Abstract

Mycoplasma gallisepticum (MG) is the most economically significant mycoplasma pathogen of poultry that causes chronic respiratory disease (CRD) in chickens. Although miRNAs have been identified as a major regulator effect on inflammatory response, it is largely unclear how they regulate MG-induced inflammation. The aim of this study was to investigate the functional roles of gga-miR-451 and identify downstream targets regulated by gga-miR-451 in MG infection of chicken. We found that the expression of gga-miR-451 was significantly up-regulated during MG infection of chicken embryo fibroblast cells (DF-1) and chicken embryonic lungs. Overexpression of gga-miR-451 decreased the MG-induced inflammatory cytokine production, including tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and interleukin-6 (IL-6), whereas inhibition of gga-miR-451 had the opposite effect. Gene expression data combined with luciferase reporter assays demonstrated that tyrosine3-monooxygenase/tryptophan5-monooxygenase activation protein zeta (YWHAZ) was identified as a direct target of gga-miR-451 in the context of MG infection. Furthermore, upregulation of gga-miR-451 significantly inhibited the MG-infected DF-1 cells proliferation, induced cell-cycle arrest, and promoted apoptosis. Collectively, our results demonstrate that gga-miR-451 negatively regulates the MG-induced production of inflammatory cytokines via targeting YWHAZ, inhibits the cell cycle progression and cell proliferation, and promotes cell apoptosis. This study provides a better understanding of the molecular mechanisms of MG infection.

Highlights

  • The host inflammatory response constitutes an essential immune defense against invasion by microbial pathogens

  • Mycoplasma gallisepticum (MG) Infection Significantly Upregulates gga-miR-451 Expression Microribonucleic acids (miRNA) sequencing was performed previously and a large variety of dysregulated miRNAs were identified in the lungs of MG-infected chicken embryos, and gga-miR-451 was down-regulated during MG infection [31]

  • We further investigated the expression of gga-miR-451 in MG-infected DF-1 cells at 48 h post-infection, and the result demonstrated that gga-miR-451 expression was up-regulated after MG infection (Figure 1B)

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Summary

Introduction

The host inflammatory response constitutes an essential immune defense against invasion by microbial pathogens. Mycoplasma gallisepticum (MG) is a common etiological cause of chronic respiratory disease (CRD) in chickens and infectious sinusitis in turkeys [2], which feature inflammation in respiratory tract (trachea, lungs, and air sacs) [3,4]. MG can invade, survive, and multiply inside chicken embryonic fibroblasts (CEF) and HeLa cells in vitro [7,8,9]. MG interacts with host respiratory epithelial cells and generates an inflammatory response, resulting in increased levels of cytokines, such as tumor necrosis factor alpha (TNF-α), interleukin-6 (IL-6), and interleukin-2 (IL-2) [10]. The increased levels of inflammatory mediators appear to play a protective role or to initiate an irreversible immune response leading to cell death [11]. MG-HS strain is a virulence strain isolated from a chicken farm in Hubei Province of China, which is used for further experiments [12,13]

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