Na+/H+ exchanger (NHE) in Pacific white shrimp (Litopenaeus vannamei): Molecular cloning, transcriptional response to acidity stress, and physiological roles in pH homeostasis

PLoS One. 2019 Feb 27;14(2):e0212887. doi: 10.1371/journal.pone.0212887. eCollection 2019.

Abstract

Na+/H+ exchangers are the most common membrane proteins involved in the regulation of intracellular pH that concurrently transport Na+ into the cells and H+ out of the cells. In this study, the full-length cDNA of the Na+/H+ exchanger (NHE) from the Pacific white shrimp (Litopenaeus vannamei) was cloned. The LvNHE cDNA is 3167 bp long, contains a 5'-untranslated region (UTR) of 74 bp and a 3'-UTR of 456 bp and an open reading frame (ORF) of 2637 bp, coding for a protein of 878 amino acids with 11 putative transmembrane domains and a long cytoplasmic tail. LvNHE shows high sequence homology with mud crab NHE at the amino acid level. LvNHE mRNA was detected in the hepatopancreas, gill, eyestalk, skin, heart, intestine, muscle, brain and stomach, with the highest abundance in the intestine. In the shrimp intestinal fragment cultures exposed to gradually declining pH medium (from pH 8.0 to pH 6.4), the LvNHE mRNA expression was significantly stimulated, with the highest response when incubated in pH 7.0 medium for 6 h. To investigate the functional roles of LvNHE in pH regulation at the physiological and cellular levels, the LvNHE mRNA expression was silenced by siRNA knockdown. Upon low-pH challenge, the hemolymph pH was significantly reduced in the LvNHE mRNA knockdown shrimp. In addition, knockdown of LvNHE mRNA reduced the recovery capacity of intracellular pH in intestinal fragment cultures after acidification. Altogether, this study demonstrates the role of NHE in shrimp response to low pH stress and provides new insights into the acid/base homeostasis mechanisms of crustaceans.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arthropod Proteins / genetics
  • Arthropod Proteins / metabolism
  • Cloning, Molecular / methods*
  • Gene Expression Regulation
  • Homeostasis
  • Hydrogen-Ion Concentration
  • Open Reading Frames
  • Penaeidae / genetics
  • Penaeidae / metabolism*
  • Sequence Analysis, DNA
  • Sodium-Hydrogen Exchangers / genetics*
  • Sodium-Hydrogen Exchangers / metabolism*
  • Stress, Physiological
  • Tissue Distribution
  • Transcription, Genetic

Substances

  • Arthropod Proteins
  • Sodium-Hydrogen Exchangers

Grants and funding

This work was supported by grants the National Natural Science Foundation of China (31402287 to Dr. Ting Chen and 31602135 to Dr. Wen Huang), the Guangdong Province Program (2015B020231007 to Prof. Chaoqun Hu and 2016A030310112 to Prof. Chaoqun Hu, 2016A020210062 to Dr. Ting Chen and 2014A020208136 to Dr. Ting Chen, 2017B030314052 to Dr. Wen Huang, 2017A030310429 to Dr. Xiao Jiang), the Program of Fishery Problem Tackling of Guangdong Province (A201701B03 to Prof. Chaoqun Hu), and the Science & Technology Promoting Projects for Oceanic & Fishery in Guangdong Province (A201601A03 to Prof. Chaoqun Hu). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.