Bacterial diversity in Buruli ulcer skin lesions: Challenges in the clinical microbiome analysis of a skin disease.

Buruli ulcer (BU) is an infectious disease caused by Mycobacterium ulcerans and considered the third most prevalent mycobacterial disease in humans. Secondary bacterial infections in open BU lesions are the main cause of pain, delayed healing and systemic illness, resulting in prolonged hospital sta...

Full description

Bibliographic Details
Main Authors: Chloé Van Leuvenhaege, Koen Vandelannoote, Dissou Affolabi, Françoise Portaels, Ghislain Sopoh, Bouke C de Jong, Miriam Eddyani, Conor J Meehan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5531519?pdf=render
id doaj-b420dd2778824559bdfba62ade1bcc64
record_format Article
spelling doaj-b420dd2778824559bdfba62ade1bcc642020-11-24T21:48:16ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01127e018199410.1371/journal.pone.0181994Bacterial diversity in Buruli ulcer skin lesions: Challenges in the clinical microbiome analysis of a skin disease.Chloé Van LeuvenhaegeKoen VandelannooteDissou AffolabiFrançoise PortaelsGhislain SopohBouke C de JongMiriam EddyaniConor J MeehanBuruli ulcer (BU) is an infectious disease caused by Mycobacterium ulcerans and considered the third most prevalent mycobacterial disease in humans. Secondary bacterial infections in open BU lesions are the main cause of pain, delayed healing and systemic illness, resulting in prolonged hospital stay. Thus, understanding the diversity of bacteria, termed the microbiome, in these open lesions is important for proper treatment. However, adequately studying the human microbiome in a clinical setting can prove difficult when investigating a neglected tropical skin disease due to its rarity and the setting.Using 16S rRNA sequencing, we determined the microbial composition of 5 BU lesions, 3 non-BU lesions and 3 healthy skin samples. Although no significant differences in diversity were found between BU and non-BU lesions, the former were characterized by an increase of Bacteroidetes compared to the non-BU wounds and the BU lesions also contained significantly more obligate anaerobes. With this molecular-based study, we were also able to detect bacteria that were missed by culture-based methods in previous BU studies.Our study suggests that BU may lead to changes in the skin bacterial community within the lesions. However, in order to determine if such changes hold true across all BU cases and are either a cause or consequence of a specific wound environment, further microbiome studies are necessary. Such skin microbiome analysis requires large sample sizes and lesions from the same body site in many patients, both of which can be difficult for a rare disease. Our study proposes a pipeline for such studies and highlights several drawbacks that must be considered if microbiome analysis is to be utilized for neglected tropical diseases.http://europepmc.org/articles/PMC5531519?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Chloé Van Leuvenhaege
Koen Vandelannoote
Dissou Affolabi
Françoise Portaels
Ghislain Sopoh
Bouke C de Jong
Miriam Eddyani
Conor J Meehan
spellingShingle Chloé Van Leuvenhaege
Koen Vandelannoote
Dissou Affolabi
Françoise Portaels
Ghislain Sopoh
Bouke C de Jong
Miriam Eddyani
Conor J Meehan
Bacterial diversity in Buruli ulcer skin lesions: Challenges in the clinical microbiome analysis of a skin disease.
PLoS ONE
author_facet Chloé Van Leuvenhaege
Koen Vandelannoote
Dissou Affolabi
Françoise Portaels
Ghislain Sopoh
Bouke C de Jong
Miriam Eddyani
Conor J Meehan
author_sort Chloé Van Leuvenhaege
title Bacterial diversity in Buruli ulcer skin lesions: Challenges in the clinical microbiome analysis of a skin disease.
title_short Bacterial diversity in Buruli ulcer skin lesions: Challenges in the clinical microbiome analysis of a skin disease.
title_full Bacterial diversity in Buruli ulcer skin lesions: Challenges in the clinical microbiome analysis of a skin disease.
title_fullStr Bacterial diversity in Buruli ulcer skin lesions: Challenges in the clinical microbiome analysis of a skin disease.
title_full_unstemmed Bacterial diversity in Buruli ulcer skin lesions: Challenges in the clinical microbiome analysis of a skin disease.
title_sort bacterial diversity in buruli ulcer skin lesions: challenges in the clinical microbiome analysis of a skin disease.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Buruli ulcer (BU) is an infectious disease caused by Mycobacterium ulcerans and considered the third most prevalent mycobacterial disease in humans. Secondary bacterial infections in open BU lesions are the main cause of pain, delayed healing and systemic illness, resulting in prolonged hospital stay. Thus, understanding the diversity of bacteria, termed the microbiome, in these open lesions is important for proper treatment. However, adequately studying the human microbiome in a clinical setting can prove difficult when investigating a neglected tropical skin disease due to its rarity and the setting.Using 16S rRNA sequencing, we determined the microbial composition of 5 BU lesions, 3 non-BU lesions and 3 healthy skin samples. Although no significant differences in diversity were found between BU and non-BU lesions, the former were characterized by an increase of Bacteroidetes compared to the non-BU wounds and the BU lesions also contained significantly more obligate anaerobes. With this molecular-based study, we were also able to detect bacteria that were missed by culture-based methods in previous BU studies.Our study suggests that BU may lead to changes in the skin bacterial community within the lesions. However, in order to determine if such changes hold true across all BU cases and are either a cause or consequence of a specific wound environment, further microbiome studies are necessary. Such skin microbiome analysis requires large sample sizes and lesions from the same body site in many patients, both of which can be difficult for a rare disease. Our study proposes a pipeline for such studies and highlights several drawbacks that must be considered if microbiome analysis is to be utilized for neglected tropical diseases.
url http://europepmc.org/articles/PMC5531519?pdf=render
work_keys_str_mv AT chloevanleuvenhaege bacterialdiversityinburuliulcerskinlesionschallengesintheclinicalmicrobiomeanalysisofaskindisease
AT koenvandelannoote bacterialdiversityinburuliulcerskinlesionschallengesintheclinicalmicrobiomeanalysisofaskindisease
AT dissouaffolabi bacterialdiversityinburuliulcerskinlesionschallengesintheclinicalmicrobiomeanalysisofaskindisease
AT francoiseportaels bacterialdiversityinburuliulcerskinlesionschallengesintheclinicalmicrobiomeanalysisofaskindisease
AT ghislainsopoh bacterialdiversityinburuliulcerskinlesionschallengesintheclinicalmicrobiomeanalysisofaskindisease
AT boukecdejong bacterialdiversityinburuliulcerskinlesionschallengesintheclinicalmicrobiomeanalysisofaskindisease
AT miriameddyani bacterialdiversityinburuliulcerskinlesionschallengesintheclinicalmicrobiomeanalysisofaskindisease
AT conorjmeehan bacterialdiversityinburuliulcerskinlesionschallengesintheclinicalmicrobiomeanalysisofaskindisease
_version_ 1725893142406758400