Zheng D, Alm E W, Stahl D A, Raskin L
Department of Civil Engineering, University of Illinois at Urbana-Champaign 61801, USA.
Appl Environ Microbiol. 1996 Dec;62(12):4504-13. doi: 10.1128/aem.62.12.4504-4513.1996.
Universal oligonucleotide hybridization probes targeting the small-subunit rRNA are commonly used to quantify total microbial representation in environmental samples. Universal probes also serve to normalize results obtained with probes targeting specific phylogenetic groups of microorganisms. In this study, six universal probes were evaluated for stability of probe-target duplexes by using rRNA from nine organisms representing the three domains of Bacteria, Archaea, and Eucarya. Domain-specific variations in dissociation temperatures were observed for all probes. This could lead to a significant bias when these probes are used to quantify microbial populations in environmental samples. We suggest lowering the posthybridization wash stringency for two of the universal probes (S--Univ-1390-a-A-18 and S--Univ-1392-a-A-15) examined. These two probes were evaluated with traditional and modified hybridization conditions to characterize defined mixtures of rRNAs extracted from pure cultures and rRNA samples obtained from anaerobic digester samples. Probe S-*-Univ-1390-a-A-18 provided excellent estimations of domain-level community composition of these samples and is recommended for future use in microbial ecology studies.
靶向小亚基rRNA的通用寡核苷酸杂交探针通常用于量化环境样品中总的微生物表现。通用探针也用于标准化使用靶向特定微生物系统发育类群的探针所获得的结果。在本研究中,通过使用来自代表细菌、古菌和真核生物三个域的9种生物体的rRNA,评估了6种通用探针的探针-靶标双链体的稳定性。观察到所有探针在解链温度上存在域特异性差异。当这些探针用于量化环境样品中的微生物种群时,这可能导致显著偏差。我们建议降低所检测的两种通用探针(S--Univ-1390-a-A-18和S--Univ-1392-a-A-15)的杂交后洗涤严谨性。使用传统和改良的杂交条件对这两种探针进行评估,以表征从纯培养物中提取的rRNA的确定混合物以及从厌氧消化器样品中获得的rRNA样品。探针S-*-Univ-1390-a-A-18对这些样品的域水平群落组成提供了出色的估计,建议在未来的微生物生态学研究中使用。