Abstract

BackgroundToll-like receptors (TLRs) are the frontline actors in the innate immune response to various pathogens and are expected to be targets of natural selection in species adapted to habitats with contrasting pathogen burdens. The recent publication of genome sequences of giraffe and okapi together afforded the opportunity to examine the evolution of selected TLRs in broad range of terrestrial ungulates and cetaceans during their complex habitat diversification. Through direct sequence comparisons and standard evolutionary approaches, the extent of nucleotide and protein sequence diversity in seven Toll-like receptors (TLR2, TLR3, TLR4, TLR5, TLR7, TLR9 and TLR10) between giraffe and closely related species was determined. In addition, comparison of the patterning of key TLR motifs and domains between giraffe and related species was performed. The quantification of selection pressure and divergence on TLRs among terrestrial ungulates and cetaceans was also performed.ResultsSequence analysis shows that giraffe has 94–99% nucleotide identity with okapi and cattle for all TLRs analyzed. Variations in the number of Leucine-rich repeats were observed in some of TLRs between giraffe, okapi and cattle. Patterning of key TLR domains did not reveal any significant differences in the domain architecture among giraffe, okapi and cattle. Molecular evolutionary analysis for selection pressure identifies positive selection on key sites for all TLRs examined suggesting that pervasive evolutionary pressure has taken place during the evolution of terrestrial ungulates and cetaceans. Analysis of positively selected sites showed some site to be part of Leucine-rich motifs suggesting functional relevance in species-specific recognition of pathogen associated molecular patterns. Notably, clade analysis reveals significant selection divergence between terrestrial ungulates and cetaceans in viral sensing TLR3. Mapping of giraffe TLR3 key substitutions to the structure of the receptor indicates that at least one of giraffe altered sites coincides with TLR3 residue known to play a critical role in receptor signaling activity.ConclusionThere is overall structural conservation in TLRs among giraffe, okapi and cattle indicating that the mechanism for innate immune response utilizing TLR pathways may not have changed very much during the evolution of these species. However, a broader phylogenetic analysis revealed signatures of adaptive evolution among terrestrial ungulates and cetaceans, including the observed selection divergence in TLR3. This suggests that long term ecological dynamics has led to species-specific innovation and functional variation in the mechanisms mediating innate immunity in terrestrial ungulates and cetaceans.

Highlights

  • Toll-like receptors (TLRs) are the frontline actors in the innate immune response to various pathogens and are expected to be targets of natural selection in species adapted to habitats with contrasting pathogen burdens

  • TLR3 recognizes doublestranded RNA, TLR7 and TLR8 are activated upon contact with single-stranded RNA while TLR9 recognizes Cytosine Phosphate Guanine (CpG) DNA from virus, fungi and other invading pathogens [9,10,11]

  • The asterisk (*) refers to residue identical to that of giraffe in our study suggest that the diversity of ecological specializations among ungulates and cetaceans has combined with the TLR4 inherent factors to accelerate adaptive evolution of TLR4 in these species

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Summary

Introduction

Toll-like receptors (TLRs) are the frontline actors in the innate immune response to various pathogens and are expected to be targets of natural selection in species adapted to habitats with contrasting pathogen burdens. Mammalian Toll-like receptors (TLRs) are membranebound proteins expressed in defense cells where they have evolved to mediate innate immune system through recognition of various pathogen-associated molecular patterns (PAMPs) [1, 2]. Other outer membrane TLRs include TLR4 which dimerize to recognize lipopolysaccharides (LPS) of gram negative bacteria [5], TLR5 which recognizes flagellins [6] and TLR10 which has recently been shown to have anti-inflammatory effects, and perhaps in combination with TLR2 may be associated with mycobacterial infections [7, 8]. TLR3 recognizes doublestranded RNA (dsRNA), TLR7 and TLR8 are activated upon contact with single-stranded RNA (ssRNA) while TLR9 recognizes CpG DNA from virus, fungi and other invading pathogens [9,10,11]

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