Short report: Comprehensive panel of real-time TaqMan™ polymerase chain reaction assays for detection and absolute quantification of filoviruses, arenaviruses, and new world hantaviruses

197Citations
Citations of this article
185Readers
Mendeley users who have this article in their library.

Abstract

Viral hemorrhagic fever is caused by a diverse group of single-stranded, negative-sense or positive-sense RNA viruses belonging to the families Filoviridae (Ebola and Marburg), Arenaviridae (Lassa, Junin, Machupo, Sabia, and Guanarito), and Bunyaviridae (hantavirus). Disease characteristics in these families mark each with the potential to be used as a biological threat agent. Because other diseases have similar clinical symptoms, specific laboratory diagnostic tests are necessary to provide the differential diagnosis during outbreaks and for instituting acceptable quarantine procedures. We designed 48 TaqMan™-based polymerase chain reaction (PCR) assays for specific and absolute quantitative detection of multiple hemorrhagic fever viruses. Forty-six assays were determined to be virus-specific, and two were designated as pan assays for Marburg virus. The limit of detection for the assays ranged from 10 to 0.001 plaque-forming units (PFU)/PCR. Although these real-time hemorrhagic fever virus assays are qualitative (presence of target), they are also quantitative (measure a single DNA/RNA target sequence in an unknown sample and express the final results as an absolute value (e.g., viral load, PFUs, or copies/mL) on the basis of concentration of standard samples and can be used in viral load, vaccine, and antiviral drug studies. Copyright © 2010 by The American Society of Tropical Medicine and Hygiene.

References Powered by Scopus

Hemorrhagic fever viruses as biological weapons: Medical and public health management

610Citations
N/AReaders
Get full text

Rapid detection and quantification of RNA of Ebola and Marburg viruses, Lassa virus, Crimean-Congo hemorrhagic fever virus, Rift Valley fever virus, dengue virus, and yellow fever virus by real-time reverse transcription-PCR

552Citations
N/AReaders
Get full text

Importance of Aeromonas Sobria in Aeromonas Bacteremia

459Citations
N/AReaders
Get full text

Cited by Powered by Scopus

Rapid metagenomic identification of viral pathogens in clinical samples by real-time nanopore sequencing analysis

399Citations
N/AReaders
Get full text

Late Ebola virus relapse causing meningoencephalitis: a case report

278Citations
N/AReaders
Get full text

Rapid and Fully Microfluidic Ebola Virus Detection with CRISPR-Cas13a

248Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Trombley, A. R., Wachter, L., Garrison, J., Buckley-Beason, V. A., Jahrling, J., Hensley, L. E., … Kulesh, D. A. (2010). Short report: Comprehensive panel of real-time TaqManTM polymerase chain reaction assays for detection and absolute quantification of filoviruses, arenaviruses, and new world hantaviruses. American Journal of Tropical Medicine and Hygiene, 82(5), 954–960. https://doi.org/10.4269/ajtmh.2010.09-0636

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 66

50%

Researcher 50

38%

Professor / Associate Prof. 14

11%

Lecturer / Post doc 3

2%

Readers' Discipline

Tooltip

Agricultural and Biological Sciences 56

46%

Medicine and Dentistry 26

21%

Immunology and Microbiology 22

18%

Biochemistry, Genetics and Molecular Bi... 18

15%

Article Metrics

Tooltip
Mentions
News Mentions: 3

Save time finding and organizing research with Mendeley

Sign up for free