<p>One challenge in point-of-care
diagnostics is the lack of room-temperature methods for RNA detection based on
enzymatic amplification and visualization steps. Here we perform a reverse
transcription ligase chain reaction using our isothermal lesion induced DNA
amplification (LIDA) technique that can be tuned to operate at any desired
temperature. Using RNA-triggered LIDA, we can detect as little as ~100 attomoles
target RNA and can distinguish RNA target from total cellular RNA. Finally, we
demonstrate that the resulting DNA amplicons can be detected colorimetrically,
also at room temperature, by rapid, target-triggered disassembly of
DNA-modified gold nanoparticles. This integrated amplification/detection
platform requires no heating or visualization instrumentation, which is an
important step towards realizing instrument-free POC testing.</p>