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Carbon dioxide shapes parasite-host interactions in a human-infective nematode.
- Source :
-
BioRxiv : the preprint server for biology [bioRxiv] 2024 Mar 31. Date of Electronic Publication: 2024 Mar 31. - Publication Year :
- 2024
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Abstract
- Skin-penetrating nematodes infect nearly one billion people worldwide. The developmentally arrested infective larvae (iL3s) seek out hosts, invade hosts via skin penetration, and resume development inside the host in a process called activation. Activated infective larvae (iL3as) traverse the host body, ending up as parasitic adults in the small intestine. Skin-penetrating nematodes respond to many chemosensory cues, but how chemosensation contributes to host seeking, intra-host development, and intra-host navigation - three crucial steps of the parasite-host interaction - remains poorly understood. Here, we investigate the role of carbon dioxide (CO <subscript>2</subscript> ) in promoting parasite-host interactions in the human-infective threadworm Strongyloides stercoralis . We show that S. stercoralis exhibits life-stage-specific preferences for CO <subscript>2</subscript> : iL3s are repelled, non-infective larvae and adults are neutral, and iL3as are attracted. CO <subscript>2</subscript> repulsion in iL3s may prime them for host seeking by stimulating dispersal from host feces, while CO <subscript>2</subscript> attraction in iL3as may direct worms toward high-CO <subscript>2</subscript> areas of the body such as the lungs and intestine. We also identify sensory neurons that detect CO <subscript>2</subscript> ; these neurons are depolarized by CO <subscript>2</subscript> in iL3s and iL3as. In addition, we demonstrate that the receptor guanylate cyclase Ss -GCY-9 is expressed specifically in CO <subscript>2</subscript> -sensing neurons and is required for CO <subscript>2</subscript> -evoked behavior . Ss -GCY-9 also promotes activation, indicating that a single receptor can mediate both behavioral and physiological responses to CO <subscript>2</subscript> . Our results illuminate chemosensory mechanisms that shape the interaction between parasitic nematodes and their human hosts and may aid in the design of novel anthelmintics that target the CO <subscript>2</subscript> -sensing pathway.<br />Competing Interests: Declaration of Interests The authors declare no competing interests.
Details
- Language :
- English
- Database :
- MEDLINE
- Journal :
- BioRxiv : the preprint server for biology
- Accession number :
- 38585813
- Full Text :
- https://doi.org/10.1101/2024.03.28.587273