A sand fly salivary protein acts as a neutrophil chemoattractant

Nat Commun. 2021 May 28;12(1):3213. doi: 10.1038/s41467-021-23002-5.

Abstract

Apart from bacterial formyl peptides or viral chemokine mimicry, a non-vertebrate or insect protein that directly attracts mammalian innate cells such as neutrophils has not been molecularly characterized. Here, we show that members of sand fly yellow salivary proteins induce in vitro chemotaxis of mouse, canine and human neutrophils in transwell migration or EZ-TAXIScan assays. We demonstrate murine neutrophil recruitment in vivo using flow cytometry and two-photon intravital microscopy in Lysozyme-M-eGFP transgenic mice. We establish that the structure of this ~ 45 kDa neutrophil chemotactic protein does not resemble that of known chemokines. This chemoattractant acts through a G-protein-coupled receptor and is dependent on calcium influx. Of significance, this chemoattractant protein enhances lesion pathology (P < 0.0001) and increases parasite burden (P < 0.001) in mice upon co-injection with Leishmania parasites, underlining the impact of the sand fly salivary yellow proteins on disease outcome. These findings show that some arthropod vector-derived factors, such as this chemotactic salivary protein, activate rather than inhibit the host innate immune response, and that pathogens take advantage of these inflammatory responses to establish in the host.

Publication types

  • Observational Study
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Cells, Cultured
  • Chemotactic Factors / metabolism*
  • Chemotaxis, Leukocyte / immunology
  • Disease Models, Animal
  • Dogs
  • Female
  • Healthy Volunteers
  • Host-Pathogen Interactions / immunology
  • Humans
  • Immunity, Innate
  • Insect Proteins / genetics
  • Insect Proteins / isolation & purification
  • Insect Proteins / metabolism*
  • Insect Vectors / immunology
  • Insect Vectors / metabolism
  • Insect Vectors / parasitology
  • Leishmania major / immunology
  • Leishmania major / pathogenicity
  • Leishmaniasis, Cutaneous / immunology*
  • Leishmaniasis, Cutaneous / parasitology
  • Leishmaniasis, Cutaneous / transmission
  • Male
  • Mice
  • Middle Aged
  • Neutrophil Infiltration / immunology
  • Neutrophils / immunology*
  • Primary Cell Culture
  • Psychodidae / immunology
  • Psychodidae / metabolism
  • Psychodidae / parasitology
  • Recombinant Proteins / genetics
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Salivary Proteins and Peptides / genetics
  • Salivary Proteins and Peptides / isolation & purification
  • Salivary Proteins and Peptides / metabolism*
  • Young Adult

Substances

  • Chemotactic Factors
  • Insect Proteins
  • Recombinant Proteins
  • Salivary Proteins and Peptides