| Literature DB >> 29290574 |
Ranadhir Dey1, Amritanshu B Joshi1, Fabiano Oliveira2, Lais Pereira3, Anderson B Guimarães-Costa2, Tiago D Serafim2, Waldionê de Castro2, Iliano V Coutinho-Abreu2, Parna Bhattacharya1, Shannon Townsend2, Hamide Aslan2, Alec Perkins2, Subir Karmakar1, Nevien Ismail1, Morgan Karetnick2, Claudio Meneses2, Robert Duncan1, Hira L Nakhasi1, Jesus G Valenzuela4, Shaden Kamhawi5.
Abstract
Leishmania donovani parasites are the cause of visceral leishmaniasis and are transmitted by bites from phlebotomine sand flies. A prominent feature of vector-transmitted Leishmania is the persistence of neutrophils at bite sites, where they protect captured parasites, leading to enhanced disease. Here, we demonstrate that gut microbes from the sand fly are egested into host skin alongside Leishmania parasites. The egested microbes trigger the inflammasome, leading to a rapid production of interleukin-1β (IL-1β), which sustains neutrophil infiltration. Reducing midgut microbiota by pretreatment of Leishmania-infected sand flies with antibiotics or neutralizing the effect of IL-1β in bitten mice abrogates neutrophil recruitment. These early events are associated with impairment of parasite visceralization, indicating that both gut microbiota and IL-1β are important for the establishment of Leishmania infections. Considering that arthropods harbor a rich microbiota, its potential egestion after bites may be a shared mechanism that contributes to severity of vector-borne disease. Published by Elsevier Inc.Entities:
Keywords: IL-1β; Leishmania; disease severity; gut microbiota; inflammasome; neutrophil; parasite dissemination; sand fly; skin inflammatory response; vector-borne disease
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Year: 2017 PMID: 29290574 PMCID: PMC5832060 DOI: 10.1016/j.chom.2017.12.002
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023