A fully automated sample-to-answer PCR system for easy and sensitive detection of dengue virus in human serum and mosquitos

被引:14
|
作者
Tsai, Jih-Jin [1 ,2 ,3 ,4 ]
Liu, Wei-Liang [5 ]
Lin, Ping-Chang [1 ,3 ]
Huang, Bo-Yi [1 ,3 ]
Tsai, Ching-Yi [1 ,3 ]
Lee, Pei-Yu Alison [6 ]
Tsai, Yun-Long [6 ]
Chou, Pin-Hsing [6 ]
Chung, Simon [6 ]
Liu, Li-Teh [1 ,7 ]
Chen, Chun-Hong [5 ,8 ]
机构
[1] Kaohsiung Med Univ, Ctr Dengue Fever Control & Res, Kaohsiung, Taiwan
[2] Kaohsiung Med Univ, Sch Med, Coll Med, Kaohsiung, Taiwan
[3] Kaohsiung Med Univ Hosp, Trop Med Ctr, Kaohsiung, Taiwan
[4] Kaohsing Med Univ, Div Infect Dis, Dept Internal Med, Kaohsiung, Taiwan
[5] Natl Hlth Res Inst, Natl Mosquitoborne Dis Control Res Ctr, Zhunan, Taiwan
[6] GeneReach Biotechnol, Taichung, Taiwan
[7] Chung Hwa Univ Med Technol, Dept Med Lab Sci & Biotechnol, Coll Med Technol, Tainan, Taiwan
[8] Natl Hlth Res Inst, Natl Inst Infect Dis & Vaccinol, Zhunan, Taiwan
来源
PLOS ONE | 2019年 / 14卷 / 07期
关键词
REVERSE TRANSCRIPTION-PCR; TIME RT-PCR; AEDES-AEGYPTI; HEMORRHAGIC-FEVER; RAPID DETECTION; ASSAY; MULTIPLEX; DIAGNOSIS;
D O I
10.1371/journal.pone.0218139
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background The insulated isothermal PCR (iiPCR) technology enables consistent PCR amplification and detection in a simple heating device. A pan-dengue virus (DENV) RT-iiPCR, targeting the 5 untranslated region, was validated previously on the semi-automated POCKIT combo system (involving separate devices for nucleic acid extraction and PCR amplification/detection) to offer performance comparable to a laboratory real-time PCR. Working on the same technologies, a compact automated sample-in-answer-out system (POCKIT Central Nucleic Acid Analyser) has been available commercially for iiPCR, minimizing human error risks and allowing easy molecular bio-detection near points of need. Here, we evaluated the analytical and clinical performance of the pan-DENV RT-iiPCR on the fully automated system by comparison to those on the semi-automated system. Methodology/Principal findings Testing sera containing serial diluted DENV-1, -2, -3, or -4 cell culture stock, the pan-DENV RT-iiPCR system had similar 100% detection endpoints on the two systems; i.e. at 1, 10, 1 and 10 PFU/ml, respectively, on the fully automated system, and at 10, 1, 10 and 10 PFU/ml, respectively, on the semi-automated system. Furthermore, both fully automated and semi-automated PCR system can detect all four DENV serotypes in mosquitos. Clinical performance of the reagent on the two systems was evaluated by testing 60 human serum samples. Both systems detected the same 40 samples (ten DENV-1, -2, -3, and -4 positive each) and did not detect the other 20; 100% agreement (kappa = 1) was found between the two systems. Conclusions/Significance With performance comparable to a previously validated system, the fully-automated PCR system allows applications of the pan-DENV reagent as a useful tool near points of need to facilitate easy, fast and effective detection of dengue virus and help mitigate versatile public health challenges in the control and management of dengue disease.
引用
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页数:12
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