Evidence map›Paper›PMID 27225403›Full record

ArticleJournal of clinical microbiology2016

Rapid Drug Susceptibility Testing of Drug-Resistant Mycobacterium tuberculosis Isolates Directly from Clinical Samples by Use of Amplicon Sequencing: a Proof-of-Concept Study.

Rebecca E Colman, Julia Anderson, Darrin Lemmer, Erik Lehmkuhl, Sophia B Georghiou, Hannah Heaton, Kristin Wiggins, John D Gillece, James M Schupp, Donald G Catanzaro and 4 more

Open access · hybridAbstract readEvaluation Study
In one paragraph

Article in Journal of clinical microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
8.0field-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

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 103 citations in OpenAlex.

  1. Pooled it
  2. Rapid drug resistance prediction in positiveEmerging microbes & infections · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Xpert MTB/RIF Ultra-resistant and MTBDRAntimicrobial agents and chemotherapy · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Molecular Capture ofInternational journal of molecular sciences · 2023
    Article
  20. Direct detection of drug-resistantFrontiers in public health · 2023
    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

14 authors at 4 institutions in 2 countries.

Rebecca E ColmanPathogen Genomics, Translational Genomics Research Institute, Flagstaff, Arizona, USA rcolman@ucsd.edu.ORCID 0000-0002-6854-2100
Julia AndersonPathogen Genomics, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Darrin LemmerPathogen Genomics, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Erik LehmkuhlPathogen Genomics, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Sophia B GeorghiouDivision of Pulmonary, Critical Care, and Sleep Medicine, University of San Diego, San Diego, California, USA.
Hannah HeatonPathogen Genomics, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Kristin WigginsPathogen Genomics, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
John D GillecePathogen Genomics, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
James M SchuppPathogen Genomics, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Donald G CatanzaroCollege of Education and Health Professions, University of Arkansas, Fayetteville, Arkansas, USA.
Valeriu CruduPhthisiopneumology Institute (PPI), Chisinau, Republic of Moldova.
Ted CohenYale School of Public Health, New Haven, Connecticut, USA.
Timothy C RodwellDivision of Pulmonary, Critical Care, and Sleep Medicine, University of San Diego, San Diego, California, USA.
David M EngelthalerPathogen Genomics, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Translational Genomics Research Institute · USUniversity of San Diego · USPhthisiopneumology Institute "Chiril Draganiuc" · MDUniversity of Arkansas at Fayetteville · US

Funding

VirologyP30AI036214 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI David Mitchell Smith · 1994 to 2026
$78.4M
Understanding and controlling antibiotic resistanceU54GM088558 · NIGMS · HARVARD SCHOOL OF PUBLIC HEALTH · PI LIPSITCH, MARC · 2009 to 2018
$26.4M
Rapid Tests for Drug Resistance to Detect Extensively Drug-Resistant TuberculosisU01AI082229 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CATANZARO, ANTONINO · 2009 to 2013
$10.9M
An Integrated Tabletop Platform for Rapid Detection of XDR-TB in Clinical SamplesR01AI111435 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RODWELL, TIMOTHY CHARLES · 2014 to 2018
$5.4M
Evolutionary and Functional Significance of Novel Mutations in MDR-XDR TBR01AI105185 · NIAID · SAN DIEGO STATE UNIVERSITY · PI VALAFAR, FARAMARZ · 2013 to 2021
$5.3M
Prevalence, risk factors and consequences of complex M. Tuberculosis infectionsDP2OD006663 · OD · BRIGHAM AND WOMEN'S HOSPITAL · PI COHEN, THEODORE H · 2010 to 2010
$2.7M
NIAID NIH HHS P30 AI036214NIAID NIH HHS R01 AI105185NIAID NIH HHS R01 AI111435NIAID NIH HHS U01 AI082229NIGMS NIH HHS U54 GM088558NIH HHS DP2 OD006663
6 · The paper itself

Abstract

Increasingly complex drug-resistant tuberculosis (DR-TB) is a major global health concern and one of the primary reasons why TB is now the leading infectious cause of death worldwide. Rapid characterization of a DR-TB patient's complete drug resistance profile would facilitate individualized treatment in place of empirical treatment, improve treatment outcomes, prevent amplification of resistance, and reduce the transmission of DR-TB. The use of targeted next-generation sequencing (NGS) to obtain drug resistance profiles directly from patient sputum samples has the potential to enable comprehensive evidence-based treatment plans to be implemented quickly, rather than in weeks to months, which is currently needed for phenotypic drug susceptibility testing (DST) results. In this pilot study, we evaluated the performance of amplicon sequencing of Mycobacterium tuberculosis DNA from patient sputum samples using a tabletop NGS technology and automated data analysis to provide a rapid DST solution (the Next Gen-RDST assay). One hundred sixty-six out of 176 (94.3%) sputum samples from the Republic of Moldova yielded complete Next Gen-RDST assay profiles for 7 drugs of interest. We found a high level of concordance of our Next Gen-RDST assay results with phenotypic DST (97.0%) and pyrosequencing (97.8%) results from the same clinical samples. Our Next Gen-RDST assay was also able to estimate the proportion of resistant-to-wild-type alleles down to mixtures of ≤1%, which demonstrates the ability to detect very low levels of resistant variants not detected by pyrosequencing and possibly below the threshold for phenotypic growth methods. The assay as described here could be used as a clinical or surveillance tool.

Indexed as

AdolescentAdultAgedAged, 80 and overChildChild, PreschoolFemaleGenotyping TechniquesHigh-Throughput Nucleotide SequencingHumansMaleMicrobial Sensitivity TestsMiddle AgedMycobacterium tuberculosisPharmaceutical PreparationsPilot ProjectsPharmaceutical Preparations

Identifiers

PMID27225403
PMCPMC4963505
OpenAlexW2400129586

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.