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Sodium-bile acid co-transporter is crucial for survival of a carcinogenic liver fluke Clonorchis sinensis in the bile

The liver fluke Clonorchis sinensis inhabits the bile ducts, where bile concentration disparities across the fluke cell membrane can cause bile intoxication. Sodium-bile acid co-transporter (SBAT) plays a crucial role in bile acid recycling. The process by which SBAT imports bile acids is electrical...

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Autores principales: Dai, Fuhong, Yoo, Won Gi, Lu, Yanyan, Song, Jin-Ho, Lee, Ji-Yun, Byun, Youngro, Pak, Jhang Ho, Sohn, Woon-Mok, Hong, Sung-Jong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746286/
https://www.ncbi.nlm.nih.gov/pubmed/33284789
http://dx.doi.org/10.1371/journal.pntd.0008952
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author Dai, Fuhong
Yoo, Won Gi
Lu, Yanyan
Song, Jin-Ho
Lee, Ji-Yun
Byun, Youngro
Pak, Jhang Ho
Sohn, Woon-Mok
Hong, Sung-Jong
author_facet Dai, Fuhong
Yoo, Won Gi
Lu, Yanyan
Song, Jin-Ho
Lee, Ji-Yun
Byun, Youngro
Pak, Jhang Ho
Sohn, Woon-Mok
Hong, Sung-Jong
author_sort Dai, Fuhong
collection PubMed
description The liver fluke Clonorchis sinensis inhabits the bile ducts, where bile concentration disparities across the fluke cell membrane can cause bile intoxication. Sodium-bile acid co-transporter (SBAT) plays a crucial role in bile acid recycling. The process by which SBAT imports bile acids is electrically coupled to sodium ion co-transportation. Here, we report that the SBAT of C. sinensis (CsSBAT) is involved in bile acid transportation. CsSBAT cDNA encoded a putative polypeptide of 546 amino acid residues. Furthermore, CsSBAT consisted of ten putative transmembrane domains, and its 3D structure was predicted to form panel and core domains. The CsSBAT had one bile acid- and three Na(+)-binding sites, enabling coordination of a symport process. CsSBAT was mainly localized in the mesenchymal tissue throughout the fluke body and sparsely localized in the basement of the tegument, intestinal epithelium, and excretory bladder wall. Bile acid permeated into the adult flukes in a short time and remained at a low concentration level. Bile acid accumulated inside the mesenchymal tissue when CsSBAT was inhibited using polyacrylic acid–tetradeoxycholic acid conjugate. The accumulated bile acid deteriorated the C. sinensis adults leading to death. CsSBAT silencing shortened the lifespan of the fluke when it was placed into bile. Taken together, we propose that CsSBAT transports bile acids in the mesenchymal tissue and coordinate with outward transporters to maintain bile acid homeostasis of C. sinensis adults, contributing to C. sinensis survival in the bile environment.
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spelling pubmed-77462862020-12-31 Sodium-bile acid co-transporter is crucial for survival of a carcinogenic liver fluke Clonorchis sinensis in the bile Dai, Fuhong Yoo, Won Gi Lu, Yanyan Song, Jin-Ho Lee, Ji-Yun Byun, Youngro Pak, Jhang Ho Sohn, Woon-Mok Hong, Sung-Jong PLoS Negl Trop Dis Research Article The liver fluke Clonorchis sinensis inhabits the bile ducts, where bile concentration disparities across the fluke cell membrane can cause bile intoxication. Sodium-bile acid co-transporter (SBAT) plays a crucial role in bile acid recycling. The process by which SBAT imports bile acids is electrically coupled to sodium ion co-transportation. Here, we report that the SBAT of C. sinensis (CsSBAT) is involved in bile acid transportation. CsSBAT cDNA encoded a putative polypeptide of 546 amino acid residues. Furthermore, CsSBAT consisted of ten putative transmembrane domains, and its 3D structure was predicted to form panel and core domains. The CsSBAT had one bile acid- and three Na(+)-binding sites, enabling coordination of a symport process. CsSBAT was mainly localized in the mesenchymal tissue throughout the fluke body and sparsely localized in the basement of the tegument, intestinal epithelium, and excretory bladder wall. Bile acid permeated into the adult flukes in a short time and remained at a low concentration level. Bile acid accumulated inside the mesenchymal tissue when CsSBAT was inhibited using polyacrylic acid–tetradeoxycholic acid conjugate. The accumulated bile acid deteriorated the C. sinensis adults leading to death. CsSBAT silencing shortened the lifespan of the fluke when it was placed into bile. Taken together, we propose that CsSBAT transports bile acids in the mesenchymal tissue and coordinate with outward transporters to maintain bile acid homeostasis of C. sinensis adults, contributing to C. sinensis survival in the bile environment. Public Library of Science 2020-12-07 /pmc/articles/PMC7746286/ /pubmed/33284789 http://dx.doi.org/10.1371/journal.pntd.0008952 Text en © 2020 Dai et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Dai, Fuhong
Yoo, Won Gi
Lu, Yanyan
Song, Jin-Ho
Lee, Ji-Yun
Byun, Youngro
Pak, Jhang Ho
Sohn, Woon-Mok
Hong, Sung-Jong
Sodium-bile acid co-transporter is crucial for survival of a carcinogenic liver fluke Clonorchis sinensis in the bile
title Sodium-bile acid co-transporter is crucial for survival of a carcinogenic liver fluke Clonorchis sinensis in the bile
title_full Sodium-bile acid co-transporter is crucial for survival of a carcinogenic liver fluke Clonorchis sinensis in the bile
title_fullStr Sodium-bile acid co-transporter is crucial for survival of a carcinogenic liver fluke Clonorchis sinensis in the bile
title_full_unstemmed Sodium-bile acid co-transporter is crucial for survival of a carcinogenic liver fluke Clonorchis sinensis in the bile
title_short Sodium-bile acid co-transporter is crucial for survival of a carcinogenic liver fluke Clonorchis sinensis in the bile
title_sort sodium-bile acid co-transporter is crucial for survival of a carcinogenic liver fluke clonorchis sinensis in the bile
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746286/
https://www.ncbi.nlm.nih.gov/pubmed/33284789
http://dx.doi.org/10.1371/journal.pntd.0008952
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