Identification of a bifunctional lipopolysaccharide sialyltransferase in Haemophilus influenzae -: Incorporation of disialic acid

被引:53
作者
Fox, Kate L.
Cox, Andrew D.
Gilbert, Michel
Wakarchuk, Warren W.
Li, Jianjun
Makepeace, Katherine
Richards, James C.
Moxon, E. Richard
Hood, Derek W.
机构
[1] Univ Oxford, John Radcliffe Hosp, Dept Paediat, Mol Infect Dis Grp,Weatherall Inst Mol Med, Oxford OX3 9DS, England
[2] Natl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, Canada
基金
英国医学研究理事会;
关键词
D O I
10.1074/jbc.M602314200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The lipopolysaccharide (LPS) of non-typeable Haemophilus influenzae (NTHi) can be substituted at various positions by N-acetylneuraminic acid (Neu5Ac). LPS sialylation plays an important role in pathogenesis. The only LPS sialyltransferase characterized biochemically to date in H. influenzae is Lic3A, an alpha-2,3-sialyltransferase responsible for the addition of Neu5Ac to a lactose acceptor (Hood, D. W., Cox, A. D., Gilbert, M., Makepeace, K., Walsh, S., Deadman, M. E., Cody, A., Martin, A., Mansson, M., Schweda, E. K., Brisson, J.R., Richards, J.C., Moxon, E.R., and Wakarchuk, W.W. (2001) Mol. Microbiol. 39, 341-350). Here we describe a second sialyltransferase, Lic3B, that is a close homologue of Lic3A and present in 60% of NTHi isolates tested. A recombinant form of Lic3B was expressed in Escherichia coli and purified by affinity chromatography. We used synthetic fluorescent acceptors with a terminal lactose or sialyllactose to show that Lic3B has both alpha-2,3- and alpha-2,8-sialyltransferase activities. Structural analysis of LPS from lic3B mutant strains of NTHi confirmed that only monosialylated species were detectable, whereas disialylated species were detected upon inactivation of lic3A. Furthermore, introduction of lic3B into a lic3B-deficient strain background resulted in a significant increase in sialylation in the recipient strain. Mass spectrometric analysis of LPS indicated that glycoforms containing two Neu5Ac residues were evident that were not present in the LPS of the parent strain. These findings characterize the activity of a second sialyltransferase in H. influenzae, responsible for the addition of di-sialic acid to the LPS. Modification of the LPS by di-sialylation conferred increased resistance of the organism to the killing effects of normal human serum, as compared with mono-sialylated or non-sialylated species, indicating that this modification has biological significance.
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收藏
页码:40024 / 40032
页数:9
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