Key result
A combined cell culture-molecular beacon assay successfully detected as little as 1 PFU of infectious coxsackievirus B6 within 6 hours postinfection.
A combined cell culture-molecular beacon assay enables rapid, sensitive detection and quantification of infectious coxsackievirus within 6 hours.
May accelerate lab-based enterovirus detection; leaves open clinical translation and validation.
Rapid detection of infectious viruses is of central importance for public health risk assessment. By directly visualizing newly synthesized viral RNA with molecular beacons (MBs), we have developed a generalized method for the rapid and sensitive detection of infectious viruses from cell culture. An MB, CVB1, specifically targeting the 5' noncoding region of the enterovirus genome was designed and synthesized. Introduction of MB CVB1 into permeabilized cells highly infected with coxsackievirus B6 resulted in brightly fluorescent cells that can be easily visualized with a fluorescence microscope. In contrast, no detectable signal was observed with noninfected cells or with nonspecific MBs. The number of fluorescent cells also increased in a dose-responsive manner, enabling the direct quantification of infectious viral dosages by direct counting of fluorescent foci. As little as 1 PFU of infectious coxsackievirus B6 was detected within 6 h postinfection. When combined with nuclease-resistant MBs, this method could be useful not only for the real-time detection of infectious viruses but is also useful to study the life cycle of viral processing in vivo.
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Wang et al. (2005) studied Coxsackievirus infection (in vitro). Molecular beacon (MB CVB1) assay vs. Traditional plaque assay / uninfected cells was evaluated on Detection and quantification of infectious coxsackievirus B6. A combined cell culture-molecular beacon assay successfully detected as little as 1 PFU of infectious coxsackievirus B6 within 6 hours postinfection.
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