Evidence map›Paper›PMID 30905290›Full record

ArticlePhilosophical transactions of the Royal Society of London. Series B, Biological sciences2019

Different genetic and morphological outcomes for phages targeted by single or multiple CRISPR-Cas spacers.

B N J Watson, R A Easingwood, B Tong, M Wolf, G P C Salmond, R H J Staals, M Bostina, P C Fineran

Open access · bronzeAbstract read
In one paragraph

Article in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 31 citations in OpenAlex.

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  18. The ecology and evolution of microbial CRISPR-Cas adaptive immune systems.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 4 countries.

B N J Watson1 Department of Microbiology and Immunology, University of Otago , PO Box 56, Dunedin 9054 , New Zealand.
R A Easingwood2 Otago Centre for Electron Microscopy, University of Otago , PO Box 56, Dunedin 9054 , New Zealand.
B Tong1 Department of Microbiology and Immunology, University of Otago , PO Box 56, Dunedin 9054 , New Zealand.
M Wolf3 Molecular Cryo-Electron Microscopy Unit, Okinawa Institute of Science and Technology, Graduate University , Onna, Okinawa , Japan.
G P C Salmond4 Department of Biochemistry, University of Cambridge , Cambridge CB2 1QW , UK.
R H J Staals1 Department of Microbiology and Immunology, University of Otago , PO Box 56, Dunedin 9054 , New Zealand.
M Bostina1 Department of Microbiology and Immunology, University of Otago , PO Box 56, Dunedin 9054 , New Zealand.
P C Fineran1 Department of Microbiology and Immunology, University of Otago , PO Box 56, Dunedin 9054 , New Zealand.
University of Otago · NZOkinawa Institute of Science and Technology Graduate University · JPUniversity of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council BB/G000298/1Biotechnology and Biological Sciences Research Council BB/H002677/1
6 · The paper itself

Abstract

CRISPR-Cas systems provide bacteria and archaea with adaptive immunity against genetic invaders, such as bacteriophages. The systems integrate short sequences from the phage genome into the bacterial CRISPR array. These 'spacers' provide sequence-specific immunity but drive natural selection of evolved phage mutants that escape the CRISPR-Cas defence. Spacer acquisition occurs by either naive or primed adaptation. Naive adaptation typically results in the incorporation of a single spacer. By contrast, priming is a positive feedback loop that often results in acquisition of multiple spacers, which occurs when a pre-existing spacer matches the invading phage. We predicted that single and multiple spacers, representative of naive and primed adaptation, respectively, would cause differing outcomes after phage infection. We investigated the response of two phages, ϕTE and ϕM1, to the Pectobacterium atrosepticum type I-F CRISPR-Cas system and observed that escape from single spacers typically occurred via point mutations. Alternatively, phages escaped multiple spacers through deletions, which can occur in genes encoding structural proteins. Cryo-EM analysis of the ϕTE structure revealed shortened tails in escape mutants with tape measure protein deletions. We conclude that CRISPR-Cas systems can drive phage genetic diversity, altering morphology and fitness, through selective pressures arising from naive and primed acquisition events. This article is part of a discussion meeting issue 'The ecology and evolution of prokaryotic CRISPR-Cas adaptive immune systems'.

Indexed as

CRISPR-Cas SystemsBacteriophagesPectobacteriumPoint MutationbacteriophagesCRISPR-Casphage evolutionphage morphologytape measure protein

Identifiers

PMID30905290
PMCPMC6452268
OpenAlexW2924195773

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.