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      Ultrastructural and Cytotoxic Effects of Metarhizium robertsii Infection on Rhipicephalus microplus Hemocytes

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          Abstract

          Metarhizium is an entomopathogenic fungus widely employed in the biological control of arthropods. Hemocytes present in the hemolymph of invertebrates are the cells involved in the immune response of arthropods. Despite this, knowledge about Rhipicephalus microplus hemocytes morphological aspects as well as their role in response to the fungal infection is scarce. The present study aimed to analyze the hemocytes of R. microplus females after Metarhizium robertsii infection, using light and electron microscopy approaches associated with the cytotoxicity evaluation. Five types of hemocytes (prohemocytes, spherulocytes, plasmatocytes, granulocytes, and oenocytoids) were described in the hemolymph of uninfected ticks, while only prohemocytes, granulocytes, and plasmatocytes were observed in fungus-infected tick females. Twenty-four hours after the fungal infection, only granulocytes and plasmatocytes were detected in the transmission electron microscopy analysis. Hemocytes from fungus-infected tick females showed several cytoplasmic vacuoles with different electron densities, and lipid droplets in close contact to low electron density vacuoles, as well as the formation of autophagosomes and subcellular material in different stages of degradation could also be observed. M. robertsii propagules were more toxic to tick hemocytes in the highest concentration tested (1.0 × 10 8 conidia mL −1). Interestingly, the lowest fungus concentration did not affect significantly the cell viability. Microanalysis showed that cells granules from fungus-infected and uninfected ticks had similar composition. This study addressed the first report of fungal cytotoxicity analyzing ultrastructural effects on hemocytes of R. microplus infected with entomopathogenic fungi. These results open new perspectives for the comprehension of ticks physiology and pathology, allowing the identification of new targets for the biological control.

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          Intestinal epithelial autophagy is essential for host defense against invasive bacteria.

          The mammalian intestine is colonized with a diverse community of bacteria that perform many beneficial functions but can threaten host health upon tissue invasion. Epithelial cell-intrinsic innate immune responses are essential to limit the invasion of both commensal and pathogenic bacteria and maintain beneficial host-bacterial relationships; however, little is known about the role of various cellular processes, notably autophagy, in controlling bacterial interactions with the intestinal epithelium in vivo. We demonstrate that intestinal epithelial cell autophagy protects against tissue invasion by both opportunistically invasive commensals and the invasive intestinal pathogen Salmonella Typhimurium. Autophagy is activated following bacterial invasion of epithelial cells through a process requiring epithelial cell-intrinsic signaling via the innate immune adaptor protein MyD88. Additionally, mice deficient in intestinal epithelial cell autophagy exhibit increased dissemination of invasive bacteria to extraintestinal sites. Thus, autophagy is an important epithelial cell-autonomous mechanism of antibacterial defense that protects against dissemination of intestinal bacteria. Copyright © 2013 Elsevier Inc. All rights reserved.
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            Exploiting the potential of insects for in vivo pathogenicity testing of microbial pathogens.

            Conventional assays for quantifying the virulence of microbial pathogens and mutants have traditionally relied upon the use of a range of mammalian species. A number of workers have demonstrated that insects can be used for evaluating microbial pathogenicity and provide results comparable to those that can be obtained with mammals since one component of the vertebrate immune system, the innate immune response, remains similar to that found in insects. Larvae of the Greater Wax Moth Galleria mellonella have been used to evaluate the virulence of a range of bacterial and fungal pathogens and a correlation with the virulence of these microbes in mice has been established. This review highlights the similarities of the vertebrate and insect innate immune responses to infection and identifies the potential use of insects for the in vivo evaluation of the microbial pathogenicity.
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              Trajectory and genomic determinants of fungal-pathogen speciation and host adaptation

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                Author and article information

                Contributors
                URI : http://loop.frontiersin.org/people/735479/overview
                URI : http://loop.frontiersin.org/people/644155/overview
                URI : http://loop.frontiersin.org/people/535783/overview
                URI : http://loop.frontiersin.org/people/739737/overview
                URI : http://loop.frontiersin.org/people/739742/overview
                URI : http://loop.frontiersin.org/people/739759/overview
                URI : http://loop.frontiersin.org/people/739807/overview
                URI : http://loop.frontiersin.org/people/634310/overview
                Journal
                Front Physiol
                Front Physiol
                Front. Physiol.
                Frontiers in Physiology
                Frontiers Media S.A.
                1664-042X
                29 May 2019
                2019
                : 10
                : 654
                Affiliations
                [1] 1Programa de Pós-Graduação em Ciências Veterinárias, Instituto de Veterinária, Universidade Federal Rural do Rio de Janeiro , Seropédica, Brazil
                [2] 2Laboratório de Biologia Celular, IOC, Fundação Oswaldo Cruz , Rio de Janeiro, Brazil
                [3] 3Departamento de Parasitologia Animal, Instituto de Veterinária, Universidade Federal Rural do Rio de Janeiro , Seropédica, Brazil
                [4] 4Laboratório de Fisiopatologia, Instituto Butantan , São Paulo, Brazil
                [5] 5Departamento de Epidemiologia e Saúde Pública, Instituto de Veterinária, Universidade Federal Rural do Rio de Janeiro , Seropédica, Brazil
                Author notes

                Edited by: Itabajara Da Silva Vaz Jr., Federal University of Rio Grande do Sul, Brazil

                Reviewed by: Renata Silva Matos, Universidade Federal de Juiz de Fora, Brazil; Karim Christina Furquim Isler, Universidade Estadual Paulista Júlio de Mesquita Filho, Brazil

                *Correspondence: Vânia Rita Elias Pinheiro Bittencourt, vaniabit@ 123456ufrrj.br

                This article was submitted to Invertebrate Physiology, a section of the journal Frontiers in Physiology

                Article
                10.3389/fphys.2019.00654
                6548823
                31191351
                76279076-150a-4c7f-a226-04acdd3718c0
                Copyright © 2019 Fiorotti, Menna-Barreto, Gôlo, Coutinho-Rodrigues, Bitencourt, Spadacci-Morena, Angelo and Bittencourt.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 04 March 2019
                : 09 May 2019
                Page count
                Figures: 12, Tables: 0, Equations: 0, References: 125, Pages: 17, Words: 0
                Categories
                Physiology
                Original Research

                Anatomy & Physiology
                entomopathogenic fungi,cell death,fungal infection,tick,immunity
                Anatomy & Physiology
                entomopathogenic fungi, cell death, fungal infection, tick, immunity

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