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对改良纽约市培养基上的淋病奈瑟菌初代分离培养物进行鉴定和青霉素酶检测。

Identification and penicillinase testing of Neisseria gonorrhoeae from primary isolation cultures on modified New York City medium.

作者信息

Young H

出版信息

J Clin Microbiol. 1978 Mar;7(3):247-50. doi: 10.1128/jcm.7.3.247-250.1978.

Abstract

The fluorescent-antibody test, rapid carbohydrate utilization test (RCUT), and a test for penicillinase production were performed on the bacterial growth from primary cultures on modified New York City medium. Of 134 gonococcal infections in men, 88.8% were diagnosed by the fluorescent-antibody test and 70.9% by the RCUT after incubation for 24 h; the corresponding figures for 75 infections in women were 86.7 and 54.7%, respectively. After incubation for 48 h, 100% of infections were diagnosed by the fluorescent-antibody test, wherease 88.8% of infected males and 86.7% of females were also diagnosed by the RCUT. Primary isolation cultures on modified New York City medium proved suitable for determining the ability of strains to produce penicillinase by a modified RCUT procedure. The method of isolation and identification by using primary cultures from modified New York City medium is both rapid and economical. The rapidity of diagnosis provided by the RCUT makes this a very useful diagnostic method, particularly in laboratories lacking immunofluorescence equipment. Since the penicillinase production test forms part of a routine identification procedure, no extra culture media or subcultures are required. The rapidity of this test should make it of value in tracing contacts of patients infected with penicillinase-producing strains.

摘要

对改良纽约市培养基上初代培养物中的细菌生长进行了荧光抗体试验、快速碳水化合物利用试验(RCUT)以及青霉素酶产生检测。在134例男性淋球菌感染中,培养24小时后,88.8%通过荧光抗体试验诊断出来,70.9%通过RCUT诊断出来;75例女性感染的相应数字分别为86.7%和54.7%。培养48小时后,100%的感染通过荧光抗体试验诊断出来,而88.8%的感染男性和86.7%的感染女性也通过RCUT诊断出来。改良纽约市培养基上的初代分离培养物经证明适用于通过改良的RCUT程序来测定菌株产生青霉素酶的能力。利用改良纽约市培养基上的初代培养物进行分离和鉴定的方法既快速又经济。RCUT提供的诊断快速性使其成为一种非常有用的诊断方法,尤其是在缺乏免疫荧光设备的实验室中。由于青霉素酶产生检测是常规鉴定程序的一部分,因此无需额外的培养基或传代培养。该检测的快速性应使其在追踪感染产青霉素酶菌株患者的接触者方面具有价值。

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The sensitivity of gonococci to penicillin.
J Antimicrob Chemother. 1977 May;3(3):197-8. doi: 10.1093/jac/3.3.197.
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Screening Neisseriae for penicillinase production.
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