Bauters T G, Nelis H J
Laboratory for Pharmaceutical Microbiology, Department of Pharmaceutical Analysis, Ghent University, Harlebekestraat 72, 9000 Ghent, Belgium.
J Clin Microbiol. 2002 May;40(5):1838-9. doi: 10.1128/JCM.40.5.1838-1839.2002.
CHROMagar Candida medium was inoculated with a variety of clinical samples (n = 282) by using membrane filtration instead of swabbing or streaking. This modified CHROMagar procedure increased the ability to detect yeast by 16.7%. Compared to an enzymatic two-step membrane filtration method with fluorogenic substrates, it yielded similar recovery but was slower.
使用膜过滤而非拭子或划线法,将多种临床样本(n = 282)接种于CHROMagar念珠菌培养基。这种改良的CHROMagar方法使酵母检测能力提高了16.7%。与使用荧光底物的酶促两步膜过滤法相比,其回收率相似,但速度较慢。