4.8 Article

Non-retroviral Endogenous Viral Element Limits Cognate Virus Replication in Aedes aegypti Ovaries

Journal

CURRENT BIOLOGY
Volume 30, Issue 18, Pages 3495-+

Publisher

CELL PRESS
DOI: 10.1016/j.cub.2020.06.057

Keywords

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Funding

  1. Netherlands Organisation for Scientific Research (VICI grant) [016.VICI.170.090]
  2. European Molecular Biology Organization (EMBO grant) [ASTF 449-2016]
  3. Agence Nationale de la Recherche [ANR-16-CE35-0004-01, ANR-17-ERC2-0016-01]
  4. City of Paris Emergence(s) program in Biomedical Research
  5. European Research Council [615220]
  6. French Government's Investissement d'Avenir program Laboratoire d'Excellence Integrative Biology of Emerging Infectious Diseases [ANR-10-LABX-62-IBEID]
  7. European Research Council (ERC) [615220] Funding Source: European Research Council (ERC)
  8. Agence Nationale de la Recherche (ANR) [ANR-17-ERC2-0016] Funding Source: Agence Nationale de la Recherche (ANR)

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Endogenous viral elements (EVEs) are viral sequences integrated in host genomes. A large number of non-retroviral EVEs was recently detected in Aedes mosquito genomes, leading to the hypothesis that mosquito EVEs may control exogenous infections by closely related viruses. Here, we experimentally investigated the role of an EVE naturally found in Aedes aegypti populations and derived from the widespread insect-specific virus, cell-fusing agent virus (CFAV). Using CRISPR-Cas9 genome editing, we created an Ae. aegypti line lacking the CFAV EVE. Absence of the EVE resulted in increased CFAV replication in ovaries, possibly modulating vertical transmission of the virus. Viral replication was controlled by targeting of viral RNA by EVE-derived P-element-induced wimpy testis-interacting RNAs (piRNAs). Our results provide evidence that antiviral piRNAs are produced in the presence of a naturally occurring EVE and its cognate virus, demonstrating a functional link between non-retroviral EVEs and antiviral immunity in a natural insect-virus interaction.

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