Evidence map›Paper›PMID 28650958›Full record

ArticlePLoS genetics2017

Dynamics and impact of homologous recombination on the evolution of Legionella pneumophila.

Sophia David, Leonor Sánchez-Busó, Simon R Harris, Pekka Marttinen, Christophe Rusniok, Carmen Buchrieser, Timothy G Harrison, Julian Parkhill

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

37 citing papers in PubMed, 57 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 3 countries.

Sophia DavidPathogen Genomics, Wellcome Trust Sanger Institute, Cambridge, United Kingdom.
Leonor Sánchez-BusóPathogen Genomics, Wellcome Trust Sanger Institute, Cambridge, United Kingdom.ORCID http://orcid.org/0000-0002-4162-0228
Simon R HarrisPathogen Genomics, Wellcome Trust Sanger Institute, Cambridge, United Kingdom.ORCID http://orcid.org/0000-0003-1512-6194
Pekka MarttinenHelsinki Institute for Information Technology HIIT, Department of Computer Science, Aalto University, Aalto, Espoo, Finland.
Christophe RusniokInstitut Pasteur, Biologie des Bactéries Intracellulaires, Paris, France.
Carmen BuchrieserInstitut Pasteur, Biologie des Bactéries Intracellulaires, Paris, France.ORCID http://orcid.org/0000-0003-3477-9190
Timothy G HarrisonRespiratory and Vaccine Preventable Bacteria Reference Unit, Public Health England, London, United Kingdom.
Julian ParkhillPathogen Genomics, Wellcome Trust Sanger Institute, Cambridge, United Kingdom.ORCID http://orcid.org/0000-0002-7069-5958
Wellcome Sanger Institute · GBCentre National de la Recherche Scientifique · FRHelsinki Institute for Information Technology · FIPublic Health England · GB

Funding

Wellcome Trust 098051
6 · The paper itself

Abstract

Legionella pneumophila is an environmental bacterium and the causative agent of Legionnaires' disease. Previous genomic studies have shown that recombination accounts for a high proportion (>96%) of diversity within several major disease-associated sequence types (STs) of L. pneumophila. This suggests that recombination represents a potentially important force shaping adaptation and virulence. Despite this, little is known about the biological effects of recombination in L. pneumophila, particularly with regards to homologous recombination (whereby genes are replaced with alternative allelic variants). Using newly available population genomic data, we have disentangled events arising from homologous and non-homologous recombination in six major disease-associated STs of L. pneumophila (subsp. pneumophila), and subsequently performed a detailed characterisation of the dynamics and impact of homologous recombination. We identified genomic "hotspots" of homologous recombination that include regions containing outer membrane proteins, the lipopolysaccharide (LPS) region and Dot/Icm effectors, which provide interesting clues to the selection pressures faced by L. pneumophila. Inference of the origin of the recombined regions showed that isolates have most frequently imported DNA from isolates belonging to their own clade, but also occasionally from other major clades of the same subspecies. This supports the hypothesis that the possibility for horizontal exchange of new adaptations between major clades of the subspecies may have been a critical factor in the recent emergence of several clinically important STs from diverse genomic backgrounds. However, acquisition of recombined regions from another subspecies, L. pneumophila subsp. fraseri, was rarely observed, suggesting the existence of a recombination barrier and/or the possibility of ongoing speciation between the two subspecies. Finally, we suggest that multi-fragment recombination may occur in L. pneumophila, whereby multiple non-contiguous segments that originate from the same molecule of donor DNA are imported into a recipient genome during a single episode of recombination.

Indexed as

Evolution, MolecularBacterial Outer Membrane ProteinsGenome, BacterialHomologous RecombinationLegionella pneumophilaLegionnaires' DiseaseLipopolysaccharidesPhylogenyRecombinant ProteinsBacterial Outer Membrane ProteinsLipopolysaccharidesRecombinant Proteins

Identifiers

PMID28650958
PMCPMC5507463
OpenAlexW2633121908

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.