Abstract

Schistosomiasis is a disease of great medical and veterinary importance in tropical and subtropical regions caused by different species of parasitic flatworms of the genus Schistosoma. The emergence of natural hybrids of schistosomes indicate the risk of possible infection to humans and their zoonotic potential, specifically for Schistosoma haematobium and S. bovis. Hybrid schistosomes have the potential to replace existing species, generate new resistances, pathologies and extending host ranges. Hybrids may also confuse the serological, molecular and parasitological diagnosis. Currently, LAMP technology based on detection of nucleic acids is used for detection of many agents, including schistosomes. Here, we evaluate our previously developed species-specific LAMP assays for S. haematobium, S. mansoni, S. bovis and also the genus-specific LAMP for the simultaneous detection of several Schistosoma species against both DNA from pure and, for the first time, S. haematobium x S. bovis hybrids. Proper operation was evaluated with DNA from hybrid schistosomes and with human urine samples artificially contaminated with parasites’ DNA. LAMP was performed with and without prior DNA extraction. The genus-specific LAMP properly amplified pure Schistosoma species and different S. haematobium-S. bovis hybrids with different sensitivity. The Schistosoma spp.-LAMP method is potentially adaptable for field diagnosis and disease surveillance in schistosomiasis endemic areas where human infections by schistosome hybrids are increasingly common.

Highlights

  • Environmental changes due to ecosystem decline, biodiversity loss and climate change are some issues with potential ecological risk that we are facing as human beings

  • The results obtained in testing the different Schisto-loop-mediated isothermal amplification (LAMP) assays against both the hybrid schistosomes Genomic DNA (gDNA) and pure Schistosoma species used as controls are shown in LAMP for detecting S. haematobium amplified all DNA samples with the exception of S

  • The species-specific LAMP for S. bovis amplified both pure S. bovis DNA and S. bovis-S. haematobium x S. bovis hybrid parasite DNA

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Summary

Introduction

Environmental changes due to ecosystem decline, biodiversity loss and climate change are some issues with potential ecological risk that we are facing as human beings. These changes driven by increasing economic development, migration, agricultural and livestock practices and deforestation have consequences in emerging infectious diseases (EIDs) [1,2,3,4,5,6]. The appearance of diseases in non-endemic areas and the increase in encounters between different species, when ecological and geographic barriers are lost, lead to the emergence of new hybrid forms [4]. The three main species infecting humans are S. haematobium, S. mansoni

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