Lanoil B D, Giovannoni S J
Molecular and Cellular Biology Program, Oregon State University, Corvallis 97331, USA.
Appl Environ Microbiol. 1997 Mar;63(3):1118-23. doi: 10.1128/aem.63.3.1118-1123.1997.
Chromosomal painting is a technique for the microscopic localization of genetic material. It has been applied at the subcellular level to identify regions of eukaryotic chromosomes. Here we describe the development of bacterial chromosomal painting (BCP), a related technology for the identification of bacterial cells. Purified genomic DNAs from six bacterial strains were labeled by nick translation with the fluorochrome Fluor-X, Cy3, or Cy5. The average size of the labeled fragments was ca. 50 to 200 bp. The probes were hybridized to formaldehyde-fixed microbial cells attached to slides and visualized by fluorescence microscopy. In reciprocal comparisons, distantly related members of the class Proteobacteria (Escherichia coli and Oceanospirillum linum), different species of the genus Bacillus (B. subtilis and B. megaterium), and different serotypes of the subspecies Salmonella choleraesuis subsp. choleraesuis (serotype typhimurium LT2 and serotype typhi Ty2) could easily be distinguished. A combination of two probes, each labeled with a different fluorochrome, was used successfully to simultaneously identify two cell types in a mixture. Lysozyme treatment was required for the identification of Bacillus spp., and RNase digestion and pepsin digestion were found to enhance signal strength and specificity for all cell types tested. Chromosome in situ suppression, a technique that removes cross-hybridizing fragments from the probe, was necessary for the differentiation of the Salmonella serotypes but was not required to distinguish the more distantly related taxa. BCP may have applications in diverse branches of microbiology where the objective is the identification of bacterial cells.
染色体涂染是一种用于遗传物质微观定位的技术。它已应用于亚细胞水平,以识别真核染色体区域。在此,我们描述了细菌染色体涂染(BCP)技术的发展,这是一种用于识别细菌细胞的相关技术。用荧光染料Fluor-X、Cy3或Cy5通过缺口平移法对来自六种细菌菌株的纯化基因组DNA进行标记。标记片段的平均大小约为50至200 bp。将探针与附着在载玻片上的甲醛固定微生物细胞杂交,并通过荧光显微镜观察。在相互比较中,变形菌纲关系较远的成员(大肠杆菌和亚麻海洋螺菌)、芽孢杆菌属的不同种(枯草芽孢杆菌和巨大芽孢杆菌)以及猪霍乱沙门氏菌亚种猪霍乱沙门氏菌的不同血清型(鼠伤寒血清型LT2和伤寒血清型Ty2)都能很容易地被区分开来。成功地使用了两种分别用不同荧光染料标记的探针组合,同时识别混合物中的两种细胞类型。鉴定芽孢杆菌属需要溶菌酶处理,并且发现核糖核酸酶消化和胃蛋白酶消化可增强所有测试细胞类型的信号强度和特异性。染色体原位抑制是一种从探针中去除交叉杂交片段的技术,它对于区分沙门氏菌血清型是必要的,但区分关系较远的分类群则不需要。BCP可能在微生物学的不同分支中有应用,其目标是识别细菌细胞。