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Updated: Mar 23, 2026

A Mouse Model for Pathogen-induced Chronic Inflammation at Local and Systemic Sites
Published on: August 8, 2014
The origin of Pasteurella multocida impacts pathology and inflammation when assessed in a mouse model
Susanne E Pors1, Mark S Chadfield2, Dorte B Sørensen1
1Department of Veterinary Disease Biology, University of Copenhagen, Denmark.
Abstract:
Host-pathogen interactions of Pasteurella multocida isolates of different origin were studied in a mouse model, focusing on pathology, bacterial load and expression of the metalloproteinase MMP9 and its inhibitor TIMP1. Intranasal inoculation with one of three doses (10(6), 10(4), 10(2)CFU) of an isolate from porcine pneumonia or fowl cholera showed marked differences between the two isolates. The avian isolate was highly pathogenic with severe signs of necrotizing pneumonia, liver necrosis and high bacterial load in lung and liver. Clinical signs and pathology related to the porcine isolate were dose dependent and consisted of exudative bronchopneumonia, abscess formation in liver and a lower bacterial load in lung and liver. Both isolates caused increased expression of MMP9 and TIMP1. In conclusion, evaluation and comparison of pathogenicity and host-pathogen interaction of P. multocida isolates from different hosts is possible in the intranasal murine model.
Insights
This study compared Pasteurella multocida isolates from pigs and poultry in mice. The avian isolate caused severe disease, while the porcine isolate
Area of Science:
- Veterinary Microbiology
- Infectious Diseases
- Immunology
Background:
- Pasteurella multocida is a significant bacterial pathogen affecting various animal species.
- Understanding host-pathogen interactions is crucial for controlling P. multocida infections.
Purpose of the Study:
- To compare the pathogenicity and host-pathogen interactions of P. multocida isolates from porcine pneumonia and fowl cholera in a murine model.
- To investigate the expression of matrix metalloproteinase 9 (MMP9) and its inhibitor TIMP1 during infection.
Main Methods:
- Intranasal inoculation of mice with different doses (10(6), 10(4), 10(2) CFU) of avian and porcine P. multocida isolates.
- Assessment of clinical signs, gross pathology, bacterial load in lung and liver, and expression of MMP9 and TIMP1.
Main Results:
- The avian isolate exhibited high pathogenicity, causing severe necrotizing pneumonia and liver necrosis with high bacterial loads.
- The porcine isolate showed dose-dependent pathogenicity, leading to bronchopneumonia and liver abscesses with lower bacterial loads.
- Both isolates increased the expression of MMP9 and TIMP1.
Conclusions:
- The intranasal murine model effectively differentiates the pathogenicity of P. multocida isolates from different hosts.
- Host-pathogen interactions, including MMP9 and TIMP1 expression, vary between avian and porcine P. multocida isolates.
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