Molecular characterization and pathogenicity of Mycoplasma capricolum subsp. capricpolum from goats in Morocco

Noha Semmate1, Zaid Zouagui2, Zouhair Elkarhat1, Zahra Bamouh2, Siham Fellahi2, Noursaid Tligui2, Zineb Boumart1, Ouafaa Fassi Fihri2, Mehdi El Harrak1
1Research and Development Department, Multi-Chemical Industry, Mohammedia, Morocco
2Agronomic and Veterinary Institute Hassan II, BP: 6202, Rabat Institutions, Rabat, Morocco

Tóm tắt

AbstractMycoplasma capricolum subsp. capricolum (Mcc) is an important etiological agent of contagious agalactia (CA). CA affects small ruminants and is characterized by inducing mastitis, arthritis, kerato-conjunctivitis and respiratory symptoms. The aim of this study was to isolate and characterize Mcc from Moroccan goats with contagious agalactia. A total of 300 Alpine goats were monitored. Serology analysis, molecular identification, and isolation of Mcc were realized from suspected goats. An experimental study was conducted for isolated Mcc to determine their pathogenicity. Thus, clinical observation showed that respiratory symptoms were predominant in young animals, and other symptoms, such as mastitis, keratoconjunctivitis and lameness, were more frequently detected in adult goats. Of the 80 tested blood samples, 28 sera were seropositive for Mcc antibodies. Mcc was identified by polymerase chain reaction (PCR) in milk, lung tissue and synovial liquid samples. The isolation of Mcc was successful through bacterial culture from lung tissue. LppA gene sequence of this strain revealed 98.1% similarity with the reference strain (ATCC 27343), with 11 missense variants. Experimental infection resulted in severe and generalized CA disease in sheep and goats, confirming the high pathogenicity of the Moroccan Mcc isolate.

Từ khóa


Tài liệu tham khảo

Ashkenazy, H., S. Abadi, E. Martz, O. Chay, I. Mayrose, T. Pupko, and N. Ben-tal. 2016. ConSurf 2016 : an improved methodology to estimate and visualize evolutionary conservation in macromolecules. Nucleic Acids Research 44: 344–350. https://doi.org/10.1093/nar/gkw408.

Bamouh, Z., F. Fakri, M. Jazouli, N. Safini, K. Omari Tadlaoui, and M. Elharrak. 2019. Peste des petits ruminants pathogenesis on experimental infected goats by the Moroccan 2015 isolate. BMC Veterinary Research 15: 1–8. https://doi.org/10.1186/s12917-019-2164-6.

Benkirane, A., S. Amghar, and H. Kirchhoff. 1993. Analysis of Membrane Proteins of Mycoplasma capricolum Strains by SDS-PAGE and Immunoblotting. Journal of Veterinary Medicine Series B 40: 119–124. https://doi.org/10.1111/j.1439-0450.1993.tb00118.x.

Bergonier, D., X. Berthelot, and F. Poumarat. 1997. Contagious agalactia of small ruminants: current knowledge concerning epidemiology, diagnosis and control. OIE Review in Scienific Techique 16 (3): 848–873.

Brown, D.R., L.A. Zacher, L.D. Wendland, and M.B. Brown. 2005. Emerging mycoplasmoses in wildlife. In Mycoplasmas, Molecular Biology, Pathogenicity and Strategies for Control, ed. A. Blanchard and G. Browning, 383–414. Norfolk: Horizon Bioscience).

DaMassa, A.J., P.S. Wakenell, and D.L. Brooks. 1992. Mycoplasmas of goats and sheep. Journal of Veterinary Diagnostic Investigation 4: 101–113. https://doi.org/10.1177/104063879200400126.

De la Fe, C., A. Gutiérrez, J.B. Poveda, P. Assunção, A.S. Ramírez, and F. Fabelo. 2007. First isolation of Mycoplasma capricolum subsp. capricolum, one of the causal agents of caprine contagious agalactia, on the island of Lanzarote (Spain). Veterinary Journal 173: 440–442. https://doi.org/10.1016/j.tvjl.2005.09.011.

Elkarhat, Z., H. Charoute, L. Elkhattabi, A. Barakat, and H. Rouba. 2020. Potential inhibitors of SARS-cov-2 RNA dependent RNA polymerase protein: molecular docking, molecular dynamics simulations and MM-PBSA analyses. Journal of Biomolecular Structure & Dynamics 0: 1–14. https://doi.org/10.1080/07391102.2020.1813628.

Fakri, F.Z., A. Elhajjam, Z. Bamouh, M. Jazouli, Z. Boumart, K. Tadlaoui, O. Fassi-Fihri, and M. Elharrak. 2017. Susceptibility of Moroccan sheep and goat breeds to peste des petits ruminants virus. Acta Veterinaria Scandinavica 59: 1–6. https://doi.org/10.1186/s13028-017-0323-y.

Heller, M., R. Schwarz, G. Noe, J. Jores, A. Fischer, E. Schubert, and K. Sachse. 2015. First human case of severe septicaemia associated with Mycoplasma capricolum subsp . capricolum infection MicroSoc. JMM Case Reports 2: 1–3. https://doi.org/10.1099/jmmcr.0.000101.

Jaÿ, M., and F. Tardy. 2019. Contagious Agalactia In Sheep And Goats: Current Perspectives. Veterinary Medicine: Research and Reports 10: 229–247. https://doi.org/10.2147/vmrr.s201847.

Kumar, P., A. Roy, B.B. Bhanderi, and B.C. Pal. 2011. Isolation, identification and molecular characterization of Mycoplasma isolates from goats of Gujarat State, India. Veterinarski Arhiv 81: 443–458.

Laws, L. 1956. A Pleuropneumonia-Like Organism causing peritonitis in goat, Peritonitis. Australian Veterinary Journal 32: 326. https://doi.org/10.1111/j.1751-0813.1956.tb08243.x.

G. Mogoş, M. Daneş, D. Daneş, 2021. Potency evaluation of two commercial vaccines against contagious agalactia of small ruminants. Scientific Works. Series C. Veterinary Medicine.

Monnerat, M.P., F. Thiaucourt, J. Nicolet, and J. Frey. 1999. Comparative analysis of the lppA locus in Mycoplasma capricolum subsp. capricolum and Mycoplasma capricolum subsp. capripneumoniae. Veterinary Microbiology 69: 157–172. https://doi.org/10.1016/S0378-1135(99)00105-4.

Nicholas, R., R. Ayling, and L. McAuliffe. 2008. Respiratory diseases of small ruminants. In Mycoplasma Diseases of Ruminants, 1st ed., 169–198. Oxfordshire: CABI International.

Perreau, P., and A. Breard. 1979. La mycoplasmose caprine a m. capricolum. Comparative Immunology, Microbiology and Infectious Diseases 2: 87–97. https://doi.org/10.1016/0147-9571(79)90062-6.

Pourbakhsh, S.A., A.R. Abtin, A. Ashtari, M.A. Bayatzadeh, S.M. Barani, and E. Asli. 2015. Detection of Mycoplasma capricolum capricolum from goats of Qom province, Iran. Archives of Razi Institute 70: 45–50. https://doi.org/10.7508/ari.2015.01.007.

Rodríguez, J.L., C. Gutiérrez, D.L. Brooks, A.J. Damassa, J. Orós, and A. Fernández. 1998. A Pathological and Immunohistochemical Study of Goat Kids Undergoing Septicaemic Disease Caused by Mycoplasma capricolum subsp. capricolum, Mycoplasma mycoides subsp. capri and Mycoplasma mycoides subsp. mycoides (Large Colony Type). Journal of Veterinary Medicine Series B 45: 141–149. https://doi.org/10.1111/j.1439-0450.1998.tb00777.x.

Taoudi, A., H. Karib, D.W. Johnson, and M.M. Fassi-Fehri. 1988. Comparaison du pouvoir pathogène de trois souches de Mycoplasma capricolum pour la chèvre et le chevreau nouveau-né. Revue d'Élevage et de Médecine Vétérinaire des Pays Tropicaux 41: 353–358. https://doi.org/10.19182/remvt.8644.

Taoudi, D.W. Johnson, and D. Kheyyali. 1987. Pathogenicity of Mycoplasma capricolum in Sheep after Experimental Infection. Veterinary Microbiology 14: 137–144. https://doi.org/10.1016/0378-1135(87)90005-8.

Ying, H., Z. Nian-Zhang, Z. Ping, C. Yue-Feng, G. Peng-Cheng, Z. Jian-Jun, and L. Zhong-Xin. 2011. Improvement of specific polymerase chain reaction (PCR) for the identification of Mycoplasma capricolum subsp. capripneumoniae. African Journal of Biotechnology 10: 17291–17296. https://doi.org/10.5897/AJB11.2016.