Development and Evaluation of a Duo Chikungunya Virus Real-Time RT-PCR Assay Targeting Two Regions within the Genome

被引:15
|
作者
Thirion, Laurence [1 ]
Pezzi, Laura [1 ,2 ]
Corcostegui, Iban [1 ]
Dubot-Peres, Audrey [1 ]
Falchi, Alessandra [2 ]
de Lamballerie, Xavier [1 ]
Charrel, Remi N. [1 ,3 ]
机构
[1] Aix Marseille Univ, UVE:, IHU Mediterranee Infect, INSERM 1207,IRD 190, F-13005 Marseille, France
[2] Univ Corse, INSERM, EA7310, Lab Virol, F-94925 Corte, France
[3] Univ Florida, Emerging Pathogens Inst, Gainesville, FL 32601 USA
来源
VIRUSES-BASEL | 2019年 / 11卷 / 08期
基金
欧盟地平线“2020”;
关键词
Alphavirus; Togaviridae; emergence; arbovirus; arthropod-borne; fever; epidemic; outbreak; tropical disease; HIV-1; TEST; TYPE-1; DENGUE; OUTBREAK; LOAD;
D O I
10.3390/v11080755
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Chikungunya virus (CHIKV) re-emerged as a globalized health threat fifteen years ago. There are dozens of RT-PCR assays published. An inventory of the latter was made, and after in silico analysis, two assays were selected for their ability to detect strains belonging to the five CHIKV genetic lineages. They were combined in order to provide a robust assay not affected by genetic point mutations and the resulting Duo CHIKV real-time RT-PCR assay was compared to the two parental single-plex tests against five strains belonging to the five genetic lineages. The Duo CHIKV assay performed equally, or better, in terms of sensitivity, specificity, linearity and signal intensity. Dual-target assays are better suited for viruses having the propensity to evolve into new variants via point mutations or major sequence deletions/insertions. Here, we demonstrated that combining two single systems into a dual-target assay did not impair sensitivity and specificity, and proved a potent diagnostic tool to face a potential emergence of CHIKV variants by newly evolving mutations.
引用
收藏
页数:12
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