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The microbiological signature of human cutaneous leishmaniasis lesions exhibits restricted bacterial diversity compared to healthy skin

Localised cutaneous leishmaniasis (LCL) is the most common form of cutaneous leishmaniasis characterised by single or multiple painless chronic ulcers, which commonly presents with secondary bacterial infection. Previous culture-based studies have found staphylococci, streptococci, and opportunistic...

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Autores principales: Salgado, Vanessa R, de Queiroz, Artur TL, Sanabani, Sabri S, de Oliveira, Camila I, Carvalho, Edgar M, Costa, Jackson ML, Barral-Netto, Manoel, Barral, Aldina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Oswaldo Cruz, Ministério da Saúde 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830113/
https://www.ncbi.nlm.nih.gov/pubmed/27074253
http://dx.doi.org/10.1590/0074-02760150436
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author Salgado, Vanessa R
de Queiroz, Artur TL
Sanabani, Sabri S
de Oliveira, Camila I
Carvalho, Edgar M
Costa, Jackson ML
Barral-Netto, Manoel
Barral, Aldina
author_facet Salgado, Vanessa R
de Queiroz, Artur TL
Sanabani, Sabri S
de Oliveira, Camila I
Carvalho, Edgar M
Costa, Jackson ML
Barral-Netto, Manoel
Barral, Aldina
author_sort Salgado, Vanessa R
collection PubMed
description Localised cutaneous leishmaniasis (LCL) is the most common form of cutaneous leishmaniasis characterised by single or multiple painless chronic ulcers, which commonly presents with secondary bacterial infection. Previous culture-based studies have found staphylococci, streptococci, and opportunistic pathogenic bacteria in LCL lesions, but there have been no comparisons to normal skin. In addition, this approach has strong bias for determining bacterial composition. The present study tested the hypothesis that bacterial communities in LCL lesions differ from those found on healthy skin (HS). Using a high throughput amplicon sequencing approach, which allows for better populational evaluation due to greater depth coverage and the Quantitative Insights Into Microbial Ecology pipeline, we compared the microbiological signature of LCL lesions with that of contralateral HS from the same individuals.Streptococcus, Staphylococcus,Fusobacterium and other strict or facultative anaerobic bacteria composed the LCL microbiome. Aerobic and facultative anaerobic bacteria found in HS, including environmental bacteria, were significantly decreased in LCL lesions (p < 0.01). This paper presents the first comprehensive microbiome identification from LCL lesions with next generation sequence methodology and shows a marked reduction of bacterial diversity in the lesions.
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spelling pubmed-48301132016-04-13 The microbiological signature of human cutaneous leishmaniasis lesions exhibits restricted bacterial diversity compared to healthy skin Salgado, Vanessa R de Queiroz, Artur TL Sanabani, Sabri S de Oliveira, Camila I Carvalho, Edgar M Costa, Jackson ML Barral-Netto, Manoel Barral, Aldina Mem Inst Oswaldo Cruz Articles Localised cutaneous leishmaniasis (LCL) is the most common form of cutaneous leishmaniasis characterised by single or multiple painless chronic ulcers, which commonly presents with secondary bacterial infection. Previous culture-based studies have found staphylococci, streptococci, and opportunistic pathogenic bacteria in LCL lesions, but there have been no comparisons to normal skin. In addition, this approach has strong bias for determining bacterial composition. The present study tested the hypothesis that bacterial communities in LCL lesions differ from those found on healthy skin (HS). Using a high throughput amplicon sequencing approach, which allows for better populational evaluation due to greater depth coverage and the Quantitative Insights Into Microbial Ecology pipeline, we compared the microbiological signature of LCL lesions with that of contralateral HS from the same individuals.Streptococcus, Staphylococcus,Fusobacterium and other strict or facultative anaerobic bacteria composed the LCL microbiome. Aerobic and facultative anaerobic bacteria found in HS, including environmental bacteria, were significantly decreased in LCL lesions (p < 0.01). This paper presents the first comprehensive microbiome identification from LCL lesions with next generation sequence methodology and shows a marked reduction of bacterial diversity in the lesions. Instituto Oswaldo Cruz, Ministério da Saúde 2016-04 /pmc/articles/PMC4830113/ /pubmed/27074253 http://dx.doi.org/10.1590/0074-02760150436 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Salgado, Vanessa R
de Queiroz, Artur TL
Sanabani, Sabri S
de Oliveira, Camila I
Carvalho, Edgar M
Costa, Jackson ML
Barral-Netto, Manoel
Barral, Aldina
The microbiological signature of human cutaneous leishmaniasis lesions exhibits restricted bacterial diversity compared to healthy skin
title The microbiological signature of human cutaneous leishmaniasis lesions exhibits restricted bacterial diversity compared to healthy skin
title_full The microbiological signature of human cutaneous leishmaniasis lesions exhibits restricted bacterial diversity compared to healthy skin
title_fullStr The microbiological signature of human cutaneous leishmaniasis lesions exhibits restricted bacterial diversity compared to healthy skin
title_full_unstemmed The microbiological signature of human cutaneous leishmaniasis lesions exhibits restricted bacterial diversity compared to healthy skin
title_short The microbiological signature of human cutaneous leishmaniasis lesions exhibits restricted bacterial diversity compared to healthy skin
title_sort microbiological signature of human cutaneous leishmaniasis lesions exhibits restricted bacterial diversity compared to healthy skin
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830113/
https://www.ncbi.nlm.nih.gov/pubmed/27074253
http://dx.doi.org/10.1590/0074-02760150436
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