Evidence map›Paper›PMID 27487956›Full record

ArticleJournal of clinical microbiology2016

Evaluation of Semiautomated IS6110-Based Restriction Fragment Length Polymorphism Typing for Mycobacterium tuberculosis in a High-Burden Setting.

Halima M Said, Keshav Krishnamani, Shaheed V Omar, Andries W Dreyer, Bianca Sansom, Dorothy Fallows, Nazir A Ismail

Open access · bronzeAbstract readComparative StudyEvaluation 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Exploring the usefulness of molecular epidemiology of tuberculosis in Africa: a systematic review.International journal of molecular epidemiology and genetics · 2020
    Review
  6. Fourier transform infrared spectroscopy: unlocking fundamentals and prospects for bacterial strain typing.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2019
    Review
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 3 institutions in 2 countries.

Halima M SaidCentre for Tuberculosis, National Institute of Communicable Diseases, Johannesburg, South Africa Department of Medical Microbiology, Faculty of Health Science, University of Free State, Bloemfontein, South Africa halimas@nicd.ac.za.
Keshav KrishnamaniDuPont Nutrition and Health, Geneva, Switzerland.
Shaheed V OmarCentre for Tuberculosis, National Institute of Communicable Diseases, Johannesburg, South Africa.
Andries W DreyerCentre for Tuberculosis, National Institute of Communicable Diseases, Johannesburg, South Africa.
Bianca SansomCentre for Tuberculosis, National Institute of Communicable Diseases, Johannesburg, South Africa.
Dorothy FallowsPublic Health Research Institute, Rutgers University, Newark, New Jersey, USA.
Nazir A IsmailCentre for Tuberculosis, National Institute of Communicable Diseases, Johannesburg, South Africa Department of Medical Microbiology, Faculty of Health Science, University of Pretoria, Pretoria, South Africa.
Rutgers, The State University of New Jersey · USUniversity of Pretoria · ZAUniversity of the Free State · ZA

Funding

Emerging XDR-TB: Host and Pathogen ContributionsR01AI080737 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI FALLOWS, DOROTHY A. · 2009 to 2013
$2.9M
NIAID NIH HHS R01 AI080737
6 · The paper itself

Abstract

The manual IS6110-based restriction fragment length polymorphism (RFLP) typing method is highly discriminatory; however, it is laborious and technically demanding, and data exchange remains a challenge. In an effort to improve IS6110-based RFLP to make it a faster format, DuPont Molecular Diagnostics recently introduced the IS6110-PvuII kit for semiautomated typing of Mycobacterium tuberculosis using the RiboPrinter microbial characterization system. This study aimed to evaluate the semiautomated RFLP typing against the standard manual method. A total of 112 isolates collected between 2013 and 2014 were included. All isolates were genotyped using manual and semiautomated RFLP typing methods. Clustering rates and discriminatory indexes were compared between methods. The overall performance of semiautomated RFLP compared to manual typing was excellent, with high discriminatory index (0.990 versus 0.995, respectively) and similar numbers of unique profiles (72 versus 74, respectively), numbers of clustered isolates (33 versus 31, respectively), cluster sizes (2 to 6 and 2 to 5 isolates, respectively), and clustering rates (21.9% and 17.1%, respectively). The semiautomated RFLP system is technically simple and significantly faster than the manual RFLP method (8 h versus 5 days). The analysis is fully automated and generates easily manageable databases of standardized fingerprints that can be easily exchanged between laboratories. Based on its high-throughput processing with minimal human effort, the semiautomated RFLP can be a very useful tool as a first-line method for routine typing of M. tuberculosis isolates, especially where Beijing strains are highly prevalent, followed by manual RFLP typing if resolution is not achieved, thereby saving time and labor.

Indexed as

DNA Transposable ElementsPolymorphism, Restriction Fragment LengthAutomation, LaboratoryCluster AnalysisHumansMolecular EpidemiologyMolecular TypingMycobacterium tuberculosisTime FactorsDNA Transposable Elements

Identifiers

PMID27487956
PMCPMC5035400
OpenAlexW2518482518

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.