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用玻片凝集技术鉴别铜绿假单胞菌主要鞭毛抗原

Differentiation of the major flagellar antigens of Pseudomonas aeruginosa by the slide coagglutination technique.

作者信息

Ansorg R A, Knoche M E, Spies A F, Kraus C J

出版信息

J Clin Microbiol. 1984 Jul;20(1):84-8. doi: 10.1128/jcm.20.1.84-88.1984.

Abstract

Antisera against the two major flagellar antigens of Pseudomonas aeruginosa were obtained by immunization of rabbits with isolated flagella and absorption of contaminating antisomatic antibodies. In the conventional slide agglutination test, the pure H antisera did not agglutinate the flagellated cells of the homologous strains. The addition of protein A-bearing staphylococci to H antiserum and homologous flagellated cells, the so-called slide coagglutination, results in a rapid development of flaky clumps. H coagglutination tests of reference strains, which formerly have been H typed by long-term tube agglutination and by the indirect fluorescent-antibody technique, yielded exactly the same subdivision of the strains in H type a and H type b as the more laborious and time-consuming methods. O grouping and H typing of 181 isolates from clinical specimens revealed a free combination of the somatic and flagellar antigens. 25 OH serovars were found. The simple and rapid coagglutination technique can promote the serovar determination of P. aeruginosa, particularly for the purpose of hospital infection control.

摘要

通过用分离的鞭毛免疫兔子并吸收污染的菌体抗体,获得了抗铜绿假单胞菌两种主要鞭毛抗原的抗血清。在传统的玻片凝集试验中,纯H抗血清不会凝集同源菌株的鞭毛细胞。在H抗血清和同源鞭毛细胞中加入携带蛋白A的葡萄球菌,即所谓的玻片协同凝集,会导致迅速形成片状凝集块。对以前通过长期试管凝集和间接荧光抗体技术进行H分型的参考菌株进行H协同凝集试验,与更费力且耗时的方法相比,菌株在H型a和H型b中的细分结果完全相同。对181份临床标本分离株进行O分组和H分型,发现菌体抗原和鞭毛抗原可自由组合。共发现25种OH血清型。这种简单快速的协同凝集技术可促进铜绿假单胞菌的血清型鉴定,特别是用于医院感染控制目的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5fe/271252/518587d536d8/jcm00120-0101-a.jpg

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