Evidence map›Paper›PMID 31226931›Full record

ArticleBMC evolutionary biology2019

Serotype-specific evolutionary patterns of antimicrobial-resistant Salmonella enterica.

Jingqiu Liao, Renato Hohl Orsi, Laura M Carroll, Jasna Kovac, Hongyu Ou, Hailong Zhang, Martin Wiedmann

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
7.4field-weighted citation impact, top 3% 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

19 citing papers in PubMed, 46 citations in OpenAlex.

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  13. Detecting Genetic Variation of ColonizingFrontiers in bioinformatics · 2022
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  16. High-Resolution Genomic Comparisons withinApplied and environmental microbiology · 2021
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  18. Monitoring the Microevolution ofFrontiers in microbiology · 2021
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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

7 authors at 4 institutions in 2 countries.

Jingqiu LiaoDepartment of Food Science, 341 Stocking Hall, Cornell University, Ithaca, NY, 14853, USA.
Renato Hohl OrsiDepartment of Food Science, 341 Stocking Hall, Cornell University, Ithaca, NY, 14853, USA.
Laura M CarrollDepartment of Food Science, 341 Stocking Hall, Cornell University, Ithaca, NY, 14853, USA.
Jasna KovacDepartment of Food Science, The Pennsylvania State University, University Park, PA, 16802, USA.
Hongyu OuSchool of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai, 200240, China.
Hailong ZhangDepartment of Computer Science & Engineering, Ohio State University, Columbus, OH, 43210, USA.
Martin WiedmannDepartment of Food Science, 341 Stocking Hall, Cornell University, Ithaca, NY, 14853, USA. mw16@cornell.edu.
Cornell University · USPennsylvania State University · USShanghai Jiao Tong University · CNThe Ohio State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe emergence of antimicrobial-resistant (AMR) strains of the important human and animal pathogen Salmonella enterica poses a growing threat to public health. Here, we studied the genome-wide evolution of 90 S. enterica AMR isolates, representing one host adapted serotype (S. Dublin) and two broad host range serotypes (S. Newport and S. Typhimurium).

resultsAMR S. Typhimurium had a large effective population size, a large and diverse genome, AMR profiles with high diversity, and frequent positive selection and homologous recombination. AMR S. Newport showed a relatively low level of diversity and a relatively clonal population structure. AMR S. Dublin showed evidence for a recent population bottleneck, and the genomes were characterized by a larger number of genes and gene ontology terms specifically absent from this serotype and a significantly higher number of pseudogenes as compared to other two serotypes. Approximately 50% of accessory genes, including specific AMR and putative prophage genes, were significantly over- or under-represented in a given serotype. Approximately 65% of the core genes showed phylogenetic clustering by serotype, including the AMR gene aac (6')-Iaa. While cell surface proteins were shown to be the main target of positive selection, some proteins with possible functions in AMR and virulence also showed evidence for positive selection. Homologous recombination mainly acted on prophage-associated proteins.

conclusionsOur data indicates a strong association between genome content of S. enterica and serotype. Evolutionary patterns observed in S. Typhimurium are consistent with multiple emergence events of AMR strains and/or ecological success of this serotype in different hosts or habitats. Evolutionary patterns of S. Newport suggested that antimicrobial resistance emerged in one single lineage, Lineage IIC. A recent population bottleneck and genome decay observed in AMR S. Dublin are congruent with its narrow host range. Finally, our results suggest the potentially important role of positive selection in the evolution of antimicrobial resistance, host adaptation and serotype diversification in S. enterica.

Indexed as

Evolution, MolecularSerogroupAnti-Bacterial AgentsHumansPhylogenySalmonella entericaAnti-Bacterial AgentsAntimicrobial resistanceGenome decayHomologous recombinationPositive selectionSalmonella entericaSerotypes

Identifiers

PMID31226931
PMCPMC6588947
OpenAlexW2952311913

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.