Evidence map›Paper›PMID 31065672›Full record

ArticleGenome biology and evolution2019

Remarkable Genome Stability among emm1 Group A Streptococcus in Belgium over 19 Years.

Jasmine Coppens, Basil Britto Xavier, Katherine Loens, Christine Lammens, Margareta Ieven, Veerle Matheeussen, Herman Goossens, Surbhi Malhotra-Kumar

Abstract read
In one paragraph

Article in Genome biology and evolution, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Consistent Biofilm Formation byFrontiers in microbiology · 2022
    Article
  3. Genetic Diversity AmongFrontiers in microbiology · 2020
    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.

Jasmine CoppensLaboratory of Medical Microbiology, Vaccine & Infectious Disease Institute, University of Antwerp, Belgium.
Basil Britto XavierLaboratory of Medical Microbiology, Vaccine & Infectious Disease Institute, University of Antwerp, Belgium.
Katherine LoensBelgian Reference Centre for Group A Streptococcus, Antwerp University Hospital, Antwerp, Belgium.
Christine LammensLaboratory of Medical Microbiology, Vaccine & Infectious Disease Institute, University of Antwerp, Belgium.
Margareta IevenLaboratory of Medical Microbiology, Vaccine & Infectious Disease Institute, University of Antwerp, Belgium.
Veerle MatheeussenBelgian Reference Centre for Group A Streptococcus, Antwerp University Hospital, Antwerp, Belgium.
Herman GoossensLaboratory of Medical Microbiology, Vaccine & Infectious Disease Institute, University of Antwerp, Belgium.
Surbhi Malhotra-KumarLaboratory of Medical Microbiology, Vaccine & Infectious Disease Institute, University of Antwerp, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the last two decades, there has been a public health concern of severe invasive infections caused by Group A Streptococcus (GAS) of the emm1 genotype. This study investigated the dynamics of emm1 GAS during 1994-2013 in Belgium. emm1 GAS isolated from blood, tissue, and wounds of patients with invasive infections (n = 23, S1-S23), and from patients with uncomplicated pharyngitis (n = 15, NS1-NS15) were subjected to whole-genome mapping (WGM; kpn) (Opgen). Whole-genome sequencing was performed on 25 strains (WGS; S1-S23 and NS6-NS7) (Illumina Inc.). Belgian GAS belonged to the M1T1 clone typified by the 36-kb chromosomal region encoding extracellular toxins, NAD+-glycohydrolase and streptolysin O. Strains from 1994-1999 clustered together with published strains (MGAS5005 and M1476). From 2001 onward, invasive GAS showed higher genomic divergence in the accessory genome and harbored on average 7% prophage content. Low evolutionary rate (2.49E-008; P > 0.05) was observed in this study, indicating a highly stable genome. The studied invasive and pharyngitis isolates were no genetically distinct populations based on the WGM and core genome phylogeny analyses. Two copies of the speJ superantigen were present in the 1999 and 2010 study strains (n = 3), one being chromosomal and one being truncated and associated with phage remnants. This study showed that emm1 GAS in Belgium, compared with Canada and UK M1 strains, were highly conserved by harboring a remarkable genome stability over a 19-year period with variations observed in the accessory genome.

Indexed as

Genome, BacterialGenomic InstabilityBelgiumDrug Resistance, BacterialEvolution, MolecularInterspersed Repetitive SequencesStreptococcal InfectionsStreptococcus pyogenesSuperantigensWhole Genome SequencingSuperantigenscgMLSTGASspeJWGMwgMLSTWGS

Identifiers

PMID31065672
PMCPMC6521816

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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.