Westerberg Sonja, Hagbom Marie, Rajan Anandi, Loitto Vesa, Persson B David, Allard Annika, Nordgren Johan, Sharma Sumit, Magnusson Karl-Eric, Arnberg Niklas, Svensson Lennart
Division of Molecular Virology, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
Department of Clinical Microbiology, Division of Virology, and Molecular Infection Medicine Sweden, Umeå University, Umeå, Sweden.
J Virol. 2018 Mar 14;92(7). doi: 10.1128/JVI.00026-18. Print 2018 Apr 1.
Human adenovirus 41 (HAdV-41) causes acute gastroenteritis in young children. The main characteristics of HAdV-41 infection are diarrhea and vomiting. Nevertheless, the precise mechanism of HAdV-41-induced diarrhea is unknown, as a suitable small-animal model has not been described. In this study, we used the human midgut carcinoid cell line GOT1 to investigate the effect of HAdV-41 infection and the individual HAdV-41 capsid proteins on serotonin release by enterochromaffin cells and on enteric glia cell (EGC) activation. We first determined that HAdV-41 could infect the enterochromaffin cells. Immunofluorescence staining revealed that the cells expressed HAdV-41-specific coxsackievirus and adenovirus receptor (CAR); flow cytometry analysis supported these findings. HAdV-41 infection of the enterochromaffin cells induced serotonin secretion dose dependently. In contrast, control infection with HAdV-5 did not induce serotonin secretion in the cells. Confocal microscopy studies of enterochromaffin cells infected with HAdV-41 revealed decreased serotonin immunofluorescence compared to that in uninfected cells. Incubation of the enterochromaffin cells with purified HAdV-41 short fiber knob and hexon proteins increased the serotonin levels in the harvested cell supernatant significantly. HAdV-41 infection could also activate EGCs, as shown in the significantly altered expression of glia fibrillary acidic protein (GFAP) in EGCs incubated with HAdV-41. The EGCs were also activated by serotonin alone, as shown in the significantly increased GFAP staining intensity. Likewise, EGCs were activated by the cell supernatant of HAdV-41-infected enterochromaffin cells. The nonenveloped human adenovirus 41 causes diarrhea, vomiting, dehydration, and low-grade fever mainly in children under 2 years of age. Even though acute gastroenteritis is well described, how human adenovirus 41 causes diarrhea is unknown. In our study, we analyzed the effect of human adenovirus 41 infection on human enterochromaffin cells and found it stimulates serotonin secretion in the cells, which is involved in regulation of intestinal secretion and gut motility and can also activate enteric glia cells, which are found in close proximity to enterochromaffin cells This disruption of gut barrier homeostasis as maintained by these cells following human adenovirus 41 infection might be a mechanism in enteric adenovirus pathogenesis in humans and could indicate a possible serotonin-dependent cross talk between human adenovirus 41, enterochromaffin cells, and enteric glia cells.
人腺病毒41型(HAdV - 41)可导致幼儿急性胃肠炎。HAdV - 41感染的主要特征是腹泻和呕吐。然而,由于尚未描述合适的小动物模型,HAdV - 41引起腹泻的确切机制尚不清楚。在本研究中,我们使用人小肠类癌细胞系GOT1来研究HAdV - 41感染以及单个HAdV - 41衣壳蛋白对肠嗜铬细胞释放5-羟色胺和对肠神经胶质细胞(EGC)激活的影响。我们首先确定HAdV - 41可感染肠嗜铬细胞。免疫荧光染色显示这些细胞表达HAdV - 41特异性的柯萨奇病毒和腺病毒受体(CAR);流式细胞术分析支持了这些发现。HAdV - 41感染肠嗜铬细胞可剂量依赖性地诱导5-羟色胺分泌。相比之下,用HAdV - 5进行对照感染未诱导这些细胞分泌5-羟色胺。对感染HAdV - 41的肠嗜铬细胞进行共聚焦显微镜研究发现,与未感染细胞相比,5-羟色胺免疫荧光降低。用纯化的HAdV - 41短纤维钮和六邻体蛋白孵育肠嗜铬细胞可显著提高收获的细胞上清液中的5-羟色胺水平。HAdV - 41感染也可激活EGC,如与HAdV - 41孵育的EGC中胶质纤维酸性蛋白(GFAP)表达的显著改变所示。单独的5-羟色胺也可激活EGC,如GFAP染色强度显著增加所示。同样,HAdV - 41感染的肠嗜铬细胞的细胞上清液也可激活EGC。无包膜的人腺病毒41型主要导致2岁以下儿童腹泻、呕吐、脱水和低热。尽管急性胃肠炎已有详细描述,但人腺病毒41型如何引起腹泻尚不清楚。在我们的研究中,我们分析了人腺病毒41型感染对人肠嗜铬细胞的影响,发现它刺激细胞分泌5-羟色胺,5-羟色胺参与肠道分泌和肠道运动的调节,还可激活与肠嗜铬细胞紧密相邻的肠神经胶质细胞。人腺病毒41型感染后这些细胞所维持的肠道屏障稳态的破坏可能是人肠道腺病毒发病机制中的一种机制,并且可能表明人腺病毒41型、肠嗜铬细胞和肠神经胶质细胞之间可能存在5-羟色胺依赖性的相互作用。