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Associated Pulmonary and Urogenital Disease and Pathology in a Colony of Enzootically Infected Il12rb2 Deficient and Stat1 Knockout Mice. | LitMetric

Associated Pulmonary and Urogenital Disease and Pathology in a Colony of Enzootically Infected Il12rb2 Deficient and Stat1 Knockout Mice.

Comp Med

Tri-Institutional Training Program in Laboratory Animal Medicine and Science, Memorial Sloan Kettering Cancer Center, Weill Cornell Medicine, and The Rockefeller University, New York, New York; Center of Comparative Medicine and Pathology, Memorial Sloan Kettering Cancer Center and Weill Cornell Medicine, New York, New York;, Email:

Published: April 2024

AI Article Synopsis

  • Researchers rediscovered the intracellular bacterium Cm, historically linked to severe pneumonia in mice, in research mouse colonies, noting its moderate prevalence.
  • They observed clinical disease in genetically engineered mouse strains with impaired immune responses, presenting symptoms like poor condition and hunched posture, along with histopathological evidence of Cm in various tissues.
  • The study suggests that Cm could negatively impact research validity, underscoring the need to exclude this bacterium from mouse colonies used in scientific studies.

Article Abstract

(Cm), an intracellular bacterium of historical importance, was recently rediscovered as moderately prevalent in research mouse colonies. Cm was first reported as a causative agent of severe pneumonia in mice about 80 y ago, and while it has been used experimentally to model infection of humans, there have been no further reports of clinical disease associated with natural infection. We observed clinical disease and pathology in 2 genetically engi- neered mouse (GEM) strains, KO and KO, with impaired interferon-γ signaling and Th1 CD4+ T cell responses in a colony of various GEM strains known to be colonized with and shedding Cm. Clinical signs included poor condition, hunched posture, and poor fecundity. Histopathology revealed disseminated Cm with lesions in pulmonary, gastrointestinal, and urogenital tissues. The presence of Cm was confirmed using both immunohistochemistry for Cm major outer membrane protein-1 antigen and in situ hybridization using a target probe directed against select regions of Cm strain Nigg. Cm was also found in association with a urothelial papilloma in one mouse. These cases provide additional support for excluding Cm from research mouse colonies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11078279PMC
http://dx.doi.org/10.30802/AALAS-CM-24-000002DOI Listing

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