Identification of circulating biomarkers in sera of Plasmodium knowlesi-infected malaria patients - comparison against Plasmodium vivax infection

BMC Infectious Diseases

Volumn 15, Issue 1, 2015, Pages

  Chen, Yeng ^a   Chan, Choon K ^b   Kerishnan, Jesinda P ^a   Lau, Yee L ^a   Wong, Yin Ling ^a   Gopinath, Subash ^a,c  

^a UNIVERSITY OF MALAYA   (Malaysia)

^b INSTITUTE FOR RESEARCH IN MOLECULAR MEDICINE INFORMM   (Malaysia)

^c UNIVERSITY MALAYSIA PERLIS   (Malaysia)

Author keywords

Antigenicity; Immunoproteomics; Malaria; Plasmodium knowlesi; Plasmodium vivax

Indexed keywords

ALPHA 1 B GLYCOPROTEIN; APOLIPOPROTEIN A1; COMPLEMENT COMPONENT C3C; FETUIN A; GLYCOPROTEIN; HAPTOGLOBIN; HEMOPEXIN; SEROTRANSFERRIN; TRANSFERRIN; UNCLASSIFIED DRUG; ZINC 2 ALPHA GLYCOPROTEIN; BIOLOGICAL MARKER; PARASITE ANTIGEN;

ANTIGEN ANTIBODY COMPLEX; ARTICLE; DISEASE MARKER; DOWN REGULATION; HUMAN; HUMAN CELL; IMMUNOBLOTTING; IMMUNOREACTIVITY; NONHUMAN; PARASITE IDENTIFICATION; PLASMODIUM KNOWLESI; PLASMODIUM KNOWLESI MALARIA; PLASMODIUM VIVAX; PLASMODIUM VIVAX MALARIA; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN INTERACTION; PROTEOMICS; VALIDITY; ADULT; BLOOD; EVALUATION STUDY; FEMALE; IMMUNOLOGY; MALARIA; MALAYSIA; MALE; MIDDLE AGED; PARASITOLOGY; PATHOGENICITY; SENSITIVITY AND SPECIFICITY; TWO DIMENSIONAL GEL ELECTROPHORESIS;

ADULT; ANTIGENS, PROTOZOAN; BIOMARKERS; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; FEMALE; HUMANS; MALARIA; MALAYSIA; MALE; MIDDLE AGED; PLASMODIUM KNOWLESI; PLASMODIUM VIVAX; SENSITIVITY AND SPECIFICITY;

EID: 84924911145     PISSN: None     EISSN: 14712334     Source Type: Journal    
DOI: 10.1186/s12879-015-0786-2     Document Type: Article

References (44)

1. Jongwutiwes S, Putaporntip C, Iwasaki T, Sata T, Kanbara H. Naturally acquired Plasmodium knowlesi malaria in human. Thailand Emerg Infect Dis. 2004;10(12):2211-3.
2. White NJ. Plasmodium knowlesi: the fifth human malaria parasite. Clin Infect Dis. 2008;46(2):172-3.
3. Singh B, Daneshvar C. Human infections and detection of Plasmodium knowlesi. Clin Microbiol Rev. 2013;26(2):165-84.
4. Singh B, Kim Sung L, Matusop A, Radhakrishnan A, Shamsul SS, Cox-Singh J, et al. A large focus of naturally acquired Plasmodium knowlesi infections in human beings. Lancet. 2004;363(9414):1017-24.
5. Cox-Singh J, Davis TM, Lee KS, Shamsul SS, Matusop A, Ratnam S, et al. Plasmodium knowlesi malaria in humans is widely distributed and potentially life threatening. Clin Infect Dis. 2008;46(2):165-71.
6. Daneshvar C, Davis TM, Cox-Singh J, Rafa'ee MZ, Zakaria SK, Divis PC, et al. Clinical and laboratory features of human Plasmodium knowlesi infection. Clin Infect Dis. 2009;49(6):852-60.
7. Lee KS, Cox-Singh J, Singh B. Morphological features and differential counts of Plasmodium knowlesi parasites in naturally acquired human infections. Malar J. 2009;8:73.
8. McCutchan TF, Piper RC, Makler MT. Use of malaria rapid diagnostic test to identify Plasmodium knowlesi infection. Emerg Infect Dis. 2008;14(11):1750-2.
9. Schaecher K, Kumar S, Yadava A, Vahey M, Ockenhouse CF. Genome-wide expression profiling in malaria infection reveals transcriptional changes associated with lethal and nonlethal outcomes. Infect Immun. 2005;73(9):6091-100.
10. Lovegrove FE, Tangpukdee N, Opoka RO, Lafferty EI, Rajwans N, Hawkes M, et al. Serum angiopoietin-1 and -2 levels discriminate cerebral malaria from uncomplicated malaria and predict clinical outcome in African children. PLoS One. 2009;4(3):e4912.
11. Lau YL, Fong MY, Mahmud R, Chang PY, Palaeya V, Cheong FW, et al. Specific, sensitive and rapid detection of human plasmodium knowlesi infection by loop-mediated isothermal amplification (LAMP) in blood samples. Malar J. 2011;10:197.
12. Chen Y, Lim BK, Peh SC, Abdul-Rahman PS, Hashim OH. Profiling of serum and tissue high abundance acute-phase proteins of patients with epithelial and germ line ovarian carcinoma. Proc Natl Acad Sci U S A. 2008;6:20.
13. Heukeshoven J, Dernick R. Improved silver staining procedure for fast staining in PhastSystem Development Unit. I. Staining of sodium dodecyl sulfate gels. Electrophoresis. 1988;9(1):28-32.
14. Shevchenko A, Wilm M, Vorm O, Mann M. Mass spectrometric sequencing of proteins silver-stained polyacrylamide gels. Anal Chem. 1996;68(5):850-8.
15. da Huang W, Sherman BT, Lempicki RA. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc. 2009;4(1):44-57.
16. da Huang W, Sherman BT, Lempicki RA. Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists. Nucleic Acids Res. 2009;37(1):1-13.
17. Franceschini A, Szklarczyk D, Frankild S, Kuhn M, Simonovic M, Roth A, et al. STRING v9.1: protein-protein interaction networks, with increased coverage and integration. Nucleic Acids Res. 2013;41(Database issue):D808-15.
18. Carlton JM, Escalante AA, Neafsey D, Volkman SK. Comparative evolutionary genomics of human malaria parasites. Trends Parasitol. 2008;24(12):545-50.
19. Bell DR, Jorgensen P, Christophel EM, Palmer KL. Malaria risk: estimation of the malaria burden. Nature. 2005;437(7056):E3-4. discussion E-5.
20. Reyburn H, Mbakilwa H, Mwangi R, Mwerinde O, Olomi R, Drakeley C, et al. Rapid diagnostic tests compared with malaria microscopy for guiding outpatient treatment of febrile illness in Tanzania: randomised trial. BMJ. 2007;334(7590):403.
21. Pain A, Bohme U, Berry AE, Mungall K, Finn RD, Jackson AP, et al. The genome of the simian and human malaria parasite Plasmodium knowlesi. Nature. 2008;455(7214):799-803.
22. Kooij TW, Carlton JM, Bidwell SL, Hall N, Ramesar J, Janse CJ, et al. A Plasmodium whole-genome synteny map: indels and synteny breakpoints as foci for species-specific genes. PLoS Pathog. 2005;1(4):e44.
23. Yeng C, Osman E, Mohamed Z, Noordin R. Detection of immunogenic parasite and host-specific proteins in the sera of active and chronic individuals infected with Toxoplasma gondii. Electrophoresis. 2010;31(23-24):3843-9.
24. Nischik N, Schade B, Dytnerska K, Dlugonska H, Reichmann G, Fischer HG. Attenuation of mouse-virulent Toxoplasma gondii parasites is associated with a decrease in interleukin-12-inducing tachyzoite activity and reduced expression of actin, catalase and excretory proteins. Microbes Infect. 2001;3(9):689-99.
25. Gastens MH, Fischer HG. Toxoplasma gondii eukaryotic translation initiation factor 4A associated with tachyzoite virulence is down-regulated in the bradyzoite stage. Int J Parasitol. 2002;32(10):1225-34.
26. Neudeck A, Stachelhaus S, Nischik N, Striepen B, Reichmann G, Fischer HG. Expression variance, biochemical and immunological properties of Toxoplasma gondii dense granule protein GRA7. Microbes Infect. 2002;4(6):581-90.
27. Couper KN, Phillips RS, Brombacher F, Alexander J. Parasite-specific IgM plays a significant role in the protective immune response to asexual erythrocytic stage Plasmodium chabaudi AS infection. Parasite Immunol. 2005;27(5):171-80.
28. Mustafa B, Jenneby M, Esther KA, Hastings OS, Michael GM. Immunity to Plasmodium knowlesi H strain malaria in olive baboons. arXiv preprint arXiv:12013232. 2012.
29. Mitchell GH, Hadley TJ, McGinniss MH, Klotz FW, Miller LH. Invasion of erythrocytes by Plasmodium falciparum malaria parasites: evidence for receptor heterogeneity and two receptors. Blood. 1986;67(5):1519-21.
30. Ray S, Renu D, Srivastava R, Gollapalli K, Taur S, Jhaveri T, et al. Proteomic investigation of falciparum and vivax malaria for identification of surrogate protein markers. PLoS One. 2012;7(8):e41751.
31. Johnson EE, Wessling-Resnick M. Iron metabolism and the innate immune response to infection. Microbes Infect. 2012;14(3):207-16.
32. Lodish HF, Small B. Membrane proteins synthesized by rabbit reticulocytes. J Cell Biol. 1975;65(1):51-64.
33. Fritsch G, Treumer J, Spira DT, Jung A. Plasmodium vinckei: suppression of mouse infections with desferrioxamine B. Exp Parasitol. 1985;60(2):171-4.
34. Clark MA, Goheen MM, Cerami C. Influence of host iron status on Plasmodium falciparum infection. Front Pharmacol. 2014;5:84.
35. Delanghe JR, Langlois MR. Hemopexin: a review of biological aspects and the role in laboratory medicine. Clin Chim Acta. 2001;312(1-2):13-23.
36. Ferreira A, Balla J, Jeney V, Balla G, Soares MP. A central role for free heme in the pathogenesis of severe malaria: the missing link? J Mol Med. 2008;86(10):1097-111.
37. Rodriguez MH, Jungery M. A protein on Plasmodium falciparum-infected erythrocytes functions as a transferrin receptor. Nature. 1986;324(6095):388-91.
38. Whitby PW, Sim KE, Morton DJ, Patel JA, Stull TL. Transcription of genes encoding iron and heme acquisition proteins of Haemophilus influenzae during acute otitis media. Infect Immun. 1997;65(11):4696-700.
39. Sikkema DJ, Brubaker RR. Outer membrane peptides of Yersinia pestis mediating siderophore-independent assimilation of iron. Biol Met. 1989;2(3):174-84.
40. Cope LD, Thomas SE, Hrkal Z, Hansen EJ. Binding of heme-hemopexin complexes by soluble HxuA protein allows utilization of this complexed heme by Haemophilus influenzae. Infect Immun. 1998;66(9):4511-6.
41. Pickett CL, Auffenberg T, Pesci EC, Sheen VL, Jusuf SS. Iron acquisition and hemolysin production by Campylobacter jejuni. Infect Immun. 1992;60(9):3872-7.
42. Cunnington AJ, Njie M, Correa S, Takem EN, Riley EM, Walther M. Prolonged neutrophil dysfunction after Plasmodium falciparum malaria is related to hemolysis and heme oxygenase-1 induction. J Immunol. 2012;189(11):5336-46.
43. Imrie H, Fowkes FJ, Michon P, Tavul L, Hume JC, Piper KP, et al. Haptoglobin levels are associated with haptoglobin genotype and alpha + -Thalassemia in a malaria-endemic area. Am J Trop Med Hyg. 2006;74(6):965-71.
44. Hunt NH, Driussi C, Sai-Kiang L. Haptoglobin and malaria. Redox Rep. 2001;6(6):389-92.