Abstract

BackgroundSchistosomiasis remains one of the most prevalent parasitic infections in the world and has significant economic and public health consequences, particularly in poor communities. Reliable and accurate diagnosis plays a key role in surveillance, prevention and control of schistosomiasis. Currently, the microscopic Kato Katz (KK) stool thick smear technique is the most commonly used method to diagnose Schistosoma mansoni infections in epidemiological surveys. It is well-known that the sensitivity of this parasitological method decreases when infection intensities are moderate to low, however. The urine-based Point-of Care Circulating Cathodic Antigen (POC-CCA) test has been extensively evaluated as a further diagnostic tool. Several studies have shown that the POC-CCA test is more sensitive but less specific than the KK method. However, to clarify the meaning of inconsistent results between KK and POC-CCA tests in clinical routine, this study compares the accuracy of microscopy and POC-CCA versus real-time polymerase chain reaction (real-time PCR) results of urine and faecal samples from African school children participants.MethodologyThis was a school-based cross-sectional study conducted in 2015 among 305 school children aged 7–16 years from two primary schools located in Ilemela and Magu Districts, north-western Tanzania. Single stool and urine samples were collected from each participant and examined for the presence of Schistosoma mansoni eggs, parasite antigen, and parasite DNA using KK thick smears, POC-CCA tests, and real-time PCR, respectively.Principal findingsThe prevalence of S. mansoni infection, calculated by KK was 85.2%, by real-time PCR 92.9% and by POC-CCA 94.9%. In comparison to KK, the POC-CCA and real-time PCR tests had sensitivities of 89.7% and 99.5% and specificities of 22.73% and 29.55%, respectively. However, due to the known limitations of the KK assay, we also used latent class analysis (LCA) that included POC-CCA, KK, and schistosome-specific real-time PCR results to determine their sensitivities and specificities. The POC-CCA test had the highest sensitivity (99.5%) and a specificity of 63.4% by LCA and the real-time PCR test had a sensitivity of 98.7% and the highest specificity (81.2%).ConclusionIn moderate and high prevalence areas, the POC-CCA cassette test is more sensitive than the KK method and can be used for screening and geographical mapping of S. mansoni infections. Real-time PCR is highly sensitive and also shows the highest specificity among the 3 investigated diagnostic procedures. It can offer added value in diagnosing schistosomiasis.

Highlights

  • Schistosomiasis is one of the poverty-related neglected tropical diseases that affects more than 230 million people worldwide [1]

  • In moderate and high prevalence areas, the Point-of Care Circulating Cathodic Antigen (POC-Cathodic Antigen (CCA)) cassette test is more sensitive than the Kato Katz (KK) method and can be used for screening and geographical mapping of S. mansoni infections

  • We present the results of a study that compares the diagnostic accuracy of microscopy (KK method) and POC-CCA versus real-time polymerase chain reaction (PCR) in urine and faecal samples of school children from an area in Tanzania that is highly endemic for S. mansoni infection

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Summary

Introduction

Schistosomiasis is one of the poverty-related neglected tropical diseases that affects more than 230 million people worldwide [1]. In SSA, schistosomiasis is caused mainly by two species, Schistosoma mansoni and Schistosoma haematobium [4,5]. Data from several studies show that the prevalence of schistosomiasis in Tanzania varies from one region to another, with a prevalence up to 80% in some areas [4,6,7]. The prevalence, infection intensity and transmission intensity is determined by various causes such as human behaviour, ecology and biological factors related to the parasite [4]. According to a research study by Colley et al (2014), in endemic areas the initial infection often occurs as early as in children aged 2 to 3 years [1]. The highest prevalence and intensity of infection are commonly described in young adolescents [1,3]

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