4.7 Article

Adhesion Characteristics and Dual Transcriptomic and Proteomic Analysis of Lactobacillus reuteri SH23 upon Gastrointestinal Fluid Stress

Journal

JOURNAL OF PROTEOME RESEARCH
Volume 20, Issue 5, Pages 2447-2457

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jproteome.0c00933

Keywords

Lactobacillus reuteri; gastrointestinal fluid; proteomics; transcriptome; mucus-binding proteins

Funding

  1. National Natural Science Foundation of China [32072192, 31671869, 31901668]
  2. Key Research and Development Project of Zhejiang Province [2020C02042]
  3. Natural Science Foundation of Zhejiang Province [LY19C200005]
  4. Natural Science Foundation of Ningbo [202003N4129]
  5. Open Project Program of State Key Laboratory of Dairy Biotechnology [SKLDB2020007]
  6. K.C. Wong Magna Fund in Ningbo University

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The study revealed that the hydrophobicity and auto-aggregation of L. reuteri SH23 were significantly reduced under simulated gastrointestinal conditions, affecting gene expression related to cell envelope, metabolic processes, stress response, regulatory systems, and transporters. Additionally, proteomics analysis showed upregulation of proteins related to ABC transporters and LPxTG anchor domain proteins on the cell surface after exposure to gastrointestinal fluid. Recombinant Mub protein was also found to enhance the survival ability of L. reuteri SH23 in the GIT. Overall, mucus-binding proteins played a crucial role in the adhesion and tolerance of L. reuteri in the gastrointestinal tract.
The ability to survive in the harsh gastrointestinal tract (GIT) environment is essential for Lactobacillus reuteri (L. reuteri) exhibiting beneficial effects. In this study, we found that the hydrophobicity and auto-aggregation of L. reuteri SH23 were significantly decreased and biofilm production was also significantly decreased when L. reuteri SH23 passes through the simulated GIT. Furthermore, according to the comparative transcriptome analysis, gene expression involved in the cell envelope, metabolic processes, common stress response, regulatory systems, and transporters were also affected. Meanwhile, label-free quantitative proteomics was used to identify the differential expression of surface proteins of L. reuteri in response to simulated gastrointestinal fluid. Proteins related to the ABC transporters (Lreu_0517, Lreu_0098, and Lreu_0296) and LPxTG anchor domain proteins were upregulated in the cell surface after gastrointestinal fluid treatment, which is useful for adherence and colonization of L. reuteri in the GIT. Additionally, the recombinant Mub protein could also enhance the survival ability of L. reuteri SH23 in GIT stress environment. This study provides a comprehensive understanding of the adaptation and adhesion mechanisms of L. reuteri SH23 under the gastrointestinal tract by the transcriptomics and proteomics analysis, and mucus-binding proteins were involved in the adhesion and GIT tolerance process.

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