Altered gene expression in the host brain caused by a trematode parasite: neuropeptide genes are preferentially affected during parasitosis

Proc Natl Acad Sci U S A. 1997 Dec 9;94(25):14072-6. doi: 10.1073/pnas.94.25.14072.

Abstract

Schistosome parasites adjust the physiology and behavior of their intermediate molluscan hosts to their own benefit. Previous studies demonstrated effects of the avian-schistosome Trichobilharzia ocellata on peptidergic centers in the brain of the intermediate snail host Lymnaea stagnalis. In particular, electrophysiological properties and peptide release of growth- and reproduction-controlling neuroendocrine neurons were affected. We now have examined the possibility that the expression of genes that control physiology and behavior of the host might be altered during parasitosis. A cDNA library of the brain of parasitized Lymnaea was constructed and differentially screened by using mRNA from the brain of both parasitized and nonparasitized snails. This screening yielded a number of clones, including previously identified cDNAs as well as novel neuronal transcripts, which appear to be differentially regulated. The majority of these transcripts encode neuropeptides. Reverse Northern blot analysis confirmed that neuropeptide gene expression is indeed affected in parasitized animals. Moreover, the expression profiles of 10 transcripts tested showed a differential, parasitic stage-specific regulation. Changes in expression could in many cases already be observed between 1.5 and 5 hr postinfection, suggesting that changes in gene expression are a direct effect of parasitosis. We suggest that direct regulation of neuropeptide gene expression is a strategy of parasites to induce physiological and behavioral changes in the host.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Brain / metabolism*
  • DNA, Complementary / genetics
  • Gene Expression
  • Host-Parasite Interactions / genetics
  • Lymnaea / genetics
  • Lymnaea / metabolism
  • Lymnaea / parasitology
  • Molecular Sequence Data
  • Neuropeptides / genetics*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Sequence Homology, Amino Acid
  • Trematoda / pathogenicity*
  • Trematode Infections / genetics*
  • Trematode Infections / metabolism
  • Trematode Infections / parasitology

Substances

  • DNA, Complementary
  • Neuropeptides
  • RNA, Messenger