Please use this identifier to cite or link to this item: https://doi.org/10.1128/IAI.73.7.4295-4301.2005
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dc.titleProduction of nontypeable Haemophilus influenzae HtrA by recombinant Bordetella pertussis with the use of filamentous hemagglutinin as a carrier
dc.contributor.authorAlonso, S.
dc.contributor.authorWillery, E.
dc.contributor.authorRenauld-Mongénie, G.
dc.contributor.authorLocht, C.
dc.date.accessioned2016-12-13T05:36:47Z
dc.date.available2016-12-13T05:36:47Z
dc.date.issued2005-07
dc.identifier.citationAlonso, S., Willery, E., Renauld-Mongénie, G., Locht, C. (2005-07). Production of nontypeable Haemophilus influenzae HtrA by recombinant Bordetella pertussis with the use of filamentous hemagglutinin as a carrier. Infection and Immunity 73 (7) : 4295-4301. ScholarBank@NUS Repository. https://doi.org/10.1128/IAI.73.7.4295-4301.2005
dc.identifier.issn00199567
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/132808
dc.description.abstractBordetella pertussis, the etiologic agent of whooping cough, is a highly infectious human pathogen capable of inducing mucosal and systemic immune responses upon a single intranasal administration. In an attenuated, pertussis toxin (PTX)-deficient recombinant form, it may therefore constitute an efficient bacterial vector that is particularly well adapted for the delivery of heterologous antigens to the respiratory mucosa. Filamentous hemagglutinin (FHA) has been used as a carrier to present foreign antigens at the bacterial surface, thereby inducing local, systemic, and protective immune responses to these antigens in mice. Both full-length and truncated (Fha44) forms of FHA have been used for antigen presentation. To investigate the effect of the carrier (FHA or Fha44) on antibody responses to passenger antigens, we genetically fused the HtrA protein of nontypeable Haemophilus influenzae to either FHA form. The fha-htrA and Fha44 gene-htrA hybrids were expressed as single copies inserted into the chromosome of PTX-deficient B. pertussis. Both chimeras were secreted into the culture supernatants of the recombinant strains and were recognized by anti-FHA and anti-HtrA antibodies. Intranasal infection with the strain producing the FHA-HtrA hybrid led to significantly higher anti-HtrA and anti-FHA antibody titers than those obtained in mice infected with the Fha44-HtrA-producing strain. Interestingly, the B. pertussis strain producing the Fha44-HtrA chimera colonized the mouse lungs more efficiently than the parental, Fha44-producing strain and gave rise to higher anti-FHA antibody titers than those induced by the parental strain. Copyright © 2005, American Society for Microbiology. All Rights Reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1128/IAI.73.7.4295-4301.2005
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentMICROBIOLOGY
dc.description.doi10.1128/IAI.73.7.4295-4301.2005
dc.description.sourcetitleInfection and Immunity
dc.description.volume73
dc.description.issue7
dc.description.page4295-4301
dc.description.codenINFIB
dc.identifier.isiut000230151100056
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