Identification and Analysis of a Four-Gene Set for Diagnosing SFTS Virus Infection Based on Machine Learning Methods and Its Association with Immune Cell Infiltration

Severe Fever with thrombocytopenia syndrome (SFTS) is a highly fatal viral infectious disease that poses a significant threat to public health. Currently, the phase and pathogenesis of SFTS are not well understood, and there are no specific vaccines or effective treatment available. Therefore, it is...

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Main Authors: Tao Huang, Xueqi Wang, Yuqian Mi, Tiezhu Liu, Yang Li, Ruixue Zhang, Zhen Qian, Yanhan Wen, Boyang Li, Lina Sun, Wei Wu, Jiandong Li, Shiwen Wang, Mifang Liang
Format: Article
Language:English
Published: MDPI AG 2023-10-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/15/10/2126
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author Tao Huang
Xueqi Wang
Yuqian Mi
Tiezhu Liu
Yang Li
Ruixue Zhang
Zhen Qian
Yanhan Wen
Boyang Li
Lina Sun
Wei Wu
Jiandong Li
Shiwen Wang
Mifang Liang
author_facet Tao Huang
Xueqi Wang
Yuqian Mi
Tiezhu Liu
Yang Li
Ruixue Zhang
Zhen Qian
Yanhan Wen
Boyang Li
Lina Sun
Wei Wu
Jiandong Li
Shiwen Wang
Mifang Liang
author_sort Tao Huang
collection DOAJ
description Severe Fever with thrombocytopenia syndrome (SFTS) is a highly fatal viral infectious disease that poses a significant threat to public health. Currently, the phase and pathogenesis of SFTS are not well understood, and there are no specific vaccines or effective treatment available. Therefore, it is crucial to identify biomarkers for diagnosing acute SFTS, which has a high mortality rate. In this study, we conducted differentially expressed genes (DEGs) analysis and WGCNA module analysis on the GSE144358 dataset, comparing the acute phase of SFTSV-infected patients with healthy individuals. Through the LASSO–Cox and random forest algorithms, a total of 2128 genes were analyzed, leading to the identification of four genes: ADIPOR1, CENPO, E2F2, and H2AC17. The GSEA analysis of these four genes demonstrated a significant correlation with immune cell function and cell cycle, aligning with the functional enrichment findings of DEGs. Furthermore, we also utilized CIBERSORT to analyze the immune cell infiltration and its correlation with characteristic genes. The results indicate that the combination of ADIPOR1, CENPO, E2F2, and H2AC17 genes has the potential as characteristic genes for diagnosing and studying the acute phase of SFTS virus (SFTSV) infection.
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spelling doaj.art-5cb4f87661954df49acc0d3f125a91d02023-11-19T18:28:42ZengMDPI AGViruses1999-49152023-10-011510212610.3390/v15102126Identification and Analysis of a Four-Gene Set for Diagnosing SFTS Virus Infection Based on Machine Learning Methods and Its Association with Immune Cell InfiltrationTao Huang0Xueqi Wang1Yuqian Mi2Tiezhu Liu3Yang Li4Ruixue Zhang5Zhen Qian6Yanhan Wen7Boyang Li8Lina Sun9Wei Wu10Jiandong Li11Shiwen Wang12Mifang Liang13National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases (NITFID), Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, ChinaCapital Institute of Pediatrics, Beijing 100020, ChinaShanxi Academy of Advanced Research and Innovation, Taiyuan 030032, ChinaNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases (NITFID), Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, ChinaChongqing Research Institute of Big Data, Peking University, Chongqing 400039, ChinaNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases (NITFID), Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, ChinaNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases (NITFID), Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, ChinaNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases (NITFID), Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, ChinaNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases (NITFID), Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, ChinaNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases (NITFID), Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, ChinaNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases (NITFID), Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, ChinaNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases (NITFID), Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, ChinaNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases (NITFID), Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, ChinaNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases (NITFID), Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, ChinaSevere Fever with thrombocytopenia syndrome (SFTS) is a highly fatal viral infectious disease that poses a significant threat to public health. Currently, the phase and pathogenesis of SFTS are not well understood, and there are no specific vaccines or effective treatment available. Therefore, it is crucial to identify biomarkers for diagnosing acute SFTS, which has a high mortality rate. In this study, we conducted differentially expressed genes (DEGs) analysis and WGCNA module analysis on the GSE144358 dataset, comparing the acute phase of SFTSV-infected patients with healthy individuals. Through the LASSO–Cox and random forest algorithms, a total of 2128 genes were analyzed, leading to the identification of four genes: ADIPOR1, CENPO, E2F2, and H2AC17. The GSEA analysis of these four genes demonstrated a significant correlation with immune cell function and cell cycle, aligning with the functional enrichment findings of DEGs. Furthermore, we also utilized CIBERSORT to analyze the immune cell infiltration and its correlation with characteristic genes. The results indicate that the combination of ADIPOR1, CENPO, E2F2, and H2AC17 genes has the potential as characteristic genes for diagnosing and studying the acute phase of SFTS virus (SFTSV) infection.https://www.mdpi.com/1999-4915/15/10/2126SFTSSFTS acute phasemachine learningLASSO–Coximmune cells infiltration
spellingShingle Tao Huang
Xueqi Wang
Yuqian Mi
Tiezhu Liu
Yang Li
Ruixue Zhang
Zhen Qian
Yanhan Wen
Boyang Li
Lina Sun
Wei Wu
Jiandong Li
Shiwen Wang
Mifang Liang
Identification and Analysis of a Four-Gene Set for Diagnosing SFTS Virus Infection Based on Machine Learning Methods and Its Association with Immune Cell Infiltration
Viruses
SFTS
SFTS acute phase
machine learning
LASSO–Cox
immune cells infiltration
title Identification and Analysis of a Four-Gene Set for Diagnosing SFTS Virus Infection Based on Machine Learning Methods and Its Association with Immune Cell Infiltration
title_full Identification and Analysis of a Four-Gene Set for Diagnosing SFTS Virus Infection Based on Machine Learning Methods and Its Association with Immune Cell Infiltration
title_fullStr Identification and Analysis of a Four-Gene Set for Diagnosing SFTS Virus Infection Based on Machine Learning Methods and Its Association with Immune Cell Infiltration
title_full_unstemmed Identification and Analysis of a Four-Gene Set for Diagnosing SFTS Virus Infection Based on Machine Learning Methods and Its Association with Immune Cell Infiltration
title_short Identification and Analysis of a Four-Gene Set for Diagnosing SFTS Virus Infection Based on Machine Learning Methods and Its Association with Immune Cell Infiltration
title_sort identification and analysis of a four gene set for diagnosing sfts virus infection based on machine learning methods and its association with immune cell infiltration
topic SFTS
SFTS acute phase
machine learning
LASSO–Cox
immune cells infiltration
url https://www.mdpi.com/1999-4915/15/10/2126
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