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<p>How antiviral immunity first arose in animals is a central question in evolutionary biology. Here, using the sea anemone <i>Nematostella vectensis</i>, we identify <i>CARDIB</i>, a previously uncharacterized gene located next to <i>RLRb</i>—a cnidarian homologue of the vertebrate RIG-I-like receptor family. This conserved genomic linkage across Anthozoa reveals an ancient coupling between immune sensing and regulation. Despite sequence similarity to vertebrate MAVS, CARDIB performs an opposing function: it represses immune genes under basal conditions yet is essential for activation upon viral challenge. CARDIB binds RLRb through a single CARD domain, forming a repressive complex. Loss of either gene abolishes antiviral transcription, disrupts apoptosis and elevates viral load under laboratory conditions. Both genes, as well as the <i>RLRb</i> paralogue <i>RLRa</i>, are essential for antiviral defence under native conditions. Phylogeny places the cnidarian CARDs distinctly from the vertebrate RLR–MAVS families, revealing an ancient mechanism that regulates the antiviral response through CARD-based signalling.</p>

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An ancient anthozoan protein reveals an alternative evolutionary path of antiviral signalling

  • 期刊论文

  • 发表日期：

    2026年6月26日

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  • Ton Sharoni,
  • Adrian Jaimes-Becerra,
  • Sydney Birch,
  • Hee-Jin Kwak,
  • Daria Aleshkina,
  • Magda Lewandowska,
  • Joachim M. Surm,
  • Hannah Justin,
  • Reuven Aharoni,
  • Adam M. Reitzel,
  • Yehu Moran

摘要

How antiviral immunity first arose in animals is a central question in evolutionary biology. Here, using the sea anemone Nematostella vectensis, we identify CARDIB, a previously uncharacterized gene located next to RLRb—a cnidarian homologue of the vertebrate RIG-I-like receptor family. This conserved genomic linkage across Anthozoa reveals an ancient coupling between immune sensing and regulation. Despite sequence similarity to vertebrate MAVS, CARDIB performs an opposing function: it represses immune genes under basal conditions yet is essential for activation upon viral challenge. CARDIB binds RLRb through a single CARD domain, forming a repressive complex. Loss of either gene abolishes antiviral transcription, disrupts apoptosis and elevates viral load under laboratory conditions. Both genes, as well as the RLRb paralogue RLRa, are essential for antiviral defence under native conditions. Phylogeny places the cnidarian CARDs distinctly from the vertebrate RLR–MAVS families, revealing an ancient mechanism that regulates the antiviral response through CARD-based signalling.