The Role of Myofibroblasts in Granulomatous Lymphadenitis in Pigs Naturally Infected with M. Avium Subsp. Hominissuis

1. Inderlied, C.B., Kemper, C.A., Bermudez, L.E. (1993). The Mycobacterium avium complex. Clin Microbiol Rev. 6 (3): 266–310. https://doi.org/10.1128/CMR.6.3.266 PMid:8358707 PMCid:PMC35828610.1128/CMR.6.3.266PMid:8358707PMCid:PMC358286Open DOISearch in Google Scholar

2. Johansen, T., Agdestein, A., Olsen, I., Nilsen, S., Holstad, G., Djønne, B., et al. (2009). Biofilm formation by Mycobacterium avium isolates originating from humans, swine and birds. BMC Microbiol. 9(1): 159. https://doi.org/10.1186/1471-2180-9-159 PMid:19660141 PMCid:PMC274146710.1186/1471-2180-9-159PMid:19660141PMCid:PMC2741467Open DOISearch in Google Scholar

3. Agdestein, A., Olsen, I., Jørgensen, A., Djønne, B., Johansen, T.B. (2014). Novel insights into transmission routes of Mycobacterium avium in pigs and possible implications for human health. Vet Res. 45, 46. https://doi.org/10.1186/1297-9716-45-46 PMid:24742183 PMCid:PMC402146510.1186/1297-9716-45-46PMid:24742183PMCid:PMC4021465Open DOISearch in Google Scholar

4. Bezos, J., Álvarez-Carrión, B., Rodríguez-Bertos, A., Fernández-Manzano, Á., de Juan, L., Huguet, C., et al. (2016). Evidence of disseminated infection by Mycobacterium avium subspecies hominissuis in a pet ferret (Mustela putorius furo). Research in Veterinary Science 109, 52-55. https://doi.org/10.1016/j.rvsc.2016.09.013 PMid:2789287310.1016/j.rvsc.2016.09.013PMid:27892873Open DOISearch in Google Scholar

5. Matlova, L., Dvorska, L., Ayele, W.Y., Bartos, M., Amemori, T., Pavlik, I. (2005). Distribution of Mycobacterium avium complex isolates in tissue samples of pigs fed peat naturally contaminated with mycobacteria as a supplement. J Clin Microbiol. 43(3): 1261–1268. https://doi.org/10.1128/JCM.43.3.1261-1268.2005 PMid:15750094 PMCid:PMC108122710.1128/JCM.43.3.1261-1268.2005PMid:15750094PMCid:PMC1081227Open DOISearch in Google Scholar

6. Biet, F., Boschiroli, M.L. (2014). Non-tuberculous mycobacterial infections of veterinary relevance. Res Vet Sci. 97, S69–77. https://doi.org/10.1016/j.rvsc.2014.08.007 PMid:2525696410.1016/j.rvsc.2014.08.007PMid:25256964Open DOISearch in Google Scholar

7. Polaček, V., Aleksić - Kovačević, S. (2016). Mycobacteriosis in pigs – an underrated threat. Acta Vet Beograd. 66(4): 429–443. https://doi.org/10.1515/acve-2016-003710.1515/acve-2016-0037Open DOISearch in Google Scholar

8. Pate, M., Zdovc, I., Pirs, T., Krt, B., Ocepek, M. (2004). Isolation and characterisation of Mycobacterium avium and Rhodococcus equi from granulomatous lesions of swine lymph nodes in Slovenia. Acta Vet Hung. 52(2): 143–150. https://doi.org/10.1556/AVet.52.2004.2.2 PMid:1516874510.1556/avet.52.2004.2.2Search in Google Scholar

9. Agdestein, A., Johansen, T.B., Kolbjørnsen, Ø., Jørgensen, A., Djønne, B., Olsen, I. (2012). A comparative study of Mycobacterium avium subsp. avium and Mycobacterium avium subsp. hominissuis in experimentally infected pigs. BMC Vet Res. 8(1): 11. https://doi.org/10.1186/1746-6148-8-11 PMid:22284630 PMCid:PMC329660310.1186/1746-6148-8-11PMid:22284630PMCid:PMC3296603Open DOISearch in Google Scholar

10. Saunders, B.M., Britton, W.J. (2007). Life and death in the granuloma: immunopathology of tuberculosis. Immunol Cell Biol. 85(2): 103–111. https://doi.org/10.1038/sj.icb.7100027 PMid:1721383010.1038/sj.icb.7100027Search in Google Scholar

11. Wangoo, A., Johnson, L., Gough, J., Ackbar, R., Inglut, S., Hicks, D., et al. (2005). Advanced granulomatous lesions in Mycobacterium bovisinfected cattle are associated with increased expression of type I procollagen, (WC1+) T cells and CD 68+ cells. J Comp Pathol. 133(4): 223–234. https://doi.org/10.1016/j.jcpa.2005.05.001 PMid:1615414010.1016/j.jcpa.2005.05.001PMid:16154140Open DOISearch in Google Scholar

12. Miković, R., Knežević, A., Milić, N., Krnjaić, D., Radojičić, M., Veljović, L., et al. (2016). Molecular detection of pseudorabies virus (PrV), porcine parvovirus (PPV) and porcine circovirus 2 (PCV2) in swine in Republic of Montenegro. Acta Vet Beograd. 66(3): 347–358. https://doi.org/10.1515/acve-2016-003010.1515/acve-2016-0030Open DOISearch in Google Scholar

13. Lukač, B., Knežević, A., Milić, N., Krnjaić, D., Veljović, L., Milićević, V., et al. (2016). Molecular detection of PCV2 and PPV in pigs in Republic of Srpska, Bosnia and Herzegovina. Acta Vet Beograd. 66(1): 51–60. https://doi.org/10.1515/acve-2016-000410.1515/acve-2016-0004Open DOISearch in Google Scholar

14. Veldhoen, M., Hocking, R.J., Flavell, R.A., Stockinger, B. (2006). Signals mediated by transforming growth factor-β initiate autoimmune encephalomyelitis, but chronic inflammation is needed to sustain disease. Nat Immunol. 7(11): 1151–1156. https://doi.org/10.1038/ni1391 PMid:1699849210.1038/ni1391PMid:16998492Open DOISearch in Google Scholar

15. Agdestein, A., Johansen, T.B., Polaček, V., Lium, B., Holstad, G., Vidanović, D., et al. (2011). Investigation of an outbreak of mycobacteriosis in pigs. BMC Vet Res. 7, 63. https://doi.org/10.1186/1746-6148-7-63 PMid:22014189 PMCid:PMC321564310.1186/1746-6148-7-63PMid:22014189PMCid:PMC3215643Open DOISearch in Google Scholar

16. Birkness, K., Guarner, J., Sable, S.B., Tripp, R., Kellar, K.L., Bartlett, J., et al. (2007). An in vitro model of the leukocyte interactions associated with granuloma formation in Mycobacterium tuberculosis infection. Immunol Cell Biol. 85(2): 160–168. https://doi.org/10.1038/sj.icb.7100019 PMid:1719911210.1038/sj.icb.7100019PMid:17199112Open DOISearch in Google Scholar

17. Hibiya, K., Kasumi, Y., Sugawara, I., Fujita, J. (2008). Histopathological classification of systemic Mycobacterium avium complex infections in slaughtered domestic pigs. Comp Immunol Microbiol Infect Dis. 31(4): 347–366. https://doi.org/10.1016/j.cimid.2007.05.001 PMid:1762956010.1016/j.cimid.2007.05.001PMid:17629560Open DOISearch in Google Scholar

18. Fujita, J., Ohtsuki, Y., Suemitsu, I., Yamadori, I., Shigeto, E., Shiode, M, et al. (2002). Immunohistochemical distribution of epithelioid cell, myofibroblast, and transforming growth factorbeta1 in the granuloma caused by Mycobacterium avium intracellulare complex pulmonary infection. Microbiol Immunol. 46(2): 67–74. https://doi.org/10.1111/j.1348-0421.2002.tb02660.x PMid:1193958010.1111/j.1348-0421.2002.tb02660.xPMid:11939580Open DOISearch in Google Scholar

19. Kaarteenaho-Wiik, R., Sademies, O., Pääkkö, P., Risteli, J., Soini, Y. (2007). Extracellular matrix proteins and myofibroblasts in granulomas of sarcoidosis, atypical mycobacteriosis, and tuberculosis of the lung. Hum Pathol. 38(1): 147–153. https://doi.org/10.1016/j.humpath.2006.07.001 PMid:1699656510.1016/j.humpath.2006.07.001PMid:16996565Open DOISearch in Google Scholar

20. Polaček, V., Vidanović, D., Vasković, N., Knežević, M., Gledić, D., Aleksić-Kovačević, S., et al. (2010). Distribution of myofibroblasts, transforming growth factor-β1 and transforming growth factor-β1 receptor-I in granulomas caused by Mycobacterium avium complex in pigs. J Comp Pathol. 143(4): 326. https://doi.org/10.1016/j.jcpa.2010.09.05110.1016/j.jcpa.2010.09.051Open DOISearch in Google Scholar

21. Cvetkovikj, I., Mrenoshki, S., Krstevski, K., Djadjovski, I., Angjelovski, B., Popova, Z., et al. (2017). Bovine tuberculosis in the republic of Macedonia: Postmortem, microbiological and molecular study in slaughtered reactor cattle. Mac Vet Rev. 40(1): 43–52. https://doi.org/10.1515/macvetrev-2016-009710.1515/macvetrev-2016-0097Open DOISearch in Google Scholar