RPB0094

Pathogen Description

Target Pathogen Pathogen Name NCBI Taxonomy ID Order Family Genus Species Pathogen type
HMPV Human metapneumovirus 162145 Mo\gavirales Pneumoviridae Metapneumovirus Human metapneumovirus 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
HmPV-N-F4 GGCATGTATCTGTGCAAGCTGA 22 \ 50 57.87 6790.47 \
HmPV-N-R4 TCCCTCTGTACATTCCTATT 20 \ 40 48.89 5968.95 \

Gene Description

Target Gene GenBank ID
N gene \

Assay Description

Application Assay Primer Designing Software Reaction Time(min) Assay Temperature(℃) Readout System(s) Limit of Detection(LoD) Sensitivity(%) Specificity(%)
detection of human metapneumovirus RT-RPA-Cas12a-LF \ 20 39 CRISPR-Cas12a-fuorescence 6.97 × 102 copies/mL \ 1

Publication Description

Year of Publication Title Author(s) Journal PMID DOI
2021 Visual detection of human metapneumovirus using CRISPR-Cas12a diagnostics Weidong Qian,Jie Huang,Ting Wang,Xiaoxian He,Guozhang Xu,Yongdong Li Virus research 34555442 10.1016/j.virusres.2021.198568

Visual detection of human metapneumovirus using CRISPR-Cas12a diagnostics

Author(s):

Weidong Qian,Jie Huang,Ting Wang,Xiaoxian He,Guozhang Xu,Yongdong Li

Journal:

Virus research

Year:

2021

Abstract:

Human metapneumovirus (HmPV) is a common and serious virus that causes respiratory tract infection. This study aimed to develop a detection technique by combining reverse transcription recombinase polymerase amplification (RT-RPA) with CRISPR-Cas12a (RT-RPA-Cas12a) for clinical diagnosis of HmPV. Herein, four primer pairs targeting partial nucleoprotein (N) gene of HmPV were designed and evaluated. Then, the products amplified by RT-RPA were detected using CRISPR-Cas12a combined with fluorescence or lateral flow (LF). RT-RPA-Cas12a-based fluorescence or LF assay can be completed within 35 min or 45 min, and the detection limit was up to 6.97 × 102 copies/mL. And there was no cross reaction with human bocavirus, respiratory syncytial virus, adenovirus and parainfluenza virus. By combining with LF, the detection results were evaluated by naked eyes. Furthermore, 28 clinical samples were applied to examine the performance of RT-RPA-Cas12a system. The detection coincidence rates of RT-RPA-Cas12a-fluorescence and RT-RPA-Cas12a-LF with quantitative RT-PCR were 96.4% and 92.9%, respectively. Together, the new method for detecting HmPV with high sensitivity and specificity based on RT-RPA-Cas12a-fluorescence or LF shows promising potential for clinical diagnosis of HmPV without professional skills or ancillary equipment.