Cargando…

Characterization of lethal inhalational infection with Francisella tularensis in the common marmoset (Callithrix jacchus)

The intracellular Gram-negative pathogen Francisella tularensis is the causative agent of tularaemia and is prevalent in many countries in the northern hemisphere. To determine whether the common marmoset (Callithrix jacchus) would be a suitable non-human primate model of inhalational tularaemia, a...

Descripción completa

Detalles Bibliográficos
Autores principales: Nelson, Michelle, Lever, Mark S., Dean, Rachel E., Savage, Victoria L., Salguero, F. Javier, Pearce, Peter C., Stevens, Daniel J., Simpson, Andrew J. H.
Formato: Texto
Lenguaje:English
Publicado: Society for General Microbiology 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052436/
https://www.ncbi.nlm.nih.gov/pubmed/20558585
http://dx.doi.org/10.1099/jmm.0.020669-0
_version_ 1782199672293556224
author Nelson, Michelle
Lever, Mark S.
Dean, Rachel E.
Savage, Victoria L.
Salguero, F. Javier
Pearce, Peter C.
Stevens, Daniel J.
Simpson, Andrew J. H.
author_facet Nelson, Michelle
Lever, Mark S.
Dean, Rachel E.
Savage, Victoria L.
Salguero, F. Javier
Pearce, Peter C.
Stevens, Daniel J.
Simpson, Andrew J. H.
author_sort Nelson, Michelle
collection PubMed
description The intracellular Gram-negative pathogen Francisella tularensis is the causative agent of tularaemia and is prevalent in many countries in the northern hemisphere. To determine whether the common marmoset (Callithrix jacchus) would be a suitable non-human primate model of inhalational tularaemia, a pathophysiology study was undertaken. Ten animals were challenged with ∼10(2) c.f.u. F. tularensis strain SCHU S4 (F. tularensis subsp. tularensis). To look for trends in the infection, pairs of animals were sacrificed at 24 h intervals between 0 and 96 h post-challenge and blood and organs were assessed for bacteriology, pathology and haematological and immunological parameters. The first indication of infection was a raised core temperature at 3 days post-challenge. This coincided with a number of other factors: a rapid increase in the number of bacteria isolated from all organs, more pronounced gross pathology and histopathology, and an increase in the immunological response. As the disease progressed, higher bacterial and cytokine levels were detected. More extensive pathology was observed, with multifocal lesions seen in the lungs, liver and spleen. Disease progression in the common marmoset appears to be consistent with human clinical and pathological features of tularaemia, indicating that this may be a suitable animal model for the investigation of novel medical interventions such as vaccines or therapeutics.
format Text
id pubmed-3052436
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Society for General Microbiology
record_format MEDLINE/PubMed
spelling pubmed-30524362011-09-01 Characterization of lethal inhalational infection with Francisella tularensis in the common marmoset (Callithrix jacchus) Nelson, Michelle Lever, Mark S. Dean, Rachel E. Savage, Victoria L. Salguero, F. Javier Pearce, Peter C. Stevens, Daniel J. Simpson, Andrew J. H. J Med Microbiol Models of Infection The intracellular Gram-negative pathogen Francisella tularensis is the causative agent of tularaemia and is prevalent in many countries in the northern hemisphere. To determine whether the common marmoset (Callithrix jacchus) would be a suitable non-human primate model of inhalational tularaemia, a pathophysiology study was undertaken. Ten animals were challenged with ∼10(2) c.f.u. F. tularensis strain SCHU S4 (F. tularensis subsp. tularensis). To look for trends in the infection, pairs of animals were sacrificed at 24 h intervals between 0 and 96 h post-challenge and blood and organs were assessed for bacteriology, pathology and haematological and immunological parameters. The first indication of infection was a raised core temperature at 3 days post-challenge. This coincided with a number of other factors: a rapid increase in the number of bacteria isolated from all organs, more pronounced gross pathology and histopathology, and an increase in the immunological response. As the disease progressed, higher bacterial and cytokine levels were detected. More extensive pathology was observed, with multifocal lesions seen in the lungs, liver and spleen. Disease progression in the common marmoset appears to be consistent with human clinical and pathological features of tularaemia, indicating that this may be a suitable animal model for the investigation of novel medical interventions such as vaccines or therapeutics. Society for General Microbiology 2010-09 /pmc/articles/PMC3052436/ /pubmed/20558585 http://dx.doi.org/10.1099/jmm.0.020669-0 Text en Copyright © 2010, Crown copyright
spellingShingle Models of Infection
Nelson, Michelle
Lever, Mark S.
Dean, Rachel E.
Savage, Victoria L.
Salguero, F. Javier
Pearce, Peter C.
Stevens, Daniel J.
Simpson, Andrew J. H.
Characterization of lethal inhalational infection with Francisella tularensis in the common marmoset (Callithrix jacchus)
title Characterization of lethal inhalational infection with Francisella tularensis in the common marmoset (Callithrix jacchus)
title_full Characterization of lethal inhalational infection with Francisella tularensis in the common marmoset (Callithrix jacchus)
title_fullStr Characterization of lethal inhalational infection with Francisella tularensis in the common marmoset (Callithrix jacchus)
title_full_unstemmed Characterization of lethal inhalational infection with Francisella tularensis in the common marmoset (Callithrix jacchus)
title_short Characterization of lethal inhalational infection with Francisella tularensis in the common marmoset (Callithrix jacchus)
title_sort characterization of lethal inhalational infection with francisella tularensis in the common marmoset (callithrix jacchus)
topic Models of Infection
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052436/
https://www.ncbi.nlm.nih.gov/pubmed/20558585
http://dx.doi.org/10.1099/jmm.0.020669-0
work_keys_str_mv AT nelsonmichelle characterizationoflethalinhalationalinfectionwithfrancisellatularensisinthecommonmarmosetcallithrixjacchus
AT levermarks characterizationoflethalinhalationalinfectionwithfrancisellatularensisinthecommonmarmosetcallithrixjacchus
AT deanrachele characterizationoflethalinhalationalinfectionwithfrancisellatularensisinthecommonmarmosetcallithrixjacchus
AT savagevictorial characterizationoflethalinhalationalinfectionwithfrancisellatularensisinthecommonmarmosetcallithrixjacchus
AT salguerofjavier characterizationoflethalinhalationalinfectionwithfrancisellatularensisinthecommonmarmosetcallithrixjacchus
AT pearcepeterc characterizationoflethalinhalationalinfectionwithfrancisellatularensisinthecommonmarmosetcallithrixjacchus
AT stevensdanielj characterizationoflethalinhalationalinfectionwithfrancisellatularensisinthecommonmarmosetcallithrixjacchus
AT simpsonandrewjh characterizationoflethalinhalationalinfectionwithfrancisellatularensisinthecommonmarmosetcallithrixjacchus