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Infection and Immunity, March 2004, p. 1700-1705, Vol. 72, No. 3
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.3.1700-1705.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Susceptibility to Tuberculosis: Clues from Studies with Inbred and Outbred New Zealand White Rabbits

Susan E. Dorman,1 Christine L. Hatem,1 Sandeep Tyagi,1 Katherine Aird,1 Javier Lopez-Molina,1 M. Louise M. Pitt,2 Bernard C. Zook,3 Arthur M. Dannenberg Jr.,4,5,6,7 William R. Bishai,1,5,8 and Yukari C. Manabe1,5,8*

Departments of Medicine,1 Pathology, School of MedicineDepartments of,4 Environmental Health Sciences,5 Molecular Microbiology and Immunology,6 International Health,8 Epidemiology, Bloomberg School of Public Health, The Johns Hopkins University, Baltimore,7 Department of Aerobiology and Product Evaluation, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland,2 Department of Pathology, George Washington University Medical Center, Washington, D.C.3

Received 26 August 2003/ Returned for modification 29 October 2003/ Accepted 11 December 2003

The rabbit model of tuberculosis (TB) is important because rabbits develop a disease that is similar to TB in humans, namely, granulomas with caseous necrosis, liquefaction, and cavities. We describe here a comparison of inbred and outbred New Zealand White rabbits infected by aerosol with either Mycobacterium tuberculosis Erdman or H37Rv strain. Five weeks after infection with either bacillary strain, the inbred rabbits had significantly larger pulmonary tubercles than did outbred rabbits (2.7 versus 1.4 mm in diameter; P < 0.01). After infection with H37Rv, the inbred rabbits had significantly more pulmonary tubercles than did the outbred rabbits (98 ± 12 versus 33 ± 13; P < 0.01), with more mycobacterial CFU per tubercle (809 ± 210 versus 215 ± 115; P = 0.027) (means ± standard errors of the means). Compared with histologic examination of lung granulomas from outbred rabbits, histologic examination of those from inbred rabbits showed more caseous necrosis, more visible bacilli, and fewer mature epithelioid cells. The delayed-type hypersensitivity (DTH) responses to intradermal tuberculin were significantly lower, and peritoneal macrophages from uninfected inbred rabbits produced significantly less tumor necrosis factor alpha after lipopolysaccharide (LPS) stimulation in vitro than those from the outbred rabbits (2,413 ± 1,154 versus 8,879 ± 966 pg/ml). We conclude that these inbred rabbits were more susceptible to TB than their outbred counterparts and had an impaired ability to contain disease, resulting in more grossly visible tubercles that were larger than those observed in outbred rabbits. Preliminary evidence is presented for a cell-mediated immune defect with lower DTH responses and macrophages that have a decreased ability to respond to in vitro stimulation with LPS or M. tuberculosis infection.


* Corresponding author. Mailing address: Johns Hopkins University School of Medicine, 1503 E. Jefferson St., Rm. 1108, Baltimore, MD 21231-1004. Phone: (410) 614-6600. Fax: (410) 614-8173. E-mail: ymanabe{at}jhmi.edu.

Editor: S. H. E. Kaufmann


Infection and Immunity, March 2004, p. 1700-1705, Vol. 72, No. 3
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.3.1700-1705.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




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