1. The APOBEC3B cytidine deaminase is an adenovirus restriction factor.
- Author
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Lejeune, Noémie, Mathieu, Sarah, Decloux, Alexandra, Poulain, Florian, Blockx, Zoé, Raymond, Kyle A., Willemart, Kévin, Vartanian, Jean-Pierre, Suspène, Rodolphe, and Gillet, Nicolas A.
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CYTIDINE deaminase , *ADENOVIRUSES , *DNA viruses , *VIRAL genomes , *RESPIRATORY infections - Abstract
Human adenoviruses (HAdVs) are a large family of DNA viruses counting more than a hundred strains divided into seven species (A to G). HAdVs induce respiratory tract infections, gastroenteritis and conjunctivitis. APOBEC3B is a cytidine deaminase that restricts several DNA viruses. APOBEC3B is also implicated in numerous cancers where it is responsible for the introduction of clustered mutations into the cellular genome. In this study, we demonstrate that APOBEC3B is an adenovirus restriction factor acting through a deaminase-dependent mechanism. APOBEC3B introduces C-to-T clustered mutations into the adenovirus genome. APOBEC3B reduces the propagation of adenoviruses by limiting viral genome replication, progression to late phase, and production of infectious virions. APOBEC3B restriction efficiency varies between adenoviral strains, the A12 strain being more sensitive to APOBEC3B than the B3 or C2 strains. In A12-infected cells, APOBEC3B clusters in the viral replication centers. Importantly, we show that adenovirus infection leads to a reduction of the quantity and/or enzymatic activity of the APOBEC3B protein depending on the strains. The A12 strain seems less able to resist APOBEC3B than the B3 or C2 strains, a characteristic which could explain the strong depletion of the APOBEC3-targeted motifs in the A12 genome. These findings suggest that adenoviruses evolved different mechanisms to antagonize APOBEC3B. Elucidating these mechanisms could benefit the design of cancer treatments. This study also identifies adenoviruses as triggers of the APOBEC3B-mediated innate response. The involvement of certain adenoviral strains in the genesis of the APOBEC3 mutational signature observed in tumors deserves further study. Author summary: The APOBEC3B protein is overexpressed in many human tumors and promotes genetic diversity and resistance to drug and oncolytic viruses. The identification of the mechanisms that lead to the dysregulation of APOBEC3B and the search for ways to abrogate its expression in tumors are intensively pursued. We have previously shown that adenoviral infection triggers APOBEC3B expression. In this study, we demonstrate that APOBEC3B mutates the genome of adenoviruses during their replication in the nucleus. These results warrant further investigation of the role of adenoviruses in APOBEC3B dysregulation. Our study also suggests that adenoviruses have evolved mechanisms to antagonize APOBEC3B and that some adenoviral strains are highly capable of decreasing the amount of APOBEC3B protein in infected cells. Identification of the viral proteins involved could be used to design better oncolytic vectors capable of propagating in tumor cells expressing high levels of APOBEC3B. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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