Zuck Meghan, Austin Laura S, Danziger Samuel A, Aitchison John D, Kaushansky Alexis
Center for Infectious Disease Research, formerly Seattle Biomedical Research Institute, Seattle, WA, United States.
Institute for Systems Biology, Seattle, WA, United States.
Front Microbiol. 2017 Nov 16;8:2183. doi: 10.3389/fmicb.2017.02183. eCollection 2017.
Despite global eradication efforts over the past century, malaria remains a devastating public health burden, causing almost half a million deaths annually (WHO, 2016). A detailed understanding of the mechanisms that control malaria infection has been hindered by technical challenges of studying a complex parasite life cycle in multiple hosts. While many interventions targeting the parasite have been implemented, the complex biology of poses a major challenge, and must be addressed to enable eradication. New approaches for elucidating key host-parasite interactions, and predicting how the parasite will respond in a variety of biological settings, could dramatically enhance the efficacy and longevity of intervention strategies. The field of systems biology has developed methodologies and principles that are well poised to meet these challenges. In this review, we focus our attention on the Liver Stage of the lifecycle and issue a "call to arms" for using systems biology approaches to forge a new era in malaria research. These approaches will reveal insights into the complex interplay between host and pathogen, and could ultimately lead to novel intervention strategies that contribute to malaria eradication.
尽管在过去一个世纪里全球都在努力根除疟疾,但疟疾仍然是一个毁灭性的公共卫生负担,每年导致近50万人死亡(世界卫生组织,2016年)。由于在多个宿主中研究复杂寄生虫生命周期存在技术挑战,对控制疟疾感染机制的详细了解受到了阻碍。虽然已经实施了许多针对该寄生虫的干预措施,但疟原虫复杂的生物学特性构成了重大挑战,要实现根除必须加以应对。阐明关键宿主-寄生虫相互作用以及预测寄生虫在各种生物学环境中如何反应的新方法,可能会显著提高干预策略的有效性和持久性。系统生物学领域已经开发出了有能力应对这些挑战的方法和原则。在本综述中,我们将注意力集中在疟原虫生命周期的肝脏阶段,并发出“战斗号召”,呼吁使用系统生物学方法开创疟疾研究的新纪元。这些方法将揭示宿主与病原体之间复杂相互作用的见解,并最终可能导致有助于根除疟疾的新型干预策略。