Differential proteomic analysis of children infected with respiratory syncytial virus

Respiratory syncytial virus (RSV) infection is the main cause of lower respiratory tract infection in children. However, there is no effective treatment for RSV infection. Here, we aimed to identify potential biomarkers to aid in the treatment of RSV infection. Children in the acute and convalescenc...

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Veröffentlicht in:Brazilian journal of medical and biological research 2021-01, Vol.54 (4), p.e9850-e9850, Article 9850
Hauptverfasser: Yin, Gen-Quan, Zeng, Hui-Xuan, Li, Zi-Long, Chen, Chen, Zhong, Jia-Yong, Xiao, Mi-Si, Zeng, Qiang, Jiang, Wen-Hui, Wu, Pei-Qiong, Zeng, Jie-Min, Hu, Xiao-Yin, Chen, Huan-Hui, Ruo-Hu, Zhao, Hai-Jin, Gao, Lin, Liu, Cong, Cai, Shao-Xi
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container_issue 4
container_start_page e9850
container_title Brazilian journal of medical and biological research
container_volume 54
creator Yin, Gen-Quan
Zeng, Hui-Xuan
Li, Zi-Long
Chen, Chen
Zhong, Jia-Yong
Xiao, Mi-Si
Zeng, Qiang
Jiang, Wen-Hui
Wu, Pei-Qiong
Zeng, Jie-Min
Hu, Xiao-Yin
Chen, Huan-Hui
Ruo-Hu
Zhao, Hai-Jin
Gao, Lin
Liu, Cong
Cai, Shao-Xi
description Respiratory syncytial virus (RSV) infection is the main cause of lower respiratory tract infection in children. However, there is no effective treatment for RSV infection. Here, we aimed to identify potential biomarkers to aid in the treatment of RSV infection. Children in the acute and convalescence phases of RSV infection were recruited and proteomic analysis was performed to identify differentially expressed proteins (DEPs). Subsequently, promising candidate proteins were determined by functional enrichment and protein-protein interaction network analysis, and underwent further validation by western blot both in clinical and mouse model samples. Among the 79 DEPs identified in RSV patient samples, 4 proteins (BPGM, TPI1, PRDX2, and CFL1) were confirmed to be significantly upregulated during RSV infection. Functional analysis showed that BPGM and TPI1 were mainly involved in glycolysis, indicating an association between RSV infection and the glycolysis metabolic pathway. Our findings provide insights into the proteomic profile during RSV infection and indicated that BPGM, TPI1, PRDX2, and CFL1 may be potential therapeutic biomarkers or targets for the treatment of RSV infection.
doi_str_mv 10.1590/1414-431X20209850
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However, there is no effective treatment for RSV infection. Here, we aimed to identify potential biomarkers to aid in the treatment of RSV infection. Children in the acute and convalescence phases of RSV infection were recruited and proteomic analysis was performed to identify differentially expressed proteins (DEPs). Subsequently, promising candidate proteins were determined by functional enrichment and protein-protein interaction network analysis, and underwent further validation by western blot both in clinical and mouse model samples. Among the 79 DEPs identified in RSV patient samples, 4 proteins (BPGM, TPI1, PRDX2, and CFL1) were confirmed to be significantly upregulated during RSV infection. Functional analysis showed that BPGM and TPI1 were mainly involved in glycolysis, indicating an association between RSV infection and the glycolysis metabolic pathway. 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subjects BIOLOGY
Biomarkers
Child
Children
Differentially expressed protein
Humans
Infection
Life Sciences & Biomedicine
Life Sciences & Biomedicine - Other Topics
MEDICINE, RESEARCH & EXPERIMENTAL
Mouse model
Protein-protein interactions
Proteins
Proteomics
Research & Experimental Medicine
Respiratory syncytial virus
Respiratory Syncytial Virus Infections
Respiratory Syncytial Virus, Human
Science & Technology
title Differential proteomic analysis of children infected with respiratory syncytial virus
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