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. 2012 Mar;28(1):61-6.
doi: 10.5625/lar.2012.28.1.61. Epub 2012 Mar 21.

Molecular identification of Mycoplasma cynos from laboratory beagle dogs with respiratory disease

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Molecular identification of Mycoplasma cynos from laboratory beagle dogs with respiratory disease

Sunhwa Hong et al. Lab Anim Res. 2012 Mar.

Abstract

In this study, we examined a colony of 20 beagle dogs in a laboratory animal facility. Mycoplasma was detected by consensus PCR assay in 1 dog with respiratory and constitutional symptoms. None of the other dogs were affected. The dog was euthanized and necropsied. In postmortem examinations, gray or plum-colored gross lesions were found on the lung, most commonly in the apical and cardiac lobes. Some lesions showed clear demarcation and consolidation. Microscopic examination showed peribronchiolar lymphoid hyperplasia and interstitial thickening, lesions pathognomonic for mycoplasma pneumonia. To identify canine Mycoplasma species, we used species-specific PCR reactions for M. arginini, M. canis, M. cynos, M. edwardii, M. felis, M. gateae, M. maculosum, M. molare, M. opalescens, M. spumans, Mycoplasma sp. HRC 689, and M. collis. As the result, we identified Mycoplasma cynos by amplification of DNA extracted from lung tissue of the laboratory beagle dog with respiratory disease.

Keywords: Beagle; Mycoplasma; Mycoplasma cynos; PCR; consensus; dog.

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Figures

Figure 1
Figure 1
Histopathological findings in the lung of dog No. 8. (A) Peribronchiolar lymphoid hyperplasia and interstitial thickening lesions. H&E stain, Bar=100 µm, (B) Infiltrating lymphocytes and mononuclear cells in peribronchiolar hyperplasia lesion. H&E stain, Bar=20 µm
Figure 2
Figure 2
Amplification of 16S rDNA gene by mycoplasma consensus PCR was confirmed on a 1.2% agarose gel electrophoresis. Lane P: positive control, N: distilled water, 1~20: Nasal swab sample of No. 1~No. 20 dog
Figure 3
Figure 3
Amplification of DNA extracted from the lung tissue of dog No. 8 with canine Mycoplasma species-specific primers was confirmed on 1.2% agarose gel electrophoresis. Lane P: positive control, N: distilled water, 1: M. arginini, 2: M. canis, 3: M. cynos, 4: M. edwardii, 5: M. felis, 6: M. gateae, 7: M. maculosum, 8: M. molare, 9: M. opalescens, 10: M. spumans, 11: Mycoplasma sp. HRC 689, 12: M. collis

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References

    1. McAuliffe L, Ellis RJ, Ayling RD, Nicholas RA. Differentiation of Mycoplasma species by 16S ribosomal DNA PCR and denaturing gradient gel electrophoresis fingerprinting. J Clin Microbiol. 2003;41(10):4844–4847. - PMC - PubMed
    1. Fox JG, Anderson LC, Loew FM, Quimby FW. Laboratory Animal Medicine. 2nd ed. Amsterdam: Academic Press; 2002. pp. 111–165.
    1. Lindsey JR, Baker HJ, Overcash RG, Cassell GH, Hunt CE. Murine chronic respiratory disease. Significance as a research complication and experimental production with Mycoplasma pulmonis. Am J Pathol. 1971;64(3):675–708. - PMC - PubMed
    1. Davis JK, Thorp RB, Maddox PA, Brown MB, Cassell GH. Murine respiratory mycoplasmosis in F344 and LEW rats: evolution of lesions and lung lymphoid cell populations. Infect Immun. 1982;36(2):720–729. - PMC - PubMed
    1. Rosendal S. Canine mycoplasmas: their ecologic niche and role in disease. J Am Vet Med Assoc. 1982;180(10):1212–1214. - PubMed