Recombinant flagellin-PAL fusion protein of Legionella pneumophila induced cell-mediated and protective immunity against bacteremia in BALB/c mice
We report a new recombinant fusion protein composed of full-length Legionella pneumophila flagellin A and peptidoglycan-associated lipoprotein (PAL), rFLA-PAL, capable of inducing protective immunity against L. pneumophila . The recombinant protein was over expressed in Escherichia coli strain BL21...
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Veröffentlicht in: | World journal of microbiology & biotechnology 2017-09, Vol.33 (9), p.175-175, Article 175 |
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Sprache: | eng |
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Zusammenfassung: | We report a new recombinant fusion protein composed of full-length
Legionella pneumophila
flagellin A and peptidoglycan-associated lipoprotein (PAL), rFLA-PAL, capable of inducing protective immunity against
L. pneumophila
. The recombinant protein was over expressed in
Escherichia coli
strain BL21 (DE3) using pET-28a (+) expression vector (pET28a-
fla
A-
pal
) and purified by Ni
2+
exchange chromatography. Immunological properties of rFLA-PAL were assessed in a mouse model. Female BALB/c mice, immunized with rFLA-PAL, exhibited a rapid increase in serum antibody concentration against each of its protein portions. Furthermore, a strong activation of both innate and adaptive cell-mediated immunity was observed as indicated by antigen-specific splenocyte proliferation, IFN-γ and IL-12 production, and early production of TNF-α in the serum and in splenocyte cultures which were separately assessed against PAL and FLA. BALB/c mice were challenged with a lethal dose of
L. pneumophila
intravenously. In a 10-days follow-up after intravenous lethal challenge with
L. pneumophila
, a 100% survival rate was observed for mice immunized with rFLA-PAL, same as for those immunized with a sublethal dose of
L. pneumophila
. Based on the potent immune responses observed in mice immunized with rFLA-PAL, this recombinant fusion protein could be a potential vaccine candidate against the intracellular pathogen
L. pneumophila
. |
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ISSN: | 0959-3993 1573-0972 |
DOI: | 10.1007/s11274-017-2315-5 |