Cited by 87Malaria Research and ControlTravel-related health issuesParasitic Infections and Diagnostics

Evaluation of the RealArt Malaria LC Real-Time PCR Assay for Malaria Diagnosis

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Farcas, Gabriella A., Zhong, Kathleen J. Y., Mazzulli, Tony, Kain, Kevin C.·2004·Journal of Clinical Microbiology

Abstract

PCR-based methods have advantages over traditional microscopic methods for the diagnosis of malaria, especially in cases of low parasitemia and mixed infections. However, current PCR-based assays are often labor-intensive and not readily quantifiable and have the potential for contamination due to a requirement for postamplification sample handling. Real-time PCR can address these limitations. This study evaluated the performance characteristics of a commercial malaria real-time PCR assay (RealArt Malaria LC Assay; Artus GmbH, Hamburg, Germany) on the LightCycler platform for the detection of malaria parasites in 259 febrile returned travelers. Compared to nested PCR as the reference standard, the real-time assay had a sensitivity of 99.5%, specificity of 100%, positive predictive value of 100%, and negative predictive value of 99.6% for the detection of malaria. Our results indicate that the RealArt assay is a rapid (<45 min), sensitive, and specific method for the detection of malaria in returned travelers.

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Crossref · 10.1128/jcm.42.2.636-638.2004

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  • In several studies using real-time PCR, either a single species was identified or no distinction between the four human parasites was made.

    “In several studies in which real-time PCR was utilized, either a single-species was identified (13) or no distinction between the four human parasites was made (8, 18).”

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Research works printed but not linked: 2

  1. [2]2. Brown, A. E., K. C. Kain, J. Pipithkul, and H. K. Webster. 1992. Demonstration by the polymerase chain reaction of mixed Plasmodium falciparum and P. vivax infections undetected by conventional microscopy. Trans. R. Soc. Trop. Med. Hyg. 86: 609-612.
  2. [14]14. Pieroni, P., C. D. Mills, C. Ohrt, M. A. Harrington, and K. C. Kain. 1998. Comparison of the ParaSight-F test and the ICT Malaria Pf test with the polymerase chain reaction for the diagnosis of Plasmodium falciparum malaria in travellers. Trans. R. Soc. Trop. Med. Hyg. 92: 166-169.

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Authors
Farcas, G. A., Zhong, K. J. Y., Mazzulli, T., & Kain, K. C.
Affiliations
  • Institute of Medical Science, Department of Medicine
  • University Health Network (CA)
  • Mount Sinai Hospital (CA)
Corresponding author
Kain, Kevin C.
Venue
Journal of Clinical Microbiology
Published
2004-02
Volume
42
Issue
2
Pages
636-638
ISSN
  • 0095-1137 (ISSN-L)
  • 1098-660X
OpenAlex
W2117478915
Cited by
87
References
0
Citations by year
2026: 1 · 2025: 2 · 2024: 2 · 2022: 3 · 2021: 2 · 2020: 1 · 2019: 1 · 2018: 2 · 2017: 1 · 2016: 3 · 2015: 3 · 2014: 4 · 2013: 5 · 2012: 6
FWCI
9.21
Type
journal article
Language
en
Open access
Locations
  • Journal of Clinical Microbiology (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Canada Research Chairs
  • Canadian Institutes of Health Research
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Malaria Research and Control
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Travel-related health issues
  • Life Sciences › Immunology and Microbiology › Parasitology › Parasitic Infections and Diagnostics
Keywords
malaria diagnosis, LightCycler, real-time PCR, returning travelers, febrile illness, nested PCR, assay sensitivity and specificity, mixed malaria infection, low parasitemia
MeSH terms
Animals, Humans, Malaria, Plasmodium falciparum, Plasmodium malariae, Plasmodium vivax, DNA, Protozoan, Polymerase Chain Reaction, Malaria, Falciparum, Malaria, Vivax, Plasmodium ovale

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