Shoji Mikio, Sato Keiko, Yukitake Hideharu, Naito Mariko, Nakayama Koji
Division of Microbiology and Oral Infection, Department of Molecular Microbiology and Immunology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, 852-8588, Japan.
Sci Rep. 2014 May 23;4:5056. doi: 10.1038/srep05056.
The periodontal pathogen Porphyromonas gingivalis has two different lipopolysaccharide (LPS) molecules, O-LPS and A-LPS. We have recently shown that P. gingivalis strain HG66 lacks A-LPS. Here, we found that introduction of a wild-type wbpB gene into strain HG66 restored formation of A-LPS. Sequencing of the wbpB gene from strain HG66 revealed the presence of a nonsense mutation in the gene. The wbpB gene product is a member of the Wbp pathway, which plays a role in the synthesis of UDP-ManNAc(3NAc)A in Pseudomonas aeruginosa; UDP-ManNAc(3NAc)A is sequentially synthesized by the WbpA, WbpB, WbpE, WbpD and WbpI proteins. We then determined the effect of the PGN_0002 gene, a wbpD homolog, on the biosynthesis of A-LPS. A PGN_0002-deficient mutant demonstrated an A-LPS biosynthesis deficiency. Taken together with previous studies, the present results suggest that the final product synthesized by the Wbp pathway is one of the sugar substrates necessary for the biosynthesis of A-LPS.
牙周病原体牙龈卟啉单胞菌有两种不同的脂多糖(LPS)分子,即O-LPS和A-LPS。我们最近发现牙龈卟啉单胞菌HG66菌株缺乏A-LPS。在此,我们发现将野生型wbpB基因导入HG66菌株可恢复A-LPS的形成。对HG66菌株的wbpB基因进行测序发现该基因存在无义突变。wbpB基因产物是Wbp途径的成员之一,该途径在铜绿假单胞菌中参与UDP-ManNAc(3NAc)A的合成;UDP-ManNAc(3NAc)A由WbpA、WbpB、WbpE、WbpD和WbpI蛋白依次合成。然后,我们确定了wbpD同源基因PGN_0002对A-LPS生物合成的影响。PGN_0002缺陷型突变体表现出A-LPS生物合成缺陷。结合之前的研究,目前的结果表明Wbp途径合成的最终产物是A-LPS生物合成所需的糖底物之一。