Hood Derek W, Randle Gaynor, Cox Andrew D, Makepeace Katherine, Li Jianjun, Schweda Elke K H, Richards James C, Moxon E Richard
Molecular Infectious Diseases Group, University of Oxford Department of Paediatrics, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DS, United Kingdom.
J Bacteriol. 2004 Nov;186(21):7429-39. doi: 10.1128/JB.186.21.7429-7439.2004.
It is generally thought that mucosal bacterial pathogens of the genera Haemophilus, Neisseria, and Moraxella elaborate lipopolysaccharide (LPS) that is fundamentally different from that of enteric organisms that express O-specific polysaccharide side chains. Haemophilus influenzae elaborates short-chain LPS that has a role in the pathogenesis of H. influenzae infections. We show that the synthesis of LPS in this organism can no longer be as clearly distinguished from that in other gram-negative bacteria that express an O antigen. We provide evidence that a region of the H. influenzae genome, the hmg locus, is involved in the synthesis of glycoforms in which tetrasaccharide units are added en bloc, not stepwise, to the normal core glycoforms, similar to the biosynthesis of an O-antigen.
一般认为,嗜血杆菌属、奈瑟菌属和莫拉克斯氏菌属的黏膜细菌病原体所产生的脂多糖(LPS)与表达O特异性多糖侧链的肠道微生物的脂多糖有根本区别。流感嗜血杆菌产生的短链LPS在流感嗜血杆菌感染的发病机制中起作用。我们发现,该生物体中LPS的合成与其他表达O抗原的革兰氏阴性细菌的合成不再能如此清晰地区分开来。我们提供的证据表明,流感嗜血杆菌基因组的一个区域,即hmg位点,参与了糖型的合成,在这种糖型中,四糖单位是作为一个整体添加到正常核心糖型上,而不是逐步添加,这类似于O抗原的生物合成。