TY - JOUR
T1 - A new approach for analyzing an adhesive bacterial protein in the mouse gastrointestinal tract using optical tissue clearing
AU - Nishiyama, Keita
AU - Sugiyama, Makoto
AU - Yamada, Hiroki
AU - Makino, Kyoko
AU - Ishihara, Sayaka
AU - Takaki, Takashi
AU - Mukai, Takao
AU - Okada, Nobuhiko
N1 - Funding Information:
This study was supported by a Grant-in-Aid for Young Scientists (B) (no. 17K15249 to K.N.) from the Japan Society for the Promotion of Science, by a Kitasato University Research Grant for Young Researchers (to K.N.), and by a Private University Research Branding Project by MEXT (Ministry of Education, Culture, Sports, Science and Technology). We thank Dr. Yuji Yamamoto (Kitasato University) for useful comments. Dr. Hiromi Ikadai (Kitasato university) and Mr. Yasuhito Tanaka (Keyence Co Ltd.) kindly helped with microscopic techniques. We are also grateful to Mr. Issei Katai, Ms. Hanae Fukasawa, and Ms. Yuka Kushida (Kitasato university) for technical assistance. The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Publisher Copyright:
© 2019, The Author(s).
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Several bacterial moonlighting proteins act as adhesion factors, which are important for bacterial colonization of the gastrointestinal (GI) tract. However, little is known about the adherence properties of moonlighting proteins in the GI tract. Here, we describe a new approach for visualizing the localization of moonlighting protein-coated fluorescent microbeads in the whole GI tract by using a tissue optical clearing method, using elongation factor Tu (EF-Tu) as an example. As a bacterial cell surface-localized protein mimic, recombinant EF-Tu from Lactobacillus reuteri was immobilized on microbeads. EF-Tu-coating promoted the interaction of the microbeads with a Caco-2 cell monolayer. Next, the microbeads were orally administered to mice. GI whole tissues were cleared in aqueous fructose solutions of increasing concentrations. At 1 h after administration, the microbeads were diffused from the stomach up to the cecum, and after 3 h, they were diffused throughout the intestinal tract. In the lower digestive tract, EF-Tu-beads were significantly more abundant than non-coated control beads, suggesting that EF-Tu plays an important role in the persistence of the microbeads in the GI tract. The new approach will help in evaluating how moonlighting proteins mediate bacterial colonization.
AB - Several bacterial moonlighting proteins act as adhesion factors, which are important for bacterial colonization of the gastrointestinal (GI) tract. However, little is known about the adherence properties of moonlighting proteins in the GI tract. Here, we describe a new approach for visualizing the localization of moonlighting protein-coated fluorescent microbeads in the whole GI tract by using a tissue optical clearing method, using elongation factor Tu (EF-Tu) as an example. As a bacterial cell surface-localized protein mimic, recombinant EF-Tu from Lactobacillus reuteri was immobilized on microbeads. EF-Tu-coating promoted the interaction of the microbeads with a Caco-2 cell monolayer. Next, the microbeads were orally administered to mice. GI whole tissues were cleared in aqueous fructose solutions of increasing concentrations. At 1 h after administration, the microbeads were diffused from the stomach up to the cecum, and after 3 h, they were diffused throughout the intestinal tract. In the lower digestive tract, EF-Tu-beads were significantly more abundant than non-coated control beads, suggesting that EF-Tu plays an important role in the persistence of the microbeads in the GI tract. The new approach will help in evaluating how moonlighting proteins mediate bacterial colonization.
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U2 - 10.1038/s41598-019-41151-y
DO - 10.1038/s41598-019-41151-y
M3 - Article
C2 - 30894579
AN - SCOPUS:85063332266
SN - 2045-2322
VL - 9
JO - Scientific reports
JF - Scientific reports
IS - 1
M1 - 4731
ER -