Key result
An optimized RT-PCR protocol using the EQ-1/EQ-2 primer set detected enterovirus in 11 of 22 recreational water sites and 6 of 9 shellfish sites around Oahu, Hawaii.
Observational (n=22)
An optimized RT-PCR protocol and the use of shellfish as bioindicators effectively detect enterovirus contamination in Hawaiian recreational waters.
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May inform enterovirus surveillance in Oahu recreational waters; leaves open validation of optimized RT-PCR and shellfish bioindicators.
Health risks associated with sewage-contaminated recreational waters are of important public health concern. Reliable water monitoring systems are therefore crucial. Current recreational water quality criteria rely predominantly on the enumeration of bacterial indicators, while potentially dangerous viral pathogens often remain undetected. Human enteric viruses have been proposed as alternative indicators; however, their detection is often hindered by low viral concentrations present in the environment. Reported here are novel and effective laboratory protocols for viral concentration and highly sensitive and optimized RT-PCR for the efficient detection of enteroviruses, an important enteric virus subset, in Hawaiian environmental waters. Eighteen published enterovirus primer pairs were comparatively evaluated for detection sensitivity. The primer set exhibiting the lowest detection limit under optimized conditions, EQ-1/EQ-2, was validated in a field survey of 22 recreational bodies of water located around the island of Oahu, Hawaii. Eleven sites tested positive for enterovirus, indicating fecal contamination at these locations. As an additional means of viral concentration, shellfish were collected from 9 sample sites and subjected to dissection, RNA extraction, and subsequent RT-PCR. Shellfish tissue from 6 of 9 sites tested positive for enterovirus. The techniques implemented here are valuable resources to aid accurate reflection of microbial contamination in Hawaii's environmental waters.
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Connell et al. (2012) conducted an observational in Environmental enterovirus contamination (n=22). Optimized RT-PCR (EQ-1/EQ-2 primer set) was evaluated on Detection of enterovirus in environmental water samples. An optimized RT-PCR protocol using the EQ-1/EQ-2 primer set detected enterovirus in 11 of 22 recreational water sites and 6 of 9 shellfish sites around Oahu, Hawaii.
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