Evidence map›Paper›PMID 25056330›Full record

ArticleJournal of clinical microbiology2014

Genome sequencing of Mycobacterium abscessus isolates from patients in the united states and comparisons to globally diverse clinical strains.

Rebecca M Davidson, Nabeeh A Hasan, Paul R Reynolds, Sarah Totten, Benjamin Garcia, Adrah Levin, Preveen Ramamoorthy, Leonid Heifets, Charles L Daley, Michael Strong

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

44 citing papers in PubMed, 77 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Rebecca M DavidsonIntegrated Center for Genes, Environment, and Health, National Jewish Health, Denver, Colorado, USA.
Nabeeh A HasanIntegrated Center for Genes, Environment, and Health, National Jewish Health, Denver, Colorado, USA Computational Bioscience Program, University of Colorado Denver, School of Medicine, Aurora, Colorado, USA.
Paul R ReynoldsDepartment of Pediatrics, National Jewish Health, Denver, Colorado, USA.
Sarah TottenMycobacteriology and Pharmacokinetics, National Jewish Health, Denver, Colorado, USA.
Benjamin GarciaIntegrated Center for Genes, Environment, and Health, National Jewish Health, Denver, Colorado, USA Computational Bioscience Program, University of Colorado Denver, School of Medicine, Aurora, Colorado, USA.
Adrah LevinDivision of Mycobacterial and Respiratory Infections, National Jewish Health, Denver, Colorado, USA.
Preveen RamamoorthyDepartment of Academic Affairs, National Jewish Health, Denver, Colorado, USA.
Leonid HeifetsMycobacteriology and Pharmacokinetics, National Jewish Health, Denver, Colorado, USA.
Charles L DaleyDivision of Mycobacterial and Respiratory Infections, National Jewish Health, Denver, Colorado, USA.
Michael StrongIntegrated Center for Genes, Environment, and Health, National Jewish Health, Denver, Colorado, USA Computational Bioscience Program, University of Colorado Denver, School of Medicine, Aurora, Colorado, USA strongm@njhealth.org.
University of Colorado Denver · USNational Jewish Health · US

Funding

Computational Bioscience Program Training GrantT15LM009451 · NLM · UNIVERSITY OF COLORADO DENVER · PI Katherina Kechris-Mays, Arjun Krishnan · 2007 to 2026
$11.7M
NLM NIH HHS 2T15LM009451-06NLM NIH HHS T15 LM009451
6 · The paper itself

Abstract

Nontuberculous mycobacterial infections caused by Mycobacterium abscessus are responsible for a range of disease manifestations from pulmonary to skin infections and are notoriously difficult to treat, due to innate resistance to many antibiotics. Previous population studies of clinical M. abscessus isolates utilized multilocus sequence typing or pulsed-field gel electrophoresis, but high-resolution examinations of genetic diversity at the whole-genome level have not been well characterized, particularly among clinical isolates derived in the United States. We performed whole-genome sequencing of 11 clinical M. abscessus isolates derived from eight U.S. patients with pulmonary nontuberculous mycobacterial infections, compared them to 30 globally diverse clinical isolates, and investigated intrapatient genomic diversity and evolution. Phylogenomic analyses revealed a cluster of closely related U.S. and Western European M. abscessus subsp. abscessus isolates that are genetically distinct from other European isolates and all Asian isolates. Large-scale variation analyses suggested genome content differences of 0.3 to 8.3%, relative to the reference strain ATCC 19977(T). Longitudinally sampled isolates showed very few single-nucleotide polymorphisms and correlated genomic deletion patterns, suggesting homogeneous infection populations. Our study explores the genomic diversity of clinical M. abscessus strains from multiple continents and provides insight into the genome plasticity of an opportunistic pathogen.

Indexed as

Genetic VariationGenome, BacterialSequence Analysis, DNAAdultAgedCluster AnalysisEvolution, MolecularFemaleGenotypeHumansMaleMiddle AgedMycobacteriumMycobacterium Infections, NontuberculousPhylogenyPolymorphism, Single Nucleotide

Identifiers

PMID25056330
PMCPMC4187745
OpenAlexW2011458298

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.