jan Cook, Mamoru Hyodo, Yoshihiro Hayakawa and David K.R. Karaolis-
dc.description.urihttp://www.elsevier.com/wps/find/journaldescription.cws_home/30521/description#description-
dc.language.isoen-
dc.publisherElsevier Sci Ltd-
dc.source.urihttp://dx.doi.org/10.1016/j.vaccine.2008.06.099-
dc.subjectLung-
dc.subjectLymph Nodes-
dc.subjectBlood-
dc.subjectAnimals-
dc.subjectMice, Inbred BALB C-
dc.subjectMice-
dc.subjectStreptococcus pneumoniae-
dc.subjectPneumococcal Infections-
dc.subjectAlum Compounds-
dc.subjectBacterial Proteins-
dc.subjectCyclic GMP-
dc.subjectStreptolysins-
dc.subjectPneumococcal Vaccines-
dc.subjectImmunologic Factors-
dc.subjectAdjuvants, Immunologic-
dc.subjectAntibodies, Bacterial-
dc.subjectColony Count, Microbial-
dc.subjectAdministration, Intranasal-
dc.subjectInjections, Intraperitoneal-
dc.subjectSurvival Analysis-
dc.subjectFemale-
dc.subjectMale-
dc.titleC-di-GMP is an effective immunomodulator and vaccine adjuvant against pneumococcal infection-
dc.typeJournal article-
dc.identifier.doi10.1016/j.vaccine.2008.06.099-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/284214-
pubs.publication-statusPublished-
dc.identifier.orcidOgunniyi, A. [0000-0001-9308-5629]-
dc.identifier.orcidPaton, J. [0000-0001-9807-5278]-
Appears in Collections:Aurora harvest 5
Molecular and Biomedical Science publications

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