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

PLoS Negl Trop Dis. 2020 Dec 7;14(12):e0008952. doi: 10.1371/journal.pntd.0008952. eCollection 2020 Dec.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Bile / metabolism
  • Bile Acids and Salts / metabolism*
  • Bile Ducts / parasitology
  • Binding Sites
  • Biological Transport
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Clonorchiasis / parasitology*
  • Clonorchis sinensis / genetics*
  • Clonorchis sinensis / physiology
  • Helminth Proteins / genetics
  • Helminth Proteins / metabolism
  • Male
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Models, Molecular*
  • Protein Domains
  • Rabbits
  • Sequence Alignment
  • Sodium / metabolism

Substances

  • Bile Acids and Salts
  • Carrier Proteins
  • Helminth Proteins
  • Membrane Glycoproteins
  • bile acid binding proteins
  • Sodium

Grants and funding

This research was supported by the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (grant no. 2014R1A2A1A11051870) to SJH. This research was supported by the Natural Science Foundation of the Jiangsu Higher Education Institutions of China (grant no. 19KJB310014) (http://jyt.jiangsu.gov.cn/) to FD. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.