Abstract

BackgroundSchistosomiasis is one of the world’s most common NTDs. Successful control operations often target snail vectors with the molluscicide niclosamide. Little is known about how niclosamide affects snails, including for Biomphalaria pfeifferi, the most important vector for Schistosoma mansoni in Africa. We used Illumina technology to explore how field-derived B. pfeifferi, either uninfected or harboring cercariae–producing S. mansoni sporocysts, respond to a sublethal treatment of niclosamide. This study afforded the opportunity to determine if snails respond differently to biotic or abiotic stressors, and if they reserve unique responses for when presented with both stressors in combination. We also examined how sporocysts respond when their snail host is treated with niclosamide.Principal findingsCercariae-producing sporocysts within snails treated with niclosamide express ~68% of the genes in the S. mansoni genome, as compared to 66% expressed by intramolluscan stages of S. mansoni in snails not treated with niclosamide. Niclosamide does not disable sporocysts nor does it seem to provoke from them distinctive responses associated with detoxifying a xenobiotic. For uninfected B. pfeifferi, niclosamide treatment alone increases expression of several features not up-regulated in infected snails including particular cytochrome p450s and heat shock proteins, glutathione-S-transferases, antimicrobial factors like LBP/BPI and protease inhibitors, and also provokes strong down regulation of proteases. Exposure of infected snails to niclosamide resulted in numerous up-regulated responses associated with apoptosis along with down-regulated ribosomal and defense functions, indicative of a distinctive, compromised state not achieved with either stimulus alone.Conclusions/SignificanceThis study helps define the transcriptomic responses of an important and under-studied schistosome vector to S. mansoni sporocysts, to niclosamide, and to both in combination. It suggests the response of S. mansoni sporocysts to niclosamide is minimal and not reflective of a distinct repertoire of genes to handle xenobiotics while in the snail host. It also offers new insights for how niclosamide affects snails.

Highlights

  • Schistosomiasis control remains elusive in many of the world’s hyperendemic foci of infection in sub-Saharan Africa, jeopardizing the goals of diminishing schistosomiasis as a public health concern, or of eliminating transmission where possible by 2025 [1]

  • Following the discovery of niclosamide’s molluscicidal properties in the 1950s, it has been incorporated into the commercial preparation known as Bayluscide [7] and is the only molluscicide approved for use in schistosomiasis control by the WHO Pesticide Evaluation Scheme (WHOPES)

  • It was evident that the response of niclosamide-exposed snails had features in common to those evoked by S. mansoni exposure, many genes were uniquely differentially expressed by exposure to just niclosamide

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Summary

Introduction

Schistosomiasis control remains elusive in many of the world’s hyperendemic foci of infection in sub-Saharan Africa, jeopardizing the goals of diminishing schistosomiasis as a public health concern, or of eliminating transmission where possible by 2025 [1]. Use of niclosamide has enjoyed a modest resurgence and its focal application in snail control is advocated by WHO [8]. It has been used widely in Egypt and China as a mainstay for control operations, and it is used in both experimental [9,10] and in new control contexts, most notably recently as part of the S. haematobium elimination program in Zanzibar [11,12]. Schistosomiasis is one of the world’s most common NTDs. Successful control operations often target snail vectors with the molluscicide niclosamide. Little is known about how niclosamide affects snails, including for Biomphalaria pfeifferi, the most important vector for Schistosoma mansoni in Africa. We examined how sporocysts respond when their snail host is treated with niclosamide

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