Clinical Microbiology Laboratory, Peking Union Medical College Hospital, Peking Union Medical College, China Academy of Medical Science, Beijing 100730, China.
Chin Med J (Engl). 2010 Oct;123(19):2706-9.
During recent years, the incidence of serious infections caused by opportunistic fungi has increased dramatically due to alterations of the immune status of patients with hematological diseases, malignant tumors, transplantations and so forth. Unfortunately, the wide use of triazole antifungal agents to treat these infections has lead to the emergence of Aspergillus spp. resistant to triazoles. The present study was to assess the in vitro activities of five antifungal agents (voriconazole, itraconazole, posaconazole, amphotericin B and caspofungin) against different kinds of Aspergillus spp. that are commonly encountered in the clinical setting.
The agar-based Etest MIC method was employed. One hundred and seven strains of Aspergillus spp. (5 species) were collected and prepared according to Etest Technique Manuel. Etest MICs were determined with RPMI agar containing 2% glucose and were read after incubation for 48 hours at 35°C. MIC(50), MIC(90) and MIC range were acquired by Whonet 5.4 software.
The MIC(90) of caspofungin against A. fumigatus, A. flavus and A. nidulans was 0.094 µg/ml whereas the MIC(90) against A. niger was 0.19 µg/ml. For these four species, the MIC(90) of caspofungin was the lowest among the five antifungal agents. For A. terrus, the MIC(90) of posaconazole was the lowest. For A. fumigatus and A. flavus, the MIC(90) in order of increasing was caspofungin, posaconazole, voriconazole, itraconazole, and amphotericin B. The MIC of amphotericin B against A. terrus was higher than 32 µg/ml in all 7 strains tested.
The in vitro antifungal susceptibility test shows the new drug caspofungin, which is a kind of echinocandins, has good activity against the five species of Aspergillus spp. and all the triazoles tested have better in vitro activity than traditional amphotericin B.
近年来,由于血液病、恶性肿瘤、移植等患者免疫状态的改变,机会性真菌感染的发病率显著增加。不幸的是,唑类抗真菌药物的广泛应用导致了对三唑类药物耐药的曲霉菌属的出现。本研究旨在评估五种抗真菌药物(伏立康唑、伊曲康唑、泊沙康唑、两性霉素 B 和卡泊芬净)对临床常见曲霉菌属的体外活性。
采用琼脂基础 Etest MIC 法。收集并按 Etest 技术手册制备 107 株曲霉菌属(5 种)。在含 2%葡萄糖的 RPMI 琼脂中进行 Etest MIC 测定,在 35°C 孵育 48 小时后读取。采用 Whonet 5.4 软件获得 MIC50、MIC90 和 MIC 范围。
卡泊芬净对烟曲霉、黄曲霉和构巢曲霉的 MIC90 为 0.094μg/ml,对黑曲霉的 MIC90 为 0.19μg/ml。对于这四种曲霉菌属,卡泊芬净的 MIC90 是五种抗真菌药物中最低的。对于土曲霉,泊沙康唑的 MIC90 最低。对于烟曲霉和黄曲霉,按 MIC90 增加的顺序依次为卡泊芬净、泊沙康唑、伏立康唑、伊曲康唑和两性霉素 B。两性霉素 B 对所有 7 株测试的土曲霉的 MIC 均高于 32μg/ml。
体外抗真菌药敏试验表明,新型棘白菌素类药物卡泊芬净对五种曲霉菌属均具有良好的活性,所有三唑类药物的体外活性均优于传统的两性霉素 B。