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Abstract

Ferroptotic cell death is a regulated process that is governed by iron-dependent membrane lipid peroxide accumulation that plays a pathogenic role in several disease-related settings. The use of ferroptosis-related genes (FRGs) to distinguish active tuberculosis (ATB) from latent tuberculosis infection (LTBI) among children, however, remains to be analysed. Tuberculosis-related gene expression data and FRG lists were obtained, respectively, from Gene Expression Omnibus (GEO) and FerrDb. Differentially expressed FRGs (DE-FRGs) detected when comparing samples from paediatric ATB and LTBI patients were explored using appropriate bioinformatics techniques, after which enrichment analyses were performed for these genes and hub genes were identified, with these genes then being used to explore potential drug interactions and construct competing endogenous RNA (ceRNA) networks. The GSE39939 dataset yielded 124 DE-FRGs that were primarily related to responses to oxidative, chemical and extracellular stimulus-associated stress. In total, the LASSO and SVM-RFE algorithms enabled the identification of nine hub genes (, , , , , , , , ) that exhibited good diagnostic utility. Functional enrichment analyses of these genes suggested that they may govern ATB transition from LTBI through the control of many pathways, including the immune response, DNA repair, transcription, RNA degradation, and glycan and energy metabolism pathways. The CIBERSORT algorithm suggested that these genes were positively correlated with inflammatory and myeloid cell activity while being negatively correlated with the activity of lymphocytes. A total of 50 candidate drugs targeting 6 hub DE-FRGs were also identified, and a ceRNA network was used to explore the complex interplay among these hub genes. The nine hub FRGs defined in this study may serve as valuable biomarkers differentiating between ATB and LTBI in young patients.

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2023-05-10
2024-12-12
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References

  1. Chen L, Hua J, Dai X, He X. Assessment of ferroptosis-associated gene signatures as potential biomarkers for differentiating latent from active tuberculosis in children. Microbiology Society. Dataset 2023 [View Article]
    [Google Scholar]
  2. Gong W, Liang Y, Wu X. The current status, challenges, and future developments of new tuberculosis vaccines. Hum Vaccin Immunother 2018; 14:1697–1716 [View Article] [PubMed]
    [Google Scholar]
  3. Khatami A, Britton PN, Marais BJ. Management of children with tuberculosis. Clin Chest Med 2019; 40:797–810 [View Article] [PubMed]
    [Google Scholar]
  4. Carvalho I, Goletti D, Manga S, Silva DR, Manissero D et al. Managing latent tuberculosis infection and tuberculosis in children. Pulmonology 2018; 24:106–114 [View Article] [PubMed]
    [Google Scholar]
  5. Floyd K, Glaziou P, Zumla A, Raviglione M. The global tuberculosis epidemic and progress in care, prevention, and research: an overview in year 3 of the End TB era. Lancet Respir Med 2018; 6:299–314 [View Article] [PubMed]
    [Google Scholar]
  6. Pai M, Behr M. Latent Mycobacterium tuberculosis infection and interferon-gamma release assays. Microbiol Spectr 2016; 4: [View Article] [PubMed]
    [Google Scholar]
  7. Jaganath D, Beaudry J, Salazar-Austin N. Tuberculosis in children. Infect Dis Clin North Am 2022; 36:49–71 [View Article] [PubMed]
    [Google Scholar]
  8. Paik S, Kim JK, Chung C, Jo EK. Autophagy: a new strategy for host-directed therapy of tuberculosis. Virulence 2019; 10:448–459 [View Article] [PubMed]
    [Google Scholar]
  9. Lam A, Prabhu R, Gross CM, Riesenberg LA, Singh V et al. Role of apoptosis and autophagy in tuberculosis. Am J Physiol Lung Cell Mol Physiol 2017; 313:L218–L229 [View Article] [PubMed]
    [Google Scholar]
  10. Amaral EP, Costa DL, Namasivayam S, Riteau N, Kamenyeva O et al. A major role for ferroptosis in Mycobacterium tuberculosis-induced cell death and tissue necrosis. J Exp Med 2019; 216:556–570 [View Article] [PubMed]
    [Google Scholar]
  11. Shu C-C, Wu M-F, Hsu C-L, Huang C-T, Wang J-Y et al. Apoptosis-associated biomarkers in tuberculosis: promising for diagnosis and prognosis prediction. BMC Infect Dis 2013; 13:45 [View Article] [PubMed]
    [Google Scholar]
  12. Stockwell BR, Jiang X, Gu W. Emerging mechanisms and disease relevance of Ferroptosis. Trends Cell Biol 2020; 30:478–490 [View Article] [PubMed]
    [Google Scholar]
  13. Amaral EP, Costa DL, Namasivayam S, Riteau N, Kamenyeva O et al. A major role for ferroptosis in Mycobacterium tuberculosis-induced cell death and tissue necrosis. J Exp Med 2019; 216:556–570 [View Article] [PubMed]
    [Google Scholar]
  14. Newman AM, Liu CL, Green MR, Gentles AJ, Feng W et al. Robust enumeration of cell subsets from tissue expression profiles. Nat Methods 2015; 12:453–457 [View Article] [PubMed]
    [Google Scholar]
  15. Zhang J, Qian X, Ning H, Eickhoff CS, Hoft DF et al. Transcriptional suppression of IL-27 production by Mycobacterium tuberculosis-activated p38 MAPK via inhibition of AP-1 binding. J Immunol 2011; 186:5885–5895 [View Article] [PubMed]
    [Google Scholar]
  16. Petrilli JD, Araújo LE, da Silva LS, Laus AC, Müller I et al. Whole blood mRNA expression-based targets to discriminate active tuberculosis from latent infection and other pulmonary diseases. Sci Rep 2020; 10:22072 [View Article] [PubMed]
    [Google Scholar]
  17. Liang T, Chen J, Xu G, Zhang Z, Xue J et al. Ferroptosis-related gene SOCS1, a marker for tuberculosis diagnosis and treatment, involves in macrophage polarization and facilitates bone destruction in tuberculosis. Tuberculosis 2022; 132:102140 [View Article] [PubMed]
    [Google Scholar]
  18. Brady PN, Goel A, Johnson MA. Poly(ADP-Ribose) polymerases in host-pathogen interactions, inflammation, and immunity. Microbiol Mol Biol Rev 2019; 83:e00038-18 [View Article] [PubMed]
    [Google Scholar]
  19. Hong T, Lei G, Chen X, Li H, Zhang X et al. PARP inhibition promotes ferroptosis via repressing SLC7A11 and synergizes with ferroptosis inducers in BRCA-proficient ovarian cancer. Redox Biol 2021; 42:101928 [View Article] [PubMed]
    [Google Scholar]
  20. Zhang L, Peng S, Dai X, Gan W, Nie X et al. Tumor suppressor SPOP ubiquitinates and degrades EglN2 to compromise growth of prostate cancer cells. Cancer Lett 2017; 390:11–20 [View Article] [PubMed]
    [Google Scholar]
  21. Yang M, Chen P, Liu J, Zhu S, Kroemer G et al. Clockophagy is a novel selective autophagy process favoring ferroptosis. Sci Adv 2019; 5:eaaw2238 [View Article] [PubMed]
    [Google Scholar]
  22. Xie B-S, Wang Y-Q, Lin Y, Mao Q, Feng J-F et al. Inhibition of ferroptosis attenuates tissue damage and improves long-term outcomes after traumatic brain injury in mice. CNS Neurosci Ther 2019; 25:465–475 [View Article] [PubMed]
    [Google Scholar]
  23. Mayer-Barber KD, Barber DL. Innate and adaptive cellular immune responses to Mycobacterium tuberculosis infection. Cold Spring Harb Perspect Med 2015; 5:12 [View Article] [PubMed]
    [Google Scholar]
  24. Berry MPR, Graham CM, McNab FW, Xu Z, Bloch SAA et al. An interferon-inducible neutrophil-driven blood transcriptional signature in human tuberculosis. Nature 2010; 466:973–977 [View Article] [PubMed]
    [Google Scholar]
  25. Rakotosamimanana N, Richard V, Raharimanga V, Gicquel B, Doherty TM et al. Biomarkers for risk of developing active tuberculosis in contacts of TB patients: a prospective cohort study. Eur Respir J 2015; 46:1095–1103 [View Article] [PubMed]
    [Google Scholar]
  26. Sibley L, Gooch K, Wareham A, Gray S, Chancellor A et al. Differences in monocyte: lymphocyte ratio and tuberculosis disease progression in genetically distinct populations of macaques. Sci Rep 2019; 9:3340 [View Article] [PubMed]
    [Google Scholar]
  27. Lindestam Arlehamn CS, Lewinsohn D, Sette A, Lewinsohn D. Antigens for CD4 and CD8 T cells in tuberculosis. Cold Spring Harb Perspect Med 2014; 4:a018465 [View Article] [PubMed]
    [Google Scholar]
  28. Achkar JM, Chan J, Casadevall A. B cells and antibodies in the defense against Mycobacterium tuberculosis infection. Immunol Rev 2015; 264:167–181 [View Article] [PubMed]
    [Google Scholar]
  29. Joosten SA, Fletcher HA, Ottenhoff THM. A helicopter perspective on TB biomarkers: pathway and process based analysis of gene expression data provides new insight into TB pathogenesis. PLoS One 2013; 8:e73230 [View Article] [PubMed]
    [Google Scholar]
  30. Tang D, Chen X, Kang R, Kroemer G. Ferroptosis: molecular mechanisms and health implications. Cell Res 2021; 31:107–125 [View Article] [PubMed]
    [Google Scholar]
  31. Sun Y, Chen P, Zhai B, Zhang M, Xiang Y et al. The emerging role of ferroptosis in inflammation. Biomed Pharmacother 2020; 127:110108 [View Article] [PubMed]
    [Google Scholar]
  32. Lo U, Selvaraj V, Plane JM, Chechneva OV, Otsu K et al. p38α (MAPK14) critically regulates the immunological response and the production of specific cytokines and chemokines in astrocytes. Sci Rep 2014; 4:7405 [View Article] [PubMed]
    [Google Scholar]
  33. Fan L, Wu X, Jin C, Li F, Xiong S et al. MptpB promotes mycobacteria survival by inhibiting the expression of inflammatory mediators and cell apoptosis in macrophages. Front Cell Infect Microbiol 2018; 8:171 [View Article] [PubMed]
    [Google Scholar]
  34. Hölscher C, Gräb J, Hölscher A, Müller AL, Schäfer SC et al. Chemical p38 MAP kinase inhibition constrains tissue inflammation and improves antibiotic activity in Mycobacterium tuberculosis-infected mice. Sci Rep 2020; 10:13629 [View Article] [PubMed]
    [Google Scholar]
  35. Sabir N, Hussain T, Shah SZA, Peramo A, Zhao D et al. miRNAs in tuberculosis: new avenues for diagnosis and host-directed therapy. Front Microbiol 2018; 9:602 [View Article] [PubMed]
    [Google Scholar]
  36. Sinigaglia A, Peta E, Riccetti S, Venkateswaran S, Manganelli R et al. Tuberculosis-associated microRNAs: from pathogenesis to disease biomarkers. Cells 2020; 9:10 [View Article] [PubMed]
    [Google Scholar]
  37. Wei L, Liu K, Jia Q, Zhang H, Bie Q et al. The roles of host noncoding RNAs in Mycobacterium tuberculosis infection. Front Immunol 2021; 12:664787 [View Article] [PubMed]
    [Google Scholar]
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