Albuquerque Pedro, Mendes Marta V, Santos Catarina L, Moradas-Ferreira Pedro, Tavares Fernando
IBMC-Instituto de Biologia Molecular e Celular, Universidade do Porto, Portugal.
Sci Total Environ. 2009 Jun 1;407(12):3641-51. doi: 10.1016/j.scitotenv.2008.10.054. Epub 2008 Dec 4.
During the late eighties, environmental microbiologists realized the potential of the polymerase chain reaction (PCR) for the design of innovative approaches to study microbial communities or to detect and identify microorganisms in diverse and complex environments. In contrast to long-established methods of cultivation-based microbial identification, PCR-based techniques allow for the identification of microorganisms regardless of their culturability. A large number of reports have been published that describe PCR-inspired methods, frequently complemented by sequencing or hybridization profiling, to infer taxonomic and clonal microbial diversity or to detect and identify microorganisms using taxa-specific genomic markers. Typing methods have been particularly useful for microbial ecology-driven studies; however, they are not suitable for diagnostic purposes, such as the detection of specific species, strains or clones. Recently, comprehensive reviews have been written describing the panoply of typing methods available and describing their advantages and limitations; however, molecular approaches for bacterial detection and identification were either not considered or only vaguely discussed. This review focuses on DNA-based methods for bacterial detection and identification, highlighting strategies for selecting taxa-specific loci and emphasizing the molecular techniques and emerging technological solutions for increasing the detection specificity and sensitivity. The massive and increasing number of available bacterial sequences in databases, together with already employed bioinformatics tools, hold promise of more reliable, fast and cost-effective methods for bacterial identification in a wide range of samples in coming years. This tendency will foster the validation and certification of these methods and their routine implementation by certified diagnostic laboratories.
在20世纪80年代后期,环境微生物学家意识到聚合酶链反应(PCR)在设计创新方法以研究微生物群落或检测和鉴定各种复杂环境中的微生物方面的潜力。与基于培养的微生物鉴定的长期方法不同,基于PCR的技术能够鉴定微生物,而不论其是否可培养。已经发表了大量报告,描述了受PCR启发的方法,这些方法经常辅以测序或杂交分析,以推断分类学和克隆微生物多样性,或使用分类群特异性基因组标记检测和鉴定微生物。分型方法在微生物生态学驱动的研究中特别有用;然而,它们不适用于诊断目的,例如检测特定物种、菌株或克隆。最近,已经撰写了全面的综述,描述了可用的分型方法的全貌,并描述了它们的优点和局限性;然而,细菌检测和鉴定的分子方法要么没有被考虑,要么只是被模糊地讨论。本综述重点关注基于DNA的细菌检测和鉴定方法,强调选择分类群特异性位点的策略,并强调提高检测特异性和灵敏度的分子技术和新兴技术解决方案。数据库中大量且不断增加的可用细菌序列,以及已经使用的生物信息学工具,有望在未来几年为广泛样本中的细菌鉴定提供更可靠、快速且经济高效的方法。这种趋势将促进这些方法的验证和认证,以及它们由认证诊断实验室的常规实施。