在恒化器中生长时,生物膜和浮游态拟杆菌中多糖利用和荚膜生物合成基因座的调控表达。

Regulated expression of polysaccharide utilization and capsular biosynthesis loci in biofilm and planktonic Bacteroides thetaiotaomicron during growth in chemostats.

机构信息

Department of Biological and Environmental Engineering, Cornell University, Ithaca, New York, 14853.

出版信息

Biotechnol Bioeng. 2014 Jan;111(1):165-73. doi: 10.1002/bit.24994. Epub 2013 Jul 30.

Abstract

Bacteroides thetaiotaomicron is a prominent member of the human distal gut microbiota that specializes in breaking down diet and host-derived polysaccharides. While polysaccharide utilization has been well studied in B. thetaiotaomicron, other aspects of its behavior are less well characterized, including the factors that allow it to maintain itself in the gut. Biofilm formation may be a mechanism for bacterial retention in the gut. Therefore, we used custom GeneChips to compare the transcriptomes of biofilm and planktonic B. thetaiotaomicron during growth in mono-colonized chemostats. We identified 1,154 genes with a fold-change greater than 2, with confidence greater than or equal to 95%. Among the prominent changes observed in biofilm populations were: (i) greater expression of genes in polysaccharide utilization loci that are involved in foraging of O-glycans normally found in the gut mucosa; and (ii) regulated expression of capsular polysaccharide biosynthesis loci. Hierarchical clustering of the data with different datasets, which were obtained during growth under a range of conditions in minimal media and in intestinal tracts of gnotobiotic mice, revealed that within this group of differentially expressed genes, biofilm communities were more similar to the in vivo samples than to planktonic cells and exhibited features of substrate limitation. The current study also validates the use of chemostats as an in vitro "gnotobiotic" model to study gene expression of attached populations of this bacterium. This is important to gut microbiota research, because bacterial attachment and the consequences of disruptions in attachment are difficult to study in vivo.

摘要

拟杆菌属是人类远端肠道微生物群中的一个重要成员,专门分解饮食和宿主来源的多糖。虽然拟杆菌属的多糖利用已经得到了很好的研究,但它的其他行为方面的特征还不太清楚,包括允许它在肠道中自我维持的因素。生物膜的形成可能是细菌在肠道中保留的一种机制。因此,我们使用定制的 GeneChips 在单定植恒化器中生长时比较了生物膜和浮游拟杆菌属的转录组。我们鉴定了 1154 个 fold-change 大于 2,置信度大于或等于 95%的基因。在生物膜群体中观察到的显著变化包括:(i)参与觅食通常存在于肠道黏膜的 O-聚糖的多糖利用基因座的表达增加;(ii)荚膜多糖生物合成基因座的调控表达。对不同数据集的层次聚类,这些数据集是在最小培养基和无菌小鼠肠道中生长的一系列条件下获得的,表明在这群差异表达的基因中,生物膜群落与体内样本更相似,而不是与浮游细胞更相似,并表现出底物限制的特征。本研究还验证了使用恒化器作为体外“无菌”模型来研究该细菌附着群体的基因表达。这对于肠道微生物组研究很重要,因为细菌附着及其附着中断的后果在体内很难研究。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索