The evolution of antimicrobial peptides in Chiroptera

Front Immunol. 2023 Sep 26:14:1250229. doi: 10.3389/fimmu.2023.1250229. eCollection 2023.

Abstract

High viral tolerance coupled with an extraordinary regulation of the immune response makes bats a great model to study host-pathogen evolution. Although many immune-related gene gains and losses have been previously reported in bats, important gene families such as antimicrobial peptides (AMPs) remain understudied. We built an exhaustive bioinformatic pipeline targeting the major gene families of defensins and cathelicidins to explore AMP diversity and analyze their evolution and distribution across six bat families. A combination of manual and automated procedures identified 29 AMP families across queried species, with α-, β-defensins, and cathelicidins representing around 10% of AMP diversity. Gene duplications were inferred in both α-defensins, which were absent in five species, and three β-defensin gene subfamilies, but cathelicidins did not show significant shifts in gene family size and were absent in Anoura caudifer and the pteropodids. Based on lineage-specific gains and losses, we propose diet and diet-related microbiome evolution may determine the evolution of α- and β-defensins gene families and subfamilies. These results highlight the importance of building species-specific libraries for genome annotation in non-model organisms and shed light on possible drivers responsible for the rapid evolution of AMPs. By focusing on these understudied defenses, we provide a robust framework for explaining bat responses to pathogens.

Keywords: bioinformatics pipelines; defensins; gene annotation; innate immunity; non-model organisms; transposable elements.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Antimicrobial Cationic Peptides
  • Antimicrobial Peptides
  • Cathelicidins
  • Chiroptera* / genetics
  • beta-Defensins* / genetics

Substances

  • beta-Defensins
  • Antimicrobial Peptides
  • Antimicrobial Cationic Peptides
  • Cathelicidins

Grants and funding

This work was funded in part by US Fish and Wildlife Service grant F14AP00737 to MM, LMD, and ALR. LMD was supported in part by NSF-IOS 2032063 and 2031906, APC was supported in part by NSF-IOS 2031926 and 2032011; NS was supported by a charitable donation by Pamela Hurst-Della Pietra to the Dávalos Lab; DAR and DM-S were supported by NSF-DEB 1838283 and IOS 2032006. FXC was funded by a fellowship granted by the Texas Tech Department of Biological Sciences. GMH was funded by a UCD Ad Astra scholarship.