The Extract of Scutellaria baicalensis Attenuates the Pattern Recognition Receptor Pathway Activation Induced by Influenza A Virus in Macrophages

Author:

Yang Mingrui1,Ma Luyao1,Su Rina1,Guo Rui1,Zhou Na1,Liu Menghua1,Wu Jun1,Wang Yi2,Hao Yu1

Affiliation:

1. School of Life Sciences, Beijing University of Chinese Medicine, Beijing 102488, China

2. Experimental Research Center, China Academy of Chinese Medical Sciences, Beijing 100700, China

Abstract

The dual strategy of inhibiting the viral life cycle and reducing the host inflammatory response should be considered in the development of therapeutic drugs for influenza A virus (IAV). In this study, an extract of Scutellaria baicalinase (SBE) containing seven flavonoids was identified to exert both antiviral and anti-inflammatory effects in macrophages infected with IAV. We performed transcriptome analysis using high-throughput RNA sequencing and identified 315 genes whose transcription levels were increased after IAV infection but were able to be decreased after SBE intervention. Combined with Gene Ontology (GO) and Kyoto encyclopedia of genes and genomes (KEGG) enrichment analysis, these genes were mainly involved in TLR3/7/8, RIG-I/MDA5, NLRP3 and cGAS pattern recognition receptor (PRR)-mediated signaling pathways. SBE inhibited the transcription of essential genes in the above pathways and nuclear translocation of NF-κB p65 as confirmed by RT-qPCR and immunofluorescence, respectively, indicating that SBE reversed PR8-induced over-activation of the PRR signaling pathway and inflammation in macrophages. This study provides an experimental basis for applying Scutellaria baicalensis and its main effects in the clinical treatment of viral pneumonia. It also provides novel targets for screening and developing novel drugs to prevent and treat IAV infectious diseases.

Funder

Innovation Team and Talents Cultivation Program of the National Administration of Traditional Chinese Medicine

National Science Foundation of China

Scientific and Technological Innovation Project of CACMS

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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