Messer J W, Dufour A P
Microbiological and Chemical Exposure Assessment Research Division, U.S. Environmental Protection Agency, Cincinnati, Ohio 45268, USA.
Appl Environ Microbiol. 1998 Feb;64(2):678-80. doi: 10.1128/AEM.64.2.678-680.1998.
A two-step membrane filter (MF) method with mE medium, upon which the membrane must be incubated for 48 h and then transferred to a substrate medium to differentiate enterococci, is recommended by the U.S. Environmental Protection Agency to measure enterococci in fresh and marine recreational waters. The original mE medium was modified by reducing the triphenyltetrazolium chloride from 0.15 to 0.02 g/liter and adding 0.75 g of indoxyl beta-D-glucoside per liter. The new MF medium, mEI medium, detected levels of enterococci in 24 h comparable to those detected by the original mE medium in 48 h, with the same level of statistical confidence. In addition, the use of mEI medium eliminated the need to transfer the membrane to a substrate medium to differentiate enterococci from other genera of the fecal streptococcal group. Colonies from mEI medium were examined to determine the rates of false-positive and false-negative occurrences. mEI medium had a false-positive rate of 6.0% and a false-negative rate of 6.5%. Interlaboratory testing of the MF method with mEI medium demonstrated that the relative reproducibility standard deviations among laboratories ranged from 2.2% for marine water to 18.9% for freshwater. The comparative recovery studies, specificity determinations, and multilaboratory evaluation indicated that mEI medium has analytical performance characteristics equivalent to those of mE medium. The simplicity of use and decreased incubation time with mEI medium will facilitate the detection and quantification of enterococci in fresh and marine recreational waters.
美国环境保护局推荐一种采用mE培养基的两步膜过滤(MF)方法来测定淡水和海洋休闲水域中的肠球菌,在该方法中,膜必须先在mE培养基中培养48小时,然后转移至底物培养基中以鉴别肠球菌。最初的mE培养基进行了改良,将氯化三苯基四氮唑的含量从每升0.15克降至0.02克,并添加每升0.75克的β-D-葡萄糖苷吲哚酚。新的MF培养基,即mEI培养基,能在24小时内检测到的肠球菌水平与原始mE培养基在48小时内检测到的水平相当,且具有相同的统计置信度。此外,使用mEI培养基无需将膜转移至底物培养基中以鉴别肠球菌与粪链球菌群的其他属。对mEI培养基上的菌落进行检查以确定假阳性和假阴性发生率。mEI培养基的假阳性率为6.0%,假阴性率为6.5%。采用mEI培养基对MF方法进行的实验室间测试表明,各实验室之间的相对重现性标准偏差范围为海水2.2%至淡水18.9%。比较回收率研究、特异性测定和多实验室评估表明,mEI培养基的分析性能特征与mE培养基相当。mEI培养基使用简便且培养时间缩短,将有助于淡水和海洋休闲水域中肠球菌的检测和定量。