Cuenca-Estrella M, Díaz-Guerra T M, Mellado E, Rodríguez-Tudela J L
Centro Nacional de Microbiologia, Instituto de Salud Carlos III, Madrid, Spain.
Antimicrob Agents Chemother. 2001 Jul;45(7):2070-4. doi: 10.1128/AAC.45.7.2070-2074.2001.
A major limitation of the National Committee for Clinical Laboratory Standards M27-A methodology is reliable detection of amphotericin B (AMB) resistance. The results obtained by using Iso-Sensitest, a synthetic medium, to detect AMB resistance were analyzed and compared with those obtained with RPMI and antibiotic medium 3 (AM3). The ability to detect AMB resistance with RPMI is not enhanced by using a higher inoculum, glucose supplementation at a final concentration of 20 g/liter, spectrophotometric reading, or 24 h of incubation time. Testing using AM3 and an inoculum of 10(3) CFU/ml detects resistance. Identification of resistant isolates is not improved by glucose supplementation, changes in reading method, or changes in incubation time. However, the use of AM3 as assay medium and an inoculum of 10(5) CFU/ml did not allow detection of AMB resistance. Testing using Iso-Sensitest medium appears to be similar to AM3 in detecting resistance. The most pronounced discrimination is achieved by testing in Iso-Sensitest supplemented with glucose and spectrophotometric reading after 24 h of incubation. The reproducibility of MIC testing was greatest for Iso-Sensitest-based procedures. Use of Iso-Sensitest produces both highly reproducible MICs and reliable identification of AMB-resistant Candida isolates.
美国国家临床实验室标准委员会M27 - A方法的一个主要局限性在于对两性霉素B(AMB)耐药性的可靠检测。分析了使用合成培养基异感测测试(Iso - Sensitest)检测AMB耐药性所获得的结果,并将其与使用RPMI和3号抗生素培养基(AM3)所获得的结果进行比较。使用更高接种量、终浓度为20克/升的葡萄糖补充、分光光度法读数或24小时孵育时间,均不能提高RPMI检测AMB耐药性的能力。使用AM3和10³CFU/ml的接种量进行检测可发现耐药性。补充葡萄糖、改变读数方法或改变孵育时间,均不能改善耐药菌株的鉴定。然而,使用AM3作为检测培养基和10⁵CFU/ml的接种量无法检测出AMB耐药性。使用Iso - Sensitest培养基进行检测在发现耐药性方面似乎与AM3相似。通过在补充葡萄糖的Iso - Sensitest中进行检测并在孵育24小时后采用分光光度法读数,可实现最显著的区分。基于Iso - Sensitest的程序,MIC检测的重现性最佳。使用Iso - Sensitest既能产生高度可重现的MIC,又能可靠地鉴定出对AMB耐药的念珠菌分离株。