Miliary Bovine Tuberculosis in Buffaloes in Al-Muthanna Governorate, Iraq
DOI:
https://doi.org/10.6000/1927-520X.2022.11.10Keywords:
Bubalus bubalis, miliary TB, M. Bovis, tuberculosis, Löwenstein-Jensen mediaAbstract
Background: Bubalus bubalis (river buffaloes) are widely distributed in the southern marshes of Iraq. This study intends to record a case of miliary tuberculosis in buffalo for the first time in Al Muthanna abattoir, Iraq, with its clinical, gross, and histopathological findings and microbiological investigations.
Case Description: Ten years old buffalo showed chronic cough, infertility, emaciation, debilitation, lower milk production, loss of weight, and loss of appetite for 2 months; during meat inspection, thousands of various size typical tubercles, yellowish, granulomatous, and caseous lesions were distributed over all the body.
Results: Microscopically, features of tuberculosis granuloma lesions were observed and revealed oval or round caseous necrosis with irregular central areas. Moreover, mineralization was enclosed by a thin to a broad layer of diverse inflammatory cells and solid collagenous connective tissue sheath. Moreover, a direct smear from the lesion stained by the Ziehl-Neelsen stain showed a slightly curved, red, and straight rod that was seen alone or in clusters, indicating the bacilli of tuberculosis. Additionally, the growing bacteria on the Löwenstein-Jensen media slant revealed flat, smooth, moist, white, not pigmented colonies suggestive of M. Bovis that revealed typical results with traditional biochemical tests, including negative reaction to nitrate reduction, niacin test, and deamination of pyrazinamide.
Conclusion: For the author’s knowledge, this is the first case report of miliary bovine tuberculosis in buffalo in Iraq. The diagnosis was made according to clinical signs, gross pathology, and histopathological features supported by Ziehl-Neelsen stain and bacterial isolation. The author recommends future epidemiological molecular studies to improve the diagnosis tools of bovine tuberculosis in Iraq and investigate the causative agent M. Bovis to establish the roles for disease control that becomes much more challenging.
References
Al-Salihi KA. An insight into veterinary education in Iraq. Downloaded from veterinaryrecord.bmj.com 2012; 316/Veterinary Record. Published by group.bmj.com https://doi.org/10.1136/vr.e5145
Batista HR, Sarturi C, Stelmachtchuk FN, Oliveira DR, Morini AC, Gennari SM, et al. Prevalence and risk factors associated with ectoparasite infestation of buffaloes in an Amazonian ecosystem. Parasit Vect 2018; 11: 335. https://doi.org/10.1186/s13071-018-2917-2
Batista HR, Passos CTS, Nunes Neto OG, Sarturi C, Coelho APL, Moreira TR, et al. Factors associated with the prevalence of antibodies against Brucella abortus in water buffaloes from Santarém, Lower Amazon region, Brazil. Transbound Emerg Dis 2020; 67: 44-8. https://doi.org/10.1111/tbed.13192
Villanueva MA, Mingala CN, Tubalinal GAS, Gaban PBV, Nakajima C, Suzuki Y. Emerging Infectious Diseases in Water Buffalo: An Economic and Public Health Concern. London: IntechOpen 2018. https://doi.org/10.5772/intechopen.73395
Khademi P, Ownagh A, Mardani K, Khalili M. Prevalence of Coxiella burnetii in milk collected from buffalo (water buffalo) and cattle dairy farms in Northwest of Iran. Comp Immunol Microbiol Infect Dis 2019; 67: 101368. https://doi.org/10.1016/j.cimid.2019.101368
Michel AL, Muller B, van Helden PD. Mycobacterium Bovis at the animal-human interface: a problem, or not? Vet Microbiol 2009; 140: 371-81. https://doi.org/10.1016/j.vetmic.2009.08.029
WHO. The End TB Strategy 2018. Retrieved from: HTTPS: //www.who.int/tb/ strategy/en/ (accessed July 1, 2019).
WHO. Roadmap for Zoonotic Tuberculosis. 2017; Retrieved from: https://www.who.int/tb/publications/2017/zoonotic_TB/ en/ (accessed July 1, 2019).
De la Rua DR. Human Mycobacterium Bovis infection in the United Kingdom: incidence, risks, control measures and review of the zoonotic aspects of bovine tuberculosis. Tuberculosis (Edinb). J Tube 2006; 86: 77-109. https://doi.org/10.1016/j.tube.2005.05.002
Thoen CO, Lobue P, Enarson AD, Kaneene BJ, de Kantor NI. Tuberculosis: a re-emerging disease of animals and humans. Vet Ital 2007; 45: 135-181.
Andreazza D, Boos GS, Boabaid FM, Wouters ATB, Wouters F, Souza SO, Menegat MB, Driemeier D. Caracterização histológica e imuno- histoquímica das lesões de tuberculose em bovinos e de linfadenite granulomatosa em suínos. Pesquisa Veterinária Brasileira 2015; 35; 2: 129-136. https://doi.org/10.1590/S0100-736X2015000200006
Nascimento UFS, Rizzo H, de Andrade RLFS, Menezes HCO, da Silva TR. Miliary tuberculosis in cattle in Sergipe State. Brazil Ciência Animal 2021; 31(2): 164-172.
Sweetline Anne N, Ronald BSM, Kumar TMAS, Kannan P, Thangavelu A. Molecular identification of Mycobacterium tuberculosis in cattle. Vet Microbiol 2017; 198: 81-87. https://doi.org/10.1016/j.vetmic.2016.12.013
Al Salihi KA. A study on tuberculosis in camelids in Al-Al Muthanna governorate / Iraq. 2016; Conference: 29th World Buiatrics Congress, Dublin, Ireland.
De Kantor IN, Kim SJ, Frieden T, Laszlo A, Luelmo F, Norval P, et al. Part I: Organization and Management. Geneva: Laboratory Services in Tuberculosis Control 1998; WHO/TB/98.258: 38-41.
Ahmed WA, Al-Gburi NM, Rassol HS. An outbreak of hemorrhagic septicemia in a vaccinated herd of domestic water buffalo in Thi Qar province, Iraq: Clinical and pathological observations. Mirror Res Vet Sci Anim (MRVSA) 2014; 3(2): 36-43.
National survey of livestock in Iraq for the year. Ministry of agriculture 2008.
dos Santos LS, Sa JC, dos Santos Ribeiro DL, Chaves NP, da Silva Mol JP, Santos RL, da Paixao TA, de Carvalho Neta AV. Detection of Brucella spp. Infection through serological, microbiological, and molecular methods applied to buffaloes in Maranhao state, Brazil. Tropical Animal Health and Production 2017. https://doi.org/10.1007/s11250-017-1238-3
Hassan AS, Farba SM, GUmel AB, Lubuma JM-S. Dynamics of mycobacterium and bovine tuberculosis in human-buffalo population. Comput Math Meth Med 2014. https://doi.org/10.1155/2014/912306
Huang ZYX, De Boer WF, Van Langevelde F, Xu C, Ben Jebara K, Berlinger F, Hht P. Dilution effect in bovine tuberculosis: Risk factors for regional disease occurrence in Africa. Proceedings of The Royal B Society 2013. https://doi.org/10.1098/rspb.2013.0624
Khattak I, Mushtaq MH, Ahmad MD, Khan MS, Chaudhry M, Sadique U. Risk factors associated with Mycobacterium Bovis skin positivity in cattle and buffalo in Peshawar, Pakistan. Tropical Animal Health and Production 2015. https://doi.org/10.1007/s11250-015-0976-3
Buddle BM, de Lisle GW, Griffin JF, Hutchings SA. Epidemiology, diagnostics, and management of tuberculosis in domestic cattle and deer in New Zealand in the face of a wildlife reservoir. N Z Vet J 2015; 63(Suppl 1): 19-27. https://doi.org/10.1080/00480169.2014.929518
Tsairidou S, Woolliams JA, Allen AR, Skuce RA, McBride SH, Wright DM, et al. Genomic Prediction for Tuberculosis Resistance in Dairy Cattle. PLoS ONE 2014; 9(5): e96728. https://doi.org/10.1371/journal.pone.0096728
Waters WR, Thacker TC, Nelson JT, DiCarlo DM, Maggioli MF, Greenwald R, et al. Virulence of two strains of Mycobacterium Bovis in cattle following aerosol infection. J Comp Pathol 2014; 151: 410-9. https://doi.org/10.1016/j.jcpa.2014.08.007
Chaddock MH. Tuberculosis. In: Smith BP (ed). Large Animal Internal Medicine. 3rd ed. Mosby Publications: London, UK, 2002; pp. 588-589.
Askar S, Askar TK, Guzel M. Effect of Mycobacterium Bovis infection in cattle on changes in appetite-related hormones. Austral J Vet Sci [online]. 2018; 50(3): 119-123. https://doi.org/10.4067/S0719-81322018000300119
Luboya LW, Malangu M, Kaleka M, Ngulu N, Nkokele B, Maryabo K, Pourrut X, Vincent T, Gonzalez JP. An assessment of caprine tuberculosis prevalence in Lubum-Bashi slaughterhouse, Democratic Republic of Congo. Trop Anim Health Prod 2017; 49(4): 875-878. https://doi.org/10.1007/s11250-017-1252-5
Amemor EA, Sackey SO, Yebuah N, Folitse RD, Emikpe BO, Afari E, et al. The prevalence of tuberculosis in cattle and their handlers in north Tongu, Volta region, Ghana. Afr J Infect Dis 2017; 11(1): 12-17. https://doi.org/10.21010/ajid.v11i1.2
Fitzgerald SD, Kaneene JB. Wildlife reservoirs of bovine tuberculosis worldwide: hosts, pathology, surveillance, and control. Vet Pathol 2013; 50(3): 488-99. https://doi.org/10.1177/0300985812467472
Renwick AR, White PCL, Bengis RG. Bovine tuberculosis in southern Africa wildlife: A multispecies host-pathogen system. Epidemiol Infect 2007; 135: 529-540. https://doi.org/10.1017/S0950268806007205
Sanchez J, Tomás L, Ortega N, Buendía AJ, del Rio L, Salinas J, Bezos J, Caro MR, Navarro JA. Microscopical and immunological features of tuberculoid granulomata and cavitary pulmonary tuberculosis in naturally infected goats. J Comp Pathol 2011; 145(2-3): 107-17. https://doi.org/10.1016/j.jcpa.2010.12.006
Galiza GJN, Silva MLCR, Dantas AFM, Simões SVD, Riet-Correa F. Doenças do sistema nervoso de bovinos no semiárido nordestino. Pesquisa Veterinária Brasileira 2010; 30(3): 267-276. https://doi.org/10.1590/S0100-736X2010000300014
Oliveira LED, Nonato IA, Nascimento GAM, Nascimento AAT, Serrano MTL, Carvalho GDC. Tuberculose bovina protaraída: Relato de caso. Jornal Brasileiro de Ciência Animal 2012; 5(10): 397-405.
Coelho AC, Pinto ML, Coelho AM, Rodrigues J. Ziehl-Neelsen staining as a fast method in the diagnosis of ovine paratuberculosis. Medicina Veterinária, Arq Bras Med Vet Zootec 2008; 60(5): 1097-1102. https://doi.org/10.1590/S0102-09352008000500009
Freitas JA, Guerra JL, Panetta JC. Características da tuberculose observada em búfalos abatidos para consumo: aspectos patológicos e identificação de micobactérias. Br J Vet Res Anim Sci 2001; 38(4): 170-176. https://doi.org/10.1590/S1413-95962001000400005
Roex Nl, Koets AP, van Helden PD, Hoal EG. Gene polymorphisms in African buffalo associated with susceptibility to bovine tuberculosis infection. PLoS One 2013; 8(5): e64494. https://doi.org/10.1371/journal.pone.0064494
Linderot de Cardona K, De Gracia Scanapeico A, Braun PG. First results on small ruminant brucellosis and tuberculosis and caprine arthritis-encephalitis in El Salvador. Trop Anim Health Prod 2016; 48(5): 1083-1087. https://doi.org/10.1007/s11250-016-1044-3
Roche B, Dobson AP, Guegan JF, Rohani P. Linking community, and disease ecology: The impact of biodiversity on pathogen transmission. Philos Trans Roy Soc B 2012; 367: 2807-2813. https://doi.org/10.1098/rstb.2011.0364
Corner LAL. The role of wild animal populations in the epidemiology of tuberculosis in domestic animals: How to assess the risk. Vet Microbiol 2006; 112: 303-312. https://doi.org/10.1016/j.vetmic.2005.11.015
Alfano F, Peletto S, Lucibelli MG, et al. Identification of single nucleotide polymorphisms in Toll-like receptor candidate genes associated with tuberculosis infection in water buffalo (Bubalus bubalis). BMC Genet 2014; (15): 139. https://doi.org/10.1186/s12863-014-0139-y
Javed MT, Shahid AL, Farooqi FA, Akhtar M, Cardenas GA, Wasiq M, Cagiola M. Association of some of the possible risk factors with tuberculosis in water buffalo around two cities of Punjab Pakistan. Acta Trop 2010; 115: 242-247. https://doi.org/10.1016/j.actatropica.2010.04.004
Downloads
Published
How to Cite
Issue
Section
License
Policy for Journals/Articles with Open Access
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgment of the work's authorship and initial publication in this journal.
- Authors are permitted and encouraged to post links to their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work