Thurnheer T, Gmür R, Giertsen E, Guggenheim B
University of Zürich, Institute of Oral Microbiology and General Immunology, Plattenstrasse 11, 8028 Zürich, Switzerland.
J Microbiol Methods. 2001 Feb 1;44(1):39-47. doi: 10.1016/s0167-7012(00)00226-8.
Our aim was to develop a rapid fluorescent in situ hybridization (FISH) assay for the identification of different oral groups of streptococci in dental plaque and to combine it with digital image analysis for the automated enumeration of target cells. Cy3-labeled oligonucleotide probes specific for 16S rRNA gene sequences of the anginosus, mitis, mutans, and salivarius groups of streptococci were hybridized under stringent conditions with bacterial cultures or supragingival plaque samples that had been permeabilized with lysozyme. Probe specificity was determined with strains from 30 different species, mainly of oral origin. Results showed that probes ANG541, MIT447, SSP001, and SAL090 with specificity for the anginosus, mitis, mutans, and salivarius groups, respectively, the pan-reactive streptococcal probe STR405, the S. mutans specific probe MUT590, and the S. sobrinus specific probe SOB174 were well-suited for the identification of cultured streptococci. Probes STR405, MIT447 and SSP001 were then successfully applied to enumerate automatically bacteria of the recognized taxa in 144 supragingival plaque samples. On the average, total streptococci accounted for 8.2%, streptococci of the mitis and mutans groups for 3.9 and 1.7%, respectively, of the plaques. The combined application of FISH and automated image analysis provides an objective time-saving alternative to culture or PCR for the enumeration of selected oral streptococci in dental plaque.
我们的目标是开发一种快速荧光原位杂交(FISH)检测方法,用于鉴定牙菌斑中不同口腔链球菌群,并将其与数字图像分析相结合,以自动计数目标细胞。针对链球菌咽峡炎组、轻链球菌组、变形链球菌组和唾液链球菌组16S rRNA基因序列的Cy3标记寡核苷酸探针,在严格条件下与经溶菌酶通透处理的细菌培养物或龈上菌斑样本进行杂交。用主要来自口腔的30个不同物种的菌株确定探针特异性。结果表明,分别对咽峡炎组、轻链球菌组、变形链球菌组和唾液链球菌组具有特异性的探针ANG541、MIT447、SSP001和SAL090,泛反应性链球菌探针STR405、变形链球菌特异性探针MUT590和远缘链球菌特异性探针SOB174非常适合鉴定培养的链球菌。然后,探针STR405、MIT447和SSP001成功应用于自动计数144个龈上菌斑样本中已识别分类群的细菌。平均而言,总链球菌占菌斑的8.2%,轻链球菌组和变形链球菌组的链球菌分别占3.9%和1.7%。FISH与自动图像分析的联合应用为牙菌斑中选定口腔链球菌的计数提供了一种客观、省时的替代培养或PCR的方法。