IgM and IgG Antibody Enzyme Linked Immunosorbent Assay Profile Detected Using Adult Schistosoma guineensis Extract In Sera from Cameroonian Infected by Schistosoma mansoni, Schistosoma haematobium and Schistosoma guineensis

IgM and IgG Antibody Enzyme Linked Immunosorbent Assay Profile Detected Using Adult Schistosoma guineensis Extract In Sera from Cameroonian Infected by Schistosoma mansoni, Schistosoma haematobium and Schistosoma guineensis

Loading document ...
Page
of
Loading page ...

Author(s)

Author(s): Thomas Kuete, Gabriel Lando, Tazoacha Asonganyi, Flobert Njiokou, Albert Same-Ekobo

Download Full PDF Read Complete Article

DOI: 10.18483/ijSci.2038 16 96 67-74 Volume 8 - May 2019

Abstract

Schistosomiasis is endemic in Cameroon with three Schistosoma species infecting human in many areas. Data from many countries endemic for S.mansoni, S.haematobium and S.japonicum reported an age-dependent antibody response profile using homologous adult schistosome antigen extract. Less is known about the antibody profile in schistosomiasis endemic areas in Cameroon. This study aimed to assess the IgM and IgG antibody profiles using adult S.guineensis extract in immune sera from Schistosoma egg positive Cameroonians from intestinal or urinary schistosomiasis endemic areas. Whole adult S.guineensis antigen was extracted from a Cameroonian S.guineensis strain maintained in laboratory. The antigen extract was a supernatant obtained after centrifugation of grinded freeze-thawed 45 days old worms in enzyme inhibitor solution. Sera were obtained from residents of schistosomiasis endemic areas with microscopically confirmed monospecific infection by S.guineensis, S.mansoni or S.haematobium and Schistosoma free control sera from non endemic area. IgM and IgG antibody titers detection was proceeded by indirect ELISA using HRP-conjugated secondary IgM or IgG antibody. Optical densities (OD) were recorded with a spectrophotometer plate reader at 495 nm and mean OD were statistically analyzed according to age using Student t-test and egg load using ANOVA test. A total of 189 sera were tested. Sera from S.haematobium, S.mansoni and S.guineensis infections represented 68, 73 and 46 respectively. Of S.mansoni infection sera, 31 were collected at Lagdo and 42 in S.mansoni monospecific focus. Age had no significant influence on mean IgM and IgG antibodies OD although mean IgM and IgG changed with age. Mean IgG antibody increased with age in the three schistosomiasis sera. According to age, mean IgM decreased in S.guineensis infections sera, decreased from young to participants aged 15 to 24 years then increased in older in schistosomiasis mansoni sera. In schistosomiasis haematobium sera, mean IgM increased from young to participants aged 15 to 24 years then decreased in older. Egg load influenced significantly mean IgM and IgG titers. Mean IgM OD decreased with egg load in each of the schistosomiasis whereas mean IgG decreased in intestinal schistosomiasis sera. Mean IgM and IgG antibody titers detected with adult S.guineensis extract using ELISA technique in either intestinal or urinary schistosomiasis endemic areas in Cameroon were not age dependent but egg load depended on egg load in urine and stool samples. Diagnostic performance of the adult S.guineensis extract in antibody detection has been tested.

Keywords

Antibody, Optical Densities, Sera, ELISA, S.Mansoni, S.Guineensis, S.Haematobium, Infections, Cameroon

References

  1. Bradford MM (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Annal Biochem, 72: 248-254.
  2. Butterworth AE, Capron M, Cordingley JS, Dalton PR, Dunne DW et al. (1985). Immunity after treatment in human schistosomiasis mansoni. II : Identification of resistant individuals, and analysis of their immune responses. Trans Roy SocTrop Med Hyg,79: 393-408.
  3. Butterworth AE, Dunne DW, Fulford AJC, Ouma JH, Sturrock RF (1996). Immunity and morbidity in Schistosoma mansoni infection: quantitative aspects. Am J Trop Med Hyg, 55(5): 109-115.
  4. Druilhe P, Richard-Lenoble D, Gentilini M (1979). Parasite immunology. Encyl Med Chir, Paris. Infectious Diseases, 8078A10,5. [French].
  5. Dunne DW, Butterworth AE, Fulford AJ, Kariuki HC, Langley JG et al (1992). Immunity after treatment of human schistosomiasis: association between IgE antibodies to adult worm antigens and resistance to reinfection. Eur J Immunol. 1992; 22(6):1483–94.
  6. ElFaki TEM, Arndts K, Wiszniewsky A, Ritter M, Goreish IA et al. (2016). Multivariable regression analysis in Schistosoma mansoni-infected individuals in the Sudan reveals unique immunoepidemiological profiles in uninfected, egg+ and non egg+ infected individuals. Negl Trop Dis 10(5): e0004629. Doi:10.1371/journal.pntd.0004629 May 6, 2016.
  7. Erickson DG (1974). An efficient technique for exposure of rodents to Schistosoma mansoni or Schistosoma haematobium. J Parasitol, 60: 553-554.
  8. Grenfell RFQ, Silva-Moraes V, Taboada D, deMattos ACA, de Castro AKS, Coelho PMZ (2012). Immunodiagnostic methods: what is their role in areas of low endemicity? The ScientificWorld Journal 2012, 5 pages. Article ID 593947. DOI:10.1100/2012/593947
  9. Hagan P, Blumenthal UJ, Dunne D, Simpson AJG, Wilkins HA (1991). Human IgE, IgG4, and resistance to reinfection with Schistosoma haematobium. Nature, 349:243-5.
  10. Hayunga EG, Sumner MP, Stek M Jr (1982a). Isolation of a Concanavalin A-binding glycoprotein from adult Schistosoma japonicum. J Parasitol, 68(5) : 960-961.
  11. Hayunga EG, Sumner MP, Stek M Jr, Stirewalt MA (1982b). Characterization of surface glycoproteins on Schistosoma mansoni by lectin affinity chromatography and metabolic labeling using hexose precursors. Mol Biochem Parasitol, Supplement : 654.
  12. Hayunga EG, Mollegard J, Duncan JF, Sumner MP, Stek M.Jr, Hunter KW Jr (1987). Early diagnosis of S. mansoni in mice using assays directed against cercarial antigens isolated by hydrophobic chromatography. J Parasitol, 73(2): 351-362.
  13. Hayunga EG, Vannier WE, Chestnut RY(1981). Partial characterization of radiolabeled antigens from. adult Schistosoma haematobium. J Parasitol, 67(4) : 589-591.
  14. Hillyer and Gomez de Rios (1979). Enzyme-Linked Immunosorbent Assay (ELISA) for the immunodiagnosis of schistosomiasis. Am J Trop Med Hyg, 28 : 237-241.
  15. Mott KE, Dixon H (1982). Collaborative study on antigens for immunodiagnosis of schistosomiasis. Bull World Health Organization, 60(5): 729-753.
  16. Mott KE, Dixon H, Carter CE, Garcia E, Ishii A et al. (1987). Collaborative study on antigens for immunodiagnosis of Schistosoma japonicum. Bull World Health Organization, 65(2) : 233-244.
  17. Naus CWA, Van Dam GJ, Kremsner PG, Krijger FW, Deelder AM (1998). Human IgE, IgG subclass, and IgM responses to worm and egg antigens in Schistosomiasis haematobium: a 12-month study of reinfection in Cameroonian children. Clinical Infectious Diseases 26:1142–7. Downloaded from http://cid.oxfordjournals.org/ by guest on September 9, 2015
  18. Naus CWA, Booth M, Jones FM, Kemijumbi J, Vennervald BJ et al. (2003). The relationship between age, sex, egg-count and specific antibody responses against Schistosoma mansoni antigens in a Ugandan fishing community. Trop Med Int Health, 8(6) : 561–568.
  19. Norden AP, Strand M (1984). Schistosoma mansoni S.haematobium and S. japonicum. Identification of genus, species and gender-specific antigenic worm glycoproteins. Exp Parasitol, 57: 110-123.
  20. Ratard RC, Kouemeni LE, Ekani Bessala MM, Damkou CN, Greer GJ, Spilsbury J, Cline BL (1990). Human schistosomiasis in Cameroon. I ; Distribution of schistosomiasis. Am J Trop Med Hyg, 42 : 561-572.
  21. Ratard RC, Kouemeni LE, Ekani Bessala MM, Damkou CN (1992). Estimation of the number of cases of schistosomiasis in a country : the example of Cameroon. Trans Roy Soc Trop Med Hyg, 86 : 274-276.
  22. Ripert C, Carrie J, Pagbe JJ, Ravinet L, Deniau M, Same-Ekobo A (1981). Epidemiological study of Eseka and Edea schistosomiasis intercalatum foci (Cameroon). Effect of praziquantel treatment. Azrmeittel Forschung,31 : 584-589.
  23. Ripert C (1987). Epidemiology of S.intercalatum schistosomiasis in Central Africa. Effect praziquantel treatment. Ixth International Congress of Infectious and parasitic Diseases. Med Chir Dig, 16(8) : 597-599.
  24. Ross AGP, Bartley PB, Sleigh AC, Olds GR, Li Y, Williams GM, Mcmanus (2002). Schistosomiasis: Current Concepts. N Engl J Med, 346(16) : 1212-1220. www.nejm.org
  25. Tchuem Tchuente LA, Ngassam RIK, Sumo l, Ngassam P, Dongmo Noumedem C et al. (2012). Mapping of schistosomiasis and soil-transmitted helminthiasis in the regions of Centre, East and West Cameroon. PLoS Negl Trop Dis 6(3): e1553. Doi:10.1371/journal.pntd.0001553.
  26. Tchuem Tchuente LA, Dongmo Noumedem C, Ngassam P, Kenfack CM, Gipwe NF et al. (2013). Mapping of schistosomiasis and soil-transmitted helminthiasis in the regions of Littoral, North-West, South and South-West Cameroon and recommendations for treatment. BMC Infectious Diseases 2013 13:602. BMC Infectious Diseases, 13:602. http://www.biomedcentral.com/1471-2334/13/602.
  27. Turner P, Lalloo K, Bligh J, Armstrong M, Whitty CJM et al. (2004). Serological speciation of human schistosome infections by ELISA with a panel of three antigens. J Clin Pathol, 57: 1193-1196. Doi: 10.1136/jcp.2003.014779. Downloaded from http://jcp.bmj.com/ on December 8, 2016.
  28. Wilkins HA, Blumenthal UJ, Hagan P, Hayes RJ, Tulloch S (1987). Resistance to reinfection after treatment of urinary schistosomiasis. Trans Roy Soc Trop Med Hyg, 81: 29-35.
  29. Wilson RA, Langermans JAM, van Dam GJ, Vervenne RA, Hall SL, Borges WC, Dilon GP, Thomas AW, Coulson PS (2008). Elimination of Schistosoma mansoni adult worms by Rhesus Macaques: basis for therapeutic vaccine? PLoS Negl Trop Dis 2(9): e290. Doi:10.1311/journal.pntd.0000290. www.plosntds.org
  30. Wilkins HA, Blumenthal UJ, Hagan P, Hayes RJ, Tulloch S (1987). Resistance to reinfection after treatment of urinary schistosomiasis. Trans Roy Soc Trop Med Hyg, 81 : 29-35.
  31. World Health Organization (2017). Schistosomiasis and soil-transmitted helminthiasis: number of people treated in 2016. Weekly Epidemiological Record, 8 December 2017, 92th Year, 49(92): 749–760. http://www.who.int/wer.

Cite this Article:

International Journal of Sciences is Open Access Journal.
This article is licensed under a Creative Commons Attribution 4.0 International (CC BY 4.0) License.
Author(s) retain the copyrights of this article, though, publication rights are with Alkhaer Publications.

Search Articles

Issue June 2023

Volume 12, June 2023


Table of Contents



World-wide Delivery is FREE

Share this Issue with Friends:


Submit your Paper