Department of Genetics, Geisel School of Medicine, Dartmouth College Hanover, NH, USA ; Department of Molecular Physiology and Biophysics, Center for Human Genetics Research, Vanderbilt University Medical Center Nashville, TN, USA.
Division of Gastroenterology, Department of Medicine, Vanderbilt University Medical Center Nashville, TN, USA.
Front Genet. 2014 Aug 25;5:290. doi: 10.3389/fgene.2014.00290. eCollection 2014.
A major goal in infectious disease research is to identify the human and pathogenic genetic variants that explain differences in microbial pathogenesis. However, neither pathogenic strain nor human genetic variation in isolation has proven adequate to explain the heterogeneity of disease pathology. We suggest that disrupted co-evolution between a pathogen and its human host can explain variation in disease outcomes, and that genome-by-genome interactions should therefore be incorporated into genetic models of disease caused by infectious agents. Genetic epidemiological studies that fail to take both the pathogen and host into account can lead to false and misleading conclusions about disease etiology. We discuss our model in the context of three pathogens, Helicobacter pylori, Mycobacterium tuberculosis and human papillomavirus, and generalize the conditions under which it may be applicable.
传染病研究的一个主要目标是确定解释微生物发病机制差异的人类和病原遗传变异体。然而,无论是病原株还是人类遗传变异体本身,都不足以充分解释疾病病理学的异质性。我们认为,病原体与其人类宿主之间的协同进化被破坏可以解释疾病结果的变异性,因此,基因组对基因组的相互作用应该被纳入传染性病原体引起的疾病的遗传模型中。遗传流行病学研究如果没有同时考虑病原体和宿主,可能会导致对疾病病因的错误和误导性结论。我们根据三种病原体,即幽门螺杆菌、结核分枝杆菌和人乳头瘤病毒,讨论了我们的模型,并概括了其适用的条件。