Literature DB >> 10479078

Development of a model of natural infection with Mycobacterium bovis in white-tailed deer.

M V Palmer1, D L Whipple, S C Olsen.   

Abstract

The objective of this study was to develop a suitable experimental model of natural Mycobacterium bovis infection in white-tailed deer (Odocoileus virginianus), describe the distribution and character of tuberculous lesions, and to examine possible routes of disease transmission. In October 1997, 10 mature female white-tailed deer were inoculated by intratonsilar instillation of 2 x 10(3) (low dose) or 2 x 10(5) (high dose) colony forming units (CFU) of M. bovis. In January 1998, deer were euthanatized, examined, and tissues were collected 84 to 87 days post inoculation. Possible routes of disease transmission were evaluated by culture of nasal, oral, tonsilar, and rectal swabs at various times during the study. Gross and microscopic lesions consistent with tuberculosis were most commonly seen in medial retropharyngeal lymph nodes and lung in both dosage groups. Other tissues containing tuberculous lesions included tonsil, trachea, liver, and kidney as well as lateral retropharyngeal, mandibular, parotid, tracheobronchial, mediastinal, hepatic, mesenteric, superficial cervical, and iliac lymph nodes. Mycobacterium bovis was isolated from tonsilar swabs from 8 of 9 deer from both dosage groups at least once 14 to 87 days after inoculation. Mycobacterium bovis was isolated from oral swabs 63 and 80 days after inoculation from one of three deer in the low dose group and none of four deer in the high dose group. Similarly, M. bovis was isolated from nasal swabs 80 and 85 days after inoculation in one of three deer from the low dose group and 63 and 80 days after inoculation from two of four deer in the high dose group. Intratonsilar inoculation with M. bovis results in lesions similar to those seen in naturally infected white-tailed deer; therefore, it represents a suitable model of natural infection. These results also indicate that M. bovis persists in tonsilar crypts for prolonged periods and can be shed in saliva and nasal secretions. These infected fluids represent a likely route of disease transmission to other animals or humans.

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Year:  1999        PMID: 10479078     DOI: 10.7589/0090-3558-35.3.450

Source DB:  PubMed          Journal:  J Wildl Dis        ISSN: 0090-3558            Impact factor:   1.535


  22 in total

1.  Analysis of immune responses directed toward a recombinant early secretory antigenic target six-kilodalton protein-culture filtrate protein 10 fusion protein in Mycobacterium bovis-infected cattle.

Authors:  Alexander C Maue; W Ray Waters; William C Davis; Mitchell V Palmer; F Chris Minion; D Mark Estes
Journal:  Infect Immun       Date:  2005-10       Impact factor: 3.441

2.  Modulation of Mycobacterium bovis-specific responses of bovine peripheral blood mononuclear cells by 1,25-dihydroxyvitamin D(3).

Authors:  W R Waters; B J Nonnecke; T E Rahner; M V Palmer; D L Whipple; R L Horst
Journal:  Clin Diagn Lab Immunol       Date:  2001-11

3.  Antibody responses in reindeer (Rangifer tarandus) infected with Mycobacterium bovis.

Authors:  W R Waters; M V Palmer; J P Bannantine; R Greenwald; J Esfandiari; P Andersen; J McNair; J M Pollock; K P Lyashchenko
Journal:  Clin Diagn Lab Immunol       Date:  2005-06

4.  Using White-tailed Deer (Odocoileus virginianus) in Infectious Disease Research.

Authors:  Mitchell V Palmer; Rebecca J Cox; W Ray Waters; Tyler C Thacker; Diana L Whipple
Journal:  J Am Assoc Lab Anim Sci       Date:  2017-07-01       Impact factor: 1.232

5.  Immune responses in cattle inoculated with Mycobacterium bovis, Mycobacterium tuberculosis, or Mycobacterium kansasii.

Authors:  W R Waters; A O Whelan; K P Lyashchenko; R Greenwald; M V Palmer; B N Harris; R G Hewinson; H M Vordermeier
Journal:  Clin Vaccine Immunol       Date:  2009-12-09

6.  Antibody responses of cervids (Cervus elaphus) following experimental Mycobacterium bovis infection and the implications for immunodiagnosis.

Authors:  Noel P Harrington; Om P Surujballi; John F Prescott; J Robert Duncan; W Ray Waters; Konstantin Lyashchenko; Rena Greenwald
Journal:  Clin Vaccine Immunol       Date:  2008-09-24

7.  Single-antigen serological testing for bovine tuberculosis.

Authors:  Lawrence R Green; Cynthia C Jones; Anne L Sherwood; Inna V Garkavi; Gerard A Cangelosi; Tyler C Thacker; Mitchell V Palmer; W Ray Waters; Chris V Rathe
Journal:  Clin Vaccine Immunol       Date:  2009-07-15

8.  T-cell mRNA expression in response to Mycobacterium bovis BCG vaccination and Mycobacterium bovis infection of white-tailed deer.

Authors:  Tyler C Thacker; Mitchell V Palmer; W Ray Waters
Journal:  Clin Vaccine Immunol       Date:  2009-06-10

9.  Use of recombinant ESAT-6:CFP-10 fusion protein for differentiation of infections of cattle by Mycobacterium bovis and by M. avium subsp. avium and M. avium subsp. paratuberculosis.

Authors:  W R Waters; B J Nonnecke; M V Palmer; S Robbe-Austermann; J P Bannantine; J R Stabel; D L Whipple; J B Payeur; D M Estes; J E Pitzer; F C Minion
Journal:  Clin Diagn Lab Immunol       Date:  2004-07

10.  Antigen recognition by serum antibodies in white-tailed deer (Odocoileus virginianus) experimentally infected with Mycobacterium bovis.

Authors:  W R Waters; M V Palmer; J P Bannantine; D L Whipple; R Greenwald; J Esfandiari; P Andersen; J McNair; J M Pollock; K P Lyashchenko
Journal:  Clin Diagn Lab Immunol       Date:  2004-09
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