Abstract

BackgroundBlack widow spiders are infamous for their neurotoxic venom, which can cause extreme and long-lasting pain. This unusual venom is dominated by latrotoxins and latrodectins, two protein families virtually unknown outside of the black widow genus Latrodectus, that are difficult to study given the paucity of spider genomes. Using tissue-, sex- and stage-specific expression data, we analyzed the recently sequenced genome of the house spider (Parasteatoda tepidariorum), a close relative of black widows, to investigate latrotoxin and latrodectin diversity, expression and evolution.ResultsWe discovered at least 47 latrotoxin genes in the house spider genome, many of which are tandem-arrayed. Latrotoxins vary extensively in predicted structural domains and expression, implying their significant functional diversification. Phylogenetic analyses show latrotoxins have substantially duplicated after the Latrodectus/Parasteatoda split and that they are also related to proteins found in endosymbiotic bacteria. Latrodectin genes are less numerous than latrotoxins, but analyses show their recruitment for venom function from neuropeptide hormone genes following duplication, inversion and domain truncation. While latrodectins and other peptides are highly expressed in house spider and black widow venom glands, latrotoxins account for a far smaller percentage of house spider venom gland expression.ConclusionsThe house spider genome sequence provides novel insights into the evolution of venom toxins once considered unique to black widows. Our results greatly expand the size of the latrotoxin gene family, reinforce its narrow phylogenetic distribution, and provide additional evidence for the lateral transfer of latrotoxins between spiders and bacterial endosymbionts. Moreover, we strengthen the evidence for the evolution of latrodectin venom genes from the ecdysozoan Ion Transport Peptide (ITP)/Crustacean Hyperglycemic Hormone (CHH) neuropeptide superfamily. The lower expression of latrotoxins in house spiders relative to black widows, along with the absence of a vertebrate-targeting α-latrotoxin gene in the house spider genome, may account for the extreme potency of black widow venom.

Highlights

  • Black widow spiders are infamous for their neurotoxic venom, which can cause extreme and longlasting pain

  • Twenty-one of the 47 full-length latrotoxin genes are distributed in tandem along two genomic scaffolds with as many as 14 tandem latrotoxin genes spanning ~300 kb of scaffold 111 and 7 spanning ~120 kb of scaffold 1821 (Fig. 1a)

  • The house spider latrotoxins lacking predicted C-terminal domain (CTD) have little to no expression in female venom glands, but most appear to have greater expression in Crustacean Hyperglycemic Hormone (CHH)/Ion Transport Peptide (ITP)/latrodectin phylogeny shows shift to venom function involved CHH domain truncation In contrast to the 47–53 latrotoxins encoded by the house spider genome, we identified only nine putative CHH/ITP/latrodectin genes on four scaffolds

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Summary

Introduction

Black widow spiders are infamous for their neurotoxic venom, which can cause extreme and longlasting pain. The development of rapid and cost-effective generation sequencing (NGS) technologies has launched many new whole genome projects focused on biomedically or agriculturally important eukaryotes An example of such efforts is the i5k (5000 arthropod genomes) initiative [8], which has recently sequenced the house spider (Parasteatoda tepidariorum) genome (NCBI Accession GCA_000365465.1). This species is an emerging developmental model that is in the same family (Theridiidae) as black widow spiders (Latrodectus spp.), but produces far less hazardous venom [9, 10]. Together with extensive tissue- and stage-specific transcriptomic data, the house spider genome provides an important resource to investigate the evolutionary basis for the extreme toxicity of black widow venom

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