Key result
Enterovirus 71 infection of HT29 cells resulted in viral RNA detection at 12 hours and a significant decrease in cell viability to 17.6% compared to 77.5% in controls at 72 hours post-infection.
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The HT29 human colorectal cell line serves as a useful in vitro model for studying the replication kinetics and pathogenesis of Enterovirus 71.
Hand, Foot and Mouth Disease (HFMD), a contagious viral disease that commonly affects infants and children with blisters and flu like symptoms, is caused by a group of enteroviruses such as Enterovirus 71 (EV71) and coxsackievirus A16 (CA16). However some HFMD caused by EV71 may further develop into severe neurological complications such as encephalitis and meningitis. The route of transmission was postulated that the virus transmit from one person to another through direct contact of vesicular fluid or droplet from the infected or via faecal-oral route. To this end, this study utilised a human colorectal adenocarcinoma cell line (HT29) with epithelioid morphology as an in vitro model for the investigation of EV71 replication kinetics. Using qPCR, viral RNA was first detected in HT29 cells as early as 12 h post infection (hpi) while viral protein was first detected at 48 hpi. A significant change in HT29 cells' morphology was also observed after 48 hpi. Furthermore HT29 cell viability also significantly decreased at 72 hpi. Together, data from this study demonstrated that co-culture of HT29 with EV71 is a useful in vitro model to study the pathogenesis of EV71.
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Lui et al. (2013) studied Enterovirus 71 infection. Enterovirus 71 (EV71) infection vs. Uninfected HT29 cells was evaluated on Cell viability at 72 hours post-infection (p=<0.05). Enterovirus 71 infection of HT29 cells resulted in viral RNA detection at 12 hours and a significant decrease in cell viability to 17.6% compared to 77.5% in controls at 72 hours post-infection.
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