دورية أكاديمية

Bacterial biodiversity drives the evolution of CRISPR-based phage resistance.

التفاصيل البيبلوغرافية
العنوان: Bacterial biodiversity drives the evolution of CRISPR-based phage resistance.
المؤلفون: Alseth EO; Environment and Sustainability Institute, Biosciences, University of Exeter, Penryn Campus, Penryn, UK. eao210@exeter.ac.uk., Pursey E; Environment and Sustainability Institute, Biosciences, University of Exeter, Penryn Campus, Penryn, UK., Luján AM; IRNASUS, CONICET, Facultad de Ciencias Químicas, Universidad Católica de Córdoba, Córdoba, Argentina., McLeod I; Environment and Sustainability Institute, Biosciences, University of Exeter, Penryn Campus, Penryn, UK., Rollie C; Environment and Sustainability Institute, Biosciences, University of Exeter, Penryn Campus, Penryn, UK., Westra ER; Environment and Sustainability Institute, Biosciences, University of Exeter, Penryn Campus, Penryn, UK. e.r.westra@exeter.ac.uk.
المصدر: Nature [Nature] 2019 Oct; Vol. 574 (7779), pp. 549-552. Date of Electronic Publication: 2019 Oct 23.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-4687 (Electronic) Linking ISSN: 00280836 NLM ISO Abbreviation: Nature Subsets: MEDLINE
أسماء مطبوعة: Publication: Basingstoke : Nature Publishing Group
Original Publication: London, Macmillan Journals ltd.
مواضيع طبية MeSH: Biodiversity* , Evolution, Molecular*, Bacteriophages/*genetics , Bacteriophages/*immunology , CRISPR-Cas Systems/*genetics , Pseudomonas aeruginosa/*immunology , Pseudomonas aeruginosa/*virology, Bacteriophages/pathogenicity ; CRISPR-Cas Systems/immunology ; Pseudomonas aeruginosa/genetics ; Pseudomonas aeruginosa/pathogenicity ; Receptors, Virus/metabolism
مستخلص: About half of all bacteria carry genes for CRISPR-Cas adaptive immune systems 1 , which provide immunological memory by inserting short DNA sequences from phage and other parasitic DNA elements into CRISPR loci on the host genome 2 . Whereas CRISPR loci evolve rapidly in natural environments 3,4 , bacterial species typically evolve phage resistance by the mutation or loss of phage receptors under laboratory conditions 5,6 . Here we report how this discrepancy may in part be explained by differences in the biotic complexity of in vitro and natural environments 7,8 . Specifically, by using the opportunistic pathogen Pseudomonas aeruginosa and its phage DMS3vir, we show that coexistence with other human pathogens amplifies the fitness trade-offs associated with the mutation of phage receptors, and therefore tips the balance in favour of the evolution of CRISPR-based resistance. We also demonstrate that this has important knock-on effects for the virulence of P. aeruginosa, which became attenuated only if the bacteria evolved surface-based resistance. Our data reveal that the biotic complexity of microbial communities in natural environments is an important driver of the evolution of CRISPR-Cas adaptive immunity, with key implications for bacterial fitness and virulence.
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معلومات مُعتمدة: 714478 International ERC_ European Research Council
المشرفين على المادة: 0 (Receptors, Virus)
تواريخ الأحداث: Date Created: 20191025 Date Completed: 20191119 Latest Revision: 20231019
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC6837874
DOI: 10.1038/s41586-019-1662-9
PMID: 31645729
قاعدة البيانات: MEDLINE
الوصف
تدمد:1476-4687
DOI:10.1038/s41586-019-1662-9