Malaria antigen detection tests

Malaria antigen detection tests
A schematic diagram of a dipstick

Malaria antigen detection tests are a group of commercially available tests that allow the rapid diagnosis of malaria by people who are not otherwise skilled in traditional laboratory techniques for diagnosing malaria or in situations where such equipment is not available. There are currently over 20 such tests commercially available (WHO product testing 2008). The first malaria antigen suitable as target for Rapid Diagnostic Tests (RDTs) was a soluble glycolytic enzyme Glutamate dehydrogenase.[1][2][3] None of the rapid tests are currently as sensitive as a thick blood film, nor as cheap. A major drawback in the use of all current dipstick methods is that the result is essentially qualitative. In many endemic areas of tropical Africa, however, the quantitative assessment of parasitaemia is important, as a large percentage of the population will test positive in any qualitative assay.


Antigen-based Malaria Rapid Diagnostic Tests

Malaria is a curable disease if the patients have access to early diagnosis and prompt treatment. Antigen-based Rapid Diagnostic Tests (RDTs) have an important role at the periphery of health services capability because none of the rural clinics has the ability to diagnose malaria on-site due to a lack of microscopes and trained technicians to evaluate blood films. Furthermore, in regions where the disease is not endemic laboratory technologists have very limited experience in detecting and identifying malaria parasites. An ever increasing numbers of travelers from temperate areas each year visit tropical countries and many of them return with a malaria infection. The RDT tests are still regarded as complements to conventional microscopy but with some improvements it may well replace the microscope. The tests are simple and the procedure can be performed on the spot in field conditions. These tests use finger-stick or venous blood, the completed test takes a total of 15–20 minutes, and a laboratory is not needed. The threshold of detection by these rapid diagnostic tests is in the range of 100 parasites/µl of blood compared to 5 by thick film microscopy.[4][5][6]


Plasmodium Glutamate dehydrogenase (pGluDH) precipitated by host antibodies[1]

An accurate diagnosis is becoming more and more important, in view of the increasing resistance of Plasmodium falciparum and the high price of alternatives to chloroquine. The enzyme pGluDH does not occur in the host red blood cell and was recommended as a marker enzyme for Plasmodium species by Picard-Maureau et al. in 1975.[7] The malaria marker enzyme test is suitable for routine work and is now a standard test in most departments dealing with malaria. Presence of pGluDH is known to represent parasite viability[2] and a rapid diagnostic test using pGluDH as antigen would have the ability to differentiate live from dead organisms. A complete RDT with pGluDH as antigen has been developed in China and is now undergoing clinical trials.[3] GluDHs are ubiquitous enzymes that occupy an important branch-point between carbon and nitrogen metabolism. Both nicotinamide adenine dinucleotide (NAD) EC] and nicotinamide adenine dinucleotide phosphate (NADP) dependent GluDH [EC] enzymes are present in Plasmodia; the NAD-dependent GluDH is relatively unstable and not useful for diagnostic purposes. Glutamate dehydrogenase provides an oxidizable carbon source used for the production of energy as well as a reduced electron carrier, NADH. Glutamate is a principal amino donor to other amino acids in subsequent transamination reactions. The multiple roles of glutamate in nitrogen balance make it a gateway between free ammonia and the amino groups of most amino acids. Its crystal structure is published.[8] The GluDH activity in P.vivax, P.ovale and P. malariae has never been tested, but given the importance of GluDH as a branch point enzyme, every cell must have a high concentration of GluDH. It is well known that enzymes with a high molecular weight (like GluDH) have many isozymes, which allows strain differentiations (given the right monoclonal antibody). The host produces antibodies against the parasitic enzyme indicating a low sequence identity.[1]

Histidine Rich Protein II

The histidine-rich protein II (HRP II) is a histidine - and alanine -rich, water-soluble protein, which is localized in several cell compartments including the parasite cytoplasm. The antigen is expressed only by P. falciparum trophozoites.[9][10] HRP II from P. falciparum has been implicated in the biocrystallization of hemozoin, an inert, crystalline form of ferriprotoporphyrin IX (Fe(3+)-PPIX) produced by the parasite. A substantial amount of the HRP II is secreted by the parasite into the host bloodstream and the antigen can be detected in erythrocytes, serum, plasma, cerebrospinal fluid and even urine as a secreted water-soluble protein.[11] These antigens persist in the circulating blood after the parasitaemia has cleared or has been greatly reduced. It generally takes around two weeks after successful treatment for HRP2-based tests to turn negative, but may take as long as one month, which compromises their value in the detection of active infection.[12] False positive dipstick results were reported in patients with rheumatoid-factor-positive rheumatoid arthritis.[9] Since HPR-2 is expressed only by P. falciparum, these tests will give negative results with samples containing only P. vivax, P. ovale, or P. malariae; many cases of non-falciparum malaria may therefore be misdiagnosed as malaria negative (some P.falciparum strains also don’t have HRP II). The variability in the results of pHRP2-based RDTs is related to the variability in the target antigen.[13]


Comparison of Plasmodium Lactate Dehydrogenase (PLDH) Malaria Antibodies

P.falciparum lactate dehydrogenase (pLDH) is a 33 kDa oxidoreductase [EC].[14] It is the last enzyme of the glycolytic pathway, essential for ATP generation and one o the most abundant enzymes expressed by P.falciparum.[15] PLDH does not persist in the blood but clears about the same time as the parasites following successful treatment.[16] The lack of antigen persistence after treatment makes the pLDH test useful in predicting treatment failure. In this respect, pLDH is similar to pGluDH. LDH from P. vivax, P.malariae, and P.ovale exhibit 90-92% identity to pLDH from P.falciparum.[17]


Fructose-bisphosphate aldolase [EC] catalyzes a key reaction in glycolysis and energy production and is produced by all four species.[18] The P.falciparum aldolase is a 41 kDa protein and has 61-68% sequence similarity to known eukaryotic aldolases.[19] Its crystal structure has been published.[20] The presence of antibodies against p41 in the sera of human adults partially immune to malaria suggest that p41 is implicated in protective immune response against the parasite.[21]

See also


  1. ^ a b c Ling IT., Cooksley S., Bates PA., Hempelmann E., Wilson RJM. (1986). "Antibodies to the glutamate dehydrogenase of Plasmodium falciparum". Parasitology 92: 313–324. doi:10.1017/S0031182000064088. PMID 3086819. 
  2. ^ a b Rodríguez-Acosta A, Domínguez NG, Aguilar I, Girón ME (1998). "Characterization of Plasmodium falciparum glutamate dehydrogenase-soluble antigen". Braz J Med Biol Res 31 (9): 1149–1155. doi:10.1590/S0100-879X1998000900008. PMID 9876282. 
  3. ^ a b Li Y, Ning YS, Li L, Peng DD, Dong WQ, Li M (2005). "Preparation of a monoclonal antibodies against Plasmodium falciparum glutamate dehydrogenase and establishment of colloidal gold-immunochromatographic assay". Di Yi Jun Yi Da Xue Xue Bao = Academic journal of the first medical college of PLA 25 (4): 435–438. PMID 15837649. 
  4. ^ Warhurst DC, Williams JE (1996). "Laboratory diagnosis of malaria". J Clin Pathol 49 (7): 533–38. doi:10.1136/jcp.49.7.533. PMC 500564. PMID 8813948. 
  5. ^ Moody A. (2002). "Rapid diagnostic tests for malaria parasites". Clin Microbiol Rev. 15 (1): 66–78. doi:10.1128/CMR.15.1.66-78.2002. PMC 118060. PMID 11781267. 
  6. ^ Murray CK, Bennett JW (2008). "Rapid Diagnosis of Malaria". Interdiscip Perspect Infect Dis 2009: 415953. doi:10.1155/2009/415953. PMC 2696022. PMID 19547702. 
  7. ^ Picard-Maureau A, Hempelmann E, Krämmer G, Jackisch R, Jung A (1975). "Glutathionstatus in Plasmodium vinckei parasitierten Erythrozyten in Abhängigkeit vom intraerythrozytären Entwicklungsstadium des Parasiten". Tropenmed Parasitol 26 (4): 405–416. PMID 1216329. 
  8. ^ Werner C, Stubbs MT, Krauth-Siegel RL, Klebe G (2005). "The crystal structure of Plasmodium falciparum glutamate dehydrogenase, a putative target for novel antimalarial drugs". J Mol Biol 349 (3): 597–607. doi:10.1016/j.jmb.2005.03.077. PMID 15878595. 
  9. ^ a b Iqbal J, Sher A, Rab A (2000). "Plasmodium falciparum histidine-rich protein 2-based immunocapture diagnostic assay for malaria: cross-reactivity with rheumatoid factors". J Clin Microbiol 38 (3): 1184–1186. PMC 86370. PMID 10699018. 
  10. ^ Beadle C, Long GW, Weiss WR, McElroy PD, Maret SM, Oloo AJ, Hoffman SL (1994). "Diagnosis of malaria by detection of Plasmodium falciparum HRP-2 antigen with a rapid dipstick antigen-capture assay". Lancet 343 (8897): 564–568. doi:10.1016/S0140-6736(94)91520-2. PMID 7906328. 
  11. ^ Rock EP, Marsh K, Saul AJ, Wellems TE, Taylor DW, Maloy WL, Howard RJ (1987). "Comparative analysis of the Plasmodium falciparum histidine-rich proteins HRP-I, HRP-II and HRP-III in malaria parasites of diverse origin". Parasitology 95: 209–227. doi:10.1017/S0031182000057681. PMID 3320887. 
  12. ^ Humar A, Ohrt C, Harrington MA, Pillai D, Kain KC (1997). "Parasight F test compared with the polymerase chain reaction and microscopy for the diagnosis of Plasmodium falciparum malaria in travelers". Am J Trop Med Hyg 56 (1): 44–48. PMID 9063360. 
  13. ^ Baker J, McCarthy J, Gatton M, Kyle DE, Belizario V, Luchavez J, Bell D, Cheng Q (2005). "Genetic diversity of Plasmodium falciparum histidine-rich protein 2 (PfHRP2) and its effect on the performance of PfHRP2-based rapid diagnostic tests". J Infect Dis 192 (5): 870–877. doi:10.1086/432010. PMID 16088837. 
  14. ^ Bzik DJ, Fox BA, Gonyer K (1993). "Expression of Plasmodium falciparum lactate dehydrogenase in Escherichia coli". Mol Biochem Parasitol 59 (1): 155–166. doi:10.1016/0166-6851(93)90016-Q. PMID 8515777. 
  15. ^ Vander Jagt DL, Hunsaker LA, Heidrich JE (1981). "Partial purification and characterization of lactate dehydrogenase from Plasmodium falciparum". Mol Biochem Parasitol 4 (5-6): 255–264. doi:10.1016/0166-6851(81)90058-X. PMID 7038478. 
  16. ^ Iqbal J, Siddique A, Jameel M, Hira PR (2004). "Persistent histidine-rich protein 2, parasite lactate dehydrogenase, and panmalarial antigen reactivity after clearance of Plasmodium falciparum monoinfection". J Clin Microbiol 42 (9): 4237–4241. doi:10.1128/JCM.42.9.4237-4241.2004. PMC 516301. PMID 15365017. 
  17. ^ Brown WM, Yowell CA, Hoard A, Vander Jagt TA, Hunsaker LA, Deck LM, Royer RE, Piper RC, Dame JB, Makler MT, Vander Jagt DL (2004). "Comparative structural analysis and kinetic properties of lactate dehydrogenases from the four species of human malarial parasites". Biochemistry 43 (20): 6219–6229. doi:10.1021/bi049892w. PMID 15147206. 
  18. ^ Meier B, Döbeli H, Certa U (1992). "Stage-specific expression of aldolase isoenzymes in the rodent malaria parasite Plasmodium berghei". Mol Biochem Parasitol 52 (1): 15–27. PMID 1625704. 
  19. ^ Knapp B, Hundt E, Küpper HA (1990). "Plasmodium falciparum aldolase: gene structure and localization". Mol Biochem Parasitol 40 (1): 1–12. PMID 2190085. 
  20. ^ Kim H, Certa U, Döbeli H, Jakob P, Hol WG (1998). "Crystal structure of fructose-1,6-bisphosphate aldolase from the human malaria parasite Plasmodium falciparum". Biochemistry 37 (13): 4388–96. doi:10.1021/bi972233h. PMID 9521758. 
  21. ^ Srivastava IK, Schmidt M, Certa U, Döbeli H, Perrin LH (1990). "Specificity and inhibitory activity of antibodies to Plasmodium falciparum aldolase". J Immunol 144 (4): 1497–503. PMID 2406342. 

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