Anti-Schistosoma IgG responses in Schistosoma haematobium single and concomitant infection with malaria parasites

• Published in: Pathogens and global health Vol. 110; no. 2; pp. 74 - 78
• Main Authors: Morenikeji, Olajumoke A., Adeleye, Olumide, Omoruyi, Ewean C., Oyeyemi, Oyetunde T.
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis 01.03.2016
• Subjects: Adolescent; Animals; Anti-Schistosoma antibodies; Antibodies, Protozoan - biosynthesis; Antibodies, Protozoan - blood; Antibody Specificity; Child; Child, Preschool; Children; Co-infection; Coinfection; Cross-Sectional Studies; Female; Humans; Immunoglobulin G - biosynthesis; Immunoglobulin G - blood; Malaria; Malaria - complications; Malaria - epidemiology; Malaria - parasitology; Male; Nigeria - epidemiology; Original; Plasmodium - immunology; Plasmodium - isolation & purification; Prevalence; Schistosoma haematobium - immunology; Schistosoma haematobium - isolation & purification; Schistosomiasis; Schistosomiasis haematobia - complications; Schistosomiasis haematobia - epidemiology; Schistosomiasis haematobia - immunology; Young Adult; Schistosomiasis; Co-infection; Children; Malaria; Anti-Schistosoma antibodies
• ISSN: 2047-7724; 2047-7732
• DOI: 10.1080/20477724.2016.1174499

Areas prone to schistosomiasis are also at risk of malaria transmission. The interaction between the causal agents of the two diseases could modulate immune responses tailored toward protecting or aggravating morbidity dynamics and impair Schistosoma diagnostic precision. This study aimed at assessing the effect of Plasmodium spp. in concomitant infection with Schistosoma haematobium in modulation of anti-Schistosoma IgG antibodies. The school-based cross-sectional study recruited a total of 322 children screened for S. haematobium and Plasmodium spp. Levels of IgG against S. haematobium-soluble egg antigen (SEA) in single S. haematobium/malaria parasites infection and co-infection of the two parasites in schoolchildren were determined. Data were analyzed using χ 2 , Fisher's exact test, and Tukey's multiple comparison test analyses. The prevalence of single infection by S. haematobium, Plasmodium spp., and concurrent infection due to the two pathogens was 27.7, 41.0, and 9.3%, respectively (p < 0.0001). Anti-Schistosoma IgG production during co-infection of the two pathogens (1.950 ± 0.742 AU) was significantly higher than the value recorded for single malaria parasites' infection (1.402 ± 0.670 AU) (p < 0.01) but not in S. haematobium infection (1.591 ± 0.604 AU) (p > 0.05). The anti-Schistosoma IgG production in co-infection status was however dependent on the intensity of Plasmodium spp. with individuals having high intensity of malaria parasites recording lower anti-Schistosoma IgG. This study has implication for diagnosis of schistosomiasis where anti-Schistosoma IgG is used as an indicator of infection. Efforts should be made to control the two infections simultaneously in order not to undermine the efforts targeted toward the control of one.