Dysregulated autophagy contributes to the pathogenesis of enterovirus A71 infection

• Main Authors: Chuanjie Zhang, Yawei Li, Jingfeng Li
• Format: Article
• Language: English
• Published: BMC 2020-12-01
• Series: Cell & Bioscience
• Subjects: Autophagy; Enterovirus A71 (EVA71); Nervous system injury; Pathogenesis; Hand, foot, and mouth disease (HFMD)
• Online Access: https://doi.org/10.1186/s13578-020-00503-2

Abstract Enterovirus A71 (EVA71) infection continues to remain a vital threat to global public health, especially in the Asia–Pacific region. It is one of the most predominant pathogens that cause hand, foot, and mouth disease (HFMD), which occurs mainly in children below 5 years old. Although EVA71 prevalence has decreased sharply in China with the use of vaccines, epidemiological studies still indicate that EVA71 infection involves severe and even fatal HFMD cases. As a result, it remains more fundamental research into the pathogenesis of EVA71 as well as to develop specific anti-viral therapy. Autophagy is a conserved, self-degradation system that is critical for maintaining cellular homeostasis. It involves a variety of biological functions, such as development, cellular differentiation, nutritional starvation, and defense against pathogens. However, accumulating evidence has indicated that EVA71 induces autophagy and hijacks the process of autophagy for their optimal infection during the different stages of life cycle. This review provides a perspective on the emerging evidence that the “positive feedback” between autophagy induction and EVA71 infection, as well as its potential mechanisms. Furthermore, autophagy may be involved in EVA71-induced nervous system impairment through mediating intracranial viral spread and dysregulating host regulator involved self-damage. Autophagy is a promising therapeutic target in EVA71 infection.