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Efficacy of Co-Trimoxazole against Experimental Melioidosis Acquired by Different Routes of Infection

Burkholderia pseudomallei is the causative agent of melioidosis and presents with diverse clinical manifestations. Naturally occurring infection occurs following contamination of cuts or skin abrasions, or ingestion of contaminated water, and occasionally through inhalational of infected soil or wat...

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Autores principales: Nelson, Michelle, Burton, Neil, Nunez, Alejandro, Butcher, Wendy, Ngugi, Sarah, Atkins, Timothy P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664850/
https://www.ncbi.nlm.nih.gov/pubmed/36226972
http://dx.doi.org/10.1128/aac.00708-22
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author Nelson, Michelle
Burton, Neil
Nunez, Alejandro
Butcher, Wendy
Ngugi, Sarah
Atkins, Timothy P.
author_facet Nelson, Michelle
Burton, Neil
Nunez, Alejandro
Butcher, Wendy
Ngugi, Sarah
Atkins, Timothy P.
author_sort Nelson, Michelle
collection PubMed
description Burkholderia pseudomallei is the causative agent of melioidosis and presents with diverse clinical manifestations. Naturally occurring infection occurs following contamination of cuts or skin abrasions, or ingestion of contaminated water, and occasionally through inhalational of infected soil or water particles. The influence of the route of disease acquisition on the efficacy of medical countermeasures has not been explored in humans or in appropriate animal models. The efficacy of co-trimoxazole against melioidosis acquired by different routes of exposure was assessed in postexposure prophylaxis (PEP) and treatment studies in marmoset models of melioidosis. Following challenge with B. pseudomallei by the inhalational, subcutaneous, or ingestion routes of administration, animals were given co-trimoxazole at 12 hourly intervals for 14 days, starting either 6 h postchallenge or at the onset of fever. Animals were then observed for 28 days. All animals that received antibiotic 6 h postchallenge survived the duration of dosing. All animals that received antibiotics at the onset of fever completed the treatment, but 10%, 57%, and 60% of those with ingestion, subcutaneous, and inhalation challenge relapsed, respectively. Bacteriological and histological differences were observed between placebo-control animals and those that relapsed. Immunological profiles indicate difference between animals given placebo and those that relapsed or survived the duration of the study. A broad T-cell activation was observed in animals that survived. Overall, these data suggest the efficacy of co-trimoxazole, as measured in the incidence of relapse, differs depending on the disease-acquisition route. Therefore, there are implications in treating this disease in regions of endemicity.
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spelling pubmed-96648502022-11-15 Efficacy of Co-Trimoxazole against Experimental Melioidosis Acquired by Different Routes of Infection Nelson, Michelle Burton, Neil Nunez, Alejandro Butcher, Wendy Ngugi, Sarah Atkins, Timothy P. Antimicrob Agents Chemother Clinical Therapeutics Burkholderia pseudomallei is the causative agent of melioidosis and presents with diverse clinical manifestations. Naturally occurring infection occurs following contamination of cuts or skin abrasions, or ingestion of contaminated water, and occasionally through inhalational of infected soil or water particles. The influence of the route of disease acquisition on the efficacy of medical countermeasures has not been explored in humans or in appropriate animal models. The efficacy of co-trimoxazole against melioidosis acquired by different routes of exposure was assessed in postexposure prophylaxis (PEP) and treatment studies in marmoset models of melioidosis. Following challenge with B. pseudomallei by the inhalational, subcutaneous, or ingestion routes of administration, animals were given co-trimoxazole at 12 hourly intervals for 14 days, starting either 6 h postchallenge or at the onset of fever. Animals were then observed for 28 days. All animals that received antibiotic 6 h postchallenge survived the duration of dosing. All animals that received antibiotics at the onset of fever completed the treatment, but 10%, 57%, and 60% of those with ingestion, subcutaneous, and inhalation challenge relapsed, respectively. Bacteriological and histological differences were observed between placebo-control animals and those that relapsed. Immunological profiles indicate difference between animals given placebo and those that relapsed or survived the duration of the study. A broad T-cell activation was observed in animals that survived. Overall, these data suggest the efficacy of co-trimoxazole, as measured in the incidence of relapse, differs depending on the disease-acquisition route. Therefore, there are implications in treating this disease in regions of endemicity. American Society for Microbiology 2022-10-13 /pmc/articles/PMC9664850/ /pubmed/36226972 http://dx.doi.org/10.1128/aac.00708-22 Text en © Crown copyright 2022. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Clinical Therapeutics
Nelson, Michelle
Burton, Neil
Nunez, Alejandro
Butcher, Wendy
Ngugi, Sarah
Atkins, Timothy P.
Efficacy of Co-Trimoxazole against Experimental Melioidosis Acquired by Different Routes of Infection
title Efficacy of Co-Trimoxazole against Experimental Melioidosis Acquired by Different Routes of Infection
title_full Efficacy of Co-Trimoxazole against Experimental Melioidosis Acquired by Different Routes of Infection
title_fullStr Efficacy of Co-Trimoxazole against Experimental Melioidosis Acquired by Different Routes of Infection
title_full_unstemmed Efficacy of Co-Trimoxazole against Experimental Melioidosis Acquired by Different Routes of Infection
title_short Efficacy of Co-Trimoxazole against Experimental Melioidosis Acquired by Different Routes of Infection
title_sort efficacy of co-trimoxazole against experimental melioidosis acquired by different routes of infection
topic Clinical Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664850/
https://www.ncbi.nlm.nih.gov/pubmed/36226972
http://dx.doi.org/10.1128/aac.00708-22
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