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基于脂多糖抗原的卡他布兰汉菌菌株血清学分型

Serological typing of Branhamella catarrhalis strains on the basis of lipopolysaccharide antigens.

作者信息

Vaneechoutte M, Verschraegen G, Claeys G, Van Den Abeele A M

机构信息

Department of Medical Microbiology, University Hospital, Ghent, Belgium.

出版信息

J Clin Microbiol. 1990 Feb;28(2):182-7. doi: 10.1128/jcm.28.2.182-187.1990.

Abstract

A total of 302 strains of Branhamella catarrhalis from different parts of the world were serologically typed according to their lipopolysaccharide (LPS) antigenicity. For this purpose, an inhibition enzyme-linked immunosorbent assay was developed using the following reagents: antisera raised against whole bacterial suspensions for a panel of 16 serotype strains and LPS prepared from these strains by phenol extraction. Antisera were absorbed with whole bacterial suspensions of the B. catarrhalis strains to be tested. The residual activity of the sera against the homologous LPS was determined by means of an enzyme-linked immunosorbent assay, using microdilution plates coated with LPS. Strains which gave greater than 90% reduction of activity were considered to carry the same LPS type as the serotype strain. It was shown that 93.4% of the strains tested carried one of three possible LPS types. LPS of B. catarrhalis are the rough type and have an apparent Mr of 5,500, as estimated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

摘要

根据其脂多糖(LPS)抗原性,对来自世界各地的302株卡他布兰汉菌进行了血清学分型。为此,使用以下试剂开发了一种抑制酶联免疫吸附测定法:针对一组16个血清型菌株的全菌悬液产生的抗血清,以及通过苯酚提取从这些菌株制备的LPS。抗血清用待测试的卡他布兰汉菌菌株的全菌悬液吸收。使用包被有LPS的微量稀释板,通过酶联免疫吸附测定法测定血清对同源LPS的残留活性。活性降低超过90%的菌株被认为与血清型菌株携带相同的LPS类型。结果表明,93.4%的测试菌株携带三种可能的LPS类型之一。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳估计,卡他布兰汉菌的LPS为粗糙型,表观分子量为5500。

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