“…Nevertheless, it has several drawbacks in point-of-care detection: namely, it is time-consuming and demands expensive instrumentation [ 10 ]. Thus, many alternative methods have been developed for simple and rapid point-of-care detection [ 11 , 12 ]. For the purpose of viral RNA detection, new techniques for rapid isothermal amplification, which is pivotal in rapid point-of-care detection, have been realized using, for example, recombinase polymerase amplification (RPA) [ 13 – 15 ], rolling circle amplification (RCA) [ 16 , 17 ], and loop-mediated isothermal amplification (LAMP) [ 18 , 19 ].…”