Filarial DAF-12 sense the host serum to resume iL3 development during infection

PLoS Pathog. 2023 Jun 20;19(6):e1011462. doi: 10.1371/journal.ppat.1011462. eCollection 2023 Jun.

Abstract

Nematode parasites enter their definitive host at the developmentally arrested infectious larval stage (iL3), and the ligand-dependent nuclear receptor DAF-12 contributes to trigger their development to adulthood. Here, we characterized DAF-12 from the filarial nematodes Brugia malayi and Dirofilaria immitis and compared them with DAF-12 from the non-filarial nematodes Haemonchus contortus and Caenorhabditis elegans. Interestingly, Dim and BmaDAF-12 exhibit high sequence identity and share a striking higher sensitivity than Hco and CelDAF-12 to the natural ligands Δ4- and Δ7-dafachronic acids (DA). Moreover, sera from different mammalian species activated specifically Dim and BmaDAF-12 while the hormone-depleted sera failed to activate the filarial DAF-12. Accordingly, hormone-depleted serum delayed the commencement of development of D. immitis iL3 in vitro. Consistent with these observations, we show that spiking mouse charcoal stripped-serum with Δ4-DA at the concentration measured in normal mouse serum restores its capacity to activate DimDAF-12. This indicates that DA present in mammalian serum participate in filarial DAF-12 activation. Finally, analysis of publicly available RNA sequencing data from B. malayi showed that, at the time of infection, putative gene homologs of the DA synthesis pathways are coincidently downregulated. Altogether, our data suggest that filarial DAF-12 have evolved to specifically sense and survive in a host environment, which provides favorable conditions to quickly resume larval development. This work sheds new light on the regulation of filarial nematodes development while entering their definitive mammalian host and may open the route to novel therapies to treat filarial infections.

MeSH terms

  • Animals
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans Proteins* / genetics
  • Helminth Proteins* / genetics
  • Helminth Proteins* / metabolism
  • Hormones / metabolism
  • Larva / metabolism
  • Mammals
  • Mice
  • Receptors, Cytoplasmic and Nuclear / metabolism

Substances

  • Helminth Proteins
  • Caenorhabditis elegans Proteins
  • Hormones
  • DAF-12 protein, C elegans
  • Receptors, Cytoplasmic and Nuclear

Grants and funding

This study was supported by the department of Animal Health at INRAE (newly recruited researchers grant) to (R.B.); and a grant from the Natural Sciences and Engineering Research Council of Canada (Grant No. RGPIN-2017-04010) to (R.P.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.