Sample-ready multiplex qPCR assay for detection of malaria

被引:25
作者
Kamau, Edwin [1 ,2 ]
Alemayehu, Saba [1 ]
Feghali, Karla C. [1 ]
Juma, Dennis W. [2 ]
Blackstone, George M. [3 ]
Marion, William R. [3 ]
Obare, Peter [2 ]
Ogutu, Bernhards [2 ]
Ockenhouse, Christian F. [1 ]
机构
[1] Walter Reed Army Inst Res, Mil Malaria Res Program, Malaria Vaccine Branch, Silver Spring, MD 20910 USA
[2] US Army, Kenya Med Res Inst KEMRI, Med Res Unit Kenya, GEIS Program, Kisumu, Kenya
[3] BioGX, Birmingham, AL USA
来源
MALARIA JOURNAL | 2014年 / 13卷
关键词
TIME PCR ASSAY; PLASMODIUM-FALCIPARUM; QUANTITATIVE PCR; IMPORTED MALARIA; DIAGNOSIS; AMPLIFICATION; MICROSCOPY; PARASITES; RNA; DNA;
D O I
10.1186/1475-2875-13-158
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Microscopy and antigen detecting rapid diagnostic tests are the diagnostic tests of choice in management of clinical malaria. However, due to their limitations, the need to utilize more sensitive methods such as real-time PCR (qPCR) is evident as more studies are now utilizing molecular methods in detection of malaria. Some of the challenges that continue to limit the widespread utilization of qPCR include lack of assay standardization, assay variability, risk of contamination, and the need for cold-chain. Lyophilization of molecular assays can overcome some of these limitations and potentially enable widespread qPCR utilization. Methods: A recently published multiplex malaria qPCR assay was lyophilized by freezing drying into Sample-Ready T format (MMSR). MMSR assay contained all the required reagents for qPCR including primers and probes, requiring only the addition of water and sample to perform qPCR. The performance of the MMSR assay was compared to the non-freeze dried, "wet" assay. Stability studies were done by maintaining the MMSR assays at four different ambient temperatures of 4 degrees C, room temperature (RT), 37 degrees C and 42 degrees C over a period of 42 days, tested at seven-day intervals. Plasmodium falciparum and Plasmodium vivax DNAs were used for analysis of the MMSR assay either as single or mixed parasites, at two different concentrations. The CT values and the standard deviations (SD) were used in the analysis of the assay performance. Results: The limit of detection for the MMSR assay was 0.244 parasites/mu L for Plasmodium spp. (PLU) and P. falciparum (FAL) assay targets compared to "wet" assay which was 0.39 and 3.13 parasites/mu L for PLU and FAL assay targets, respectively. The MMSR assay performed with high efficiencies similar to those of the "wet" assay and was stable at 37 degrees C for 42 days, with estimated shelf-life of 5 months. When used to analyse field clinical samples, MMSR assay performed with 100% sensitivity and specificity compared to the "wet" assay. Conclusion: The MMSR assay has the same robust performance characteristics as the "wet" assay and is highly stable. Availability of MMSR assay allows flexibility and provides an option in choosing assay for malaria diagnostics depending on the application, needs and budget.
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页数:8
相关论文
共 24 条
[1]   Rapid detection of methicillin-resistant Staphylococcus aureus by a newly developed dry reagent-based polymerase chain reaction assay [J].
Al-Talib, Hassanain ;
Yean, Chan Yean ;
Al-Khateeb, Alyaa ;
Hasan, Habsah ;
Ravichandran, Manickam .
JOURNAL OF MICROBIOLOGY IMMUNOLOGY AND INFECTION, 2014, 47 (06) :484-490
[2]  
[Anonymous], 2010, Guidelines for the treatment of Malaria, DOI DOI 10.1080/03630269.2023.2168201
[3]   Amplification of ST50 gene using dry-reagent-based polymerase chain reaction for the detection of Salmonella typhi [J].
Aziah, Ismail ;
Ravichandran, Manickam ;
Ismail, Asma .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2007, 59 (04) :373-377
[4]   PCR-based methods to the diagnosis of imported malaria [J].
Berry, A. ;
Benoit-Vical, F. ;
Fabre, R. ;
Cassaing, S. ;
Magnaval, J. F. .
PARASITE, 2008, 15 (03) :484-488
[5]   The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments [J].
Bustin, Stephen A. ;
Benes, Vladimir ;
Garson, Jeremy A. ;
Hellemans, Jan ;
Huggett, Jim ;
Kubista, Mikael ;
Mueller, Reinhold ;
Nolan, Tania ;
Pfaffl, Michael W. ;
Shipley, Gregory L. ;
Vandesompele, Jo ;
Wittwer, Carl T. .
CLINICAL CHEMISTRY, 2009, 55 (04) :611-622
[6]   Evaluation of novel H1N1-specific primer-probe sets using commercial RT-PCR mixtures and a premixed reaction stored in a lyophilized format [J].
Cheung, Timothy K. W. ;
Chin, Alex W. H. ;
Chan, Kwok H. ;
Schumaker, Michael ;
Mak, Polly W. Y. ;
Leung, Horasis S. Y. ;
Wong, Ada ;
Peiris, J. S. Malik ;
Petrauskene, Olga V. ;
Poon, Leo L. M. .
JOURNAL OF VIROLOGICAL METHODS, 2010, 165 (02) :302-304
[7]   Comparison of PCR and microscopy for the detection of asymptomatic malaria in a Plasmodium falciparum/vivax endemic area in Thailand [J].
Coleman, Russell E. ;
Sattabongkot, Jetsumon ;
Promstaporm, Sommai ;
Maneechai, Nongnuj ;
Tippayachai, Bousaraporn ;
Kengluecha, Ampornpan ;
Rachapaew, Nattawan ;
Zollner, Gabriela ;
Miller, Robert Scott ;
Vaughan, Jefferson A. ;
Thimasarn, Krongtong ;
Khuntirat, Benjawan .
MALARIA JOURNAL, 2006, 5 (1)
[8]   Development of an internal positive control for rapid diagnosis of avian influenza virus infections by real-time reverse transcription-PCR with lyophilized reagents [J].
Das, Arnaresh ;
Spackman, Erica ;
Senne, Dennis ;
Pedersen, Jan ;
Suarez, David L. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2006, 44 (09) :3065-3077
[9]   Cytochrome b Gene Quantitative PCR for Diagnosing Plasmodium falciparum Infection in Travelers [J].
Farrugia, Cecile ;
Cabaret, Odile ;
Botterel, Francoise ;
Bories, Christian ;
Foulet, Francoise ;
Costa, Jean-Marc ;
Bretagne, Stephane .
JOURNAL OF CLINICAL MICROBIOLOGY, 2011, 49 (06) :2191-2195
[10]   Advances in malaria diagnosis [J].
Hawkes, Michael ;
Kain, Kevin C. .
EXPERT REVIEW OF ANTI-INFECTIVE THERAPY, 2007, 5 (03) :485-495