Multiplexed colorimetric detection of SARS-CoV-2 and other pathogens in wastewater on a 3D printed integrated microfluidic chip

A sensitive multiplexed colorimetric analysis platform for the detection of SARS-CoV-2 and human enteric pathogens in wastewater. [Display omitted] •Multiplexed colorimetric detection was developed for detection of SARS-CoV-2 and human enteric pathogens in wastewater.•3D printed microfluidic chip wa...

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Veröffentlicht in:Sensors and actuators. B, Chemical Chemical, 2021-10, Vol.344, p.130242-130242, Article 130242
Hauptverfasser: Yin, Kun, Ding, Xiong, Xu, Zhiheng, Li, Ziyue, Wang, Xingyu, Zhao, Hui, Otis, Clifford, Li, Baikun, Liu, Changchun
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Sprache:eng
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Zusammenfassung:A sensitive multiplexed colorimetric analysis platform for the detection of SARS-CoV-2 and human enteric pathogens in wastewater. [Display omitted] •Multiplexed colorimetric detection was developed for detection of SARS-CoV-2 and human enteric pathogens in wastewater.•3D printed microfluidic chip was designed and fabricated to detect multiple pathogens.•A real-time colorimetric LAMP assay was conducted by smartphone on the microfluidic chip.•Using a portable detection platform, SARS-CoV-2 and human enteric pathogens in wastewater can be monitored in the field. Severe acute respiratory coronavirus 2 (SARS-CoV-2) pandemic has become a global public health emergency. The detection of SARS-CoV-2 and human enteric pathogens in wastewater can provide an early warning of disease outbreak. Herein, a sensitive, multiplexed, colorimetric detection (termed “SMCD”) method was established for pathogen detection in wastewater samples. The SMCD method integrated on-chip nucleic acid extraction, two-stage isothermal amplification, and colorimetric detection on a 3D printed microfluidic chip. The colorimetric signal during nucleic acid amplification was recorded in real-time and analyzed by a programmed smartphone without the need for complicated equipment. By combining two-stage isothermal amplification assay into the integrated microfluidic platform, we detected SARS-CoV-2 and human enteric pathogens with sensitivities of 100 genome equivalent (GE)/mL and 500 colony-forming units (CFU)/mL, respectively, in wastewater within one hour. Additionally, we realized smart, connected, on-site detection with a reporting framework embedded in a portable detection platform, which exhibited potential for rapid spatiotemporal epidemiologic data collection regarding the environmental dynamics, transmission, and persistence of infectious diseases.
ISSN:0925-4005
1873-3077
0925-4005
DOI:10.1016/j.snb.2021.130242