Research Article | Vol. 6, Issue 2 | Journal of Clinical Immunology & Microbiology | Open Access

Prevalence of Bovine Tuberculosis in Cattle Slaughtered at the Gwagwalada Abattoir in the Federal Capital Territory (FCT), Nigeria: A One Year Retrospective Study

Mairabo Rebecca Rabi1, Abdullahi Musa2, Mailafia Samuel3*, Adah Bridget Jessica Maria3, Echioda- Ogbole Martha3
1Department of Veterinary Public Health, Faculty of Veterinary Medicine, University of Abuja, Nigeria
2Ministry of Agriculture and Natural Resources, Nasarawa State, Nigeria
3Department of Veterinary Microbiology, Faculty of Veterinary Medicine, University of Abuja, Nigeria

*Correspondence author: Mailafia Samuel, Department of Veterinary Microbiology, Faculty of Veterinary Medicine, University of Abuja, Nigeria; Email: [email protected]; [email protected] 

Citation: Rabi MR, et al. Prevalence of Bovine Tuberculosis in Cattle Slaughtered at the Gwagwalada Abattoir in the Federal Capital Territory (FCT), Nigeria: A One Year Retrospective Study. J Clin Immunol Microbiol. 2025;6(2):1-8.

Copyright© 2025 by Rabi MR, et al. All rights reserved. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Received
13 July, 2025
Accepted
28 July, 2025
Published
04 August, 2025

Abstract

Bovine Tuberculosis (BTB) remains a significant zoonotic disease with implications for public health, food safety, and livestock productivity. This retrospective study aimed at determining the prevalence of BTB in cattle slaughtered at the Gwagwalada Abattoir, FCT, Nigeria based on gross pathological lesions for a period of one year ranging from April 2024 to April 2025. A total of 4,492 cattle were randomly sampled based on convenience. They were examined post-mortem for caseous or granulomatous lesions which were suggestive of Bovine Tuberculosis. Records were obtained from the veterinary record books in the abattoir and analysed based on descriptive statistics. Out of 4,492 cases examined, 17 cases (0.38%) exhibited gross pathologic lesions typical of BTB. Prevalence based on organ distribution showed that the lungs was the most frequently affected organ, accounting for 14 of the 17 cases (82.4%); while the liver was involved in 3 cases (17.6%). The monthly distribution showed the highest number of cases were reported in April 2024 which had 3 cases with a 1.26% prevalence. There were no cases reported between February and April 2025. Our findings highlight the endemicity of BTB among slaughtered cattle in the Gwagwalada area, despite intervention programs. The prevalence therefore underscores the need for increased routine surveillance, testing and pre-testing of animals before slaughter, implementation of adequate government control programs with improved meat inspection techniques and public awareness campaigns to mitigate zoonotic transmission risks.

Keywords: Bovine Tuberculosis; Abattoir Surveillance; Gross Lesions; Gwagwalada; Cattle; Nigeria

Introduction

Bovine Tuberculosis (BTB) is a chronic infectious disease of cattle caused by Mycobacterium bovis. It is a major zoonotic disease, and cattle are the main reservoir for infection in humans. The disease is widespread to the human population primarily through the consumption of raw or improperly pasteurized milk. It is well known that meat and meat products from infected animals are sources of infections in man [1]. The disease also affects domestic, wild, laboratory and aquatic animals and is globally associated with huge economic losses and adverse public health implications [2-4]. The disease has a critical public health burden and causes severe economic losses including impairment of animal health, production losses, high costs of eradication programs and trade restrictions [5]. In developing countries such as Nigeria, the disease poses a significant challenge and setbacks to livestock productivity, public health, and the economy in general.

Bovine Tuberculosis has significant zoonotic and economic implications as a result of the disease burden globally. Over 50 million cattle are estimated to be infected with M. bovis and M.tuberculosis. BTB is a worldwide endemic disease resulting in production loss costing the tune of about 3 billion USD [2]. Annual losses in Nigeria ranging between 13-24 billion Naira are due to condemnation of TB affected meat or carcasses [6,7]. The African region carries the heaviest burden of tuberculosis cases followed by the South-East Asian region [8]. BTB is endemic in Nigeria with the prevalence estimated at 2.94% according to a study conducted between 2020 and 2022 by Danladi, et al [9]. There are many limitations associated with the animal disease reporting system in Nigeria as seen in cases of disease reporting of BTB [10]. Reports from most states of the federation are inconsistent, not giving a true picture of BTB in their region.

In humans, BTB causes pulmonary and extrapulmonary tuberculosis leading to a weakened immune system [11]. A 10% tuberculosis prevalence was recorded in a cross- section of sputum sampled from Nigerian livestock traders, with M. bovis strains detected in two of the seven TB cases from these occupational exposure individuals 12[. Since the disease is mostly detected at slaughter during meat inspection and occasionally during sporadic screening for the disease, people who attend to, and are in close contact with cattle such as herdsmen, butchers, and veterinarians, as well as the general public that consume fresh milk or infected meat are exposed to BTB [13]. In cattle BTB is characterised by chronic granulomatous lesions with formation of tubercles or nodules in various organs most commonly the lungs and associated lymph nodes. Lesions can also be spread to other organs such as liver, spleen, Gastrointestinal Tract (GIT), kidneys, uterus and body [14]. BTB is re-emerging in most developing countries including Nigeria, due to inadequate facilities and weak or non-existent surveillance, control measures and established control programs.

Despite ongoing national efforts to control zoonotic diseases, including BTB, abattoir-based surveillance remains underutilized in many parts of Nigeria. Limited data exists on the prevalence of BTB in cattle slaughtered within Abuja and its environs, and there is insufficient documentation to support risk assessment and control measures. This lack of data hinders effective disease control and public health interventions, contributing to the potential risk of zoonotic transmission. Understanding the prevalence and distribution of BTB in slaughtered cattle is essential for improving meat inspection protocols, guiding policy for disease control, and protecting public health. This study provides baseline epidemiological data critical for livestock health management and zoonotic risk reduction in the Gwagwalada region. Abattoir surveillance is relatively cheap and large number of diagnostic specimens from slaughtered animals are available compared to live animals in the field [15]. It encourages a better detection of infection by skilled manpower than livestock owners [15]. Early detection through abattoir surveillance can help inform national and local control strategies. This study was therefore carried out to determine the prevalence of BTB in the Gwagwalada abattoir with the view of analysing the disease epidemiology in the study area.

Methodology

Study Area

The study was conducted in the Gwagwalada abattoir located in Gwagwalada Area Council, one of the 6 area councils in the FCT Abuja, between the months of April 2024-April 2025. The Gwagwalada area council falls within latitude 8°56′ 29″ North and longitude 7°5′ 31″ and 7° 39′ East and has a land area of 1043 km2 [16]. Gwagwalada town has a hot, humid, and tropical climate. Its major elements have regimes that are intermediate from those of the Southern and Northern regions of the country [17]. The average annual temperature in this region is between 30 and 37 °C, with March being the hottest month. The average annual rainfall in this region is about 1,650 mm [18].

Figure 1: Map of the Federal Capital Territory, Nigeria showing Gwagwalada Area Council where the study was carried out. Source [19].

Study Design

A retrospective study was conducted on cattle slaughtered at the Gwagwalada Abattoir, Abuja, between April 2024 and April 2025. A total of 4,492 cattle were inspected post-mortem for tuberculous lesions. The sample size was calculated using the formula developed by Thrusfield [20].

Where:

N = required sample size

Z = standard normal deviate at 95% confidence level (1.96) P = expected prevalence (50%)

q=1-p

d= desired absolute precision (1.5%)

Substituting the values:

N =1.96 2 x 0.5 x (1 – 0.5)/0.015 2

= 3.8416 x 0.5 x 0.5/0.000225

= 0.9604/0.000225 = 4,268

A minimum sample size of 4,268 animals was calculated. To increase the precision, the sample size was increased to 4,492.

Sampling Techniques

Sampling was done based on convenience and availability of records. Data for the study was obtained from the veterinary inspection record books in the abattoir to cover the period of the study. The records included daily post mortem inspection records of cattle during the period of slaughter. Gross pathology reports were also reviewed. Post mortem examinations were carried out by veterinarians in the abattoirs as described by Corner and Grist [21]. Visual post-mortem inspection was carried out to identify tuberculosis lesions based on characteristic granulomas, caseation, and calcification in organs focusing on lymph nodes, lungs and liver amongst others. Cattle found with typical tuberculous lesions were recorded. No laboratory confirmation was performed. Prevalence was calculated as the number of cattle with visible BTB lesions divided by the total number inspected. Monthly case distribution was tabulated.

Results

The study revealed that out of a total of 4,492 cattle sampled at the Gwagwalada abattoir from April 2024 to April 2025, a total of 17 showed gross lesions consistent with BTB, giving an overall prevalence of 0.38. Table 1 shows the monthly distribution of the prevalence of BTB in the Gwagwalada abattoir within the study period. The results show the highest prevalence of 1.26 for the month of April, 2024 while the lowest prevalence in 2024 was 0.30 in June. In 2025, the highest prevalence was reported only in January with a prevalence rate of 0.27. However, the months of February, March and April of 2025 had no reported cases of BTB. Fig. 1 depicts the relationship between the number of cattle sampled for each month and the number of reported cases of BTB recorded. The chart clearly shows the highest number (3) of the cases was recorded in April 2024. This was followed by 2 cases each for the months of May, July, September, October and November in 2024. The least cases (1) with the lowest prevalences were recorded for the months of June, August and December in 2024 and January of 2025 respectively. There were no cases recorded for the months of February, March and April of 2025. Table 2 shows the distribution of the prevalences of BTB in Gwagwalada abattoir based on the organs that were affected. The lungs recorded the highest prevalence of BTB at 82.35(14 cases) while the lowest prevalence was recorded in the liver (17.65). Other organs examined such as the lymph nodes, tissues, kidneys and gastrointestinal tract (GIT) had no prevalence rates.

Month

Year

Number of Cattle Sampled

Number of BTB Cases Identified

Prevalence (%)

April

2024

239

3

1.26

May

2024

398

2

0.50

June

2024

328

1

0.30

July

2024

497

2

0.40

August

2024

294

1

0.34

September

2024

341

2

0.59

October

2024

371

2

0.54

November

2024

476

2

0.42

December

2024

245

1

0.41

January

2025

367

1

0.27

February

2025

330

0

0.00

March

2025

339

0

0.00

April

2025

267

0

0.00

Total

4492

17

0.38

Total

Table 1: Monthly distribution of cases of Bovine Tuberculosis in Gwagwalada Abattoir from April 2024-April 2025

Figure 2: Dissipation of reported cases of Bovine Tuberculosis in Gwagwalada abattoir from April 2024-April 2025.

Organ Affected

Number of Cases

Prevalence (%)

Lungs

14

82.35

Liver

3

17.65

Others

0

0

TOTAL

17

100

Table 2: Distribution of prevalence of Bovine Tuberculosis in Gwagwalada Abattoir from April 2024-April 2025 based on affected organs.

Discussion

The systematic study of BTB in slaughtered cattle in Gwagwalada abattoir revealed the prevalence rate of 0.38% .This finding partially agrees with a retrospective study carried out by Danladi, et al., across all the states in Nigeria between 2020-2022 which revealed that across the FCT ,the BTB prevalence ranged from 0.36 to 2.19% [9]. However, this prevalence rate is low when compared to a retrospective study carried out across abattoirs in the FCT from 2015 to 2019 where Adamu, et al., reported a higher prevalence of 0.92% in the Gwagwalada abattoir for slaughtered cattle that had tuberculous lesions [22]. The reason behind the differences in prevalence rates might be due to climate change and seasonal variations within the years. Also, emerging strains of Mycobacterium bovis might adapt to these environmental factors thereby leading to higher preponderance of these microorganisms in different geographical locations. The relatively lower prevalence observed in our study may imply adequate meat inspection procedures by veterinarians and proper identification of suspected lesions by meat inspectors. The change in patterns of selecting cattle by the butchers has also a major role in reducing cases of tuberculous lesions in our abattoir. Also, the present economic challenges in the country entails that the butchers may be very watchful in the selection of animals brought for slaughter. This aims at evading carcass condemnation by meat inspectors or veterinarians.

In Nigeria, most of the studies that were based on gross pathological examination at the abattoir have reported varying prevalences in different parts of the country. Okeke, et al., reported an 11% prevalence of BTB lesions in cattle slaughtered at Jos abattoir Plateau State, a peak prevalence of 12.73% was reported in Yola, Adamawa by Ejeh, et al., a 4.47% prevalence in Oyo by Jenkins, et al., and a 0.54% prevalence in Ogbomoso, Oyo State by Ameen, et al. [2,23-25]. In other African countries like Cameroon and Rwanda, a 0.18 to 0.82% and a 0.9% (148/16753) prevalence rates were reported by Awah Ndukum, et al., and Habarugira, et al., respectively [26,27]. Our study only covered Gwagwalada abattoir which indicates that a larger epidemiological survey of BTB is required in the FCT and other parts of Nigeria where this study has not been conducted. Detailed information is required to understand the disease pattern, transmission and spread of BTB in Nigeria.

The predominance of tuberculous lesions in the lungs of the slaughtered cattle recorded in our studies was 82.35%. Reports have shown that the pulmonary parenchyma serves as a very noble predilection site for the proliferation of Mycobacterium bovis [28,29]. There is however limited evidence of studies reporting BTB lesions found exclusively in the lungs without involvement of lymph nodes in cattle. However, one retrospective study from Bauchi State, Nigeria, specifically noted that during a 10-year abattoir survey, tuberculous lesions were observed in the lungs (11.87%), liver, and heart, but none were observed in the lymph nodes or intestines [30]. This suggests that, at least in this population and time frame, BTB lesions can be found in the lungs alone during abattoir inspection.

The distribution of prevalence of tuberculous lesions also implicated tuberculous lesions in the liver of the cattle to be 17.65% The presence of lesions in the liver agrees with similar studies that have documented tuberculosis lesions in the liver of cattle, often as part of generalized or extrapulmonary tuberculosis. Jajere, et al., reported a prevalence of 5.93% of all BTB lesions were found in the liver in a retrospective study carried out in the Bauchi Municipal abattoir, which is lower than the prevalence reported in our study [30]. In Ibadan, Nigeria, Adelakun, et al., reported a higher prevalence of 26.1% for condemned livers with suspected BTB lesions [31]. This indicates that though the primary route of BTB infection is through the respiratory route, its spread to other parts of the body is possible as described by Radostits, et al. This also highlights the liver as a significant site for BTB pathology in advanced or disseminated cases [32-36]. Our result may also indicate the possibility of systemic spread or misidentification without laboratory confirmation. The lack of a clear trend across the months studied implies that environmental or climatic factors may not be major contributors to case fluctuations in this context. This agrees with Dauda, et al., who reported that BTB cases along with other diseases detected in the Kubwa abattoir in the F.C.T (Contagious Bovine Pleuropneumonia, Dermatophilosis, Abscess, and Moneziasis) did not show significant variations across the months [37]. This also agrees with reports from Ameen, et al., Raufu and Ameh and Awah Ndukum et al. [7,25,26]. Cattle sourced from various regions with differing climates and management practices may contribute to the dilution of any specific trend or pattern.

The variation in monthly case numbers could also be due to changes in cattle supply sources. This is especially evident in the last 3 months of this study where no TB cases were reported. This could also be due to the inability of visual inspection techniques only to detect early infections or infections presented sub clinically. Certain months may have higher inflows from regions with more prevalent TB infections. Furthermore, increased slaughter activities around festive or market periods can elevate the chance of detecting cases, though this pattern was not strongly evident in the data.

Limitations

It is important to note that this study relied solely on gross pathological inspection, which may under-detect early or less advanced cases of tuberculosis. The absence of laboratory confirmation may also result in misclassification or underestimation of true prevalence.

Conclusion

The objectives of this research have been greatly achieved. We were able to identify the overall prevalence of tuberculous lesions in slaughtered cattle to be of 0.38%.The results of the dissipation of reported tuberculous lesions in Gwagwalada showed that the highest tuberculous lesion were recorded in April 2024 with a prevalence rate of 1.26% while the lowest prevalence rate was recorded in January 2025.The months of February, March and April of 2025 recorded no prevalence of tuberculous lesions .Based on the distribution of the tuberculous lesions in affected organs, the lungs harbours the highest with the prevalence rate of 82.35% while the liver recorded the lowest with the prevalence rate of 17.65%. Other organs such as the kidneys, lymph nodes, GIT had no recorded prevalence. BTB is therefore endemic in the cattle in areas covered by this study. The presence of BTB remains a public health concern given its zoonotic potential and the risk it poses to abattoir workers and consumers. This study underscores the need for enhanced surveillance measures, including laboratory confirmation and traceback systems using higher molecular technology to better understand the epidemiology of BTB in the region. Retrospective studies of this nature should be conducted in other parts of the F.C.T and Nigeria at large to reveal the true status of BTB in the country.

Conflict of Interest

The authors have declared no conflict of interest.

Funding

The research was carried out by Rabi Rebecca Mairabo under the supervision of Samuel Mailafia and contributions of Abdullahi Musa, Bridget Maria Jessica Adah and Martha Edioche-Ogbole. All authors contributed to the success of this publication.

References

  1. Ayele W, Neill S, Zinsstag J, Weiss M, Pavlik I. Bovine tuberculosis: an old disease but a new threat to Africa. Int J Tuberc Lung Dis. 2004;8(8):924-37.
  2. Ejeh E, Raji M, Bello M, Lawan F, Francis M, Kudi A, et al. Prevalence and direct economic losses from bovine tuberculosis in Makurdi, Nigeria. Vet Med Int. 2014;2014:904861.
  3. Ibironke AA, Fasina FO. Socio-economic implications of bovine liver rejection in a major abattoir in south-western Nigeria. Rev Cienc Agrar. 2010;33(2):211-6.
  4. Kwaghe AV, Ameh AJ, Ambali AG, Kudi AC, Kachalla MG. Prevalence and economic losses from bovine tuberculosis in Maiduguri, Borno State, Nigeria. Int J Life Sci. 2015;4(4):283-7.
  5. Terrestrial Manual of Bovine Tuberculosis: Chapter 2.4.7. World Health Organization for Animal Health, Paris; 2009.
  6. Cadmus S, Adesokan H, Adejuwon T, Adeyemi M. Retrospective study on bovine tuberculosis and other diseases of public health importance at Oko-Oba Abattoir, Lagos State. 2010
  7. Raufu I, Ameh J. Prevalence of Bovine Tuberculosis in Maidguri Nigeria–an abbattoire study. Bull Anim Health Prod Afr. 2010;58(2).
  8. Hauer A, De Cruz K, Cochard T, Godreuil S, Karoui C, Henault S, et al. Genetic evolution of Mycobacterium bovis causing tuberculosis in livestock and wildlife in France since 1978. PLoS One. 2015;10(2):e0117103.
  9. Danladi J, Kwaghe AV, Olasoju T, Ibrahim HI, Buba MI, Dakogi AY, et al. Prevalence, trends, and magnitude of bovine tuberculosis in slaughtered cattle across States in Nigeria, 2020-2022: a retrospective study. PAMJ One Health. 2024;15(20).
  10. Ihekweazu C, Michael CA, Nguku PM, Waziri NE, Habib AG, Muturi M, et al. Prioritization of zoonotic diseases of public health significance in Nigeria using the one-health approach. One Health. 2021;13:100257.
  11. Pal M, Berhanu G, Feyisa D, Mideksa B, Kandi V. Bovine Tuberculosis: A Review of Molecular Diagnostic Methods and Impact on Public Health. Am J Microbiol Res. 2021;9(1):1-8.
  12. Adesokan H, Jenkins A, Van Soolingen D, Cadmus S. Mycobacterium bovis infection in livestock workers in Ibadan, Nigeria: evidence of occupational exposure. Int J Tuberc Lung Dis. 2012;16(10):1388-92
  13. Bilal S, Iqbal M, Murphy P, Power J. Human bovine tuberculosis–remains in the differential. J Med Microbiol. 2010;59(11):1379-82.
  14. Mailafia S, Olabode HOK. Prevalence of Tuberculosis in Cattle in FCT Nigeria Using Prima TB STAT-PAK® Assay. Niger Vet J. 2016;35(4).
  15. Cameron A. Manual of basic animal disease surveillance. AusVet Anim Health Serv. 2012:1-92.
  16. Oluwatuyi F. Environmental issues in Gwagwalada Area Council of the federal capital territory. J Environ Stud. 2018;13(4):43-55.
  17. Abdullahi M, Okobia E, Hassan S. Assessment of ambient atmospheric concentration of volatile organic compounds in Abuja-Nigeria. J Chem Biol Phys Sci. 2012;2(3):1637-47.
  18. Kanee AK, Bello M, Olabode SM. Climate and weather patterns in Gwagwalada: A comprehensive review. Niger J Climate Change. 2020;5(2):65-78.
  19. Oguntade E, Shamarina S, Meenakshii N, Alaba LS. Factors influencing malaria knowledge, attitude and practice in Gwagwalada. Int J Sci Healthc Res. 2019;3:168-78.
  20. Thrusfield M. Veterinary epidemiology. 4th John Wiley & Sons; 2013.
  21. Corner L. Post mortem diagnosis of Mycobacterium bovis infection in cattle. Vet Microbiol. 1994;40(1-2):53-63.
  22. Adamu A, Adikwu A, Yikawe S, Mambula S, Idoko S, Garba B, et al. Prevalence of bovine tuberculosis lesions in cattle slaughtered in the Federal Capital Territory Abattoirs, Nigeria.
  23. Okeke LA, Fawole O, Muhammad M, Okeke IO, Nguku P, Wasswa P, et al. Bovine tuberculosis: a retrospective study at Jos abattoir, Plateau State, Nigeria. Pan Afr Med J. 2016;25:202.
  24. Jenkins AO, Cadmus SI, Venter EH, Pourcel C, Hauk Y, Vergnaud G, et al. Molecular epidemiology of human and animal tuberculosis in Ibadan, Southwestern Nigeria. Vet Microbiol. 2011;151(1-2):139-47.
  25. Ameen S, Adedeji O, Raheem A, Leigh O, Rafiu T, Ige A. Current status of bovine tuberculosis in Ogbomoso area of Oyo state. Middle-East J Sci Res. 2008;3(4):207-10.
  26. Awah Ndukum J, Kudi AC, Bradley G, Ane-Anyangwe I, Fon-Tebug S, Tchoumboue J. Prevalence of bovine tuberculosis in abattoirs of the littoral and Western highland regions of Cameroon: a cause for public health concern. Vet Med Int. 2010;2010:495015.
  27. Habarugira G, Rukelibuga J, Nanyingi MO, Mushonga B. Bovine tuberculosis in Rwanda: prevalence and economic impact evaluation by meat inspection at Societe d’Abattoir de Nyabugogo-Nyabugogo Abattoir, Kigali. J S Afr Vet Assoc. 2014;85(1):1-5.
  28. Baloch J, Leghari SASRA. Prevalence and pathological lesions of bovine tuberculosis assessment through routine procedures of meat inspection in infected cattle in Karachi metropolitan corporation abattoirs. Pure Appl Biol. 2019.
  29. Saidu A, Okolocha E, Gamawa A, Babashani M, Bakari N. Occurrence and Distribution of bovine tuberculosis (Mycobacterium bovis) in Slaughtered cattle in the abattoirs of Bauchi State, Nigeria. Vet World. 2015;8:432-7.
  30. Jajere S, Atsanda N, Bitrus A, Hamisu T, Goni M. A retrospective study of bovine tuberculosis at the municipal abattoir of Bauchi State, Northeastern Nigeria. Vet World. 2018;11:598-605.
  31. Adelakun O, Akinseye V, Adesokan H, Cadmus S. Prevalence and economic losses due to bovine tuberculosis in cattle slaughtered at Bodija Municipal Abattoir, Ibadan, Nigeria. Folia Vet. 2019;63:41-7.
  32. Hamid A, Abdelali B, Mohammed H, Hind Y, Mohammed B. Prevalence of bovine tuberculosis gross lesions in Doukkala slaughterhouses, Morocco. Eur Sci J. 2019;15:38.
  33. Jawahar A, Raj GD, Pazhanivel N, Karthik K. Gross and histopathological features of tuberculosis in cattle, buffalo and spotted deer (Axis axis) caused by Mycobacterium orygis. J Comp Pathol. 2024;208:15-9.
  34. Nuru A, Zewude A, Mohammed T, Wondale B, Teshome L, Getahun M, et al. Nontuberculosis mycobacteria are the major causes of tuberculosis like lesions in cattle slaughtered at Bahir Dar Abattoir, northwestern Ethiopia. BMC Vet Res. 2017;13:1-6.
  35. Ozturk-Gurgen H, Rieseberg B, Leipig-Rudolph M, Straubinger R, Hermanns W. Morphology of naturally-occurring tuberculosis in cattle caused by Mycobacterium caprae. J Comp Pathol. 2020;174:120-39.
  36. Xu F, Tian L, Li Y, Zhang X, Qi Y, Jing Z, et al. High prevalence of extrapulmonary tuberculosis in dairy farms: Evidence for possible gastrointestinal transmission. PLoS One. 2021;16(3):e0249341.
  37. Dauda ID, Binhambali A, Jibril AH, Idris ZO, Akorede FR. Economic impact of fetal wastage and common diseases, along with their incidence rates and seasonal variations, at an abattoir in FCT, Nigeria. PLoS One. 2025;20(2):e0310806.

Mairabo Rebecca Rabi1, Abdullahi Musa2, Mailafia Samuel3*, Adah Bridget Jessica Maria3, Echioda- Ogbole Martha3
1Department of Veterinary Public Health, Faculty of Veterinary Medicine, University of Abuja, Nigeria
2Ministry of Agriculture and Natural Resources, Nasarawa State, Nigeria
3Department of Veterinary Microbiology, Faculty of Veterinary Medicine, University of Abuja, Nigeria

*Correspondence author: Mailafia Samuel, Department of Veterinary Microbiology, Faculty of Veterinary Medicine, University of Abuja, Nigeria; Email: [email protected]; [email protected] 

Mairabo Rebecca Rabi1, Abdullahi Musa2, Mailafia Samuel3*, Adah Bridget Jessica Maria3, Echioda- Ogbole Martha3
1Department of Veterinary Public Health, Faculty of Veterinary Medicine, University of Abuja, Nigeria
2Ministry of Agriculture and Natural Resources, Nasarawa State, Nigeria
3Department of Veterinary Microbiology, Faculty of Veterinary Medicine, University of Abuja, Nigeria

*Correspondence author: Mailafia Samuel, Department of Veterinary Microbiology, Faculty of Veterinary Medicine, University of Abuja, Nigeria; Email: [email protected]; [email protected] 

Copyright© 2025 by Rabi MR, et al. All rights reserved. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Citation: Rabi MR, et al. Prevalence of Bovine Tuberculosis in Cattle Slaughtered at the Gwagwalada Abattoir in the Federal Capital Territory (FCT), Nigeria: A One Year Retrospective Study. J Clin Immunol Microbiol. 2025;6(2):1-8.