Datta K, Jain N, Sethi S, Rattan A, Casadevall A, Banerjee U
Department of Microbiology, All India Institute of Medical Sciences, New Delhi 110029, India.
J Antimicrob Chemother. 2003 Oct;52(4):683-6. doi: 10.1093/jac/dkg399. Epub 2003 Sep 1.
In cryptococcosis, fluconazole is a standard prophylactic, therapeutic and maintenance option, particularly in the expanding HIV/AIDS group. However, its excessive use may lead to resistance in Cryptococcus neoformans. Variations in clinical response to fluconazole have already been noted elsewhere, and cases of post-therapy relapse are not uncommon. To assess azole antifungal susceptibility profiles of clinical cryptococcal isolates in India, the All India Institute of Medical Sciences (AIIMS) has recently initiated preliminary studies using NCCLS M27-A.
Twenty-eight randomly chosen AIIMS clinical isolates (spanning 1997-2000), 16 isolates from other institutions in North India, and six reference strains of C. neoformans were subjected to susceptibility testing to fluconazole and itraconazole.
Among clinical isolates, susceptibilities to fluconazole and itraconazole were 84.1% and 93.2%, respectively. MICs for all clinical isolates were 0.25-32 mg/L for fluconazole and <0.03-0.25 mg/L for itraconazole. MIC50 and MIC90 values for fluconazole were 4 and 16 mg/L, respectively, and those for itraconazole were 0.032 and 0.125 mg/L, respectively. Out of 28 AIIMS clinical isolates, 22 had minimum fungicidal concentrations (MFCs) of fluconazole at 128 mg/L. Moderately high fluconazole MICs (16-32 mg/L) were observed in 16% of clinical isolates--probably the first such report from India. MIC/MFC ratios for fluconazole and itraconazole were 1:32 or more in 16 AIIMS clinical isolates, indicating possible azole tolerance. There was good agreement between MIC values obtained by the micro- and macro-broth dilution techniques of M27-A compared in this study.
The observed MIC data warrant continued surveillance of susceptibility values of clinical cryptococcal isolates in India.
在隐球菌病中,氟康唑是一种标准的预防、治疗和维持用药选择,尤其适用于不断扩大的艾滋病毒/艾滋病群体。然而,其过度使用可能导致新型隐球菌产生耐药性。在其他地方已经注意到对氟康唑的临床反应存在差异,治疗后复发的病例并不罕见。为了评估印度临床分离的隐球菌对唑类抗真菌药物的敏感性谱,全印度医学科学研究所(AIIMS)最近启动了使用NCCLS M27 - A的初步研究。
选取28株随机选择的AIIMS临床分离株(时间跨度为1997 - 2000年)、16株来自印度北部其他机构的分离株以及6株新型隐球菌参考菌株,进行氟康唑和伊曲康唑的药敏试验。
在临床分离株中,对氟康唑和伊曲康唑的敏感性分别为84.1%和93.2%。所有临床分离株对氟康唑的MIC为0.25 - 32mg/L,对伊曲康唑的MIC为<0.03 - 0.25mg/L。氟康唑的MIC50和MIC90值分别为4mg/L和16mg/L,伊曲康唑的MIC50和MIC90值分别为0.032mg/L和0.125mg/L。在28株AIIMS临床分离株中,22株的氟康唑最低杀菌浓度(MFC)为128mg/L。16%的临床分离株观察到氟康唑的MIC中度偏高(16 - 32mg/L)——这可能是印度的首个此类报告。在16株AIIMS临床分离株中,氟康唑和伊曲康唑的MIC/MFC比值为1:32或更高,表明可能存在唑类耐受性。本研究中比较的M27 - A微量肉汤稀释法和常量肉汤稀释法获得的MIC值之间具有良好的一致性。
观察到的MIC数据表明有必要继续监测印度临床分离的隐球菌的药敏值。