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Antimicrob Agents Chemother. 1994 Jul;38(7):1688-91. doi: 10.1128/AAC.38.7.1688.
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Quinolone-resistant Neisseria gonorrhoeae: correlation of alterations in the GyrA subunit of DNA gyrase and the ParC subunit of topoisomerase IV with antimicrobial susceptibility profiles.耐喹诺酮淋病奈瑟菌:DNA 回旋酶 GyrA 亚基和拓扑异构酶 IV 的 ParC 亚基改变与抗菌药物敏感性谱的相关性
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In vitro activity of a new fluoroquinolone, CP-99,219, against strains of Neisseria gonorrhoeae.新型氟喹诺酮CP-99,219对淋病奈瑟菌菌株的体外活性
Antimicrob Agents Chemother. 1995 Apr;39(4):987-9. doi: 10.1128/AAC.39.4.987.

本文引用的文献

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Antimicrobial susceptibilities of Neisseria gonorrhoeae strains representing five distinct resistance phenotypes.代表五种不同耐药表型的淋病奈瑟菌菌株的抗菌药敏性。
Antimicrob Agents Chemother. 1994 Jan;38(1):155-8. doi: 10.1128/AAC.38.1.155.
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Ceftriaxone for treatment of uncomplicated gonorrhea: routine use of a single 125-mg dose in a sexually transmitted disease clinic.
Sex Transm Dis. 1987 Oct-Dec;14(4):227-30.
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Trends in resistance of Neisseria gonorrhoeae to antimicrobial agents in the United States.
Sex Transm Dis. 1988 Oct-Dec;15(4):202-10. doi: 10.1097/00007435-198810000-00006.
4
Penicillinase-producing Neisseria gonorrhoeae in Dade County, Florida: phenotypic characterization of isolates from 1983, 1984, and 1986.佛罗里达州戴德县产青霉素酶淋病奈瑟菌:1983年、1984年及1986年分离株的表型特征
Sex Transm Dis. 1988 Jul-Sep;15(3):158-63. doi: 10.1097/00007435-198807000-00010.
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National surveillance of antimicrobial resistance in Neisseria gonorrhoeae. The Gonococcal Isolate Surveillance Project.淋病奈瑟菌抗菌药物耐药性的全国监测。淋球菌分离株监测项目。
JAMA. 1990 Sep 19;264(11):1413-7.
6
A comparison of single-dose cefixime with ceftriaxone as treatment for uncomplicated gonorrhea. The Gonorrhea Treatment Study Group.单剂量头孢克肟与头孢曲松治疗单纯性淋病的比较。淋病治疗研究组。
N Engl J Med. 1991 Nov 7;325(19):1337-41. doi: 10.1056/NEJM199111073251903.
7
Antibiotic susceptibility survey of Neisseria gonorrhoeae in Thailand.泰国淋病奈瑟菌的抗生素敏感性调查。
Antimicrob Agents Chemother. 1992 Aug;36(8):1682-7. doi: 10.1128/AAC.36.8.1682.

与盆腔炎相关的淋病奈瑟菌对头孢西丁、头孢曲松、克林霉素、庆大霉素、多西环素、阿奇霉素及其他抗菌药物的敏感性。

Susceptibility of Neisseria gonorrhoeae associated with pelvic inflammatory disease to cefoxitin, ceftriaxone, clindamycin, gentamicin, doxycycline, azithromycin, and other antimicrobial agents.

作者信息

Rice R J, Knapp J S

机构信息

Division of Sexually Transmitted Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30333.

出版信息

Antimicrob Agents Chemother. 1994 Jul;38(7):1688-91. doi: 10.1128/AAC.38.7.1688.

DOI:10.1128/AAC.38.7.1688
PMID:7979312
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC284620/
Abstract

We determined the susceptibilities, by the agar dilution method, of 84 recent clinical isolates of Neisseria gonorrhoeae obtained from women with pelvic inflammatory disease in the United States to the following antimicrobial agents: penicillin, cefoxitin, cefotetan, ceftriaxone, ceftizoxime, cefixime, tetracycline, doxycycline, ciprofloxacin, ofloxacin, erythromycin, azithromycin, clindamycin, and gentamicin. Twenty-five percent of the isolates were resistant to penicillin and 20% were resistant to tetracycline. In comparison, doxycycline was more active than tetracycline and azithromycin was more active than erythromycin in vitro. Ceftriaxone, ceftizoxime, and cefixime were equally active against penicillin-susceptible isolates, but they had different in vitro activities against gonococcal isolates possessing chromosomally mediated resistance to penicillin. Overall, cefoxitin was slightly more active than cefotetan and ciprofloxacin was more active in vitro than ofloxacin, especially against N. gonorrhoeae with chromosomally mediated resistance. Criteria for the interpretation of susceptibility data for N. gonorrhoeae are not available for clindamycin or gentamicin, but for at least half of all isolates, including penicillin-susceptible isolates, at least 4 micrograms of clindamycin or gentamicin per ml was required to inhibit growth in vitro.

摘要

我们采用琼脂稀释法,测定了从美国盆腔炎女性患者中分离出的84株近期淋病奈瑟菌临床分离株对以下抗菌药物的敏感性:青霉素、头孢西丁、头孢替坦、头孢曲松、头孢唑肟、头孢克肟、四环素、多西环素、环丙沙星、氧氟沙星、红霉素、阿奇霉素、克林霉素和庆大霉素。25%的分离株对青霉素耐药,20%对四环素耐药。相比之下,多西环素在体外比四环素活性更强,阿奇霉素比红霉素活性更强。头孢曲松、头孢唑肟和头孢克肟对青霉素敏感分离株的活性相同,但它们对具有染色体介导的青霉素耐药性的淋病奈瑟菌分离株的体外活性不同。总体而言,头孢西丁比头孢替坦活性略强,环丙沙星在体外比氧氟沙星活性更强,尤其是对具有染色体介导耐药性的淋病奈瑟菌。目前尚无针对克林霉素或庆大霉素的淋病奈瑟菌药敏数据解读标准,但对于至少一半的分离株,包括青霉素敏感分离株,体外抑制生长至少需要每毫升4微克的克林霉素或庆大霉素。