Bialowas Sonja, Hagbom Marie, Nordgren Johan, Karlsson Thommie, Sharma Sumit, Magnusson Karl-Eric, Svensson Lennart
Department of Clinical and Experimental Medicine, Division of Molecular Virology, Linköping University, Linköping, Sweden.
Department of Clinical and Experimental Medicine, Division of Medical Microbiology, Linköping University, Linköping, Sweden.
PLoS One. 2016 Jul 26;11(7):e0159660. doi: 10.1371/journal.pone.0159660. eCollection 2016.
Rotavirus (RV) has been shown to infect and stimulate secretion of serotonin from human enterochromaffin (EC) cells and to infect EC cells in the small intestine of mice. It remains to identify which intracellularly expressed viral protein(s) is responsible for this novel property and to further establish the clinical role of serotonin in RV infection. First, we found that siRNA specifically silencing NSP4 (siRNANSP4) significantly attenuated secretion of serotonin from Rhesus rotavirus (RRV) infected EC tumor cells compared to siRNAVP4, siRNAVP6 and siRNAVP7. Second, intracellular calcium mobilization and diarrhoeal capacity from virulent and avirulent porcine viruses correlated with the capacity to release serotonin from EC tumor cells. Third, following administration of serotonin, all (10/10) infants, but no (0/8) adult mice, responded with diarrhoea. Finally, blocking of serotonin receptors using Ondansetron significantly attenuated murine RV (strain EDIM) diarrhoea in infant mice (2.9 vs 4.5 days). Ondansetron-treated mice (n = 11) had significantly (p < 0.05) less diarrhoea, lower diarrhoea severity score and lower total diarrhoea output as compared to mock-treated mice (n = 9). Similarly, Ondansetron-treated mice had better weight gain than mock-treated animals (p < 0.05). A most surprising finding was that the serotonin receptor antagonist significantly (p < 0.05) also attenuated total viral shedding. In summary, we show that intracellularly expressed NSP4 stimulates release of serotonin from human EC tumor cells and that serotonin participates in RV diarrhoea, which can be attenuated by Ondansetron.
轮状病毒(RV)已被证明可感染并刺激人肠嗜铬(EC)细胞分泌5-羟色胺,并感染小鼠小肠中的EC细胞。仍有待确定哪种细胞内表达的病毒蛋白负责这种新特性,并进一步确定5-羟色胺在RV感染中的临床作用。首先,我们发现与针对病毒蛋白VP4、VP6和VP7的小干扰RNA(siRNA)相比,特异性沉默NSP4的小干扰RNA(siRNANSP4)显著减弱了恒河猴轮状病毒(RRV)感染的EC肿瘤细胞中5-羟色胺的分泌。其次,强毒和无毒猪病毒的细胞内钙动员及致腹泻能力与从EC肿瘤细胞释放5-羟色胺的能力相关。第三,给予5-羟色胺后,所有(10/10)婴儿出现腹泻反应,但成年小鼠无一(0/8)出现腹泻。最后,使用昂丹司琼阻断5-羟色胺受体可显著减轻幼鼠的鼠源RV(EDIM株)腹泻(2.9天对4.5天)。与模拟处理的小鼠(n = 9)相比,昂丹司琼处理的小鼠(n = 11)腹泻显著减少(p < 0.05),腹泻严重程度评分更低,总腹泻量也更低。同样,昂丹司琼处理的小鼠体重增加情况优于模拟处理的动物(p < 0.05)。一个最令人惊讶的发现是,5-羟色胺受体拮抗剂也显著(p < 0.05)减少了病毒的总排出量。总之,我们表明细胞内表达的NSP4刺激人EC肿瘤细胞释放5-羟色胺,且5-羟色胺参与RV腹泻,而昂丹司琼可减轻这种腹泻。