Coyne M J, Kalka-Moll W, Tzianabos A O, Kasper D L, Comstock L E
Channing Laboratory, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Infect Immun. 2000 Nov;68(11):6176-81. doi: 10.1128/IAI.68.11.6176-6181.2000.
Bacteroides fragilis produces a capsular polysaccharide complex (CPC) that is directly involved in its ability to induce abscesses. Two distinct capsular polysaccharides, polysaccharide A (PS A) and PS B, have been shown to be synthesized by the prototype strain for the study of abscesses, NCTC9343. Both of these polysaccharides in purified form induce abscesses in animal models. In this study, we demonstrate that the CPC of NCTC9343 is composed of at least three distinct capsular polysaccharides: PS A, PS B, and PS C. A previously described locus contains genes whose products are involved in the biosynthesis of PS C rather than PS B as was originally suggested. The actual PS B biosynthesis locus was cloned, sequenced, and found to contain 22 genes in an operon-type structure. A mutant with a large chromosomal deletion of the PS B biosynthesis locus was created so that the contribution of PS B to the formation of abscesses could be assessed in a rodent model. Although purified PS B can induce abscesses, removal of this polysaccharide does not attenuate the organism's ability to induce abscesses.
脆弱拟杆菌产生一种荚膜多糖复合物(CPC),该复合物直接参与其诱导脓肿形成的能力。研究脓肿形成的原型菌株NCTC9343已被证明能合成两种不同的荚膜多糖,即多糖A(PS A)和PS B。纯化形式的这两种多糖均可在动物模型中诱导脓肿形成。在本研究中,我们证明NCTC9343的CPC至少由三种不同的荚膜多糖组成:PS A、PS B和PS C。一个先前描述的基因座包含的基因产物参与PS C的生物合成,而不是如最初所认为的参与PS B的生物合成。实际的PS B生物合成基因座被克隆、测序,发现其在一个操纵子型结构中包含22个基因。构建了一个PS B生物合成基因座发生大片段染色体缺失的突变体,以便在啮齿动物模型中评估PS B对脓肿形成的贡献。尽管纯化的PS B可诱导脓肿形成,但去除这种多糖并不会减弱该生物体诱导脓肿形成的能力。