Meadow P M, Rowe P S, Wells P L
J Gen Microbiol. 1984 Mar;130(3):631-44. doi: 10.1099/00221287-130-3-631.
Mutants of Pseudomonas aeruginosa PAC1R (serotype O:3) which were resistant to bacteriophage D were isolated and shown to react with O:5d, O:9 and O:13 antisera as well as O:3. Antisera to the parent strain and to the three polyagglutinating (PA) mutants also showed cross-reactions. The mutants differed from the parent strain in their lipopolysaccharide (LPS) composition. The LPS from two of the three mutants yielded high molecular weight polysaccharide fractions. Although the high molecular weight fraction from one of the mutants contained the amino sugars and other components characteristic of the O:3 serotype strains, its mobility on Sephadex G75 was different from that of the parent strain. The high molecular weight material from the second mutant lacked the O-antigenic determinants but these were present in a semi-rough LPS fraction. The third mutant appeared rough and completely lacked the O-antigenic components. These three mutants were compared with the parent strain and with a non-agglutinating LPS-defective mutant which lacked both O-antigenic side chains and all neutral sugars in the outer core. Agglutination with absorbed sera and haemagglutination using purified LPS and ELISA detection suggested that wall components other than LPS were responsible for some of the cross-reactions observed. The components responsible were detected after SDS-PAGE of crude outer membrane fractions by a combination of Coomassie blue and silver-staining and antigenic components were detected by immunoelectrophoresis and ELISA-linked immunoblotting of the gels. The main antigenic determinants detected by antiserum to the parent strain were in the high molecular weight O-polysaccharide fractions and in the semirough fractions of the LPS, with some activity due to the H protein of the outer membrane. O:5d antisera reacted with unidentified high molecular weight polysaccharide fractions. Cross-reactions with the O:9 antiserum appeared to be due mainly to the F porin and, to a lesser extent, to the G and E proteins of the outer membrane. O:13 antiserum reacted with high molecular weight polysaccharide fractions but also with the rough core and F and H protein. Cross-reactivity of the other three mutant antisera could largely be interpreted in terms of the outer membrane components exposed in each strain. One reacted strongly with the F porin and the rough core, while the others reacted with a number of protein and LPS-derived fractions.(ABSTRACT TRUNCATED AT 400 WORDS)
分离出了对噬菌体D具有抗性的铜绿假单胞菌PAC1R(血清型O:3)突变体,结果显示它们能与O:5d、O:9和O:13抗血清以及O:3抗血清发生反应。亲本菌株和三个多凝集性(PA)突变体的抗血清也显示出交叉反应。这些突变体在脂多糖(LPS)组成上与亲本菌株不同。三个突变体中两个的LPS产生了高分子量多糖组分。尽管其中一个突变体的高分子量组分含有O:3血清型菌株特有的氨基糖和其他成分,但其在Sephadex G75上的迁移率与亲本菌株不同。第二个突变体的高分子量物质缺乏O抗原决定簇,但这些决定簇存在于一个半粗糙的LPS组分中。第三个突变体看起来很粗糙,完全缺乏O抗原成分。将这三个突变体与亲本菌株以及一个不凝集的LPS缺陷突变体进行了比较,该缺陷突变体既缺乏O抗原侧链,在外核中也缺乏所有中性糖。用吸收后的血清进行凝集反应,以及使用纯化的LPS进行血凝反应和ELISA检测表明,除LPS外的细胞壁成分是观察到的一些交叉反应的原因。通过考马斯亮蓝和银染相结合的方法,在粗外膜组分的SDS-PAGE后检测到了相关成分,通过对凝胶进行免疫电泳和ELISA连接免疫印迹检测到了抗原成分。亲本菌株抗血清检测到的主要抗原决定簇存在于高分子量O多糖组分和LPS的半粗糙组分中,外膜的H蛋白也有一些活性。O:5d抗血清与未鉴定的高分子量多糖组分发生反应。与O:9抗血清的交叉反应似乎主要归因于F孔蛋白,在外膜的G和E蛋白中程度较小。O:13抗血清与高分子量多糖组分发生反应,但也与粗糙核心以及F和H蛋白发生反应。其他三个突变体抗血清的交叉反应在很大程度上可以根据每个菌株中暴露的外膜成分来解释。其中一个与F孔蛋白和粗糙核心强烈反应,而其他的与一些蛋白质和LPS衍生组分发生反应。(摘要截短至400字)