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Intestinal epithelial cell-derived components regulate transcriptome of Lactobacillus rhamnosus GG

dc.contributor.authorSchalich, Kasey
dc.contributor.authorRajagopala, Seesandra
dc.contributor.authorDas, Suman
dc.contributor.authorO'Connell, Ryan
dc.contributor.authorYan, Fang
dc.date.accessioned2023-02-09T00:10:52Z
dc.date.available2023-02-09T00:10:52Z
dc.date.issued2023-01-04
dc.identifier.citationSchalich K, Rajagopala S, Das S, O’Connell R and Yan F (2023) Intestinal epithelial cell-derived components regulate transcriptome of Lactobacillus rhamnosus GG. Front. Microbiol. 13:1051310. doi: 10.3389/fmicb.2022.1051310en_US
dc.identifier.othereISSN 1664-302X
dc.identifier.otherPubMed ID36687654
dc.identifier.urihttp://hdl.handle.net/1803/17991
dc.description.abstractIntroductionIntestinal epithelial cells (IECs) provide the frontline responses to the gut microbiota for maintaining intestinal homeostasis. Our previous work revealed that IEC-derived components promote the beneficial effects of a commensal and probiotic bacterium, Lactobacillus rhamnosus GG (LGG). This study aimed to elucidate the regulatory effects of IEC-derived components on LGG at the molecular level. MethodsDifferential gene expression in LGG cultured with IEC-derived components at the timepoint between the exponential and stationary phase was studied by RNA sequencing and functional analysis. ResultsThe transcriptomic profile of LGG cultured with IEC-derived components was significantly different from that of control LGG, with 231 genes were significantly upregulated and 235 genes significantly down regulated (FDR <0.05). The Clusters of Orthologous Groups (COGs) and Gene Ontology (GO) analysis demonstrated that the predominant genes enriched by IEC-derived components are involved in nutrient acquisition, including transporters for amino acids, metals, and sugars, biosynthesis of amino acids, and in the biosynthesis of cell membrane and cell wall, including biosynthesis of fatty acid and lipoteichoic acid. In addition, genes associated with cell division and translation are upregulated by IEC-derived components. The outcome of the increased transcription of these genes is supported by the result that IEC-derived components significantly promoted LGG growth. The main repressed genes are associated with the metabolism of amino acids, purines, carbohydrates, glycerophospholipid, and transcription, which may reflect regulation of metabolic mechanisms in response to the availability of nutrients in bacteria. DiscussionThese results provide mechanistic insight into the interactions between the gut microbiota and the host.en_US
dc.description.sponsorshipThis work was supported by the National Institutes of Health (NIH) grants, R01DK081134-12 (FY) and R21AI149262 (SD), the Crohn’s & Colitis Foundation Senior Research Award (FY), Training Grant in Gastroenterology (T32DK007673-21) (KS), and Vanderbilt University Medical Center’s Digestive Disease Research Center supported by NIH grant P30DK058404.en_US
dc.language.isoen_USen_US
dc.publisherFrontiers In Microbiologyen_US
dc.rights© 2023 Schalich, Rajagopala, Das, O’Connell and Yan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
dc.source.urihttps://www.frontiersin.org/articles/10.3389/fmicb.2022.1051310/full
dc.subjectbacterial transporteren_US
dc.subjectbacterial metabolismen_US
dc.subjectcommensal bacteriumen_US
dc.subjectintestinal epithelial cellen_US
dc.subjectRNA sequencingen_US
dc.subjectthe microbial-host interactionen_US
dc.subjecttranscriptomeen_US
dc.titleIntestinal epithelial cell-derived components regulate transcriptome of Lactobacillus rhamnosus GGen_US
dc.typeArticleen_US
dc.identifier.doi10.3389/fmicb.2022.1051310


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