McSweeney C S, Mackie R I, Odenyo A A, Stahl D A
Long Pocket Laboratories, CSIRO Division of Tropical Animal Production, Indooroopilly, Queensland, Australia.
Appl Environ Microbiol. 1993 May;59(5):1607-12. doi: 10.1128/aem.59.5.1607-1612.1993.
Radiolabelled and fluorescent-dye-conjugated oligonucleotide probes which targeted rRNA sequences were developed for the enumeration of the ruminal bacterium Synergistes jonesii 78-1 in mixed culture. Two probes were tested, and both were highly specific for the respective complementary sequences of the target organism. Individual cells of S. jonesii in pure and mixed cultures were clearly visualized in situ by hybridization with the fluorescent-dye-conjugated probe but could not be detected in natural samples. Therefore the radiolabelled probe was used to monitor the population of S. jonesii introduced into a chemostat which simulated the rumen ecosystem. The S. jonesii probe did not hybridize to RNA extracted from the culture prior to inoculation with the target organism. After inoculation, S. jonesii rRNA represented 4.5% of the total bacterial rRNA and then rapidly declined to < 0.2% before increasing to about 1% of the total bacterial rRNA during the following 3 weeks. This study demonstrates that rRNA-targeted probes could be used for tracking organisms introduced into the rumen ecosystem.
为了对混合培养物中瘤胃细菌琼斯氏协同杆菌78-1进行计数,开发了靶向rRNA序列的放射性标记和荧光染料偶联的寡核苷酸探针。测试了两种探针,它们对目标生物体各自的互补序列都具有高度特异性。通过与荧光染料偶联的探针杂交,纯培养物和混合培养物中的琼斯氏协同杆菌的单个细胞在原位清晰可见,但在天然样品中无法检测到。因此,使用放射性标记的探针来监测引入模拟瘤胃生态系统的恒化器中的琼斯氏协同杆菌种群。在接种目标生物体之前,琼斯氏协同杆菌探针未与从培养物中提取的RNA杂交。接种后,琼斯氏协同杆菌rRNA占总细菌rRNA的4.5%,然后迅速下降至<0.2%,随后在接下来的3周内增加至总细菌rRNA的约1%。这项研究表明,靶向rRNA的探针可用于追踪引入瘤胃生态系统的生物体。