Abstract

BackgroundHard ticks (family Ixodidae) are obligatory hematophagous ectoparasites of worldwide medical and veterinary importance. The haploid genomes of multiple species of ixodid ticks exceed 1 Gbp, prompting questions regarding gene, segmental and whole genome duplication in this phyletic group. The availability of the genome assembly for the black legged tick, Ixodes scapularis, and transcriptome datasets for multiple species of ticks offers an opportunity to assess the contribution of gene duplication to the genome. Here we developed a bioinformatics pipeline to identify and analyze duplicated genes (paralogs) using gene models from the prostriate tick, I. scapularis IscaW1.1 annotation and expressed sequence tags (ESTs) from I. scapularis and the metastriate ticks, Rhipicephalus microplus (southern cattle tick), R. appendiculatus (brown ear tick) and Amblyomma variegatum (tropical bont tick).ResultsApproximately 1-2 % of I. scapularis gene models and 2-14 % of ESTs from the four species represent duplicated genes. The ratio of non-synonymous to synonymous nucleotide substitution rates suggests ~ 25 % of duplicated genes are under positive selection pressure in each species. Analyses of synonymous substitution rates provide evidence for two duplication events in I. scapularis and R. microplus involving several hundred genes. Conservative molecular clock estimates based on synonymous substitution rates for species of Anopheles mosquitoes and the fruit fly, Drosophila melanogaster, suggest these events occurred within the last 50 MYA. Mapping of paralogs to the I. scapularis genome assembly supports tandem, or possibly segmental duplication events.ConclusionsThe present study marks the first genome-level analyses of gene duplication for the Ixodidae and provides insights into mechanisms shaping genome evolution in this group. At least two duplication events involving hundreds of genes may have occurred independently in the lineages prostriata and metastriata, with tandem and segmental duplication the most likely mechanisms for paralog generation. Duplicated genes under positive selection pressure may be linked to emerging functions in the tick and represent important candidates for further study.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-2350-2) contains supplementary material, which is available to authorized users.

Highlights

  • Hard ticks are obligatory hematophagous ectoparasites of worldwide medical and veterinary importance

  • 20,901 tentative consensus (TC) generated from the alignment of 192,461 I. scapularis expressed sequence tag (EST) produced as part of the genome project and ESTs from the metastriate ticks R. microplus, R. appendiculatus and A. variegatum, were included in analyses

  • Identification of gene duplicates in I. scapularis, R. microplus, R. appendiculatus and A. variegatum Clusters of two or more paralogous sequences identified by the program Vmatch using different stringency parameters represent between 1.55-3.41 % of I. scapularis gene model (GM) and 7.54-22.90 % of TCs (Additional file 1: Table S1)

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Summary

Introduction

Hard ticks (family Ixodidae) are obligatory hematophagous ectoparasites of worldwide medical and veterinary importance. The haploid genomes of multiple species of ixodid ticks exceed 1 Gbp, prompting questions regarding gene, segmental and whole genome duplication in this phyletic group. Duplicated genes may confer advantages by increasing protein diversity through accumulation of non-synonymous mutations and alternative splicing or by changes in expression levels or spatio-temporal expression patterns [9, 10]. These genes may serve as a buffer against deleterious mutations or as targets for retro-transposition. Evaluation of gene duplicates in ixodid ticks is fundamental in order to understand genome organization and evolution, and may aid the selection of genes for development of targeted pest control

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