Horz Hans-Peter
Division of Virology, Institute of Medical Microbiology, RWTH Aachen University Hospital, Pauwelsstrasse 30, 52057 Aachen, Germany.
Life (Basel). 2015 May 5;5(2):1333-45. doi: 10.3390/life5021333.
Archaea are well-recognized components of the human microbiome. However, they appear to be drastically underrepresented compared to the high diversity of bacterial taxa which can be found on various human anatomic sites, such as the gastrointestinal environment, the oral cavity and the skin. As our "microbial" view of the human body, including the methodological concepts used to describe them, has been traditionally biased on bacteria, the question arises whether our current knowledge reflects the actual ratio of archaea versus bacteria or whether we have failed so far to unravel the full diversity of human-associated archaea. This review article hypothesizes that distinct archaeal lineages within humans exist, which still await our detection. First, previously unrecognized taxa might be quite common but they have eluded conventional detection methods. Two recent prime examples are described that demonstrate that this might be the case for specific archaeal lineages. Second, some archaeal taxa might be overlooked because they are rare and/or in low abundance. Evidence for this exists for a broad range of phylogenetic lineages, however we currently do not know whether these sporadically appearing organisms are mere transients or important members of the so called "rare biosphere" with probably basic ecosystem functions. Lastly, evidence exists that different human populations harbor different archaeal taxa and/or the abundance and activity of shared archaeal taxa may differ and thus their impact on the overall microbiome. This research line is rather unexplored and warrants further investigation. While not recapitulating exhaustively all studies on archaeal diversity in humans, this review highlights pertinent recent findings that show that the choice of appropriate methodological approaches and the consideration of different human populations may lead to the detection of archaeal lineages previously not associated with humans. This in turn will help understand variations found in the overall microbiomes from different individuals and ultimately may lead to the emergence of novel concepts/mechanisms impacting human health.
古菌是人类微生物组中被充分认识的组成部分。然而,与在人体各个解剖部位(如胃肠道环境、口腔和皮肤)发现的高度多样的细菌类群相比,它们的数量似乎严重不足。由于我们对人体的“微生物”观点,包括用于描述它们的方法概念,传统上一直偏向于细菌,因此问题就出现了:我们目前的知识是否反映了古菌与细菌的实际比例,或者我们到目前为止是否未能揭示与人类相关的古菌的全部多样性。这篇综述文章假设,人类体内存在尚未被发现的独特古菌谱系。首先,以前未被识别的类群可能相当常见,但它们躲过了传统的检测方法。文中描述了两个最近的主要例子,表明特定古菌谱系可能就是这种情况。其次,一些古菌类群可能被忽视,因为它们很罕见和/或丰度很低。对于广泛的系统发育谱系都有相关证据,但我们目前不知道这些偶尔出现的生物体仅仅是过客,还是具有可能的基本生态系统功能的所谓“稀有生物圈”的重要成员。最后,有证据表明,不同的人类群体含有不同的古菌类群,和/或共享古菌类群的丰度和活性可能不同,因此它们对整体微生物组的影响也不同。这条研究路线尚未得到充分探索,值得进一步研究。虽然没有详尽地概括所有关于人类古菌多样性的研究,但这篇综述强调了相关的最新发现,即选择合适的方法和考虑不同的人类群体可能会导致发现以前与人类无关的古菌谱系。这反过来将有助于理解不同个体的整体微生物组中发现的差异,并最终可能导致影响人类健康的新概念/机制的出现。