Differential expression of liver fluke β-tubulin isotypes at selected life cycle stages

Int J Parasitol. 2013 Dec;43(14):1133-9. doi: 10.1016/j.ijpara.2013.08.007. Epub 2013 Oct 24.

Abstract

We have shown that Fasciola hepatica expresses at least six β-tubulins in the adult stage of its life cycle, designated F.hep-β-tub1-6 (Ryan et al., 2008). Here we show that different complements of tubulin isotypes are expressed in different tissues and at different life cycle stages; this information may inform the search for novel anthelmintics. The predominant (as judged by quantitative PCR) isotype transcribed at the adult stage was F.hep-β-tub1 and immunolocalisation studies revealed that this isotype occurred mainly in mature spermatozoa and vitelline follicles. Quantitative PCR indicated that changes occurred in the transcription levels of β-tubulin isotypes at certain life cycle stages and may be of importance in the efficacy of benzimidazole-based anthelmintic drugs, but there were no significant differences between the triclabendazole-susceptible Leon isolate and the triclabendazole-resistant Oberon isolate in the transcription levels of each of the isotypes. When three well-characterised isolates with differing susceptibilities to triclabendazole were compared, only one amino acid change resulting from a homozygous coding sequence difference (Gly269Ser) in isotype 4 was observed. However, this change was not predicted to alter the overall structure of the protein. In conclusion, these findings indicate that there is tissue-specific expression of tubulin isotypes in the liver fluke but the development of resistance to triclabendazole is not associated with changes in its presumed target molecule.

Keywords: Anthelmintic resistance; Fasciola hepatica; Microtubule; Tubulin isotype.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anthelmintics / pharmacology
  • Benzimidazoles / pharmacology
  • Drug Resistance
  • Fasciola hepatica / drug effects
  • Fasciola hepatica / genetics*
  • Fasciola hepatica / growth & development*
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental*
  • Life Cycle Stages*
  • Protein Isoforms / biosynthesis
  • Protein Isoforms / genetics
  • Real-Time Polymerase Chain Reaction
  • Transcription, Genetic
  • Triclabendazole
  • Tubulin / biosynthesis*
  • Tubulin / genetics*

Substances

  • Anthelmintics
  • Benzimidazoles
  • Protein Isoforms
  • Tubulin
  • Triclabendazole