Identification of differentially expressed genes and signaling pathways with Candida infection by bioinformatics analysis

Abstract Background Opportunistic Candida species causes severe infections when the human immune system is weakened, leading to high mortality. Methods In our study, bioinformatics analysis was used to study the high-throughput sequencing data of samples infected with four kinds of Candida species....

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Main Authors: Guo-Dong Zhu, Li-Min Xie, Jian-Wen Su, Xun-Jie Cao, Xin Yin, Ya-Ping Li, Yuan-Mei Gao, Xu-Guang Guo
Format: Article
Language:English
Published: BMC 2022-03-01
Series:European Journal of Medical Research
Subjects:
Online Access:https://doi.org/10.1186/s40001-022-00651-w
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author Guo-Dong Zhu
Li-Min Xie
Jian-Wen Su
Xun-Jie Cao
Xin Yin
Ya-Ping Li
Yuan-Mei Gao
Xu-Guang Guo
author_facet Guo-Dong Zhu
Li-Min Xie
Jian-Wen Su
Xun-Jie Cao
Xin Yin
Ya-Ping Li
Yuan-Mei Gao
Xu-Guang Guo
author_sort Guo-Dong Zhu
collection DOAJ
description Abstract Background Opportunistic Candida species causes severe infections when the human immune system is weakened, leading to high mortality. Methods In our study, bioinformatics analysis was used to study the high-throughput sequencing data of samples infected with four kinds of Candida species. And the hub genes were obtained by statistical analysis. Results A total of 547, 422, 415 and 405 differentially expressed genes (DEGs) of Candida albicans, Candida glabrata, Candida parapsilosis and Candida tropicalis groups were obtained, respectively. A total of 216 DEGs were obtained after taking intersections of DEGs from the four groups. A protein–protein interaction (PPI) network was established using these 216 genes. The top 10 hub genes (FOSB, EGR1, JUNB, ATF3, EGR2, NR4A1, NR4A2, DUSP1, BTG2, and EGR3) were acquired through calculation by the cytoHubba plug-in in Cytoscape software. Validated by the sequencing data of peripheral blood, JUNB, ATF3 and EGR2 genes were  significant statistical significance. Conclusions In conclusion, our study demonstrated the potential pathogenic genes in Candida species and their underlying mechanisms by bioinformatic analysis methods. Further, after statistical validation, JUNB, ATF3 and EGR2 genes were attained, which may be used as potential biomarkers with Candida species infection.
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spelling doaj.art-c31cecc3e7d6430ba59e61502eb5e4182022-12-22T02:37:46ZengBMCEuropean Journal of Medical Research2047-783X2022-03-0127111110.1186/s40001-022-00651-wIdentification of differentially expressed genes and signaling pathways with Candida infection by bioinformatics analysisGuo-Dong Zhu0Li-Min Xie1Jian-Wen Su2Xun-Jie Cao3Xin Yin4Ya-Ping Li5Yuan-Mei Gao6Xu-Guang Guo7Department of Oncology, Guangzhou Geriatric HospitalDepartment of Clinical Laboratory Medicine, The Third Affiliated Hospital of Guangzhou Medical UniversityDepartment of Clinical Laboratory Medicine, The Third Affiliated Hospital of Guangzhou Medical UniversityDepartment of Clinical Laboratory Medicine, The Third Affiliated Hospital of Guangzhou Medical UniversityDepartment of Pediatrics, The Pediatrics School of Guangzhou Medical UniversityDepartment of Clinical Medicine, The Second Clinical School of Guangzhou Medical UniversityDepartment of Clinical Laboratory Medicine, The Third Affiliated Hospital of Guangzhou Medical UniversityDepartment of Clinical Laboratory Medicine, The Third Affiliated Hospital of Guangzhou Medical UniversityAbstract Background Opportunistic Candida species causes severe infections when the human immune system is weakened, leading to high mortality. Methods In our study, bioinformatics analysis was used to study the high-throughput sequencing data of samples infected with four kinds of Candida species. And the hub genes were obtained by statistical analysis. Results A total of 547, 422, 415 and 405 differentially expressed genes (DEGs) of Candida albicans, Candida glabrata, Candida parapsilosis and Candida tropicalis groups were obtained, respectively. A total of 216 DEGs were obtained after taking intersections of DEGs from the four groups. A protein–protein interaction (PPI) network was established using these 216 genes. The top 10 hub genes (FOSB, EGR1, JUNB, ATF3, EGR2, NR4A1, NR4A2, DUSP1, BTG2, and EGR3) were acquired through calculation by the cytoHubba plug-in in Cytoscape software. Validated by the sequencing data of peripheral blood, JUNB, ATF3 and EGR2 genes were  significant statistical significance. Conclusions In conclusion, our study demonstrated the potential pathogenic genes in Candida species and their underlying mechanisms by bioinformatic analysis methods. Further, after statistical validation, JUNB, ATF3 and EGR2 genes were attained, which may be used as potential biomarkers with Candida species infection.https://doi.org/10.1186/s40001-022-00651-wCandidaHigh-throughput sequencingDifferentially expressed genesSignaling pathwaysBioinformatics analysis
spellingShingle Guo-Dong Zhu
Li-Min Xie
Jian-Wen Su
Xun-Jie Cao
Xin Yin
Ya-Ping Li
Yuan-Mei Gao
Xu-Guang Guo
Identification of differentially expressed genes and signaling pathways with Candida infection by bioinformatics analysis
European Journal of Medical Research
Candida
High-throughput sequencing
Differentially expressed genes
Signaling pathways
Bioinformatics analysis
title Identification of differentially expressed genes and signaling pathways with Candida infection by bioinformatics analysis
title_full Identification of differentially expressed genes and signaling pathways with Candida infection by bioinformatics analysis
title_fullStr Identification of differentially expressed genes and signaling pathways with Candida infection by bioinformatics analysis
title_full_unstemmed Identification of differentially expressed genes and signaling pathways with Candida infection by bioinformatics analysis
title_short Identification of differentially expressed genes and signaling pathways with Candida infection by bioinformatics analysis
title_sort identification of differentially expressed genes and signaling pathways with candida infection by bioinformatics analysis
topic Candida
High-throughput sequencing
Differentially expressed genes
Signaling pathways
Bioinformatics analysis
url https://doi.org/10.1186/s40001-022-00651-w
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