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用于确认耐青霉素和产青霉素酶淋病奈瑟菌的培养基。

Culture medium for confirmation of penicillin-resistant and penicillinase-producing Neisseria gonorrhoeae.

作者信息

Perine P L, Westbrook W G, Biddle J W, Lewis J S, Martin J E

出版信息

J Clin Microbiol. 1982 May;15(5):865-8. doi: 10.1128/jcm.15.5.865-868.1982.

Abstract

A culture method for the isolation and identification of penicillinase (beta-lactamase)-producing Neisseria gonorrhoeae (PPNG) was evaluated in the Philippines where PPNG are common. The method uses plastic biplates containing standard Martin-Lewis gonorrhea culture medium in one side of the biplate and PPNG-selective medium containing 1.5 microgram of penicillin G per ml and a suspension of Sarcina lutea (Micrococcus lutea) that was susceptible to 0.01 microgram of penicillin G per ml in the other side. Penicillin-resistant gonococci grow on both sides of the biplate. The hydrolysis of penicillin by beta-lactamase permits the growth of S. lutea around PPNG colonies. With this medium we successfully identified 11 of 12 PPNG strains growing on primary isolation plates. A 48- to 72-h incubation period was needed, however, for visible growth of S. lutea around PPNG colonies. A unique advantage of this method was the identification of non-PPNG strains which also grew on penicillin-containing medium but did not allow growth of S. lutea. These relatively penicillin-resistant strains were the cause of infections which were not cured by penicillin treatment in 2 of 11 patients.

摘要

在菲律宾,对一种用于分离和鉴定产青霉素酶(β-内酰胺酶)淋病奈瑟菌(PPNG)的培养方法进行了评估,在该国PPNG很常见。该方法使用塑料双板,双板一侧含有标准马丁-刘易斯淋病培养基,另一侧含有每毫升含1.5微克青霉素G的PPNG选择性培养基以及对每毫升0.01微克青霉素G敏感的藤黄八叠球菌(藤黄微球菌)悬液。耐青霉素淋球菌在双板两侧生长。β-内酰胺酶对青霉素的水解使得在PPNG菌落周围藤黄八叠球菌得以生长。使用这种培养基,我们成功鉴定出在初次分离平板上生长的12株PPNG菌株中的11株。然而,需要48至72小时的培养期,PPNG菌落周围才能见到藤黄八叠球菌生长。该方法的一个独特优势是能够鉴定出那些同样能在含青霉素培养基上生长但不允许藤黄八叠球菌生长的非PPNG菌株。这些相对耐青霉素的菌株是11名患者中2名患者青霉素治疗未治愈感染的病因。

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Disc agar diffusion antimicrobial susceptibility tests with beta-lactamase producing Neisseria gonorrhoeae.
J Antibiot (Tokyo). 1978 Apr;31(4):352-8. doi: 10.7164/antibiotics.31.352.

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