We amplified and sequenced the complete genome of enterovirus D68 (EV-D68) that had been collected from classroom air using a filter-based air sampling method and by swab sampling of environmental surfaces. Relatively high levels of EV-D68 genome equivalents were found per cubic meter of air by quantitative real-time reverse transcription-PCR (RT-PCR).
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|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911490 | PMC |
| http://dx.doi.org/10.1128/genomeA.00579-16 | DOI Listing |
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