Pasteurellaceae isolated from bighorn sheep (Ovis canadensis) from Idaho, Oregon, and Wyoming

David S. Miller Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO 80523.

Search for other papers by David S. Miller in
Current site
Google Scholar
PubMed
Close
 DVM, PhD; DACZM
,
Glen C. Weiser Caine Veterinary Teaching Center, College of Agricultural and Life Sciences, University of Idaho, Caldwell, ID 83607.

Search for other papers by Glen C. Weiser in
Current site
Google Scholar
PubMed
Close
 PhD
,
Alton C. S. Ward Caine Veterinary Teaching Center, College of Agricultural and Life Sciences, University of Idaho, Caldwell, ID 83607.

Search for other papers by Alton C. S. Ward in
Current site
Google Scholar
PubMed
Close
 PhD
,
Mark L. Drew Idaho Department of Fish and Game, Wildlife Health Laboratory, 16569 S 10th Ave, Caldwell, ID 83607.

Search for other papers by Mark L. Drew in
Current site
Google Scholar
PubMed
Close
 MS, DVM; DACZM
, and
Phillip L. Chapman Department of Statistics, College of Natural Sciences, Colorado State University, Fort Collins, CO 80523.

Search for other papers by Phillip L. Chapman in
Current site
Google Scholar
PubMed
Close
 PhD

Abstract

Objective—To elucidate the species and biovariants of Pasteurellaceae isolated from clinically normal bighorn sheep (Ovis canadensis) or bighorn sheep with evidence of respiratory disease.

Sample—675 Pasteurellaceae isolates from 290 free-ranging bighorn sheep in Idaho, Oregon and Wyoming.

Procedures—Nasal and oropharyngeal swab specimens were inoculated onto selective and nonselective blood agar media. Representatives of each colony type were classified via a biovariant scheme. The association of respective β-hemolytic isolates with respiratory disease was evaluated via χ2 analyses.

Results—Bacterial isolates belonged to 4 species: Histophilus somni, Mannheimia haemolytica, Pasteurella multocida, and Bibersteinia (Pasteurella) trehalosi. Within the latter 3 species, 112 subspecies, biotypes, and biovariants were identified. Bibersteinia trehalosi 2 and B trehalosi 2B constituted 345 of 675 (51%) isolates. Most (597/618 [97%]) isolates from adult sheep were from clinically normal animals, whereas most (47/57 [82%]) isolates from lambs were from animals with evidence of respiratory disease. Twenty-two Pasteurellaceae biovariants were isolated from sheep with respiratory disease; 17 of these biovariants were also isolated from clinically normal sheep. The ability of isolates to cause β-hemolysis on blood agar was associated with respiratory disease in adult bighorn sheep (OR, 2.59; 95% confidence interval, 1.10 to 6.07).

Conclusions and Clinical Relevance—Bighorn lambs appeared more susceptible to respiratory disease caused by Pasteurellaceae than did adult sheep. β-Hemolytic Pasteurellaceae isolates were more likely to be associated with respiratory disease than were non–β-hemolytic isolates in adult sheep. Identification of Pasteurellaceae with the greatest pathogenic potential will require studies to estimate the risk of disease from specific biovariants.

Abstract

Objective—To elucidate the species and biovariants of Pasteurellaceae isolated from clinically normal bighorn sheep (Ovis canadensis) or bighorn sheep with evidence of respiratory disease.

Sample—675 Pasteurellaceae isolates from 290 free-ranging bighorn sheep in Idaho, Oregon and Wyoming.

Procedures—Nasal and oropharyngeal swab specimens were inoculated onto selective and nonselective blood agar media. Representatives of each colony type were classified via a biovariant scheme. The association of respective β-hemolytic isolates with respiratory disease was evaluated via χ2 analyses.

Results—Bacterial isolates belonged to 4 species: Histophilus somni, Mannheimia haemolytica, Pasteurella multocida, and Bibersteinia (Pasteurella) trehalosi. Within the latter 3 species, 112 subspecies, biotypes, and biovariants were identified. Bibersteinia trehalosi 2 and B trehalosi 2B constituted 345 of 675 (51%) isolates. Most (597/618 [97%]) isolates from adult sheep were from clinically normal animals, whereas most (47/57 [82%]) isolates from lambs were from animals with evidence of respiratory disease. Twenty-two Pasteurellaceae biovariants were isolated from sheep with respiratory disease; 17 of these biovariants were also isolated from clinically normal sheep. The ability of isolates to cause β-hemolysis on blood agar was associated with respiratory disease in adult bighorn sheep (OR, 2.59; 95% confidence interval, 1.10 to 6.07).

Conclusions and Clinical Relevance—Bighorn lambs appeared more susceptible to respiratory disease caused by Pasteurellaceae than did adult sheep. β-Hemolytic Pasteurellaceae isolates were more likely to be associated with respiratory disease than were non–β-hemolytic isolates in adult sheep. Identification of Pasteurellaceae with the greatest pathogenic potential will require studies to estimate the risk of disease from specific biovariants.

Contributor Notes

Dr. Miller's present address is PO Box 2786, Loveland, CO 80539.

Supported in part by the College of Agricultural and Life Sciences, University of Idaho; the Idaho Department of Fish and Game; and the Program of Economically Important Infectious Animal Diseases, Colorado State University.

Address correspondence to Dr. Weiser (gweiser@uidaho.edu).
  • 1. Bunch TD, Boyce W, Hibler CP, et al. Diseases of North American wild sheep. In: Valdez R, Krausman PR, eds. Mountain sheep of North America. Tucson: University of Arizona Press, 1999;209238.

    • Search Google Scholar
    • Export Citation
  • 2. Miller MW. Pasteurellosis. In: Williams ES, Barker IK, eds. Infectious diseases of wild mammals. 3rd ed. London: Manson Publishing, 2001;330349.

    • Search Google Scholar
    • Export Citation
  • 3. Gross JE, Singer FJ, Moses ME. Effects of disease, dispersal, and area on bighorn sheep restoration. Restor Ecol 2000; 8:2537.

  • 4. Cassirer EF, Sinclair ARE. Dynamics of pneumonia in a bighorn sheep metapopulation. J Wildl Manag 2007; 71:10801088.

  • 5. George JL, Martin DJ, Lukacs PM, et al. Epidemic pasteurellosis in a bighorn sheep population coinciding with the appearance of a domestic sheep. J Wildl Dis 2008; 44:388403.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 6. Nolen RS. Severe pneumonia outbreak kills bighorn sheep. J Am Vet Med Assoc 2010; 236:936.

  • 7. Onderka DK, Rawluk SA, Wishart WD. Susceptibility of Rocky Mountain bighorn sheep and domestic sheep to pneumonia induced by bighorn and domestic livestock strains of Pasteurella haemolytica. Can J Vet Res 1988; 52:439444.

    • Search Google Scholar
    • Export Citation
  • 8. Foreyt WJ, Snipes KP, Kasten RW. Fatal pneumonia following inoculation of healthy bighorn sheep with Pasteurella haemolytica from healthy domestic sheep. J Wildl Dis 1994; 30:137145.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 9. Dassanayake RP, Shanthalingam S, Herndon CN, et al. Mannheimia haemolytica serotype A1 exhibits differential pathogenicity in two related species, Ovis canadensis and Ovis aries. Vet Microbiol 2009; 133:366371.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 10. Angen O, Mutters R, Caugant D, et al. Taxonomic relationships of the [Pasteurella] haemolytica complex as evaluated by DNA-DNA hybridizations and 16S rRNA sequencing with proposal of Mannheimia haemolytica gen. nov., comb. nov., Mannheimia granulomatis comb. nov., Mannheimia glucosida sp. nov., Mannheimia ruminalis sp. nov., and Mannheimia varigena sp. nov. Int J Syst Bacteriol 1999; 49:6786.

    • Search Google Scholar
    • Export Citation
  • 11. Sneath PHA, Stevens M. Actinobacillus seminis sp. nov., nom. rev., Pasteurella betti sp. nov., Pasteurella lymphangitidis sp. nov., Pasteurella mairi sp. nov., and Pasteurella trehalosi sp. nov. Int J Syst Bacteriol 1990; 40:148153.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 12. Blackall PJ, Bojesen AM, Christensen H, et al. Reclassification of [Pasteurella] trehalosi as Bibersteinia trehalosi gen nov, comb nov. Int J Syst Evol Microbiol 2007; 57:666674.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 13. Weiser GC, DeLong WJ, Paz JL, et al. Characterization of Pasteurella multocida associated with pneumonia in bighorn sheep. J Wildl Dis 2003; 39:536544.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 14. Evans HF. Bighorn at many glacier. Glacial Drift 1937; 10:23.

  • 15. Marsh H. Pneumonia in Rocky Mountain bighorn sheep. J Mammal 1938; 19:214219.

  • 16. Post G. Pasteurellosis of Rocky Mountain bighorn sheep (Ovis canadensis canadensis). Wildl Dis 1962; 23:114.

  • 17. Onderka DK, Wishart WD. Experimental contact transmission of Pasteurella haemolytica from clinically normal domestic sheep causing pneumonia in Rocky Mountain bighorn sheep. J Wildl Dis 1988; 24:663667.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 18. Lawrence PK, Shanthalingam S, Dassanayake RP, et al. Transmission of Mannheimia haemolytica from domestic sheep (Ovis aries) to bighorn sheep (Ovis canadensis): unequivocal demonstration with green fluorescent protein-tagged organisms. J Wildl Dis 2010; 46:706717.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 19. Confer AW. Immunogens of Pasteurella. Vet Microbiol 1993; 37:353368.

  • 20. Bisgaard M, Mutters R. Re-investigations of selected bovine and ovine strains previously classified as Pasteurella-haemolytica and description of some new taxa within the Pasteurella-haemolytica-complex. Acta Pathol Microbiol Immunol Scand [B] 1986; 94:185193.

    • Search Google Scholar
    • Export Citation
  • 21. Jaworski MD, Hunter DL, Ward AC. Biovariants of isolates of Pasteurella from domestic and wild ruminants. J Vet Diagn Invest 1998; 10:4955.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 22. Jaworski MD, Ward AC, Hunter DL, et al. Use of DNA analysis of Pasteurella haemolytica biotype T isolates to monitor transmission in bighorn sheep (Ovis canadensis canadensis). J Clin Microbiol 1993; 31:831835.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 23. Rudolph KM, Hunter DL, Rimler RB, et al. Microorganisms associated with a pneumonic epizootic in Rocky Mountain bighorn sheep (Ovis canadensis canadensis). J Zoo Wildl Med 2007; 38:548558.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 24. Rudolph KM, Hunter DL, Foreyt WJ, et al. Sharing of Pasteurella spp. between free-ranging bighorn sheep and feral goats. J Wildl Dis 2003; 39:897903.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 25. Yates WD. A review of infectious bovine rhinotracheitis, shipping fever pneumonia and viral-bacterial synergism in respiratory disease of cattle. Can J Comp Med 1982; 46:225263.

    • Search Google Scholar
    • Export Citation
  • 26. Fisher MA, Weiser GC, Hunter DL, et al. Use of a polymerase chain reaction method to detect the leukotoxin gene lktA in bio-group and biovariant isolates of Pasteurella haemolytica and P trehalosi. Am J Vet Res 1999; 60:14021406.

    • Search Google Scholar
    • Export Citation
  • 27. Nizet V. Streptococcal β-hemolysins: genetics and role in disease pathogenesis. Trends Microbiol 2002; 10:575580.

  • 28. Confer AW, Panciera RJ, Mosier DA. Bovine pneumonic pasteurellosis: immunity to Pasteurella haemolytica. J Am Vet Med Assoc 1988; 193:13081316.

    • Search Google Scholar
    • Export Citation
  • 29. Schwabe CW, Riemann HP, Franti CE. Diseases in populations. In: Schwabe CW, Riemann HP, Franti CE, eds. Epidemiology in veterinary practice. Philadelphia: Lea and Febiger, 1977;1221.

    • Search Google Scholar
    • Export Citation
  • 30. Casadevall A, Pirofski LA. Host-pathogen interactions: redefining the basic concepts of virulence and pathogenicity. Infect Immun 1999; 67:37033713.

    • Crossref
    • Search Google Scholar
    • Export Citation

Advertisement