Reverse Transcription-Polymerase Chain Reaction Testing on Filter Paper-Dried Serum for Laboratory-Based Dengue Surveillance-American Samoa, 2018.
Autor: | Curren EJ; Epidemic Intelligence Service, CDC, Atlanta, Georgia.; Division of Vector-Borne Diseases, Centers for Disease Control and Prevention (CDC), Fort Collins, Colorado., Tufa AJ; American Samoa Department of Health, Pago Pago, American Samoa., Hancock WT; Division of State and Local Readiness, CDC, Hagatna, Guam., Biggerstaff BJ; Division of Vector-Borne Diseases, Centers for Disease Control and Prevention (CDC), Fort Collins, Colorado., Vaifanua-Leo JS; American Samoa Department of Health, Pago Pago, American Samoa., Montalbo CA; American Samoa Department of Health, Pago Pago, American Samoa., Sharp TM; Division of Vector-Borne Diseases, Centers for Disease Control and Prevention (CDC), Fort Collins, Colorado., Fischer M; Division of Vector-Borne Diseases, Centers for Disease Control and Prevention (CDC), Fort Collins, Colorado., Hills SL; Division of Vector-Borne Diseases, Centers for Disease Control and Prevention (CDC), Fort Collins, Colorado., Gould CV; Division of Vector-Borne Diseases, Centers for Disease Control and Prevention (CDC), Fort Collins, Colorado. |
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Jazyk: | angličtina |
Zdroj: | The American journal of tropical medicine and hygiene [Am J Trop Med Hyg] 2020 Mar; Vol. 102 (3), pp. 622-624. |
DOI: | 10.4269/ajtmh.19-0800 |
Abstrakt: | Laboratory-based surveillance for arboviral diseases is challenging in resource-limited settings. We evaluated the use of filter paper-dried sera for detection of dengue virus (DENV) RNA during an outbreak in American Samoa. Matched liquid and filter paper-dried sera were collected from patients with suspected dengue and shipped to a reference laboratory for diagnostic testing. RNA was extracted from each sample and tested for DENV RNA by real-time reverse transcription-polymerase chain reaction (RT-PCR). Of 18 RT-PCR-positive liquid specimens, 14 matched filter paper-dried specimens were positive for a sensitivity of 78% (95% CI, 55-91%). Of 82 RT-PCR-negative liquid specimens, all filter paper-dried specimens were negative for a specificity of 100% (95% CI, 96-100%). Shipping of filter paper-dried specimens was similarly timely but less expensive than shipping liquid sera. Using filter paper-dried serum or blood can be a cost-effective and sustainable approach to surveillance of dengue and other arboviral diseases in resource-limited settings. |
Databáze: | MEDLINE |
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