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实验性化疗期间对大环内酯类耐药的鸟分枝杆菌菌群的出现

Emergence of Mycobacterium avium populations resistant to macrolides during experimental chemotherapy.

作者信息

Bermudez L E, Petrofsky M, Kolonoski P, Young L S

机构信息

Kuzell Institute for Arthritis & Infectious Diseases, California Pacific Medical Center Research Institute, San Francisco 94115, USA.

出版信息

Antimicrob Agents Chemother. 1998 Jan;42(1):180-3. doi: 10.1128/AAC.42.1.180.

Abstract

Macrolide resistance is an emerging problem in AIDS patients who receive these agents for treatment or prophylaxis against Mycobacterium avium (MAC) infection. We compared the emergence of resistant MAC strains during therapy with clarithromycin (clarithromycin resistance was defined as MIC > or = 32 microg/ml) and azithromycin (azithromycin resistance was defined as MIC > or = 128 microg/ml) in C57BL/6 beige mice. Treatment with clarithromycin and azithromycin resulted in a decrease of 98.5% in the number of viable bacteria in spleens at week 8 and 99% at week 12 compared with the number of bacteria present in spleen before the initiation of therapy (P < 0.001). Splenic homogenates were also plated onto 7H11 agar plus clarithromycin at 32 microg/ml or azithromycin at 128 microg/ml. Resistance emerged significantly more often in mice treated with clarithromycin (100% of treated mice at both 8 and 12 weeks) than in those receiving azithromycin (0% at week 8 and 14% at week 12). The frequencies of resistance of the MAC population in the spleen to clarithromycin were 2.1 x 10(-3) at week 8 and 1.1 x 10(-2) at week 12, whereas resistance to azithromycin was absent at week 8 (all mice) and was approximately 3.5 x 10(-5) (mean for the three positive animals) at week 12. Clarithromycin was more effective in initial reduction of MAC burden in tissue after 8 and 12 weeks of treatment, but resistant strains emerged significantly more frequently after treatment with clarithromycin than after treatment with azithromycin.

摘要

大环内酯类耐药性在接受这些药物治疗或预防鸟分枝杆菌(MAC)感染的艾滋病患者中是一个新出现的问题。我们比较了C57BL/6米色小鼠在接受克拉霉素(克拉霉素耐药定义为MIC≥32μg/ml)和阿奇霉素(阿奇霉素耐药定义为MIC≥128μg/ml)治疗期间耐药MAC菌株的出现情况。与治疗开始前脾脏中的细菌数量相比,克拉霉素和阿奇霉素治疗在第8周时使脾脏中活菌数量减少了98.5%,在第12周时减少了99%(P<0.001)。脾脏匀浆也接种在含32μg/ml克拉霉素或128μg/ml阿奇霉素的7H11琼脂上。接受克拉霉素治疗的小鼠(第8周和第12周时治疗小鼠的100%)比接受阿奇霉素治疗的小鼠(第8周时为0%,第12周时为14%)出现耐药的情况明显更频繁。脾脏中MAC群体对克拉霉素的耐药频率在第8周时为2.1×10⁻³,在第12周时为1.1×10⁻²,而对阿奇霉素的耐药在第8周时不存在(所有小鼠),在第12周时约为3.5×10⁻⁵(三只阳性动物的平均值)。克拉霉素在治疗8周和12周后对组织中MAC负荷的初始降低更有效,但克拉霉素治疗后耐药菌株出现的频率明显高于阿奇霉素治疗后。

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