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Comparison of PCR-based detection of Plasmodium falciparum infections based on single and multicopy genes
- Source :
- Malaria Journal, Malaria Journal, Vol 6, Iss 1, p 112 (2007)
- Publication Year :
- 2007
- Publisher :
- Springer Science and Business Media LLC, 2007.
-
Abstract
- PCR-based assays are the most sensitive and specific methods to detect malaria parasites. This study compared the diagnostic accuracy of three PCR-based assays that do not only differ in their sequence target, but also in the number of copies of their target region, for the detection of Plasmodium falciparum in 401 individuals living in a malaria-endemic area in Nigeria. Compared to a composite reference generated from results of all the 3 PCR assays, the stevor gene amplification had a sensitivity of 100% (Kappa = 1; 95% CI = 1.000–1.000), 83% (Kappa = 0.718; 95% CI = 0.648–0.788) by SSUrRNA gene PCR and 71% (Kappa = 0.552; 95% CI = 0.478–0.627) by the msa-2 gene amplification. Results from this study indicate that the stevor gene amplification is the most sensitive technique for the detection of P. falciparum. This assay may be an important reference standard, especially when a confirmatory technique with high sensitivity and specificity is needed for ruling out P. falciparum infection.
- Subjects :
- Male
lcsh:Arctic medicine. Tropical medicine
lcsh:RC955-962
Plasmodium falciparum
Polymerase Chain Reaction
Sensitivity and Specificity
lcsh:Infectious and parasitic diseases
law.invention
Reference Values
law
parasitic diseases
Gene duplication
medicine
Animals
Humans
lcsh:RC109-216
Malaria, Falciparum
Child
Gene
Polymerase chain reaction
biology
Research
Infant
medicine.disease
biology.organism_classification
Virology
Molecular biology
Infectious Diseases
Parasitology
Falciparum infection
Child, Preschool
Female
Malaria
Kappa
Subjects
Details
- ISSN :
- 14752875
- Volume :
- 6
- Database :
- OpenAIRE
- Journal :
- Malaria Journal
- Accession number :
- edsair.doi.dedup.....af42040c8f6c8cd7d8f68fdf934013f1
- Full Text :
- https://doi.org/10.1186/1475-2875-6-112