Amann Rudolf, Fuchs Bernhard M
Department of Molecular Ecology, Max Planck Institute for Marine Microbiology, Celsiusstr. 1, D-28359 Bremen, Germany.
Nat Rev Microbiol. 2008 May;6(5):339-48. doi: 10.1038/nrmicro1888.
The ribosomal-RNA (rRNA) approach to microbial evolution and ecology has become an integral part of environmental microbiology. Based on the patchy conservation of rRNA, oligonucleotide probes can be designed with specificities that range from the species level to the level of phyla or even domains. When these probes are labelled with fluorescent dyes or the enzyme horseradish peroxidase, they can be used to identify single microbial cells directly by fluorescence in situ hybridization. In this Review, we provide an update on the recent methodological improvements that have allowed more reliable quantification of microbial populations in situ in complex environmental samples, with a particular focus on the usefulness of group-specific probes in this era of ever-growing rRNA databases.
核糖体RNA(rRNA)方法在微生物进化与生态学研究中已成为环境微生物学不可或缺的一部分。基于rRNA的零散保守性,可以设计出特异性范围从物种水平到门甚至域水平的寡核苷酸探针。当这些探针用荧光染料或辣根过氧化物酶标记后,可通过荧光原位杂交直接用于鉴定单个微生物细胞。在本综述中,我们介绍了近期方法学上的改进,这些改进使得在复杂环境样品中更可靠地原位定量微生物群体成为可能,尤其关注在这个rRNA数据库不断增长的时代,群体特异性探针的实用性。