Faculty of Medicine, Pompeu Fabra University, Barcelona, Spain.
Faculty of Medicine, Universitat Autònoma de Barcelona, Bellaterra, Spain.
Rev Med Virol. 2021 Nov;31(6):e2232. doi: 10.1002/rmv.2232. Epub 2021 Mar 31.
Infectious diseases occur worldwide with great frequency in both adults and children, causing 350,000 deaths in 2017, according to the latest World Health Organization reports. Both infections and their treatments trigger mitochondrial interactions at multiple levels: (i) incorporation of damaged or mutated proteins into the complexes of the electron transport chain; (ii) impact on mitochondrial genome (depletion, deletions and point mutations) and mitochondrial dynamics (fusion and fission); (iii) membrane potential impairment; (iv) apoptotic regulation; and (v) generation of reactive oxygen species, among others. Such alterations may result in serious adverse clinical events with considerable impact on the quality of life of the children and could even cause death. Herein, we use a systematic review to explore the association between mitochondrial alterations in paediatric infections including human immunodeficiency virus, cytomegalovirus, herpes viruses, various forms of hepatitis, adenovirus, T-cell lymphotropic virus and influenza. We analyse how these paediatric viral infectious processes may cause mitochondrial deterioration in this especially vulnerable population, with consideration for the principal aspects of research and diagnosis leading to improved disease understanding, management and surveillance.
传染病在全球范围内频繁发生,无论在成人还是儿童中,据世界卫生组织的最新报告显示,2017 年有 35 万人因此死亡。感染及其治疗都会在多个层面引发线粒体相互作用:(i)将受损或突变的蛋白质纳入电子传递链复合物中;(ii)对线粒体基因组(耗竭、缺失和点突变)和线粒体动力学(融合和裂变)的影响;(iii)膜电位损伤;(iv)细胞凋亡调节;以及(v)活性氧的产生等。这些改变可能导致严重的不良临床事件,对儿童的生活质量产生重大影响,甚至可能导致死亡。在这里,我们使用系统评价来探讨儿科感染(包括人类免疫缺陷病毒、巨细胞病毒、疱疹病毒、各种形式的肝炎、腺病毒、T 细胞白血病病毒和流感)中线粒体改变的相关性。我们分析了这些儿科病毒感染过程如何导致这一特别脆弱人群的线粒体恶化,并考虑了主要的研究和诊断方面,以提高对疾病的理解、管理和监测。