Evidence map›Paper›PMID 31462296›Full record

ArticleBMC infectious diseases2019

Development of a combined RLEP/16S rRNA (RT) qPCR assay for the detection of viable M. leprae from nasal swab samples.

Marcus Beissner, Anna Woestemeier, Malkin Saar, Kossi Badziklou, Issaka Maman, Charlotte Amedifou, Magdalena Wagner, Franz X Wiedemann, Komi Amekuse, Basile Kobara and 4 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Buruli ulcer.Nature reviews. Disease primers · 2025
    Review
  3. A rare case of lepromatous leprosy in Germany.Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG · 2025
    Article
  4. Molecular Detection ofTropical medicine and infectious disease · 2025
    Review
  5. qPCR detection ofFrontiers in molecular biosciences · 2024
    Article
  6. Article
  7. Challenges and advances in serological and molecular tests to aid leprosy diagnosis.Experimental biology and medicine (Maywood, N.J.) · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Ultrasensitive Detection ofInternational journal of molecular sciences · 2021
    Article
  14. Observational
  15. Article
  16. 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.

Marcus BeissnerDepartment of Infectious Diseases and Tropical Medicine (DITM), Medical Center of the University of Munich (LMU), Munich, Germany. beissner@lrz.uni-muenchen.de.ORCID http://orcid.org/0000-0001-9238-2998
Anna WoestemeierDepartment of Infectious Diseases and Tropical Medicine (DITM), Medical Center of the University of Munich (LMU), Munich, Germany.
Malkin SaarDepartment of Infectious Diseases and Tropical Medicine (DITM), Medical Center of the University of Munich (LMU), Munich, Germany.
Kossi BadziklouMinistère de la Santé, Institut National d'Hygiène (INH), Lomé, Togo.
Issaka MamanMinistère de la Santé, Institut National d'Hygiène (INH), Lomé, Togo.
Charlotte AmedifouGerman Leprosy and Tuberculosis Relief Association, Togo office (DAHW-T), Lomé, Togo.
Magdalena WagnerDepartment of Infectious Diseases and Tropical Medicine (DITM), Medical Center of the University of Munich (LMU), Munich, Germany.
Franz X WiedemannGerman Leprosy and Tuberculosis Relief Association, Togo office (DAHW-T), Lomé, Togo.
Komi AmekuseGerman Leprosy and Tuberculosis Relief Association, Togo office (DAHW-T), Lomé, Togo.
Basile KobaraProgramme National de Lutte contre l'Ulcère de Buruli, la Lèpre et le Pian (PNLUB-LP), Lomé, Togo.
Karl-Heinz HerbingerDepartment of Infectious Diseases and Tropical Medicine (DITM), Medical Center of the University of Munich (LMU), Munich, Germany.
Abiba Banla KereMinistère de la Santé, Institut National d'Hygiène (INH), Lomé, Togo.
Thomas LöscherLudwig-Maximilians-University (LMU), Munich, Germany.
Gisela BretzelDepartment of Infectious Diseases and Tropical Medicine (DITM), Medical Center of the University of Munich (LMU), Munich, Germany.

Funding

German Leprosy and Tuberculosis Relief Association ILEP Project No.: 7.01.02.50
6 · The paper itself

Abstract

backgroundLeprosy continues to be a health problem in endemic areas. More than 200,000 new cases of leprosy per year suggest that transmission of the disease is still ongoing, presumably as airborne infection through nasal droplets. Late diagnosis supports continued transmission and increases the individual risk for functional disabilities. Laboratory tools are considered beneficial to facilitate early detection and clinical assessment of cases. The aim of this study was to validate molecular tools allowing detection, quantification and assessment of viability of M. leprae from nasal swab samples which are easy to obtain without the need of any invasive procedures.

methodsValidation of two real-time PCRs detecting M. leprae DNA (RLEP qPCR) and RNA (16S rRNA RT qPCR) was conducted on "must not detect"/"must detect" samples and 160 pre-treatment nasal swab samples from 20 clinically diagnosed multibacillary (MB) leprosy patients from Togo.

resultsBoth assays were 100% M. leprae specific and showed analytical sensitivities of three templates each. Out of 20 clinically diagnosed MB leprosy patients, 15 (75.0%) had a positive RLEP qPCR result from nasal swab samples. The 16S rRNA RT qPCR detected viable bacilli in nasal swab samples of ten out of these 15 RLEP positive patients (66.7%).

conclusionThe combined RLEP/16S rRNA (RT) qPCR assay provides a sensitive and specific tool to determine the bacterial load and viability of M. leprae from nasal swab samples and is applicable for early diagnosis, monitoring treatment response and investigating the role of nasal carriage of M. leprae in human-to-human transmission through aerosol infection.

Indexed as

RNA, Ribosomal, 16SAdolescentAdultAgedAged, 80 and overChildChild, PreschoolDNA, BacterialHumansLeprosyLeprosy, MultibacillaryMiddle AgedMycobacterium lepraeNasal CavityReal-Time Polymerase Chain ReactionReproducibility of ResultsDNA, BacterialRNA, Ribosomal, 16S16 rRNA RT qPCRBacillary loadMycobacterium lepraeNasal swab samplesRLEP qPCRViability

Identifiers

PMID31462296
PMCPMC6714382

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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.