Identification of an anti-CRISPR protein that inhibits the CRISPR-Cas type I-B system in Clostridioides difficile

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Título: Identification of an anti-CRISPR protein that inhibits the CRISPR-Cas type I-B system in Clostridioides difficile
Autor/es: Muzyukina, Polina | Shkaruta, Anton | Guzmán, Noemí M. | Andreani, Jessica | Borges, Adair L. | Bondy-Denomy, Joseph | Maikova, Anna | Semenova, Ekaterina | Severinov, Konstantin | Soutourina, Olga
Grupo/s de investigación o GITE: Microbiología Molecular
Centro, Departamento o Servicio: Universidad de Alicante. Departamento de Fisiología, Genética y Microbiología
Palabras clave: Clostridioides difficile | Type I-B CRISPR-Cas interference | Cas operons | Enteropathogen | Anti-CRISPR | DNA mimicry | Phage
Fecha de publicación: 27-nov-2023
Editor: American Society for Microbiology
Cita bibliográfica: mSphere. 2023, 8(6). https://doi.org/10.1128/msphere.00401-23
Resumen: CRISPR-Cas systems provide prokaryotic hosts with adaptive immunity against mobile genetic elements. Many bacteriophages encode anti-CRISPR (Acr) proteins that inhibit host defense. The identification of Acr proteins is challenging due to their small size and high sequence diversity, and only a limited number has been characterized to date. In this study, we report the discovery of a novel Acr protein, AcrIB2, encoded by the φCD38-2 Clostridioides difficile phage that efficiently inhibits interference by the type I-B CRISPR-Cas system of the host and likely acts as a DNA mimic. Most C. difficile strains contain two cas operons, one encoding a full set of interference and adaptation proteins and another encoding interference proteins only. Unexpectedly, we demonstrate that only the partial operon is required for interference and is subject to inhibition by AcrIB2.
Patrocinador/es: This work was supported by the Institut Universitaire de France (to O.S.), the Institute for Integrative Biology of the Cell, the University Paris-Saclay, Graduate School Life Sciences and Health, and OI MICROBES funding and Vernadski fellowship (to P.M.). This work was also supported by NIH grant R01 GM10407 (to K.S.), the Russian Science Foundation grant 19-14-00323, and the Ministry of Science and Higher Education of the Russian Science Federation agreement no. 075-10-2021-114.
URI: http://hdl.handle.net/10045/138968
ISSN: 2379-5042
DOI: 10.1128/msphere.00401-23
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: © 2023 Muzyukina et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.
Revisión científica: si
Versión del editor: https://doi.org/10.1128/msphere.00401-23
Aparece en las colecciones:INV - Microbiología Molecular - Artículos de Revistas

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