Sekhon A S, Padhye A A, Garg A K
National Reference Center for Human Mycotic Diseases, University of Alberta, Edmonton, Canada.
Eur J Epidemiol. 1992 May;8(3):427-32. doi: 10.1007/BF00158578.
Ten isolates of Penicillium marneffei and eight of Pythium insidiosum were tested for their in vitro sensitivity to amphotericin B, hamycin (a polyene heptaene), two water-soluble analogs of amphotericin B and hamycin, namely, JAI-Amb, and JAI-hamycin,5-fluorocytosine, fluconazole, itraconazole,ketoconazole and miconazole. Itraconazole manifested the strongest activity against all of the 10 isolates of P. marneffei and would be the drug of choice in the treatment of penicilliosis due to P. marneffei. The polyene antibiotics amphotericin B and hamycin and their water-soluble analogs showed no appreciable activity against P. insidiosum. Pytium insidiosum isolates were sensitive to fluconazole, ketoconazole, and miconazole. Miconazole exhibited the strongest in vitro activity against all of the 8 isolates of P. insidiosum, followed by ketoconazole.
对10株马尔尼菲青霉和8株隐秘腐霉进行了体外药敏试验,检测它们对两性霉素B、哈霉素(一种多烯七烯)、两性霉素B和哈霉素的两种水溶性类似物(即JAI-Amb和JAI-哈霉素)、5-氟胞嘧啶、氟康唑、伊曲康唑、酮康唑和咪康唑的敏感性。伊曲康唑对所有10株马尔尼菲青霉表现出最强活性,将是治疗马尔尼菲青霉病的首选药物。多烯抗生素两性霉素B和哈霉素及其水溶性类似物对隐秘腐霉无明显活性。隐秘腐霉分离株对氟康唑、酮康唑和咪康唑敏感。咪康唑对所有8株隐秘腐霉表现出最强的体外活性,其次是酮康唑。