Skip to main content

Sero-prevalence of brucellosis among slaughterhouse workers in Bahr el Ghazal region, South Sudan



Brucellosis is an infectious zoonotic disease and is common especially among pastoral communities in most low and middle-income countries. The aim of this study was to determine sero-prevalence, and risk factors of Brucella infection among Slaughterhouse workers, in Bahr el Ghazal region, South Sudan.


A cross sectional study was conducted among Slaughterhouse workers in Bahr el Ghazal region, South Sudan from December 2015 to May 2016. A pre-tested questionnaire was used in data collection. Each randomly selected participant was interviewed and a venous blood sample collected. The blood samples were screened for Brucellosis infection using Rose Bengal Plate Test (RBPT) and confirmed using Competitive Enzyme link Immuno Sorbet Assay (c-ELISA). Data was analyzed using Stata version 13 at 95% level of confidence.


A total of 234 Slaughterhouse workers were screen for Brucella infection. Overall, a third, 32.1% (75/234) of the participants were sero-positive for brucellosis. The prevalence of brucellosis was higher, 17.1% (40/234) in Wau state compared to other states. There was high prevalence among males, 28.6% (67/234) compared to females 3.4% (8/234). The mean age of study participants was 34.4 ± 9.6 years. A high proportion, 12.8% (30/234) of participants with confirmed brucellosis infection were 31–40 years of age. Brucellosis prevalence was high among butchers, 14.5% (34/234), and meat handlers, 9.0% (21/234).


Brucellosis is common among animal slaughterhouse workers in Bahr el Ghazal region, South Sudan. There is need for public awareness campaigns and educational programs to help sensitize communities on Brucella infection.

Peer Review reports


Brucellosis is an infectious zoonotic disease caused by Brucella [1]. Humans get infected with Brucella through consumption of infected animal products, direct contact with infected animal secretions and excreta [2]. In some cases, brucellosis is acquired directly through contact with contaminated laboratory materials (specimens or cultures) during diagnostic or vaccination procedures [3].

Brucellosis is prevalent globally especially among pastoral and agro pastoral communities. A study by McDermott & Arimi, (2002) reported 5% prevalence of Brucellosis in Sub-Saharan Africa. The disease is mostly misdiagnosed and/or underreported among humans in most low and middle-income countries. This is likely to contribute to spread of the disease due to limited awareness and inadequate health care infrastructure especially in low and middle income countries [4]. Brucellosis has been reported among nomads, veterinary staff, abattoir workers and butchers [5]. A previous study by Hashim, 2007 reported positive Brucella test among abattoir workers in Omdurman city slaughterhouse in Sudan [6].

Brucella grows intracellularly producing variable bacteremia phases followed by localization of infections in tissues of the genital tract, mammary glands and reticulo-endothelial system [7]. Brucella species known to cause human Brucellosis include Brucella melitensis, Brucella suis, Brucella abortus and Brucella canis. Brucellosis is diagnosed by isolation of Brucella organism or by a combination of serological tests and clinical findings [8]. Human brucellosis cannot be diagnosed solely based on clinical grounds due to a wide variety of clinical manifestations. In addition, performing bacteriological culture take long time and the bacteria some time difficult to recover from the samples. This leaves use of serological tests as the only viable means of screening and confirming Brucellosis in clinical samples. The Rose Bengal plate test can be used as a sensitive rapid screening test but results should be confirmed by bacteriological and other serological tests. Tests like serum (tube) agglutination test (SAT), or micro-titre plate and Enzyme-linked immunosorbent assay (ELISA), for directions of antibodies like IgM and IgG [3].

Human brucellosis can be prevented through control of animal brucellosis using vaccines, and imposing fastidious hygiene measures on handling and processing of animal products. Effective use of preventive strategies like vaccination programs and education of communities has helped significantly in reducing the prevalence of Brucellosis especially in high-income countries [9]. However, the main challenge of human Brucella treatment is inadequate laboratory diagnosis. This is further complicated by Brucellosis having symptoms similar to malaria, a common disease in Sub-Saharan Africa. As such, there is high likelihood of misdiagnosis and potentially inappropriate treatment. Which could delay patients from obtaining definitive treatment, and thus worsen the disease and increase risk of unwanted outcomes such as death.

Individuals working in slaughterhouses are likely to have an increased risk of getting Brucella infection especially in endemic areas. However, in South Sudan the prevalence of Brucellosis is not known especially among high-risk groups such as veterinary staff, pastoralists and animal slaughterhouse employees. This study was thus intended to establish the prevalence of Brucellosis and associated risk factors among slaughterhouse workers in Greater Bahr el Ghazal, South Sudan.


Study area

The study was done in Greater Bahr el Ghazal region which is located northwest of the capital Juba. Four states (Gogrial, Tonj, North and Western Bahr el Ghazal) were randomly selected. From each state, one city was purposively selected (Tonj, Kuajok, Aweil and wau) where an abattoir per city was randomly selected.

Study population

The study was conducted among individuals who work in abattoirs in Bahr el Ghazal region, South Sudan. Each of the abattoirs has about 30-to-80 employees. Veterinary staff or community health workers supervise each slaughterhouse.

Study design and sample size

This was a cross sectional study. A sample size of 138 individual was estimated using a standard formula for cross-sectional studies [10]. In calculating the sample size, prevalence of Brucellosis in the study area was assumed to be 10% as reported from a previous study [11], 95% level of significance and a Z value of 1.96.

Data collection methods

Data was collected using interviewer administered questionnaire and laboratory experiments. Variables in the questionnaire included; socio-demographic information (gender, marital status, religious affiliation, education attainment, occupation and ethnicity), location/area where participant comes from, and annual general medical check-up. A structured questionnaire was developed using information from literature and was pre-tested on 20 individuals from Juba town. Information from the pre-test was used in adjusting the tool. Five research assistants who were fluent in the local language and English were trained for field data collection using the study questionnaire. Laboratory data was collected using serological tests RBPT and c-ELISA. This method according to [12, 13].

Sampling criteria and sample collection

In each of the selected abattoirs, employees were recruited using consecutive sampling method. 5 ml of venous blood was collected into purple top vacutainer bottles, which were kept at room temperature tilted at an angle of 45°c overnight to allow for clotting. The sera from vacutainer tubes were pipetted and transferred to a new set of Eppendorf tubes. The tubes were then uniquely labeled, stored on ice pack and transferred to EPI center in Wau teaching hospital laboratory where they were kept at -80 °C. After collecting all the samples, the serum was then transported to the central laboratory at Makerere University, College of Veterinary Medicine and Biosecurity. At the central laboratory, the serum samples were stored at -80 °C until analysis.

Laboratory methods

Rose Bengal plate test

This was done following a procedure reported in a previous study [14]. Briefly, samples (serum and antigen) were brought to room temperature. 30 Microliter of each serum sample was placed on a white plastic plate. After shaking the antigen bottle, an equal volume of the antigen was added on the plastic plate. These were then mixed uniformly using a clean glass rod. The mixture was agitated gently for 4 min at an ambient temperature on a rocker, after which the agglutination was read. Any visible agglutination was considered positive.

Enzyme linked immune sorbent assay (ELISA) competitive ELISA

The Brucellosis Antibody Test Kit (IDEXX – laboratories, Italia) and positive control Brucellosis Serum (P04130–13) used in this study were adopted from a study by [15, 16]. The test was performed following manufacturer’s guidelines. The results were reported as negative, suspected, or positive when the ratio of sample optical density to the positive –control optical density (S/P ratio) was less than 70, 70to 100%, more than 100%, respectively.

Data analysis

Data analysis was done, using Stata version 13. Chi-square test was used and statistical significance was taken as P < 0.05.


Socio-demographic characteristics of animal slaughterhouse workers

A total of 234 Slaughterhouse workers were screened for Brucella antibodies. The majority, 89.3% (209/234) of animal slaughterhouse workers were males. The mean age of study participants was 34.4 ± 9.6 years. The majority of respondents, 73.9% (173/234) were married. Most, 43.6% (102/234) of the slaughterhouse workers didn’t have any formal education. The majority, 40.2% (94/234) of animal slaughterhouse workers were butchers. Over half, 50.6% (119/234) of the animal slaughterhouse workers were Nilotic (Table 1).

Table 1 Demographic characteristics of animal slaughterhouse workers

Sero-prevalence of brucellosis among animal slaughterhouse workers in Bahr el Ghazal region, South Sudan

A third, 32.1% (75/234) of animal slaughterhouse workers in Bahr el Ghazal region had Brucella Antibodies. Sero-prevalence of Brucellosis was high among slaughterhouse workers from Wau state, 18.8% (44/234). Slaughterhouse workers who were 31-to-40 years of age had a higher prevalence of Brucella antibodies, 12.8% (30/234). Most, 22.2% (52/234) of the butchers had Brucella infection. The rate of Brucella antibodies was higher, 42.6% among males compared to females 36%. Brucella antibodies was higher among the married animal slaughterhouse workers, 26.5% (62/234) (Table 1).

Factors associated with Brucella infection among animal slaughterhouse workers in Bahr el Ghazal region, South Sudan

The factors significantly associated with Brucella sero-prevalence included; occupation (P = 0.04), Ethnicity (P = 0.033), locality (P = 0.027) (Table 1). Annual medical checkup (P = 0.049) had boarder line association with Brucella infection (Table 2).

Table 2 Brucella sero – prevalence versus risk factors and known symptoms

On bivariate analysis, Nilotic slaughterhouse workers were twice more likely to have Brucella infection compared to Arab slaughterhouse workers (Table 3).

Table 3 Bivariate analysis of factors associated with brucellosis

On Multivariate analysis of the risk factors of Brucella infection, there were no significant predictors of Brucella sero-prevalence among animal slaughterhouse workers in Bahr el Ghazal region (Table 4).

Table 4 Multivariate logistic regression analysis of the predictors of Brucellosis


In this study, total of 234 Slaughterhouse workers were screened for Brucella antibodies, from slaughterhouses in Bahr el Ghazal region. There were more male slaughterhouse workers than females. This could be due to the working conditions in the slaughterhouse especially the amount of effort or labor required. In this study the average age of workers was 34.5 years, a finding similar to that of previous studies [17, 18].

The study found a third of animal slaughterhouse workers in Bahr el Ghazal to be having Brucellosis. This is similar to 35.7% prevalence reported in previous studies [17, 19]. The prevalence rate in our study was higher than that the 8% reported in India and Sudan [20,21,22]. The poor condition of animal slaughterhouses in South Sudan and lack of regulatory framework could have contributed to the high risk of contracting Brucella infection among animal slaughterhouse workers. This finding is important especially for health care providers as it helps draw attention to Brucellosis as a common disease in the region. Other endemic diseases like malaria in the region may complicate Brucella diagnosis in the region. There is a high risk of mistreatment as a result of inadequate diagnosis. This is especially likely as most physicians manage patients based on clinical presentation. As a result, most patients may delay in getting appropriate treatment and thus worsening of disease condition, increasing cost of care and potentially lead to death.

Brucella sero-prevalence was high in Wau state compared to other states in Bahr-el-Ghazal region, South Sudan. This could be attributed to the large number of animals slaughtered in Wau since it previously acted as the capital before creation of new states and is still one of the largest cities in South Sudan. Brucellosis sero-prevalence was high among screened males compared to females. This could be due to high exposure to contaminated animal products among males due to their involvement in most slaughterhouse activities compared to females [23]. Furthermore inadequate hygiene practices and poor adherence to correct use of protective gears could potentially increase the risk of infection and may explain the high prevalence of Brucellosis among slaughterhouse workers reported in this study [17].

In this study, Brucellosis prevalence was higher among butchers, meat handlers and veterinarians. This finding is similar to that of previous studies [17, 24] and could be attributed to the increased contact with infected animals products in the slaughterhouse. Consumption of raw animal products like meat, milk and urine was associated with Brucellosis infections [24].

Limitation of the study

As a result of the Instability in the region due to the civil war, we had to restrict the study to only four cities, which were stable at the time of data collection.


A third of the animal slaughterhouse workers in Bahr el Ghazal have Brucellosis infection. There is need to sensitize animal Slaughterhouse workers about zoonotic diseases, and enforcement of hygiene practices and use of protective gear. In addition, the health workers in hospitals need to be sensitized to increase screening for Brucellosis among patients presenting to hospitals especially with symptoms similar to those of malaria like fever, a common disease in the region.



Competitive enzyme-linked immuno sorbent assay


Confidence interval


Rose bengal plate agglutination test


  1. Boukary AR, Saegerman C, Abatih E, Fretin D, Bada RA, De Deken R, Harouna HA, Yenikoye A, Thys E. Seroprevalence and potential risk factors for Brucella spp. infection in traditional cattle, sheep and goats reared in urban, periurban and rural areas of Niger. PLoS One. 2013;8(12):e83175.

    Article  Google Scholar 

  2. Lado D, Maina N, Lado M, Abade A, Amwayi S, Omolo J, Oundo J. Brucellosis in Terekeka counTy, cenTral equaToria sTaTe, souThern Sudan. East Afr Med J. 2012;89(1):28–33.

    CAS  PubMed  Google Scholar 

  3. Corbel MJ. Brucellosis in humans and animals: World Health Organization; 2006.

    Google Scholar 

  4. McDermott JJ, Arimi S. Brucellosis in sub-Saharan Africa: epidemiology, control and impact. Vet Microbiol. 2002;90(1–4):111–34.

    Article  Google Scholar 

  5. Musa M, Eisa M, El Sanousi E, Wahab MA, Perrett L. Brucellosis in camels (Camelus dromedarius) in Darfur, western Sudan. J Comp Pathol. 2008;138(2–3):151–5.

    Article  CAS  Google Scholar 

  6. Hashim N, Hassabo A, Yagoub S. Serological detection of brucellosis in cattle and human. Res J Microbiol. 2007;2(11):861–5.

    Article  Google Scholar 

  7. Ko J, Splitter GA. Molecular host-pathogen interaction in brucellosis: current understanding and future approaches to vaccine development for mice and humans. Clin Microbiol Rev. 2003;16(1):65–78.

    Article  CAS  Google Scholar 

  8. Al-Sekait MA. Seroepidemiology survey of brucellosis antibodies in Saudi Arabia. Annals of Saudi medicine. 1998;19(3):219–22.

    Article  Google Scholar 

  9. Pappas G. Treatment of brucellosis. BMJ. 2008;336(7646):678–9.

    Article  Google Scholar 

  10. Thrusfield M. Diagnostic testing. Veterinary epidemiology, vol. 2; 1995. p. 266–85.

    Google Scholar 

  11. Al Sharif F. Prevalence of brucellosis among slaughterhouse workers and milkers: MSc. Thesis, Faculty of Medicine, University of Khartoum; 1994.

  12. Gupte S, Kaur T. Diagnosis of human brucellosis. Journal of Tropical Diseases & Public Health. 2015.

  13. Lucero NE, Foglia L, Ayala SM, Gall D, Nielsen K. Competitive enzyme immunoassay for diagnosis of human brucellosis. J Clin Microbiol. 1999;37(10):3245–8.

    CAS  PubMed  PubMed Central  Google Scholar 

  14. Nour BY, Tawor BYB, Saeed OK, Gebril AA, Smits HI, Mohamedani AA. Evaluation of simple and rapid specific IgM/IgG flow assay and some methods used in diagnosis of brucellosis in Gezira and Blue Nile states, Sudan. Clinical Microbiology: Open Access. 2015;2015.

  15. Edwards JM, Tannahill AJ, Bradstreet CP. Comparison of the indirect fluorescent antibody test with agglutination, complement-fixation, and coombs tests for Brucella antibody. J Clin Pathol. 1970;23(2):161–5.

    Article  CAS  Google Scholar 

  16. Al-Zhaidy AAN, Al-Khafaji JKT, Al-Yasari AKS. Efficacy of immunological tests in diagnosis of acute human brucellosis. Kerbala Jorunal of Medicine. 2006;1:81–9.

    Google Scholar 

  17. Mukhtar F, Kokab F. Brucella serology in abattoir workers. J Ayub Med Coll Abbottabad. 2008;20(3):57–61.

    PubMed  Google Scholar 

  18. Frost P, Andersen JH, Nielsen VK. Occurrence of carpal tunnel syndrome among slaughterhouse workers. Scand J Work Environ Health. 1998:285–92.

    Article  CAS  Google Scholar 

  19. Karimi A, Al Borzi A, Rasouli M, Kadivar M, Nateghian A. Prevalence of antibody to Brucella species in butchers, slaughterers and others; 2003.

    Google Scholar 

  20. Mangalgi S, Sajjan A, Mohite ST. Seroprevalence of brucellosis among blood donors of Satara district, Maharashtra. J Krishna Institute of Medical Sciences University. 2012(1, 1):55–60.

  21. Mohamed A, Salih S. A note of livestock brucellosis in Blue Nile state, Sudan. Sud J Vet Sc Anim Husb. 2004;19:89–90.

    Google Scholar 

  22. Musa M. A serological study on equine brucellosis in Darfur, Western Sudan. The Sudan Journal of Veterinary Research. 2004:7–11.

  23. Minas M, Minas A, Gourgulianis K, Stournara A. Epidemiological and clinical aspects of human brucellosis in Central Greece. Jpn J Infect Dis. 2007;60(6):362.

    PubMed  Google Scholar 

  24. Aworh MK, Okolocha E, Kwaga J, Fasina F, Lazarus D, Suleman I, Poggensee G, Nguku P, Nsubuga P. Human brucellosis: seroprevalence and associated exposure factors among abattoir workers in Abuja, Nigeria-2011. Pan African medical journal. 2013(103):16.

Download references


The National Ministry of Health, South-Sudan deserves due thanks for ethical approval of this study without it, it be impossible. Moreover, we are indebted to Veterinary Research Institute (VRI), Soba-Khartoum-Sudan for providing Rose Bengal Antigen. Also the authors are grateful to all the interview respondents who participate in the study, the general director of ministry of health Wau state, South Sudan. And all research assistants for contribution to the success of this research. Special thanks go to field research assistances Mr. Samuel Julio Daba, Dr. Mohammed Adam and the slaughterhouses administrators in (Wau, Tonj, Kuajok and Aweil).


The funding body (CAPAZOMININTICO project) under NORHED program. The funder did not take any role in the design, conduct, analysis and interpretation of data for this study.

Availability of data and materials

The data-sets used and/or analysed during the current study available from the corresponding author on reasonable request.

Author information

Authors and Affiliations



NM contributed to the design, data collection, drafting and writing of the manuscript. MO, AM, and GWN contributed to data analysis, drafting and reviewing of the manuscript. AJ contributed data collection and drafting of the manuscript. JBM, CK contributed to conceptualization, design, and drafting and writing of the manuscript, and J G: contributed to the design and drafting and writing of the manuscript. All authors have read and approved the final manuscript.

Corresponding author

Correspondence to Nuol Aywel Madut.

Ethics declarations

Ethics approval and consent to participate

The study protocol (SBLS/REC/15/133), was assessed and approved by the Ethical Review Committee of the College of veterinary medicine, Animal Resources and Biosecurity (COVAB), Makerere University, Kampala, Uganda the reference number of SBLS.NA.2015 and the National Ministry of Health, Juba South Sudan. The study objective was explained to participants and written informed consent was obtained. Any participants under 18 years of age written informed consent was obtained from his parents or custodian. Each participant was interviewed independently and the collected data was kept confidential. Study numbers were used instead of participants’ names to ensure confidentiality. Moreover, import and export permits of the biological samples were obtained from Ministry of Agriculture, Animal Industry and Fisheries (MAAIF) - LHE 46/172/406, Uganda, Ministries of Health (MOH), and Livestock and Fisheries Industry (MLFI), South Sudan - RSS/MLFI/DVS/J/39, respectively, prior to shipment from and to designate country.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Madut, N.A., Ocan, M., Muwonge, A. et al. Sero-prevalence of brucellosis among slaughterhouse workers in Bahr el Ghazal region, South Sudan. BMC Infect Dis 19, 450 (2019).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: