4.8 Article

A multi-adenylate cyclase regulator at the flagellar tip controls African trypanosome transmission

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NATURE COMMUNICATIONS
卷 13, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41467-022-33108-z

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资金

  1. BioNa young scientists award of LMU
  2. MC-IEF Fellowship [PIEF-GA-2013-626034]
  3. IN.WBI excellence fellowship
  4. CNPq/Universal Grant [725 422022/2016-0]
  5. Deutsche Forschungsgemeinschaft (DFG) [268759902, 443931024]
  6. Institut Pasteur
  7. Institut National pour la Sante et le Recherche Medicale (INSERM)
  8. French Government Investissement d'Avenir programme - Laboratoire d'Excellence Integrative Biology of Emerging Infectious Diseases [ANR-10-LABX-62-IBEID]
  9. French National Agency for Scientific Research [ANR-14-CE14-0019-01 EnTrypa, ANR-18-CE15-0012 TrypaDerm]
  10. LMU

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Researchers have discovered that social motility and cAMP signaling are linked to migration of trypanosomes in the salivary glands of tsetse flies. Trypanosomes can sense environmental signals and coordinate their movement by interacting with adenylate cyclases and other proteins. These findings provide insights into the mechanisms of trypanosome migration and transmission in tsetse flies.
Trypanosomes can sense signal molecules and coordinate their movement in response to such signals, a phenomenon termed social motility (SoMo). Here, Bachmaier et al show that cyclic AMP response protein 3 (CARP3) localization to the flagellar tip and its interaction with a number of different adenylate cyclases is essential for migration to tsetse fly salivary glands and for SoMo, therewith linking SoMo and cAMP signaling to trypanosome transmission. Signaling from ciliary microdomains controls developmental processes in metazoans. Trypanosome transmission requires development and migration in the tsetse vector alimentary tract. Flagellar cAMP signaling has been linked to parasite social motility (SoMo) in vitro, yet uncovering control of directed migration in fly organs is challenging. Here we show that the composition of an adenylate cyclase (AC) complex in the flagellar tip microdomain is essential for tsetse salivary gland (SG) colonization and SoMo. Cyclic AMP response protein 3 (CARP3) binds and regulates multiple AC isoforms. CARP3 tip localization depends on the cytoskeletal protein FLAM8. Re-localization of CARP3 away from the tip microdomain is sufficient to abolish SoMo and fly SG colonization. Since intrinsic development is normal in carp3 and flam8 knock-out parasites, AC complex-mediated tip signaling specifically controls parasite migration and thereby transmission. Participation of several developmentally regulated receptor-type AC isoforms may indicate the complexity of the in vivo signals perceived.

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