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肠道上皮细胞的 Parechovirus A 感染:基因型 A1 和 A3 的差异。

Parechovirus A Infection of the Intestinal Epithelium: Differences Between Genotypes A1 and A3.

机构信息

OrganoVIR Labs, Department of Medical Microbiology, Amsterdam University Medical Centers (UMC), location Academic Medical Center, Amsterdam Institute for Infection and Immunity, University of Amsterdam, Amsterdam, Netherlands.

Emma Children's Hospital Department of Pediatrics Infectious Diseases, Amsterdam University Medical Centers (UMC), location Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands.

出版信息

Front Cell Infect Microbiol. 2021 Nov 1;11:740662. doi: 10.3389/fcimb.2021.740662. eCollection 2021.

Abstract

Human parechovirus (PeV-A), one of the species within the family, is known to cause disease in humans. The most commonly detected genotypes are PeV-A1, associated with mild gastrointestinal disease in young children, and PeV-A3, linked to severe disease with neurological symptoms in neonates. As PeV-A are detectable in stool and nasopharyngeal samples, entry is speculated to occur the respiratory and gastro-intestinal routes. In this study, we characterized PeV-A1 and PeV-A3 replication and tropism in the intestinal epithelium using a primary 2D model based on human fetal enteroids. This model was permissive to infection with lab-adapted strains and clinical isolates of PeV-A1, but for PeV-A3, infection could only be established with clinical isolates. Replication was highest with infection established from the basolateral side with apical shedding for both genotypes. Compared to PeV-A1, replication kinetics of PeV-A3 were slower. Interestingly, there was a difference in cell tropism with PeV-A1 infecting both Paneth cells and enterocytes, while PeV-A3 infected mainly goblet cells. This difference in cell tropism may explain the difference in replication kinetics and associated disease in humans.

摘要

人类肠道病毒(PeV-A)是肠道病毒科的一个种,已知可引起人类疾病。最常检测到的基因型是 PeV-A1,与幼儿轻度胃肠道疾病有关,PeV-A3 与新生儿有神经症状的严重疾病有关。由于 PeV-A 可在粪便和鼻咽样本中检测到,因此推测其通过呼吸道和胃肠道途径进入人体。在这项研究中,我们使用基于人胎儿类肠上皮细胞的二维原代模型,对肠道上皮细胞中 PeV-A1 和 PeV-A3 的复制和嗜性进行了表征。该模型允许实验室适应株和 PeV-A1 的临床分离株感染,但对于 PeV-A3,只能用临床分离株建立感染。两种基因型均从基底外侧侧建立感染,顶端脱落,其复制率最高。与 PeV-A1 相比,PeV-A3 的复制动力学较慢。有趣的是,PeV-A1 感染潘氏细胞和肠上皮细胞,而 PeV-A3 主要感染杯状细胞,两种病毒在细胞嗜性上存在差异。这种细胞嗜性的差异可能解释了人类中复制动力学和相关疾病的差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a622/8591172/613eb3cd33db/fcimb-11-740662-g001.jpg

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