Evidence map›Paper›PMID 22769602›Full record

ArticleBMC microbiology2012

Complete genome sequence of Enterococcus faecium strain TX16 and comparative genomic analysis of Enterococcus faecium genomes.

Xiang Qin, Jessica R Galloway-Peña, Jouko Sillanpaa, Jung Hyeob Roh, Sreedhar R Nallapareddy, Shahreen Chowdhury, Agathe Bourgogne, Tina Choudhury, Donna M Muzny, Christian J Buhay and 11 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

84 citing papers in PubMed, 164 citations in OpenAlex.

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  17. Antibiotics (Basel, Switzerland) · 2022
    Review
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  19. Genomic analysis of group AJournal of the Association of Medical Microbiology and Infectious Disease Canada = Journal officiel de l'Association pour la microbiologie medicale et l'infectiologie Canada · 2022
    Article
  20. Acquisition of Daptomycin Resistance byFrontiers in microbiology · 2022
    Article

24 more citing papers are in PubMed but not listed here.

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

21 authors at 1 institution in 1 country.

Xiang QinHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
Jessica R Galloway-Peña
Jouko Sillanpaa
Jung Hyeob Roh
Sreedhar R Nallapareddy
Shahreen Chowdhury
Agathe Bourgogne
Tina Choudhury
Donna M Muzny
Christian J Buhay
Yan Ding
Shannon Dugan-Rocha
Wen Liu
Christie Kovar
Erica Sodergren
Sarah Highlander
Joseph F Petrosino
Kim C Worley
Richard A Gibbs
George M Weinstock
Barbara E Murray
Baylor College of Medicine · US

Funding

The Human Genome Sequencing CenterU54HG003273 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI GIBBS, RICHARD A · 2004 to 2015
$341.3M
Molecular Basis of Infectious Diseases Training GrantT32AI055449 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI LORENZ, MICHAEL C · 2005 to 2025
$2.6M
Importance of adhesin-like proteins of Enteroccocus faeciumR01AI067861 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MURRAY, BARBARA E · 2006 to 2010
$1.8M
A Microbial Genome Reference Platform for MetagenomicsU54HG004973 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI GIBBS, RICHARD A, HIGHLANDER, SARAH KATHERINE · 2009 to 2010
$1.8M
VIRULENCE OF VANCOMYCIN RESISTANT AND OTHER E FAECIUMR01AI042399 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MURRAY, BARBARA E · 1998 to 2003
$982k
Defining the Role of WxL Proteins in Enterococcus faeciumF31AI092891 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI GALLOWAY-PENA, JESSICA RHEA · 2011 to 2013
$63k
NHGRI NIH HHS 1U54HG004973-0NHGRI NIH HHS U54 HG003273NIAID NIH HHS F31 AI092891NIAID NIH HHS R01 AI067861NIAID NIH HHS R01 AI42399NIAID NIH HHS T32 AI055449NIAID NIH HHS T32 AI55449
6 · The paper itself

Abstract

backgroundEnterococci are among the leading causes of hospital-acquired infections in the United States and Europe, with Enterococcus faecalis and Enterococcus faecium being the two most common species isolated from enterococcal infections. In the last decade, the proportion of enterococcal infections caused by E. faecium has steadily increased compared to other Enterococcus species. Although the underlying mechanism for the gradual replacement of E. faecalis by E. faecium in the hospital environment is not yet understood, many studies using genotyping and phylogenetic analysis have shown the emergence of a globally dispersed polyclonal subcluster of E. faecium strains in clinical environments. Systematic study of the molecular epidemiology and pathogenesis of E. faecium has been hindered by the lack of closed, complete E. faecium genomes that can be used as references.

resultsIn this study, we report the complete genome sequence of the E. faecium strain TX16, also known as DO, which belongs to multilocus sequence type (ST) 18, and was the first E. faecium strain ever sequenced. Whole genome comparison of the TX16 genome with 21 E. faecium draft genomes confirmed that most clinical, outbreak, and hospital-associated (HA) strains (including STs 16, 17, 18, and 78), in addition to strains of non-hospital origin, group in the same clade (referred to as the HA clade) and are evolutionally considerably more closely related to each other by phylogenetic and gene content similarity analyses than to isolates in the community-associated (CA) clade with approximately a 3-4% average nucleotide sequence difference between the two clades at the core genome level. Our study also revealed that many genomic loci in the TX16 genome are unique to the HA clade. 380 ORFs in TX16 are HA-clade specific and antibiotic resistance genes are enriched in HA-clade strains. Mobile elements such as IS16 and transposons were also found almost exclusively in HA strains, as previously reported.

conclusionsOur findings along with other studies show that HA clonal lineages harbor specific genetic elements as well as sequence differences in the core genome which may confer selection advantages over the more heterogeneous CA E. faecium isolates. Which of these differences are important for the success of specific E. faecium lineages in the hospital environment remain(s) to be determined.

Indexed as

Genome, BacterialSequence Analysis, DNADNA, BacterialEnterococcus faeciumHumansMolecular Sequence DataDNA, Bacterial

Identifiers

PMID22769602
PMCPMC3433357
OpenAlexW2025228378

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.