RPB0089

Pathogen Description

Target Pathogen Pathogen Name NCBI Taxonomy ID Order Family Genus Species Pathogen type
HAdV Human adenovirus 1907210 Rowavirales Adenoviridae Mastadenovirus Human adenovirus 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
HAdV3-F3 GCCATATTCCGGCACAGCTTACAATTCACT 30 0.42 46.7 62.66 9085.97 \
HAdV3-R1 Biotin-TTCTTCTCCAACTTGAGGCTCTGGCTGATA 30 0.42 46.7 62.52 9138.98 \
HAdV3-Probe FAM-ATAGTTACAACGAATCGAGACAATGCAGTA-[THF]-CTACCACCACAAACA-PO4 45 0.03 40 64.84 13777.07 \

Gene Description

Target Gene GenBank ID
\ AB330084.1

Assay Description

Application Assay Primer Designing Software Reaction Time(min) Assay Temperature(℃) Readout System(s) Limit of Detection(LoD) Sensitivity(%) Specificity(%)
Detection of HAdV3 RPA-LF DNAman software、Primer Premier 5 software 15 37 LF 280 copies/reaction 1 0.98

Publication Description

Year of Publication Title Author(s) Journal PMID DOI
2021 Development of Rapid and Visual Nucleic Acid Detection Methods towards Four Serotypes of Human Adenovirus Species B Based on RPA-LF Test Yong Qi,Wei Li,Xiaoling Li,Wanpeng Shen,Jinhai Zhang,Jiameng Li,Ruichen Lv,Nianhong Lu,Liqiang Zong,Susu Zhuang,Qiyuan Gui,Dongming Zhou,Jing Li,Yingjia Xu,Hongbing Shen,Yuexi Li BioMed research international 34646888 10.1155/2021/9957747

Development of Rapid and Visual Nucleic Acid Detection Methods towards Four Serotypes of Human Adenovirus Species B Based on RPA-LF Test

Author(s):

Yong Qi,Wei Li,Xiaoling Li,Wanpeng Shen,Jinhai Zhang,Jiameng Li,Ruichen Lv,Nianhong Lu,Liqiang Zong,Susu Zhuang,Qiyuan Gui,Dongming Zhou,Jing Li,Yingjia Xu,Hongbing Shen,Yuexi Li

Journal:

BioMed research international

Year:

2021

Abstract:

Objectives: Human adenoviruses (HAdV) are classified as 7 HAdV species, and some serotypes in species B like HAdV 3, HAdV 7, HAdV 21, and HAdV 55 caused severe symptoms, even fatalities. Patients may be misdiagnosed and inadequately treated without reliable and practical methods for HAdV serotyping. Developing rapid, sensitive, and specific diagnostic methods for HAdV is critical. Methods: Detection methods were established based on a recombinase polymerase amplification (RPA) assay and lateral flow (LF) test. Specific target sequence was screened, targeting which, primers and probes were designed, synthesized, and screened for establishing assay with high amplification efficiency. Primer or probe concentrations and amplification time were optimized. Detection limit, sensitivity, and specificity were evaluated. Results and Conclusions. Simple, sensitive, and specific RPA-LF methods for detection of four serotypes of HAdV together or separately were established, which had detection limits of 10 to 280 copies/reaction comparable to real-time PCR without recognizing other pathogens. The sensitivity and specificity were >92% and >98%, respectively, evaluated by limited clinical samples. The detection can be completed in 25 min without requirement of any instrument except a constant temperature equipment, showing superior detection performance and promising for a wide use in the field and resource-limited area.