Carter C J
Polygenic Pathways, Flat 2, 40 Baldslow Road, Hastings, East Sussex TN34 2EY, UK.
J Pathog. 2013;2013:965046. doi: 10.1155/2013/965046. Epub 2013 Mar 4.
Toxoplasma gondii is not only implicated in schizophrenia and related disorders, but also in Alzheimer's or Parkinson's disease, cancer, cardiac myopathies, and autoimmune disorders. During its life cycle, the pathogen interacts with ~3000 host genes or proteins. Susceptibility genes for multiple sclerosis, Alzheimer's disease, schizophrenia, bipolar disorder, depression, childhood obesity, Parkinson's disease, attention deficit hyperactivity disorder (P from 8.01E - 05 (ADHD) to 1.22E - 71) (multiple sclerosis), and autism (P = 0.013), but not anorexia or chronic fatigue are highly enriched in the human arm of this interactome and 18 (ADHD) to 33% (MS) of the susceptibility genes relate to it. The signalling pathways involved in the susceptibility gene/interactome overlaps are relatively specific and relevant to each disease suggesting a means whereby susceptibility genes could orient the attentions of a single pathogen towards disruption of the specific pathways that together contribute (positively or negatively) to the endophenotypes of different diseases. Conditional protein knockdown, orchestrated by T. gondii proteins or antibodies binding to those of the host (pathogen derived autoimmunity) and metabolite exchange, may contribute to this disruption. Susceptibility genes may thus be related to the causes and influencers of disease, rather than (and as well as) to the disease itself.
弓形虫不仅与精神分裂症及相关疾病有关,还与阿尔茨海默病或帕金森病、癌症、心肌病和自身免疫性疾病有关。在其生命周期中,该病原体与约3000个宿主基因或蛋白质相互作用。多发性硬化症、阿尔茨海默病、精神分裂症、双相情感障碍、抑郁症、儿童肥胖症、帕金森病、注意力缺陷多动障碍(P值从8.01E - 05(注意力缺陷多动障碍)到1.22E - 71)(多发性硬化症)以及自闭症(P = 0.013)的易感基因,但不包括厌食症或慢性疲劳的易感基因,在这个相互作用组的人类部分中高度富集,并且18%(注意力缺陷多动障碍)到33%(多发性硬化症)的易感基因与之相关。易感基因/相互作用组重叠中涉及的信号通路相对特异且与每种疾病相关,这表明一种方式,即易感基因可以引导单个病原体的注意力指向特定通路的破坏,这些通路共同(正向或负向)促成不同疾病的内表型。由弓形虫蛋白质或与宿主蛋白质结合的抗体(病原体衍生的自身免疫)精心安排的条件性蛋白质敲低以及代谢物交换,可能导致这种破坏。因此,易感基因可能与疾病的病因和影响因素有关,而不仅仅(以及也)与疾病本身有关。