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MicroRNAs Contribute to Host Response to Coxiella burnetii.
Sachan, Madhur; Brann, Katelynn R; Fullerton, Marissa S; Voth, Daniel E; Raghavan, Rahul.
Afiliação
  • Sachan M; Department of Biology, Portland State University, Portland, Oregon, USA.
  • Brann KR; Department of Medicine, Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Fullerton MS; Department of Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
  • Voth DE; Department of Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
  • Raghavan R; Department of Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Infect Immun ; 91(1): e0019922, 2023 01 24.
Article em En | MEDLINE | ID: mdl-36537791
ABSTRACT
MicroRNAs (miRNAs), a class of small noncoding RNAs, are critical to gene regulation in eukaryotes. They are involved in modulating a variety of physiological processes, including the host response to intracellular infections. Little is known about miRNA functions during infection by Coxiella burnetii, the causative agent of human Q fever. This bacterial pathogen establishes a large replicative vacuole within macrophages by manipulating host processes such as apoptosis and autophagy. We investigated miRNA expression in C. burnetii-infected macrophages and identified several miRNAs that were down- or upregulated during infection. We further explored the functions of miR-143-3p, an miRNA whose expression is downregulated in macrophages infected with C. burnetii, and show that increasing the abundance of this miRNA in human cells results in increased apoptosis and reduced autophagy-conditions that are unfavorable to C. burnetii intracellular growth. In sum, this study demonstrates that C. burnetii infection elicits a robust miRNA-based host response, and because miR-143-3p promotes apoptosis and inhibits autophagy, downregulation of miR-143-3p expression during C. burnetii infection likely benefits the pathogen.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Febre Q / Coxiella burnetii / MicroRNAs Limite: Humans Idioma: En Revista: Infect Immun Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Febre Q / Coxiella burnetii / MicroRNAs Limite: Humans Idioma: En Revista: Infect Immun Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos