Expanding Diversity of Firmicutes Single-Strand Annealing Proteins: A Putative Role of Bacteriophage-Host Arms Race

التفاصيل البيبلوغرافية
العنوان: Expanding Diversity of Firmicutes Single-Strand Annealing Proteins: A Putative Role of Bacteriophage-Host Arms Race
المؤلفون: Elena Bidnenko, Agnieszka K. Szczepankowska, Eric Prestel, Kamil Steczkiewicz
المساهمون: MICrobiologie de l'ALImentation au Service de la Santé (MICALIS), AgroParisTech-Université Paris-Saclay-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), This work was in part supported by the joint research project between Institut National de la Recherche Agronomique (INRA), France and the Ministry of Science and Higher Education (MSHE), Poland (number P260/N/INRA/2008/0).
المصدر: Frontiers in Microbiology
Frontiers in Microbiology, Frontiers Media, 2021, 12, ⟨10.3389/fmicb.2021.644622⟩
Frontiers in Microbiology, Vol 12 (2021)
بيانات النشر: HAL CCSD, 2021.
سنة النشر: 2021
مصطلحات موضوعية: Microbiology (medical), In silico, [SDV]Life Sciences [q-bio], phage recombinase, Context (language use), Computational biology, Biology, single strand annealing proteins (SSAP), Microbiology, DNA sequencing, Firmicutes bacteriophages, Bacteriophage, 03 medical and health sciences, CLANS, Recombinase, CRISPR, Gene, 030304 developmental biology, abortive intection, 0303 health sciences, 030306 microbiology, biology.organism_classification, QR1-502, CRISPR/cas, Horizontal gene transfer, Sak3/DUF1071, phage-bacteria arms race
الوصف: Bacteriophage-encoded single strand annealing proteins (SSAPs) are recombinases which can substitute the classical, bacterial RecA and manage the DNA metabolism at different steps of phage propagation. SSAPs have been shown to efficiently promote recombination between short and rather divergent DNA sequences and were exploited for in vivo genetic engineering mainly in Gram-negative bacteria. In opposition to the conserved and almost universal bacterial RecA protein, SSAPs display great sequence diversity. The importance for SSAPs in phage biology and phage-bacteria evolution is underlined by their role as key players in events of horizontal gene transfer (HGT). All of the above provoke a constant interest for the identification and study of new phage recombinase proteins in vivo, in vitro as well as in silico. Despite this, a huge body of putative ssap genes escapes conventional classification, as they are not properly annotated. In this work, we performed a wide-scale identification, classification and analysis of SSAPs encoded by the Firmicutes bacteria and their phages. By using sequence similarity network and gene context analyses, we created a new high quality dataset of phage-related SSAPs, substantially increasing the number of annotated SSAPs. We classified the identified SSAPs into seven distinct families, namely RecA, Gp2.5, RecT/Redβ, Erf, Rad52/22, Sak3, and Sak4, organized into three superfamilies. Analysis of the relationships between the revealed protein clusters led us to recognize Sak3-like proteins as a new distinct SSAP family. Our analysis showed an irregular phylogenetic distribution of ssap genes among different bacterial phyla and specific phages, which can be explained by the high rates of ssap HGT. We propose that the evolution of phage recombinases could be tightly linked to the dissemination of bacterial phage-resistance mechanisms (e.g., abortive infection and CRISPR/Cas systems) targeting ssap genes and be a part of the constant phage-bacteria arms race.
اللغة: English
تدمد: 1664-302X
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fef54e770b901531f94d083123f0766
https://hal.inrae.fr/hal-03343061
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....4fef54e770b901531f94d083123f0766
قاعدة البيانات: OpenAIRE