CELL-REPORTS-D-20-01909_De Souza-Vieira, Iniguez et al., 2020. Raw Data

Published: 28 October 2020| Version 1 | DOI: 10.17632/b6kj7rj6vb.1
Shaden Kamhawi


Heme oxygenase-1 induction by blood feeding arthropods controls skin inflammation and promotes disease tolerance. Hematophagous vectors lacerate host skin and capillaries to acquire a blood meal resulting in leakage of red blood cells (RBCs) and inflammation. Here, we show that heme oxygenase-1 (HO-1), a pleiotropic cytoprotective isoenzyme that mitigates heme-mediated tissue damage, is induced after bites of sand flies, mosquitoes and ticks. Further, we demonstrate that erythrophagocytosis by macrophages, including a skin-residing CD163+CD91+ professional iron recycling subpopulation, produces HO-1 after insect bites. Importantly, we establish that global deletion or transient inhibition of HO-1 in mice increases inflammation and pathology following Leishmania-infected sand fly bites without affecting parasite number; whereas CO, an end-product of the HO-1 enzymatic reaction suppresses skin inflammation. This indicates that HO-1 induction by blood feeding sand flies promotes tolerance to Leishmania infection. Collectively, our data demonstrate that HO-1 induction through erythrophagocytosis is a universal mechanism that regulates skin inflammation following blood feeding by arthropods thus promoting early-stage disease tolerance to vector-borne pathogens.



Immunology, Parasitology, Vector Borne Disease, Leishmaniasis