Microbiome Metabolic Engineering Theme, Carl R. Woese Institute for Genomic Biology, Urbana, Illinois, USA.
Department of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Appl Environ Microbiol. 2019 Mar 22;85(7). doi: 10.1128/AEM.00052-19. Print 2019 Apr 1.
In the human gut, ATCC 35704 is a predominant bacterium and one of the major bile acid 7α-dehydroxylating anaerobes. While this organism is well-studied relative to bile acid metabolism, little is known about the basic nutrition and physiology of ATCC 35704. To determine the amino acid and vitamin requirements of , the leave-one-out (one amino acid group or vitamin) technique was used to eliminate the nonessential amino acids and vitamins. With this approach, the amino acid tryptophan and three vitamins (riboflavin, pantothenate, and pyridoxal) were found to be required for the growth of In the newly developed defined medium, fermented glucose mainly to ethanol, acetate, formate, and H The genome of ATCC 35704 was completed through PacBio sequencing. Pathway analysis of the genome sequence coupled with transcriptome sequencing (RNA-Seq) under defined culture conditions revealed consistency with the growth requirements and end products of glucose metabolism. Induction with bile acids revealed complex and differential responses to cholic acid and deoxycholic acid, including the expression of potentially novel bile acid-inducible genes involved in cholic acid metabolism. Responses to toxic deoxycholic acid included expression of genes predicted to be involved in DNA repair, oxidative stress, cell wall maintenance/metabolism, chaperone synthesis, and downregulation of one-third of the genome. These analyses provide valuable insight into the overall biology of which may be important in treatment of disease associated with increased colonic secondary bile acids. is one of a few identified gut bacterial species capable of converting host cholic acid into disease-associated secondary bile acids such as deoxycholic acid. The current work represents an important advance in understanding the nutritional requirements and response to bile acids of the medically important human gut bacterium, ATCC 35704. A defined medium has been developed which will further the understanding of bile acid metabolism in the context of growth substrates, cofactors, and other metabolites in the vertebrate gut. Analysis of the complete genome supports the nutritional requirements reported here. Genome-wide transcriptomic analysis of gene expression in the presence of cholic acid and deoxycholic acid provides a unique insight into the complex response of ATCC 35704 to primary and secondary bile acids. Also revealed are genes with the potential to function in bile acid transport and metabolism.
在人类肠道中,ATCC 35704 是一种主要的细菌,也是主要的胆汁酸 7α-脱羟厌氧菌之一。虽然该生物体相对于胆汁酸代谢研究得很好,但对于 ATCC 35704 的基本营养和生理学知之甚少。为了确定 ATCC 35704 的氨基酸和维生素需求,采用逐个排除(一种氨基酸组或维生素)技术来排除非必需氨基酸和维生素。通过这种方法,发现必需氨基酸色氨酸和三种维生素(核黄素、泛酸和吡哆醛)是该细菌生长所必需的。在新开发的定义培养基中,ATCC 35704 发酵葡萄糖主要生成乙醇、乙酸盐、甲酸盐和 H2。通过 PacBio 测序完成了 ATCC 35704 的基因组。在定义培养条件下,对基因组序列进行途径分析并结合转录组测序(RNA-Seq),发现其与葡萄糖代谢的生长要求和终产物一致。用胆汁酸诱导显示出对胆酸和脱氧胆酸的复杂和差异反应,包括涉及胆酸代谢的潜在新的胆汁酸诱导基因的表达。对有毒脱氧胆酸的反应包括参与 DNA 修复、氧化应激、细胞壁维护/代谢、伴侣合成的基因的表达,以及三分之一基因组的下调。这些分析为理解 ATCC 35704 的整体生物学提供了有价值的见解,这可能对治疗与结肠中次级胆汁酸增加相关的疾病很重要。ATCC 35704 是少数几种能够将宿主胆酸转化为疾病相关的次级胆汁酸(如脱氧胆酸)的肠道细菌之一。目前的工作是在理解医学上重要的人类肠道细菌 ATCC 35704 的营养需求以及对胆汁酸的反应方面的重要进展。已经开发出一种定义培养基,这将有助于在脊椎动物肠道中的生长底物、辅助因子和其他代谢物的背景下理解胆汁酸代谢。完整基因组的分析支持这里报道的营养需求。在存在胆酸和脱氧胆酸的情况下,对全基因组转录组分析基因表达,为 ATCC 35704 对初级和次级胆汁酸的复杂反应提供了独特的见解。还揭示了具有在胆汁酸转运和代谢中发挥作用潜力的基因。