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Simultaneous detection of Zika, Chikungunya and Dengue viruses by a multiplex real-time RT-PCR assay
被引:77
|作者:
Pabbaraju, Kanti
[1
]
Wong, Sallene
[1
]
Gill, Kara
[1
]
Fonseca, Kevin
[1
,2
]
Tipples, Graham A.
[1
,3
]
Tellier, Raymond
[1
,2
]
机构:
[1] Prov Lab Publ Hlth, 3030 Hosp Dr, Calgary, AB T2N 4W4, Canada
[2] Univ Calgary, Dept Microbiol Immunol & Infect Dis, Calgary, AB T2N 1N4, Canada
[3] Univ Alberta, Dept Pathol & Lab Med, Edmonton, AB, Canada
关键词:
Arbovirus;
Zika;
Chikungunya;
Dengue;
Multiplex real-time RT-PCR;
Molecular diagnosis;
URINE;
TRAVELER;
AMERICA;
SALIVA;
SERUM;
RNA;
D O I:
10.1016/j.jcv.2016.09.001
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Background: In the recent past, arboviruses such as Chikungunya (CHIKV) and Zika (ZIKV) have increased their area of endemicity and presented as an emerging global public health threat. Objectives: To design an assay for the simultaneous detection of ZIKV, CHIKV and Dengue (DENV) 1-4 from patients with symptoms of arboviral infection. This would be advantageous because of the similar clinical presentation typically encountered with these viruses and their co-circulation in endemic areas. Study design: In this study we have developed and validated a triplex real time reverse transcription PCR assay using hydrolysis probes targeting the non-structural 5 (NS5) region of ZIKV, non-structural protein 4 (nsP4) from CHIKV and 3' untranslated region (3'UTR) of DENV 1-4. Results and conclusions: The 95% LOD by the triplex assay was 15 copies/reaction for DENV-1 and less than 10 copies/reaction for all other viruses. The triplex assay was 100% specific and did not amplify any of the other viruses tested. The assay was reproducible and adaptable to testing different specimen types including serum, plasma, urine, placental tissue, brain tissue and amniotic fluid. This assay can be easily implemented for diagnostic testing of patient samples, even in a high throughput laboratory. (C) 2016 Elsevier B.V. All rights reserved.
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页码:66 / 71
页数:6
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