# A neuregulin-like ligand and EGF receptor underpin Echinococcus multilocularis development

**Authors:** Akito Koike, Monika Bergmann, Katia Cailliau, Jérôme Vicogne, Frank Becker, Colette Dissous, Stefan Hannus, Klaus Brehm

PMC · DOI: 10.3389/fcimb.2026.1742233 · Frontiers in Cellular and Infection Microbiology · 2026-02-20

## TL;DR

A neuregulin-like ligand and EGF receptor are crucial for the development of Echinococcus multilocularis, a parasite causing a severe zoonotic disease.

## Contribution

The discovery of a neuregulin-like ligand (EmNRG) and its receptor (EmER1) as key regulators of parasite stem cell division in Echinococcus multilocularis.

## Key findings

- EmER1 is essential for metacestode vesicle formation from germinative cells and is inhibited by afatinib.
- EmNRG, a neuregulin-like ligand, interacts with EmER1 and is upregulated during stem cell clonal expansion.
- Knockdown of EmNRG encoding gene impairs metacestode vesicle generation by germinative cells.

## Abstract

Alveolar echinococcosis (AE), a neglected zoonotic disease, is caused by the infiltrative growth of the metacestode larval stage of the cestode Echinococcus multilocularis within host organs. We previously showed that metacestode development relies on the mitotic activity of a population of parasite stem cells known as germinative cells. However, the molecular mechanisms that control Echinococcus stem cell dynamics such as cell-cycle progression, self-renewal, and differentiation remain poorly understood. Building on earlier reports implicating epidermal growth factor (EGF) signalling in stem cell regulation, we here characterize the parasite’s repertoire of three EGF receptors. Using RNAi and inhibitor assays, we identify one receptor, EmER1, as essential for the formation of metacestode vesicles from germinative cells. We further demonstrate that EmER1 is targeted by afatinib, an EGF receptor inhibitor with potent anti-parasitic activity both in vitro and in vivo. Through bioinformatic analyses and membrane-bound yeast two-hybrid assays, we identified a parasite-derived, neuregulin-like ligand for EmER1, termed EmNRG, whose expression is strongly upregulated in metacestode vesicles during clonal expansion of germinative cells. RNAi-mediated knockdown of the EmNRG encoding gene severely impaired the capacity of germinative cells to generate metacestode vesicles. Our data support that EmNRG and EmER1 constitute a cognate ligand - receptor system regulating the balance between asymmetric and symmetric stem cell division in E. multilocularis. These findings provide new insights into Echinococcus stem cell biology and highlight EGF signalling as a promising avenue for developing novel anti-echinococcosis therapeutics.

## Linked entities

- **Chemicals:** afatinib (PubChem CID 10184653), epidermal growth factor (PubChem CID 56841751)
- **Diseases:** Alveolar echinococcosis (MONDO:0017282), echinococcosis (MONDO:0005738)
- **Species:** Echinococcus multilocularis (taxon 6211), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, egfr.S (epidermal growth factor receptor S homeolog) [NCBI Gene 108719997] {aka XEgfr, erbb, erbb1, her1}, AUR1 (inositol phosphorylceramide synthase) [NCBI Gene 853866], TGFA (transforming growth factor alpha) [NCBI Gene 7039] {aka TFGA}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, NRG1 (neuregulin 1) [NCBI Gene 3084] {aka ARIA, GGF, GGF2, HGL, HRG, HRG1}, PCSK1 (proprotein convertase subtilisin/kexin type 1) [NCBI Gene 5122] {aka BMIQ12, NEC1, PC1, PC1/3, PC3, SPC3}, CXCR4 (C-X-C motif chemokine receptor 4) [NCBI Gene 7852] {aka CD184, D2S201E, FB22, HM89, HSY3RR, LCR1}, NCKIPSD (NCK interacting protein with SH3 domain) [NCBI Gene 51517] {aka AF3P21, DIP, DIP1, ORF1, SPIN90, VIP54}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, CXCL12 (C-X-C motif chemokine ligand 12) [NCBI Gene 6387] {aka IRH, PBSF, SCYB12, SDF1, TLSF, TPAR1}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}
- **Diseases:** echinococcosis (MESH:D004443), cancer (MESH:D009369), toxicity (MESH:D064420), AE (MESH:C536591)
- **Chemicals:** Trizol (MESH:C411644), Leu (MESH:D007930), tyrosine (MESH:D014443), aniline (MESH:C023650), 5-ethynyl-2'-deoxyuridine (MESH:C031086), progesterone (MESH:D011374), mebendazole (MESH:D008463), osimertinib (MESH:C000596361), His (MESH:D006639), quinazoline (MESH:D011799), Cys (MESH:D003545), paraformaldehyde (MESH:C003043), Afatinib (MESH:D000077716), ATP (MESH:D000255), albendazole (MESH:D015766), DMSO (MESH:D004121), DAPI (MESH:C007293), HU (MESH:D006918), Trp (MESH:D014364), disulfide (MESH:D004220), DIG (-), benzimidazoles (MESH:D001562), MC (MESH:C061001), Dacomitinib (MESH:C525726), Amino Acid (MESH:D000596)
- **Species:** Schistosoma mansoni (species) [taxon 6183], Meriones unguiculatus (Mongolian gerbil, species) [taxon 10047], Hofstenia miamia (species) [taxon 442651], Echinococcus multilocularis (species) [taxon 6211], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Mus musculus (house mouse, species) [taxon 10090], Platyhelminthes (flatworm, phylum) [taxon 6157], Xenopus laevis (African clawed frog, species) [taxon 8355], Macaca fascicularis (crab eating macaque, species) [taxon 9541], Vulpes vulpes (red fox, species) [taxon 9627], Schmidtea mediterranea (freshwater planarian, species) [taxon 79327], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Ile13Gly, C797S, (F) for 30
- **Cell lines:** -5 — Mus musculus (Mouse), Transformed cell line (CVCL_5U93), S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232), HEK293T — Homo sapiens (Human), Transformed cell line (CVCL_0063), PC3 — Homo sapiens (Human), Prostate carcinoma, Cancer cell line (CVCL_0035), H95 — Mus musculus (Mouse), Hybrid cell line (CVCL_J820)

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12963305/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12963305/full.md

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Source: https://tomesphere.com/paper/PMC12963305