Chou S, Chedore P, Haddad A, Paul N R, Kasatiya S
Public Health Laboratory, Ontario Ministry of Health, Ottawa, Canada.
J Clin Microbiol. 1996 May;34(5):1317-20. doi: 10.1128/jcm.34.5.1317-1320.1996.
Twenty-nine Mycobacterium reference strains representing 10 species and 60 mycobacterial cultures isolated from sputum specimens were studied. These cultures were grown in Bactec 7H12B medium (Becton Dickinson and Co., Paramus, N.J.) supplemented with oleic acid-albumin-dextrose-catalase enrichment broth (Becton Dickinson and Co., Cockeysville, Md.). The cultures were analyzed by gas-liquid chromatography for their fatty acids, secondary alcohols, and mycolic acid cleavage products. All of the clinical isolates could be identified by comparing their gas-liquid chromatography profiles with those of the reference strains. The data indicate that this method significantly shortens the turnaround time and could be used for the early detection and identification of mycobacterial species.
对代表10个物种的29株分枝杆菌参考菌株以及从痰液标本中分离出的60株分枝杆菌培养物进行了研究。这些培养物在添加了油酸-白蛋白-葡萄糖-过氧化氢酶富集肉汤(Becton Dickinson and Co., Cockeysville, Md.)的Bactec 7H12B培养基(Becton Dickinson and Co., Paramus, N.J.)中生长。通过气液色谱法分析这些培养物的脂肪酸、仲醇和分枝菌酸裂解产物。通过将临床分离株的气液色谱图谱与参考菌株的图谱进行比较,所有临床分离株均可得到鉴定。数据表明,该方法显著缩短了周转时间,可用于分枝杆菌物种的早期检测和鉴定。