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首页> 外文期刊>Infection and immunity >A high-molecular-weight fraction of smooth lipopolysaccharide in Klebsiella serotype O1:K20 contains a unique O-antigen epitope and determines resistance to nonspecific serum killing.
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A high-molecular-weight fraction of smooth lipopolysaccharide in Klebsiella serotype O1:K20 contains a unique O-antigen epitope and determines resistance to nonspecific serum killing.

机译:O1:K20克雷伯菌血清型中的高分子量平滑脂多糖含有独特的O抗原表位,并确定了对非特异性血清杀伤的抵抗力。

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The lipopolysaccharide (LPS) O-antigen side chains of Klebsiella serotype O1 have been studied by using mutants selected by resistance to a Klebsiella bacteriophage designated O1-A. Two classes of LPS mutants were identified. The major group (90%) synthesized rough LPS. The remaining 10% of the mutants produced a novel LPS profile that lacked the highest-molecular-weight O-substituted molecules (HMW-LPS) but still produced lower-molecular-weight O-substituted species (LMW-LPS). By using antisera raised against mutant Klebsiella strains and antiserum specific for Pasteurella haemolytica serotype 4, it was demonstrated that HMW-LPS and LMW-LPS contain shared epitopes. HMW-LPS also contained an epitope absent in LMW-LPS. This unique epitope was recognized by a monoclonal antibody (O1-52.6) and appears to be responsible for the serological cross-reaction between the O antigens of Klebsiella O1 and Escherichia coli O19. This HMW-LPS epitope was present in eight other Klebsiella O1 isolates which were examined. Electron microscopy demonstrated that HMW-LPS excluded overlying capsular polysaccharide for a distance of 25 to 40 nm. The distance was reduced to 10 to 18 nm in strains which synthesized only LMW-LPS and to zero in rough LPS strains. The HMW-LPS of Klebsiella O1 was shown to be an important virulence determinant, since this molecule was responsible for the resistance of the bacterium to nonspecific, complement-mediated serum killing.
机译:通过使用被命名为O1-A的克雷伯氏菌噬菌体的抗性选择的突变体,研究了克雷伯氏菌血清型O1的脂多糖(LPS)O抗原侧链。鉴定出两类LPS突变体。主要组(90%)合成了粗糙的LPS。其余的10%的突变体产生了一个新颖的LPS谱,该谱缺少最高分子量的O-取代的分子(HMW-LPS),但仍然产生了较低分子量的O-取代的分子(LMW-LPS)。通过使用针对突变克雷伯菌菌株产生的抗血清和溶血巴斯德氏菌血清型4特异的抗血清,证明了HMW-LPS和LMW-LPS包含共享的表位。 HMW-LPS还包含LMW-LPS中不存在的表位。这种独特的表位被单克隆抗体(O1-52.6)识别,似乎是导致克雷伯菌O1和大肠杆菌O19的O抗原之间发生血清学交叉反应的原因。该HMW-LPS表位存在于另外八个被检查的克雷伯菌O1分离株中。电子显微镜显示,HMW-LPS在25至40 nm的距离内排除了覆盖的荚膜多糖。在仅合成LMW-LPS的菌株中,距离减小到10至18 nm,在粗糙的LPS菌株中,距离减小到零。 Klebsiella O1的HMW-LPS被证明是重要的毒力决定因素,因为该分子负责细菌对非特异性补体介导的血清杀伤的抗性。

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