Evidence map›Paper›PMID 29279044›Full record

ArticlePathogens and global health2018

Evaluation of 16S rRNA qPCR for detection of Mycobacterium leprae DNA in nasal secretion and skin biopsy samples from multibacillary and paucibacillary leprosy cases.

Lívia Érika Carlos Marques, Cristiane Cunha Frota, Josiane da Silva Quetz, Alexandre Havt Bindá, Rosa Maria Salane Mota, Maria Araci de Andrade Pontes, Heitor de Sá Gonçalves, Carl Kendall, Ligia Regina Franco Sansigolo Kerr

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Pathogens and global health, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 31% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Molecular Detection ofTropical medicine and infectious disease · 2025
    Review
  4. Article
  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. Review
  10. 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

9 authors at 3 institutions in 2 countries.

Lívia Érika Carlos Marquesa Department of Pathology and Legal Medicine, Medicine School , Federal University of Ceará , Fortaleza , Brazil.
Cristiane Cunha Frotaa Department of Pathology and Legal Medicine, Medicine School , Federal University of Ceará , Fortaleza , Brazil.ORCID 0000-0003-0018-7736
Josiane da Silva Quetzb Biomedicine Institute of the Brazilian Semiarid and Clinical Research Unit , Federal University of Ceará , Fortaleza , Brazil.ORCID 0000-0001-7889-003X
Alexandre Havt Bindáb Biomedicine Institute of the Brazilian Semiarid and Clinical Research Unit , Federal University of Ceará , Fortaleza , Brazil.
Rosa Maria Salane Motac Department of Statistics and Applied Mathematics , Federal University of Ceará , Fortaleza , Brazil.
Maria Araci de Andrade Pontesd Dona Libânia National Reference Centre for Sanitary Dermatology , Fortaleza , Brazil.
Heitor de Sá Gonçalvesd Dona Libânia National Reference Centre for Sanitary Dermatology , Fortaleza , Brazil.
Carl Kendalle Department of Global Community Health and Behavioral Sciences , Tulane University , New Orleans , LA , USA.
Ligia Regina Franco Sansigolo Kerrf Department of Community Health, Medicine School , Federal University of Ceará , Fortaleza , Brazil.
Universidade Federal do Ceará · BRInstituto de Dermatologia Dona Libania · BRTulane University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycobacterium leprae bacilli are mainly transmitted by the dissemination of nasal aerosols from multibacillary (MB) patients to susceptible individuals through inhalation. The upper respiratory tract represents the main entry and exit routes of M. leprae. Therefore, this study aimed to evaluate the sensitivity and specificity of real-time quantitative polymerase chain reaction (qPCR) in detecting M. leprae in nasal secretion (NS) and skin biopsy (SB) samples from MB and paucibacillary (PB) cases. Fifty-four NS samples were obtained from leprosy patients at the Dona Libânia National Reference Centre for Sanitary Dermatology in Ceará, Brazil. Among them, 19 MB cases provided both NS and SB samples. Bacilloscopy index assays were conducted and qPCR amplification was performed using specific primers for M. leprae 16S rRNA gene, generating a 124-bp fragment. Primer specificity was verified by determining the amplicon melting temperature (T

Indexed as

BiopsyBody FluidsBrazilDNA, BacterialDNA, RibosomalHumansLeprosyMolecular Diagnostic TechniquesMycobacterium lepraeNasal CavityReal-Time Polymerase Chain ReactionRNA, Ribosomal, 16SSensitivity and SpecificitySkinDNA, BacterialDNA, RibosomalRNA, Ribosomal, 16SbiopsyMycobacterium lepraenasal cavitypaucibacillary leprosyquantitative real-time PCR

Identifiers

PMID29279044
PMCPMC6056823
OpenAlexW2780184241

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.