Summary
The use of the polymerase chain reaction (PCR) for the detection of human adenoviruses in diluted stool samples was investigated. Several primers, including ones specific for the hexon-coding region and for enteric adenovirus (EAd) types 40 and 41, were evaluated. The primers constitute three different PCR systems designed for the detection of all six adenovirus subgenera (A-F), the two EAds Ad40 and Ad41, and Ad40, respectively. The general system and the EAd-specific system also include nested primers for a two-step amplification. The limit of detection of the PCR assay in a two-step amplification was 1 single virus particle when the two sets of general hexon primers or EAd-specific primers were used. The sensitivity of the PCR, together with its simplicity and reduced time-scale compared with other detection methods, emphasize the potential of this technique as an additional method for routine diagnosis of human adenovirus infections.
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© 1992 Springer-Verlag Berlin Heidelberg
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Allard, A., Wadell, G. (1992). Polymerase Chain Reaction for the Detection of Adenoviruses. In: Becker, Y., Darai, G. (eds) Diagnosis of Human Viruses by Polymerase Chain Reaction Technology. Frontiers of Virology, vol 1. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-84766-0_23
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DOI: https://doi.org/10.1007/978-3-642-84766-0_23
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