PCR amplification and microarray detection of alphaviruses.
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Viral RNA derived from cell culture or infected mosquitoes were PCR amplified using GSPs. Amplicons were analyzed using the ArboChip5.1 microarray. VEE, Venezuelan equine encephalitis; WEE, western equine encephalomyelitis; POS, positive PCR amplification; NEG, negative PCR amplification; yes, detected by microarray; no, not detected by microarray; n.t., not tested. aViruses propagated in cell culture and identified by microarray to species unless otherwise noted. bVirus-infected mosquito used for microarray evaluations, microarray detected at least one target for each virus. cPCR amplification produced a weak visible band. dArboChip5.1 does not include probes specific to the target. eMicroarray detection with genus-level probes only. fTarget was detected but could not be differentiated between BBKV, OCKV, and SINV. gTarget was detected but could not be differentiated between ONNV and IOV.



