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|Title:||Development of live attenuated Bordetella pertussis strains expressing the universal influenza vaccine candidate M2e||Authors:||Li, R.
|Issue Date:||26-Jul-2011||Citation:||Li, R., Lim, A., Ow, S.T.L., Phoon, M.C., Locht, C., Chow, V.T., Alonso, S. (2011-07-26). Development of live attenuated Bordetella pertussis strains expressing the universal influenza vaccine candidate M2e. Vaccine 29 (33) : 5502-5511. ScholarBank@NUS Repository. https://doi.org/10.1016/j.vaccine.2011.05.052||Abstract:||The attenuated Bordetella pertussis BPZE1 vaccine strain represents an attractive platform for the delivery of heterologous vaccine candidates via the nasal route. The filamentous hemagglutinin (FHA) has been used to secrete or expose the foreign antigens at the bacterial surface. In this study, one, two and three copies of the Cys-containing ectodomain of matrix protein 2 (M2e) from influenza A virus were genetically fused to full length FHA and expressed in BPZE1. The secretion efficacy of the FHA-(M2e)1,2,3 chimera in the extracellular milieu and the ability of the recombinant bacteria to colonize the mouse lungs inversely correlated with the number of M2e copies fused to FHA. Nevertheless FHA-(M2e)3-producing bacteria (BPLR3) triggered the highest systemic anti-M2e antibody response upon nasal administration to BALB/c mice. Nasal immunization with BPLR3 bacteria resulted in a significant reduction in the viral loads upon challenge with H1N1/PR8 influenza A virus, but did not improve the survival rate compared to BPZE1-immunized mice. Furthermore, since previous work reported that disulfide bond formation in Cys-containing passenger antigens affects the secretion efficacy of the FHA chimera, the dsbA gene encoding a periplasmic disulfide isomerase was deleted in the FHA-(M2e)3-producing strain. Despite improving significantly the secretion efficacy of the FHA-(M2e)3 chimera, the dsbA deletion did not result in higher anti-M2e antibody titers in mice, due to impaired bacterial fitness and colonization ability. © 2011 Elsevier Ltd.||Source Title:||Vaccine||URI:||http://scholarbank.nus.edu.sg/handle/10635/126718||ISSN:||0264410X||DOI:||10.1016/j.vaccine.2011.05.052|
|Appears in Collections:||Staff Publications|
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