Serodiagnosis of Schistosoma mansoni infections in an endemic area of Burkina Faso: performance of several immunological tests with different parasite antigens

• Published in: Acta tropica 2005-02, Vol.93 (2), p.169-180
• Main Authors: Sorgho, Hermann, Bahgat, Mahmoud, Poda, Jean-Noel, Song, Wenjian, Kirsten, Christa, Doenhoff, Michael J., Zongo, Issaka, Ouédraogo, Jean-Bosco, Ruppel, Andreas
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Animals; Antibodies, Helminth - blood; Antigens, Helminth - chemistry; Biological and medical sciences; Burkina Faso; Burkina Faso - epidemiology; Child; Cross-Sectional Studies; Diseases caused by trematodes; Endemic Diseases; Enzyme-Linked Immunosorbent Assay; Enzyme-linked immunosorbent assay (ELISA); Feces - parasitology; Female; Fluorescent Antibody Technique, Indirect; Helminthic diseases; Hemagglutination Tests; Humans; Indirect haemagglutination assay (IHA); Indirect immunofluorescent antibody test (IFAT); Infectious diseases; Male; Medical sciences; Parasite Egg Count; Parasitic diseases; Schistosoma mansoni; Schistosoma mansoni - isolation & purification; Schistosomiases; Schistosomiasis mansoni - diagnosis; Schistosomiasis mansoni - epidemiology; Schistosomiasis mansoni - immunology; Serodiagnosis
• ISSN: 0001-706X; 1873-6254
• DOI: 10.1016/j.actatropica.2004.10.006

The performance of indirect haemagglutination assays (IHA), enzyme-linked immunosorbent assays (ELISA) and indirect immunofluorescent antibody tests (IFAT) were compared with 450 sera from a Schistosoma mansoni-endemic area in Burkina Faso. All participants in this survey provided at least one sample each of stool, urine and serum. From those with an egg-negative Kato–Katz thick smear, a second stool sample was examined. IHA was based on either extracts of adult S. mansoni worms (SmIHA) or S. japonicum egg antigen (SjIHA). For ELISA, three antigen preparations were used, namely: (i) soluble S. mansoni adult worm antigens (SWAP); (ii) soluble S. mansoni egg antigens (SEA); and (iii) a cationic exchange fraction of S. mansoni eggs (CEF6). IFAT was performed with S. mansoni male worm sections. Among the egg-excretors, the sensitivity of ELISA was high and egg antigens performed slightly better (SEA, 96%; CEF6, 97%) than worm antigen (94%). Sensitivity of IHA was satisfactory with homologous (Sm, >85%), but not heterologous (Sj, 56%) parasite antigen. In IFAT, the parenchyma-associated fluorescence showed high sensitivity (95%), but gut-associated fluorescence, which is known to be a sensitive diagnostic marker for schistosome-infected European travelers, was observed only in 76% of a sub-sample of 100 of the endemic sera. Among sera from egg-negative individuals, many gave positive reactions in several or all of the tests employed. These reactions (formally “false positive”) are considered to represent true infections, since chemotherapy had not yet been delivered to this population. For the purpose of further surveys in Burkina Faso or other resource-poor settings, we suggest IHA as an accurate diagnostic test and propose to further improve its performance by including egg rather than worm antigens.