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High frequency of M. leprae DNA detection in asymptomatic household contacts

BACKGROUND: Characterization of the Mycobacterium leprae genome has made possible the development of Polymerase Chain Reaction (PCR) systems that can amplify different genomic regions. Increased reliability and technical efficiency of quantitative PCR (qPCR) makes it a promising tool for early diagn...

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Autores principales: Gama, Rafael Silva, Gomides, Thalisson Artur Ribeiro, Gama, Chaiana Fróes Magalhães, Moreira, Suelen Justo Maria, de Neves Manta, Fernanda Saloum, de Oliveira, Lorena Bruna P., Marçal, Pedro Henrique Ferreira, Sarno, Euzenir Nunes, Moraes, Milton Ozório, Garcia, Raúl Marcel González, de Oliveira Fraga, Lucia Alves
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5879567/
https://www.ncbi.nlm.nih.gov/pubmed/29609530
http://dx.doi.org/10.1186/s12879-018-3056-2
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author Gama, Rafael Silva
Gomides, Thalisson Artur Ribeiro
Gama, Chaiana Fróes Magalhães
Moreira, Suelen Justo Maria
de Neves Manta, Fernanda Saloum
de Oliveira, Lorena Bruna P.
Marçal, Pedro Henrique Ferreira
Sarno, Euzenir Nunes
Moraes, Milton Ozório
Garcia, Raúl Marcel González
de Oliveira Fraga, Lucia Alves
author_facet Gama, Rafael Silva
Gomides, Thalisson Artur Ribeiro
Gama, Chaiana Fróes Magalhães
Moreira, Suelen Justo Maria
de Neves Manta, Fernanda Saloum
de Oliveira, Lorena Bruna P.
Marçal, Pedro Henrique Ferreira
Sarno, Euzenir Nunes
Moraes, Milton Ozório
Garcia, Raúl Marcel González
de Oliveira Fraga, Lucia Alves
author_sort Gama, Rafael Silva
collection PubMed
description BACKGROUND: Characterization of the Mycobacterium leprae genome has made possible the development of Polymerase Chain Reaction (PCR) systems that can amplify different genomic regions. Increased reliability and technical efficiency of quantitative PCR (qPCR) makes it a promising tool for early diagnosis of leprosy. Index cases that are multibacillary spread the bacillus silently, even before they are clinically diagnosed. Early detection and treatment could prevent transmission in endemic areas. METHODS: In this study, the qPCR technique is used to detect DNA of M. leprae in samples of slit skin smears (SSS) of the ear lobe and blood of leprosy patients and their asymptomatic household contacts residing in Governador Valadares, MG, Brazil, a hyperendemic area for leprosy. A total of 164 subjects participated in the study: 43 index cases, 113 household contacts, and, as negative controls, 8 individuals who reported no contact with patients nor history of leprosy in the family. The qPCR was performed to amplify 16S rRNA fragments and was specifically designed for M. leprae. RESULTS: Of asymptomatic household contacts, 23.89% showed bacillary DNA by qPCR in samples of SSS and blood. Also, 48.84% of patients diagnosed with leprosy were positive for qPCR while the bacillary load was positive in only 30.23% of patients. It is important to note that most patients were already receiving treatment when the collection of biological material for qPCR was performed. The level of bacillary DNA from household contacts was similar to the DNA levels detected in the group of paucibacillary patients. CONCLUSION: Considering that household contacts comprise a recognizable group of individuals with a high risk of disease, as they live in close proximity to a source of infection, qPCR can be used to estimate the risk of progress towards leprosy among household contacts and as a routine screening method for a chemoprophylactic protocol. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-018-3056-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-58795672018-04-04 High frequency of M. leprae DNA detection in asymptomatic household contacts Gama, Rafael Silva Gomides, Thalisson Artur Ribeiro Gama, Chaiana Fróes Magalhães Moreira, Suelen Justo Maria de Neves Manta, Fernanda Saloum de Oliveira, Lorena Bruna P. Marçal, Pedro Henrique Ferreira Sarno, Euzenir Nunes Moraes, Milton Ozório Garcia, Raúl Marcel González de Oliveira Fraga, Lucia Alves BMC Infect Dis Research Article BACKGROUND: Characterization of the Mycobacterium leprae genome has made possible the development of Polymerase Chain Reaction (PCR) systems that can amplify different genomic regions. Increased reliability and technical efficiency of quantitative PCR (qPCR) makes it a promising tool for early diagnosis of leprosy. Index cases that are multibacillary spread the bacillus silently, even before they are clinically diagnosed. Early detection and treatment could prevent transmission in endemic areas. METHODS: In this study, the qPCR technique is used to detect DNA of M. leprae in samples of slit skin smears (SSS) of the ear lobe and blood of leprosy patients and their asymptomatic household contacts residing in Governador Valadares, MG, Brazil, a hyperendemic area for leprosy. A total of 164 subjects participated in the study: 43 index cases, 113 household contacts, and, as negative controls, 8 individuals who reported no contact with patients nor history of leprosy in the family. The qPCR was performed to amplify 16S rRNA fragments and was specifically designed for M. leprae. RESULTS: Of asymptomatic household contacts, 23.89% showed bacillary DNA by qPCR in samples of SSS and blood. Also, 48.84% of patients diagnosed with leprosy were positive for qPCR while the bacillary load was positive in only 30.23% of patients. It is important to note that most patients were already receiving treatment when the collection of biological material for qPCR was performed. The level of bacillary DNA from household contacts was similar to the DNA levels detected in the group of paucibacillary patients. CONCLUSION: Considering that household contacts comprise a recognizable group of individuals with a high risk of disease, as they live in close proximity to a source of infection, qPCR can be used to estimate the risk of progress towards leprosy among household contacts and as a routine screening method for a chemoprophylactic protocol. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-018-3056-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-02 /pmc/articles/PMC5879567/ /pubmed/29609530 http://dx.doi.org/10.1186/s12879-018-3056-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Gama, Rafael Silva
Gomides, Thalisson Artur Ribeiro
Gama, Chaiana Fróes Magalhães
Moreira, Suelen Justo Maria
de Neves Manta, Fernanda Saloum
de Oliveira, Lorena Bruna P.
Marçal, Pedro Henrique Ferreira
Sarno, Euzenir Nunes
Moraes, Milton Ozório
Garcia, Raúl Marcel González
de Oliveira Fraga, Lucia Alves
High frequency of M. leprae DNA detection in asymptomatic household contacts
title High frequency of M. leprae DNA detection in asymptomatic household contacts
title_full High frequency of M. leprae DNA detection in asymptomatic household contacts
title_fullStr High frequency of M. leprae DNA detection in asymptomatic household contacts
title_full_unstemmed High frequency of M. leprae DNA detection in asymptomatic household contacts
title_short High frequency of M. leprae DNA detection in asymptomatic household contacts
title_sort high frequency of m. leprae dna detection in asymptomatic household contacts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5879567/
https://www.ncbi.nlm.nih.gov/pubmed/29609530
http://dx.doi.org/10.1186/s12879-018-3056-2
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