Abstract

BackgroundAspartic proteases are known to play an important role in the biology of nematode parasitism. This role is best characterised in blood-feeding nematodes, where they digest haemoglobin, but they are also likely to play important roles in the biology of nematode parasites that do not feed on blood. In the present work, we investigate the evolution and expression of aspartic proteases in Strongyloides ratti, which permits a unique comparison between parasitic and free-living adult forms within its life-cycle.ResultsWe identified eight transcribed aspartic protease sequences and a further two genomic sequences and compared these to homologues in Caenorhabditis elegans and other nematode species. Phylogenetic analysis demonstrated a complex pattern of gene evolution, such that some S. ratti sequences had a one-to-one correspondence with orthologues of C. elegans but that lineage-specific expansions have occurred for other aspartic proteases in these two nematodes. These gene duplication events may have contributed to the adaptation of the two species to their different lifestyles. Among the set of S. ratti aspartic proteases were two closely-related isoforms that showed differential expression during different life stages: ASP-2A is highly expressed in parasitic females while ASP-2B is predominantly found in free-living adults. Molecular modelling of the ASP-2 isoforms reveals that their substrate specificities are likely to be very similar, but that ASP-2B is more electrostatically negative over its entire molecular surface than ASP-2A. This characteristic may be related to different pH values of the environments in which these two isoforms operate.ConclusionsWe have demonstrated that S. ratti provides a powerful model to explore the genetic adaptations associated with parasitic versus free-living life-styles. We have discovered gene duplication of aspartic protease genes in Strongyloides and identified a pair of paralogues differentially expressed in either the parasitic or the free-living phase of the nematode life-cycle, consistent with an adaptive role for aspartic proteases in the evolution of nematode parasitism.

Highlights

  • Aspartic proteases are known to play an important role in the biology of nematode parasitism

  • We identified a pair of paralogous aspartic proteases in S. ratti that have arisen as a result of a recent duplication event but for which ASP2A is highly expressed in parasitic females while ASP-2B is highly expressed in free-living females, and we present a molecular model that allows this pair of paralogous genes to be placed in a structural context

  • Two further putative asparatic protease genes, asp-8 and asp-11, were identified within the draft genome sequence for S. ratti. 5' RACE was used to complete full length coding sequences for ASP-2A and ASP-2B, while the full length for other transcripts were obtained using the genome sequences for S. ratti, when necessary

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Summary

Introduction

Aspartic proteases are known to play an important role in the biology of nematode parasitism. Aspartic proteases have been associated with digestion of host haemoglobin in the trichostrongylid Haemonchus contortus and in the hookworms Ancylostoma caninum and Necator americanus [4]. The aspartic proteases of A. caninum and N. americanus each exhibit specificity in their ability to digest haemoglobin from natural versus unnatural hosts, indicating evolutionary adaptation to their host species [4]. Aspartic proteases have been shown to degrade skin macromolecules and aid skin penetration in hookworms, suggesting that their role in nematode parasitism is not limited to digestion of haemoglobin [7]. The aspartic proteases may play a role in the biology of nematode parasites that do not feed on blood, such as Strongyloides stercoralis, Onchocerca volvulus and Brugia malayi in which aspartic proteases have previously been identified [7,8]

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