Application of whole genome data for in silico evaluation of primers and probes routinely employed for the detection of viral species by RT-qPCR using dengue virus as a case study

被引:20
|
作者
Vanneste, Kevin [1 ]
Garlant, Linda [1 ]
Broeders, Sylvia [1 ,3 ]
Van Gucht, Steven [2 ]
Roosens, Nancy H. [1 ]
机构
[1] Sciensano, Transversal Act Appl Genom, B-1050 Brussels, Belgium
[2] Sciensano, Viral Dis, B-1050 Brussels, Belgium
[3] Sciensano, Qual Labs, B-1050 Brussels, Belgium
来源
BMC BIOINFORMATICS | 2018年 / 19卷
关键词
Dengue virus; RT-qPCR; BLAST; Virus detection; TRANSCRIPTASE PCR ASSAYS; TEMPLATE MISMATCHES; RAPID DETECTION; VALIDATION; INFECTION; DIAGNOSIS; TYPE-1; FEVER; RNA;
D O I
10.1186/s12859-018-2313-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Viral infection by dengue virus is a major public health problem in tropical countries. Early diagnosis and detection are increasingly based on quantitative reverse transcriptase real-time polymerase chain reaction (RT-qPCR) directed against genomic regions conserved between different isolates. Genetic variation can however result in mismatches of primers and probes with their targeted nucleic acid regions. Whole genome sequencing allows to characterize and track such changes, which in turn enables to evaluate, optimize, and (re-)design novel and existing RT-qPCR methods. The immense amount of available sequence data renders this however a labour-intensive and complex task. Results: We present a bioinformatics approach that enables in silico evaluation of primers and probes intended for routinely employed RT-qPCR methods. This approach is based on analysing large amounts of publically available whole genome data, by first employing BLASTN to mine the genomic regions targeted by the RT-qPCR method(s), and afterwards using BLASTN-SHORT to evaluate whether primers and probes will anneal based on a set of simple in silico criteria. Using dengue virus as a case study, we evaluated 18 published RT-qPCR methods using more than 3000 publically available genomes in the NCBI Virus Variation Resource, and provide a systematic overview of method performance based on in silico sensitivity and specificity. Conclusions: We provide a comprehensive overview of dengue virus RT-qPCR method performance that will aid appropriate method selection allowing to take specific measures that aim to contain and prevent viral spread in afflicted regions. Notably, we find that primer-template mismatches at their 3' end may represent a general issue for dengue virus RT-qPCR detection methods that merits more attention in their development process. Our approach is also available as a public tool, and demonstrates how utilizing genomic data can provide meaningful insights in an applied public health setting such as the detection of viral species in human diagnostics.
引用
收藏
页数:18
相关论文
共 4 条
  • [1] Application of whole genome data for in silico evaluation of primers and probes routinely employed for the detection of viral species by RT-qPCR using dengue virus as a case study
    Kevin Vanneste
    Linda Garlant
    Sylvia Broeders
    Steven Van Gucht
    Nancy H. Roosens
    BMC Bioinformatics, 19
  • [2] Use of Whole Genome Sequencing Data for a First in Silico Specificity Evaluation of the RT-qPCR Assays Used for SARS-CoV-2 Detection
    Gand, Mathieu
    Vanneste, Kevin
    Thomas, Isabelle
    Van Gucht, Steven
    Capron, Arnaud
    Herman, Philippe
    Roosens, Nancy H. C.
    De Keersmaecker, Sigrid C. J.
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (15) : 1 - 25
  • [3] In silico evaluation of the impact of Omicron variant of concern sublineage BA.4 and BA.5 on the sensitivity of RT-qPCR assays for SARS-CoV-2 detection using whole genome sequencing
    Sharma, Divya
    Notarte, Kin, I
    Fernandez, Rey A.
    Lippi, Giuseppe
    Gromiha, Michael M.
    Henry, Brandon M.
    JOURNAL OF MEDICAL VIROLOGY, 2023, 95 (01)
  • [4] An Assay Design Pipeline for Massively Parallel, Nano-Scale Syndromic Panels: A Case Study Using a Viral RT-qPCR Respiratory Panel Paired with Virus-Like Particle (VLP) RNA Quantitative Controls
    Tang, N.
    Maharjan, M.
    Nguyen, S.
    Bao, Y.
    Fujino, Y.
    Sontag, C.
    Fisher, T.
    Kadam, R.
    Wang, J.
    Farmer, A.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2023, 25 (11): : S63 - S63