Evidence map›Paper›PMID 26968508›Full record

ArticleBMC infectious diseases2016

Differentiation of Mycobacterium tuberculosis complex from non-tubercular mycobacteria by nested multiplex PCR targeting IS6110, MTP40 and 32kD alpha antigen encoding gene fragments.

Pallavi Sinha, Anamika Gupta, Pradyot Prakash, Shampa Anupurba, Rajneesh Tripathi, G N Srivastava

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in BMC infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. African journal of infectious diseases · 2023
    Article
  7. Disseminated Ulcerated Nodules: A Quiz.Acta dermato-venereologica · 2022
    Article
  8. Article
  9. TB Antigen-Stimulated CXCR3 Ligand Assay for Diagnosis of Tuberculous Lymphadenitis.International journal of environmental research and public health · 2021
    Article
  10. Article
  11. Article
  12. Accurate Identification of Closely RelatedFrontiers in cellular and infection microbiology · 2021
    Article
  13. Article
  14. Review
  15. Veterinary world · 2020
    Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

6 authors at 2 institutions in 1 country.

Pallavi SinhaDepartment of Microbiology, Institute of Medical Sciences, Banaras Hindu University, 221 005, Varanasi, India.
Anamika GuptaDepartment of Microbiology, Institute of Medical Sciences, Banaras Hindu University, 221 005, Varanasi, India.
Pradyot PrakashDepartment of Microbiology, Institute of Medical Sciences, Banaras Hindu University, 221 005, Varanasi, India.
Shampa AnupurbaDepartment of Microbiology, Institute of Medical Sciences, Banaras Hindu University, 221 005, Varanasi, India. shampa_anupurba@yahoo.co.in.
Rajneesh TripathiDepartment of Microbiology, Institute of Medical Sciences, Banaras Hindu University, 221 005, Varanasi, India.
G N SrivastavaDepartmrnt of TB and Respiratory Diseases, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
Institute of Medical Sciences · INBanaras Hindu University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundControl of the global burden of tuberculosis is obstructed due to lack of simple, rapid and cost effective diagnostic techniques that can be used in resource poor-settings. To facilitate the early diagnosis of TB directly from clinical specimens, we have standardized and validated the use of nested multiplex PCR, targeting gene fragments IS6110, MTP40 and 32kD α-antigen encoding genes specific for Mycobacterium tuberculosis complex and non-tubercular mycobacteria (NTM), in comparison to smear microscopy, solid culture and single step multiplex PCR. The results were evaluated in comparison to a composite reference standard (CRS) comprising of microbiological results (smear and culture), clinical, radiological and cytopathological findings, clinical treatment and response to anti-tubercular therapy.

methodsThe nested multiplex PCR (nMPCR) assay was evaluated to test its utility in 600 (535 pulmonary and 65 extra-pulmonary specimens) clinically suspected TB cases. All specimens were processed for smear, culture, single step multiplex PCR and nested multiplex PCR testing.

resultsOut of 535 screened pulmonary and 65 extra-pulmonary specimens, 329 (61.5%) and 19 (29.2%) cases were culture positive for M. tuberculosis. Based on CRS, 450 patients had "clinical TB" (definitive-TB, probable-TB and possible-TB). Remaining 150 were confirmed "non-TB" cases. For culture, the sensitivity was low, 79.3% for pulmonary and 54.3% for extra-pulmonary cases. The sensitivity and specificity results for nMPCR test were evaluated taken composite reference standard as a gold standard. The sensitivity of the nMPCR assay was 97.1% for pulmonary and 91.4% for extra-pulmonary TB cases with specificity of 100% and 93.3% respectively.

conclusionNested multiplex PCR using three gene primers is a rapid, reliable and highly sensitive and specific diagnostic technique for the detection and differentiation of M. tuberculosis complex from NTM genome and will be useful in diagnosing paucibacillary samples. Nested multiplex PCR assay was found to be better than single step multiplex PCR for assessing the diagnosis of TB.

Indexed as

AdolescentAdultAgedAged, 80 and overAntigens, BacterialBronchoalveolar Lavage FluidChildChild, PreschoolDNA PrimersFemaleHumansIndiaMaleMiddle AgedMultiplex Polymerase Chain ReactionMycobacterium tuberculosisAntigens, BacterialDNA PrimersComposite reference standardMycobacterium tuberculosis complexNested multiplex PCRNon-tubercular mycobacteria

Identifiers

PMID26968508
PMCPMC4788904
OpenAlexW2295582201

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.