Abstract

BackgroundToxocara canis is the causative agent of toxocariasis of humans and other animals. This parasitic nematode (roundworm) has a complex life cycle, in which substantial developmental changes and switches occur. As small non-coding RNAs (sRNAs) are key regulators of gene expression in a wide range of organisms, we explored these RNAs in T. canis to provide a basis for future studies of its developmental biology as well as host interactions and disease at the molecular level.MethodsWe conducted high-throughput RNA sequencing and bioinformatic analyses to define sRNAs in individual male and female adults of T. canis.ResultsApart from snRNA and snoRNA, 560 and 619 microRNAs (miRNAs), including 5 and 2 novel miRNAs, were identified in male and female worms, respectively, without piRNAs being detected in either sex. An analysis of transcriptional profiles showed that, of 564 miRNAs predicted as being differentially transcribed between male and female individuals of T. canis, 218 miRNAs were transcribed exclusively in male and 277 in female worms. Functional enrichment analysis predicted that both male and female miRNAs were mainly involved in regulating embryonic morphogenesis, hemidesmosome assembly and genetic information processing. The miRNAs differentially transcribed between the sexes were predicted to be associated with sex determination, embryonic morphogenesis and nematode larval development. The roles of miRNAs were predicted based on gene ontology (GO) and KEGG pathway annotations. The miRNAs Tc-miR-2305 and Tc-miR-6090 are proposed to have roles in reproduction, embryo development and larval development, and Tc-let-7-5p, Tc-miR-34 and Tc-miR-100 appear to be involved in host-parasite interactions. Together with published information from previous studies, some miRNAs (such as Tc-miR-2861, Tc-miR-2881 and Tc-miR-5126) are predicted to represent drug targets and/or associated with drug resistance.ConclusionsThis is the first exploration of miRNAs in T. canis, which could provide a basis for fundamental investigations of the developmental biology of the parasite, parasite-host interactions and toxocariasis as well as applied areas, such as the diagnosis of infection/disease, drug target discovery and drug resistance detection.Electronic supplementary materialThe online version of this article (doi:10.1186/s13071-016-1508-3) contains supplementary material, which is available to authorized users.

Highlights

  • Toxocara canis is the causative agent of toxocariasis of humans and other animals

  • SnoRNA, small nuclear RNA (snRNA) and miRNA accounted for 0.01 %, 0.07 % and 24.92 % of all male small non-coding RNAs (sRNAs), compared with 0.01 %, 0.04 % and 32.86 % of female sRNAs, respectively (Table 1)

  • The present study of miRNAs in T. canis provides exciting prospects and delivers a resource to deepen and broaden our understanding of gene regulation in this enigmatic parasitic nematode. It provides a basis for experimental investigations of the developmental biology of the parasite, parasite-host interactions and disease, and might assist in developing tools for the diagnosis of infection/disease, drug target discovery and drug resistance detection

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Summary

Introduction

Toxocara canis is the causative agent of toxocariasis of humans and other animals. This parasitic nematode (roundworm) has a complex life cycle, in which substantial developmental changes and switches occur. As small non-coding RNAs (sRNAs) are key regulators of gene expression in a wide range of organisms, we explored these RNAs in T. canis to provide a basis for future studies of its developmental biology as well as host interactions and disease at the molecular level. Toxocara canis is an important intestinal nematode of dogs and the principal causative agent of human toxocariasis worldwide [1, 2]. There is no information on these RNAs for any ascaridoid nematode, except Ascaris [21]

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