In-vitro activity of avermectins against Mycobacterium ulcerans.

Mycobacterium ulcerans causes Buruli ulcer (BU), a debilitating infection of subcutaneous tissue. There is a WHO-recommended antibiotic treatment requiring an 8-week course of streptomycin and rifampicin. This regime has revolutionized the treatment of BU but there are problems that include reliance...

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Main Authors: Till F Omansen, Jessica L Porter, Paul D R Johnson, Tjip S van der Werf, Ymkje Stienstra, Timothy P Stinear
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-03-01
Series:PLoS Neglected Tropical Diseases
Online Access:http://europepmc.org/articles/PMC4351077?pdf=render
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spelling doaj-d5ebd057d10a43278211a48eb99518762020-11-24T20:52:51ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352015-03-0193e000354910.1371/journal.pntd.0003549In-vitro activity of avermectins against Mycobacterium ulcerans.Till F OmansenJessica L PorterPaul D R JohnsonTjip S van der WerfYmkje StienstraTimothy P StinearMycobacterium ulcerans causes Buruli ulcer (BU), a debilitating infection of subcutaneous tissue. There is a WHO-recommended antibiotic treatment requiring an 8-week course of streptomycin and rifampicin. This regime has revolutionized the treatment of BU but there are problems that include reliance on daily streptomycin injections and side effects such as ototoxicity. Trials of all-oral treatments for BU show promise but additional drug combinations that make BU treatment safer and shorter would be welcome. Following on from reports that avermectins have activity against Mycobacterium tuberculosis, we tested the in-vitro efficacy of ivermectin and moxidectin on M. ulcerans. We observed minimum inhibitory concentrations of 4-8 μg/ml and time-kill assays using wild type and bioluminescent M. ulcerans showed a significant dose-dependent reduction in M. ulcerans viability over 8-weeks. A synergistic killing-effect with rifampicin was also observed. Avermectins are well tolerated, widely available and inexpensive. Based on our in vitro findings we suggest that avermectins should be further evaluated for the treatment of BU.http://europepmc.org/articles/PMC4351077?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Till F Omansen
Jessica L Porter
Paul D R Johnson
Tjip S van der Werf
Ymkje Stienstra
Timothy P Stinear
spellingShingle Till F Omansen
Jessica L Porter
Paul D R Johnson
Tjip S van der Werf
Ymkje Stienstra
Timothy P Stinear
In-vitro activity of avermectins against Mycobacterium ulcerans.
PLoS Neglected Tropical Diseases
author_facet Till F Omansen
Jessica L Porter
Paul D R Johnson
Tjip S van der Werf
Ymkje Stienstra
Timothy P Stinear
author_sort Till F Omansen
title In-vitro activity of avermectins against Mycobacterium ulcerans.
title_short In-vitro activity of avermectins against Mycobacterium ulcerans.
title_full In-vitro activity of avermectins against Mycobacterium ulcerans.
title_fullStr In-vitro activity of avermectins against Mycobacterium ulcerans.
title_full_unstemmed In-vitro activity of avermectins against Mycobacterium ulcerans.
title_sort in-vitro activity of avermectins against mycobacterium ulcerans.
publisher Public Library of Science (PLoS)
series PLoS Neglected Tropical Diseases
issn 1935-2727
1935-2735
publishDate 2015-03-01
description Mycobacterium ulcerans causes Buruli ulcer (BU), a debilitating infection of subcutaneous tissue. There is a WHO-recommended antibiotic treatment requiring an 8-week course of streptomycin and rifampicin. This regime has revolutionized the treatment of BU but there are problems that include reliance on daily streptomycin injections and side effects such as ototoxicity. Trials of all-oral treatments for BU show promise but additional drug combinations that make BU treatment safer and shorter would be welcome. Following on from reports that avermectins have activity against Mycobacterium tuberculosis, we tested the in-vitro efficacy of ivermectin and moxidectin on M. ulcerans. We observed minimum inhibitory concentrations of 4-8 μg/ml and time-kill assays using wild type and bioluminescent M. ulcerans showed a significant dose-dependent reduction in M. ulcerans viability over 8-weeks. A synergistic killing-effect with rifampicin was also observed. Avermectins are well tolerated, widely available and inexpensive. Based on our in vitro findings we suggest that avermectins should be further evaluated for the treatment of BU.
url http://europepmc.org/articles/PMC4351077?pdf=render
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