Evidence map›Paper›PMID 32813724›Full record

ArticlePloS one2020

Mycobacterium tuberculosis polyclonal infections through treatment and recurrence.

Pooja Pandey, Anuj K Bhatnagar, Anant Mohan, Kuldeep S Sachdeva, Jyotish C Samantaray, Randeep Guleria, Urvashi B Singh

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.1field-weighted citation impact, top 48% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Understanding recurrence inJournal of clinical microbiology · 2026
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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

7 authors at 2 institutions in 1 country.

Pooja PandeyDepartment of Microbiology, All India Institute of Medical Sciences, New Delhi, India.
Anuj K BhatnagarRajan Babu Institute for Pulmonary Medicine and Tuberculosis, Delhi, India.
Anant MohanDepartment of Pulmonary Medicine and Sleep Disorders, All India Institute of Medical Sciences, New Delhi, India.
Kuldeep S SachdevaCentral TB Division, Government of India, New Delhi, India.
Jyotish C SamantarayDepartment of Microbiology, All India Institute of Medical Sciences, New Delhi, India.
Randeep GuleriaDepartment of Pulmonary Medicine and Sleep Disorders, All India Institute of Medical Sciences, New Delhi, India.
Urvashi B SinghDepartment of Microbiology, All India Institute of Medical Sciences, New Delhi, India.ORCID 0000-0001-8753-9743
All India Institute of Medical Sciences · INGovernment of India · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMixed/polyclonal infections due to different genotypes are reported in Tuberculosis. The current study was designed to understand the fate of mixed infections during the course of treatment and follow-up and its role in disease pathogenesis.

methodsSputum samples were collected on 0,1,2,3,6,12 and 24 months from 157 treatment-naïve patients, cultures subjected to Drug-Susceptibility-testing (MGIT 960), spoligotyping, MIRU-VNTR and SNP genotyping. All isolated colonies on thin layer agar (7H11) were subjected to spoligotyping.

findingsOne thirty three baseline cultures were positive (133/157, 84.7%), 43(32.3%) had mixture of genotypes. Twenty-four of these patients (55.8%) showed change in genotype while six showed different drug-susceptibility patterns while on treatment. Twenty-three (53.5%) patients with polyclonal infections showed resistance to at least one drug compared to 10/90 (11.1%) monoclonal infections (P<0.0001). Eight patients had recurrent TB, two with a new genotype and two with altered phenotypic DST.

conclusionsThe coexistence of different genotypes and change of genotypes during the same disease episode, while on treatment, confirms constancy of polyclonal infections. The composition of the mixture of genotypes and the relative predominance may be missed by culture due to its limit of detection. Polyclonal infections in TB could be a rule rather than exception and challenges the age-old dogma of reactivation/reinfection.

Indexed as

AdolescentAdultAntitubercular AgentsBacterial Typing TechniquesClonal EvolutionCoinfectionDNA, BacterialDrug Resistance, Multiple, BacterialFemaleFollow-Up StudiesGenotyping TechniquesHumansLimit of DetectionMaleMicrobial Sensitivity TestsMiddle AgedAntitubercular AgentsDNA, Bacterial

Identifiers

PMID32813724
PMCPMC7437862
OpenAlexW3051429039

What OpenQuestion holds

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LicenceCC BY
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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.