AI Article Synopsis

  • The evolution of blood-feeding insects, like mosquitoes, involves adaptations that help them consume blood while avoiding the host's immune responses.
  • Anopheles gambiae salivary apyrase (AgApyrase) plays a key role in blood meal hemostasis by inhibiting platelet aggregation and facilitating the conversion of plasminogen to plasmin, which helps in degrading fibrin and promotes Plasmodium transmission.
  • Immunizing against AgApyrase can inhibit Plasmodium infection and transmission, suggesting potential strategies for preventing malaria spread.

Article Abstract

The evolution of hematophagy involves a series of adaptations that allow blood-feeding insects to access and consume blood efficiently while managing and circumventing the host's hemostatic and immune responses. Mosquito, and other insects, utilize salivary proteins to regulate these responses at the bite site during and after blood feeding. We investigated the function of Anopheles gambiae salivary apyrase (AgApyrase) in regulating hemostasis in the mosquito blood meal and in Plasmodium transmission. Our results demonstrate that salivary apyrase, a known inhibitor of platelet aggregation, interacts with and activates tissue plasminogen activator, facilitating the conversion of plasminogen to plasmin, a human protease that degrades fibrin and facilitates Plasmodium transmission. We show that mosquitoes ingest a substantial amount of apyrase during blood feeding, which reduces coagulation in the blood meal by enhancing fibrin degradation and inhibiting platelet aggregation. AgApyrase significantly enhanced Plasmodium infection in the mosquito midgut, whereas AgApyrase immunization inhibited Plasmodium mosquito infection and sporozoite transmission. This study highlights a pivotal role for mosquito salivary apyrase for regulation of hemostasis in the mosquito blood meal and for Plasmodium transmission to mosquitoes and to the mammalian host, underscoring the potential for strategies to prevent malaria transmission.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11410810PMC
http://dx.doi.org/10.1038/s41467-024-52502-3DOI Listing

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