Ultrasensitive detection porcine transmissible gastroenteritis virus based on the dual-photoelectrode photofuel cell with in-situ isothermal amplification.

• CdS hollow spheres as photoanode and Cu 2 O/CuO as photocathode materials. • Dual-photoelectrode photocatalytic fuel cell based self-powered biosensor. • In-situ loop-mediated isothermal amplification of TGEV. • No complex thermal cycles, no need for expensive instruments. • LAMP PFC-SPBs with a lower detection limit of 0.025 fg μL−1. Loop-mediated isothermal amplification (LAMP) as a nucleic acid detection technology has many advantages than conventional polymerase chain reaction in terms of sensitivity, specificity, and equipment requirements. And combining photocatalytic fuel cell (PFC) power density readout with high sensitivity, we developed a LAMP-based dual-photoelectrode photocatalytic fuel cell based self-powered biosensors (LAMP PFC-SPBs) for the ultra-sensitive detection of transmissible gastroenteritis virus (TGEV). In this sensor, the specially designed primers were immobilized on the photosensitive material CdS-modified sensing substrate with a distinct electrochemical signal and amplified TGEV within 1 h. A wide detection range of the LAMP PFC-SPBs was demonstrated, ranging from 0.075 fg μL−1 to 7.5 ng μL−1, with a lower detection limit of 0.025 fg μL−1. In-situ LAMP PFC-SPBS had great merits in simplicity (no complex thermal cycles, no need for expensive instruments), sensitivity, specificity, and provides a new perspective on the combination of nucleic acid amplification and electrochemistry. [ABSTRACT FROM AUTHOR]