RPB0309

Pathogen Description

Target Pathogen Pathogen Name NCBI Taxonomy ID Order Family Genus Species Pathogen type
SARS-CoV-2 SARS-CoV-2, 2019-nCoV, COVID-19, COVID-19 virus, SARS2, Wuhan coronavirus, Human coronavirus 2019, COVID19, HCoV-19, SARS-2, SARS-CoV4 2697049 Nidovirales Coronaviridae Betacoronavirus Severe acute respiratory syndrome-related coronavirus virus

Primer Description

Primer Name Sequence(5'-3') Length(bp) Primer Final Concentration(μM) GC Content(%) Predicted Melting Temperature(℃) Molecular Weight(g/moles) Positions in GenBank accession number
F TCAGCTGATGCACAATCGTT 20 10 μM 45 54.5 6092.03 \
R GTCATCTTCGTCCTTTTCTTGGAAGC 26 10 μM 46.15 58.04 7894.17 \

Gene Description

Target Gene GenBank ID
orflab gene \

Assay Description

Application Assay Primer Designing Software Reaction Time(min) Assay Temperature(℃) Readout System(s) Limit of Detection(LoD) Sensitivity(%) Specificity(%)
a feasible, convenient and low-cost detection scheme, providing an alternative biosensor for rapid virus detection. RPA-microfluidic chip and integrated system \ 27 minRPA20 min 42°C microfluidic chip and integrated system 10°copies/μL 1 1

Publication Description

Year of Publication Title Author(s) Journal PMID DOI
2024 A compact microfluidic platform for rapid multiplex detection of respiratory viruses via centrifugal polar-absorbance spectroscopy Ya Su,Xiangyu Jin,Fan Yang,Xuekai Liu,Fenggang Li,Qingchen Zhao,Jialu Hou,Shuailong Zhang,Hang Li,Guoliang Huang,Rongxin Fu Talanta 39173249 10.1016/j.talanta.2024.126733

A compact microfluidic platform for rapid multiplex detection of respiratory viruses via centrifugal polar-absorbance spectroscopy

Author(s):

Ya Su,Xiangyu Jin,Fan Yang,Xuekai Liu,Fenggang Li,Qingchen Zhao,Jialu Hou,Shuailong Zhang,Hang Li,Guoliang Huang,Rongxin Fu

Journal:

Talanta

Year:

2024

Abstract:

Nucleic acid detection technology has become a crucial tool in cutting-edge research within the life sciences and clinical diagnosis domains. Its significance is particularly highlighted during the respiratory virus pandemic, where nucleic acid testing plays a pivotal role in accurately detecting the virus. Isothermal amplification technologies have been developed and offer advantages such as rapidity, mild reaction conditions and excellent stability. Among these methods, recombinase polymerase amplification (RPA) has gained significant attention due to its simple primer design and resistance to multiple reaction inhibitors. However, the detection of RPA amplicons hinders the widespread adoption of this technology, leading to a research focus on cost-effective and convenient detection methods for RPA nucleic acid testing. In this study, we propose a novel computational absorption spectrum approach that utilizes the polar GelRed dye to efficiently detect RPA amplicons. By exploiting the asymmetry of GelRed molecules upon binding with DNA, polar electric dipoles are formed, leading to precipitate formation through centrifugal vibration and electrostatic interaction. The quantification of amplicon content is achieved by measuring the residual GelRed concentration in the supernatant. Our proposed portable and integrated microfluidic device successfully detected five respiratory virus genes simultaneously. The optimized linear detection was achieved and the sensitivity for all the targets reached 100 copies/μL. The total experiment could be finished in 27 min. The clinical experiments demonstrated the practicality and accuracy. This cost-effective and convenient detection scheme presents a promising biosensor for rapid virus detection, contributing to the advancement of RPA technology.