News Release

How herpes infection may impair human fetal brain development

Peer-Reviewed Publication

PLOS

Three cell-based models shed light on how herpes simplex virus type 1 (HSV-1) infection, which can spread to the fetal brain during pregnancy, may contribute to various neurodevelopmental disabilities and long-term neurological problems into adulthood, according to a study published October 22, 2020 in the open-access journal PLOS Pathogens by Pu Chen and Ying Wu of Wuhan University, and colleagues.

HSV-1 is a highly prevalent pathogen that can cause lifelong neurological problems such as cognitive dysfunction, learning disabilities, and dementia. But progress in understanding the role of HSV-1 in human fetal brain development has been hampered by restricted access to fetal human brain tissue as well as limitations of existing animal models. To address this gap in knowledge, the researchers generated three different cell-based neurodevelopmental disorder models, including a 2D layer of cells and a 3D brain-like structure. These models are based on human induced pluripotent stem cells (hiPSCs) - immature, embryonic stem cell-like cells that are generated by genetically reprogramming specialized adult cells.

HSV-1 infection in neural stem cells derived from hiPSCs resulted in activation of the caspase-3 apoptotic pathway, which initiates programmed cell death. HSV-1 infection also impaired the production of new neurons, and hindered the ability of hiPSC-derived neural stem cells to convert into mature neurons through a process called neuronal differentiation. Moreover, the HSV-1-infected brain organoids mimicked the pathological features of neurodevelopmental disorders in the human fetal brain, including impaired neuronal differentiation and abnormalities in brain structure. In addition, the 3D model showed that HSV-1 infection promotes the abnormal proliferation and activation of non-neuronal cells called microglia, accompanied by the activation of inflammatory molecules, such as TNF-α, IL-6, IL-10, and IL-4. According to the authors, the findings open new therapeutic avenues for targeting viral reservoirs relevant to neurodevelopmental disorders.

The authors add, "This study provides novel evidence that HSV-1 infection impaired human brain development and contributed to the neurodevelopmental disorder pathogen hypothesis".

###

Research Article

Peer reviewed; Experimental study; Cells

Funding: This study was supported in part by grants from the National Natural Science Foundation of China (Grant No. 31871018, http://www.nsfc.gov.cn/), received by P.C. and the National Science and Technology Major Project (Grant No. 2018ZX10733403, http://www.most.gov.cn/), received by Y.W. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing Interests: The authors have declared that no competing interests exist.

Citation: Qiao H, Guo M, Shang J, Zhao W, Wang Z, Liu N, et al. (2020) Herpes simplex virus type 1 infection leads to neurodevelopmental disorder-associated neuropathological changes. PLoS Pathog 16(10): e1008899. https://doi.org/10.1371/journal.ppat.1008899

Author Affiliations:

Department of Biomedical Engineering, Wuhan University School of Basic Medical Sciences, Wuhan, Hubei, China,

Hubei Province Key Laboratory of Allergy and Immunology, Wuhan, Hubei, China,

State Key Laboratory of Virology, Wuhan University, Wuhan, Hubei, China,

Institute of Medical Virology, Wuhan University School of Basic Medical Sciences, Wuhan, Hubei, China,

Research Center for Medicine and Structural Biology of Wuhan University, Wuhan University, Wuhan, Hubei, China,

Hubei Province Key Laboratory of Allergy and Immunology, Wuhan, Hubei, China.

In your coverage please use this URL to provide access to the freely available paper: http://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1008899


Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.