Regulated expression of polysaccharide utilization and capsular biosynthesis loci in biofilm and planktonic Bacteroides thetaiotaomicron during growth in chemostats. Issue 1 (30th July 2013)

• Record Type: Journal Article
• Authors: TerAvest, Michaela A.; He, Zhen; Rosenbaum, Miriam A.; Martens, Eric C.; Cotta, Michael A.; Gordon, Jeffrey I.; Angenent, Largus T.
• Is Part Of: Biotechnology and bioengineering. Volume 111:Issue 1(2014:Jan.)
• Page Start: 165
• Page End: 173
• Publication Date: 2013-07-30
• Subjects: Biotechnology -- Periodicals; Bioengineering -- Periodicals; 660.6
• DOI: 10.1002/bit.24994
• Languages: English
• ISSNs: 0006-3592

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="bit24994-sec-0001" sec-type="section"> <p> <italic>Bacteroides thetaiotaomicron</italic> 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 <italic>B. thetaiotaomicron</italic>, 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 <italic>B. thetaiotaomicron</italic> 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. Biotechnol. Bioeng. 2014;111: 165–173. © 2013 Wiley Periodicals, Inc.</p> </sec> </abstract>