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Characterization of lesion formation in marmosets following inhalational challenge with different strains of Burkholderia pseudomallei

The marmoset model of melioidosis was used to explore whether there was any difference in the disease presentation and/or the lesion formation following inhalational challenge with one of four strains of Burkholderia pseudomallei (K96243, 1026b, HBPUB10303a and HBPUB10134a). Marmosets were challenge...

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Autores principales: Nelson, Michelle, Nunez, Alejandro, Ngugi, Sarah A., Sinclair, Adam, Atkins, Timothy P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744822/
https://www.ncbi.nlm.nih.gov/pubmed/26852689
http://dx.doi.org/10.1111/iep.12161
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author Nelson, Michelle
Nunez, Alejandro
Ngugi, Sarah A.
Sinclair, Adam
Atkins, Timothy P.
author_facet Nelson, Michelle
Nunez, Alejandro
Ngugi, Sarah A.
Sinclair, Adam
Atkins, Timothy P.
author_sort Nelson, Michelle
collection PubMed
description The marmoset model of melioidosis was used to explore whether there was any difference in the disease presentation and/or the lesion formation following inhalational challenge with one of four strains of Burkholderia pseudomallei (K96243, 1026b, HBPUB10303a and HBPUB10134a). Marmosets were challenged with a range of bacterial doses and bacterial load, histological and physiological features were determined temporally following lethal disease. Melioidosis presented as an acute, febrile disease with bacteraemia, bacterial dissemination, necrotizing hepatitis, splenitis and pneumonia which was independent of the challenge strain. Generally, there were no major differences in the manifestation of melioidosis following challenge by the different strains of B. pseudomallei; however, there were some differences in the time to death and the severity of the pathological features. The pathological features observed in the liver and spleen of animals challenged with B. pseudomallei strain 1026b were statistically less severe (P < 0.05) and less frequent. However, more severe foci of disease were evident in the lungs of animals challenged with strain 1026b. In all cases, the lesions developed from small areas of bacteria‐infected macrophages surrounded by non‐infected neutrophils into large lesions with both immune cell types infected. The marmoset model was a useful tool enabling the distinction of subtle difference in the pathological response to B. pseudomallei.
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spelling pubmed-47448222016-11-29 Characterization of lesion formation in marmosets following inhalational challenge with different strains of Burkholderia pseudomallei Nelson, Michelle Nunez, Alejandro Ngugi, Sarah A. Sinclair, Adam Atkins, Timothy P. Int J Exp Pathol Original Articles The marmoset model of melioidosis was used to explore whether there was any difference in the disease presentation and/or the lesion formation following inhalational challenge with one of four strains of Burkholderia pseudomallei (K96243, 1026b, HBPUB10303a and HBPUB10134a). Marmosets were challenged with a range of bacterial doses and bacterial load, histological and physiological features were determined temporally following lethal disease. Melioidosis presented as an acute, febrile disease with bacteraemia, bacterial dissemination, necrotizing hepatitis, splenitis and pneumonia which was independent of the challenge strain. Generally, there were no major differences in the manifestation of melioidosis following challenge by the different strains of B. pseudomallei; however, there were some differences in the time to death and the severity of the pathological features. The pathological features observed in the liver and spleen of animals challenged with B. pseudomallei strain 1026b were statistically less severe (P < 0.05) and less frequent. However, more severe foci of disease were evident in the lungs of animals challenged with strain 1026b. In all cases, the lesions developed from small areas of bacteria‐infected macrophages surrounded by non‐infected neutrophils into large lesions with both immune cell types infected. The marmoset model was a useful tool enabling the distinction of subtle difference in the pathological response to B. pseudomallei. John Wiley and Sons Inc. 2016-01-19 2015-12 /pmc/articles/PMC4744822/ /pubmed/26852689 http://dx.doi.org/10.1111/iep.12161 Text en © 2016 Crown copyright. International Journal of Experimental Pathology published by John Wiley & Sons Ltd on behalf of Company of the International Journal of Experimental Pathology (CIJEP). This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Nelson, Michelle
Nunez, Alejandro
Ngugi, Sarah A.
Sinclair, Adam
Atkins, Timothy P.
Characterization of lesion formation in marmosets following inhalational challenge with different strains of Burkholderia pseudomallei
title Characterization of lesion formation in marmosets following inhalational challenge with different strains of Burkholderia pseudomallei
title_full Characterization of lesion formation in marmosets following inhalational challenge with different strains of Burkholderia pseudomallei
title_fullStr Characterization of lesion formation in marmosets following inhalational challenge with different strains of Burkholderia pseudomallei
title_full_unstemmed Characterization of lesion formation in marmosets following inhalational challenge with different strains of Burkholderia pseudomallei
title_short Characterization of lesion formation in marmosets following inhalational challenge with different strains of Burkholderia pseudomallei
title_sort characterization of lesion formation in marmosets following inhalational challenge with different strains of burkholderia pseudomallei
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744822/
https://www.ncbi.nlm.nih.gov/pubmed/26852689
http://dx.doi.org/10.1111/iep.12161
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