Saleh Mohammed Jajere1, Naphtali Nayamanda Atsanda2, Asinamai Athliamai Bitrus3, Tasiu Mallam Hamisu4, Ajurojo Oluwaseun Ayo2. 1. Department of Pathology and Microbiology, Faculty of Veterinary Medicine, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia; Department of Veterinary Public Health and Preventive Medicine, Faculty of Veterinary Medicine, University of Maiduguri, P.M.B 1069 Maiduguri, Borno state, Nigeria. 2. Department of Veterinary Public Health and Preventive Medicine, Faculty of Veterinary Medicine, University of Maiduguri, P.M.B 1069 Maiduguri, Borno state, Nigeria. 3. Department of Pathology and Microbiology, Faculty of Veterinary Medicine, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia. 4. Department of Veterinary Microbiology and Parasitology, Faculty of Veterinary Medicine, University of Maiduguri, P.M.B 1069 Maiduguri, Borno state, Nigeria.
Abstract
AIM: A cross-sectional study was conducted to determine the seroprevalence of bovine brucellosis among cattle slaughtered at three municipal abattoirs of Gombe State, Nigeria. MATERIALS AND METHODS: A total of 200 blood samples collected from slaughtered cattle of different breeds (Sokoto Gudali - 50, White Fulani - 102, Red bororo - 34, and Crossbreeds - 14), sex (males - 19 and females - 181), and from different locations (Billiri - 30, Yamaltu Deba - 50, and Gombe - 120) were screened for brucellosis using rose bengal plate test (RBPT), serum agglutination test (SAT), and microtiter agglutination test (MAT). RESULTS: Of the 200 serum samples analyzed, 7 (3.5%), 10 (5.0%) and 18 (9.0%) were positive by RBPT, SAT and MAT, respectively. The results showed no statistically significant association between sex and seropositivity to bovine brucellosis. However, seropositivity of bovine brucellosis was higher in females than in males. Similarly, no statistically significant association was observed between breed and occurrence of bovine brucellosis. Moreover, the prevalence of brucellosis was higher in Sokoto Gudali as compared with the other breeds. Based on the study locations, higher seroprevalence was observed in animals screened from Billiri as compared with those from other locations (p<0.05). CONCLUSION: The presence of Brucella abortus antigen in the sera of slaughtered cattle in Gombe state poses a significant public health risk. Therefore, it is important to carry out further epidemiological studies on fulani herdsmen and cattle herds in the study area, in order to explore the risk factors associated with the occurrence and perpetuation of brucellosis among cattle herds, ascertain the prevalence and status of the disease among both farms and nomadic herds.
AIM: A cross-sectional study was conducted to determine the seroprevalence of bovinebrucellosis among cattle slaughtered at three municipal abattoirs of Gombe State, Nigeria. MATERIALS AND METHODS: A total of 200 blood samples collected from slaughtered cattle of different breeds (Sokoto Gudali - 50, White Fulani - 102, Red bororo - 34, and Crossbreeds - 14), sex (males - 19 and females - 181), and from different locations (Billiri - 30, Yamaltu Deba - 50, and Gombe - 120) were screened for brucellosis using rose bengal plate test (RBPT), serum agglutination test (SAT), and microtiter agglutination test (MAT). RESULTS: Of the 200 serum samples analyzed, 7 (3.5%), 10 (5.0%) and 18 (9.0%) were positive by RBPT, SAT and MAT, respectively. The results showed no statistically significant association between sex and seropositivity to bovinebrucellosis. However, seropositivity of bovinebrucellosis was higher in females than in males. Similarly, no statistically significant association was observed between breed and occurrence of bovinebrucellosis. Moreover, the prevalence of brucellosis was higher in Sokoto Gudali as compared with the other breeds. Based on the study locations, higher seroprevalence was observed in animals screened from Billiri as compared with those from other locations (p<0.05). CONCLUSION: The presence of Brucella abortus antigen in the sera of slaughtered cattle in Gombe state poses a significant public health risk. Therefore, it is important to carry out further epidemiological studies on fulani herdsmen and cattle herds in the study area, in order to explore the risk factors associated with the occurrence and perpetuation of brucellosis among cattle herds, ascertain the prevalence and status of the disease among both farms and nomadic herds.
Entities:
Keywords:
Gombe state; Nigeria; bovine brucellosis; microtiter agglutination test; rose bengal plate test; serum agglutination test
Bovinebrucellosis is a disease with a significant economic and public health importance due to losses incurred as a result of infertility in animals and extensive chronic morbidity in humans [1]. In Nigeria, bovinebrucellosis is a major animal health problem affecting the growth of the cattle industry. It remains a significant disease in animals and humans worldwide and an important cause of reproductive failure such as abortion in cows and sterility in bulls [2-4]. Bovinebrucellosis still remains the most widespread form of brucellosis even though reported incidences and prevalence of the disease showed that it varies from country to country. The geographical distribution of the disease is limited. However, it is still a major problem in livestock industry in the Asia, Africa, Latin American, and the Mediterranean regions [5,6].The disease is transmitted through contamination of feed and water with discharges from infected animals, aerosols, contaminated equipment, fetal fluids, and placental discharges. Infection can also be transmitted via break in the integrity of the skin and mucous membrane [7]. In endemic areas, humans get infected with brucellosis through close contact with infected animals or after birth content of animals, consumption of unpasteurized milk or milk products obtained from either dairy cows, sheep or goats [8,9]. Over the past decades, factors - such as socioeconomic, sanitary, political, and international travel - have greatly impacted on the epidemiology of brucellosis. The occurrence of brucellosis is worldwide, except in Australia, Cyprus, Canada, Norway, New Zealand, Finland, Denmark, and Sweden where the etiologic agent of bovinebrucellosis has been eradicated [10].Bovinebrucellosis is responsible for huge economic losses in animal production. This is manifested as abortions, reduced milk yield, and delayed conception; in addition to its zoonotic and public health threat [9]. For instance, an estimated loss of 600 million US dollar due to bovinebrucellosis was reported in Latin America. While in the US, an estimated loss due to abortion and reduced milk production was 400 million US dollars [10]. Economic losses due to brucellosis in Nigeria are as a result of abortion, reduced milk production, sterility in bulls, and loss of man-hour in people infected with Brucella abortus [11].Brucellosis is endemic in Nigeria; and the prevalence of bovinebrucellosis varies significantly between herds located in the same area, with an estimated seroprevalence in cattle ranging from as low as 0.2% to about 80%. The prevalence of brucellosis in institutional and dairy farms, abattoir surveys and ranches in southern Nigeria ranges from 3.7% to 48.8%. However, the prevalence was low in herd of cattle belonging to the traditional nomadic Fulani than those in the farms and ranches. Similarly, the prevalence of 32.2% was recorded in a herd of cattle belonging to a prison farm. In Northern Nigeria, 25.3% and 19.5% of milk and serum samples were, respectively, reported positive for bovinebrucellosis [11].The occurrence of the disease is influenced by the use of common grazing areas, herding animals of different breeds, age and sex together. Other factors reported to facilitate the occurrence of bovinebrucellosis includes, season of the year, lactation, and pregnancy [7,12]. The occurrence of brucellosis in animals has been reported to be a factor limiting the growth and success of livestock in Nigeria [11]. Serological diagnosis of brucellosis in livestock using a well-standardized kit specifically designed for B. abortus is considered an important component of disease surveillance and eradication. These tests are also available for use in other livestock other than cattle [13,14]. Despite studies on bovinebrucellosis in northeastern Nigerian states such as Yobe, Borno, Bauchi, Adamawa, and Taraba, only a few were conducted in Gombe state and therefore the need for this study.It is important, therefore, to adopt the use of effective control measures through early and accurate diagnosis of the disease aimed at reducing the prevalence of the disease to boost production. This study was designed to investigate the seroprevalence of bovinebrucellosis in three Municipal abattoirs of Gombe state, Northeastern Nigeria.
Materials and Methods
Ethical approval
The study to determine the seroprevalence of bovinebrucellosis was designed and performed according to the global standard guidelines to care and use of experimental animals described by Ochei and Kolhatkar [15]. Approval was duly obtained from the Institutional Ethics and Research Committee, Faculty of Veterinary Medicine, University of Maiduguri.
Study area
Gombe state is located in the northeastern geopolitical zone of Nigeria (Figure-1). It shares a common boundary line with Borno, Adamawa, Bauchi, Yobe, and Taraba state along the expansive savannah zone. The state is situated at latitude 9°30’ and 12°30’N and longitudes 8°45’ and 11°45’E. It has an area of 20,265 km2 and a population of about 2,353,000 people (NPC, 2006). The state has two different climatic conditions, the dry season ranging from November to March and the rainy season spanning from April to October. It has an average rainfall of 850 mm (https://en.wikipedia.org/wiki/Gombe_State).
Figure-1
Map of Nigeria showing Gombe state (Source: Google maps).
Map of Nigeria showing Gombe state (Source: Google maps).
Sample collection
A total of 200 blood samples were obtained from slaughtered cattle in the municipal abattoirs located in the three agro-ecological zones of Gombe state (Figure-2). Of these, about 91%, 51% and 60% were, respectively, females, males, White fulani breeds and sampled from Gombe metropolis council (Table-1). About 10 mL each of blood was aseptically collected in a well-labeled plain tube without anticoagulant, from the anterior jugular vein of cows slaughtered in these abattoirs. The blood was kept in a transport container and allowed to clot. The sera were collected in 2 mL cryovials after centrifugation at 3000 ×g for 5 min and stored at −20°C.
Figure-2
Map of Gombe state showing the three municipal abattoirs.
Table-1
Baseline characteristics of slaughtered cattle sampled from the three municipal abattoirs in Gombe state, Northeastern Nigeria.
Variables
Categories
Frequency (%)
Sex
Male
19 (9.5)
Female
181 (90.5)
Breeds
Sokoto Gudali
50 (25)
White Fulani
102 (51)
Red Bororo
34 (17)
Cross breed
14 (7)
Location
Billiri
30 (15)
Yamaltu Deba
50 (25)
Gombe
120 (60)
Overall
200 (100)
Map of Gombe state showing the three municipal abattoirs.Baseline characteristics of slaughtered cattle sampled from the three municipal abattoirs in Gombe state, Northeastern Nigeria.
Serological reaction
Blood sera was analyzed for B. abortus antibodies using rose bengal plate test (RBPT), serum agglutination test (SAT), and microtiter agglutination test (MAT) as described by Adamu et al. [7] and Gómez et al. [16]. Positive and negative reactions were recorded based on the presence or absence of agglutination reaction. The samples were considered positive for infection with brucellosis if the antigen-antibody titer is three-fold (1.40) or more (one part of the antigen and four parts of the antibody). Antigen for SAT and RBPT standard B. abortus antigen Surry KT15 3NB (New Haw Weybridge, UK.) and S99 CVL (Indian Veterinary Research Institute, Izatnagar, Uttar Pradesh, India) were used. The preparation of cocktail was assessed by titration and carried out according to the standard guidelines recommended by the World Organization for Animal Health (OIE) [17]. For SAT, Brucella antigen was prepared in a 1:50 dilution in 0.85% saline solution. A 1:10 to 1:1280 double dilution of serum was carried in tubes containing saline solutions. Appropriate titers of high, low, and negative sera were used as controls. Tubes containing 0.5 ml of diluted serum were mixed with equal amount of 1:50 dilution of Brucella antigen and then incubated at 37°C overnight.
Statistical analysis
Factors considered to assess their association with seroprevalence of bovinebrucellosis include sex, geographical location, and breeds. The results were considered statistically significant at p<0.05. Chi-square test using SPSS version 22.0 (SPSS Chicago, USA), was used to determine the strength of association between the seroprevalence of bovinebrucellosis and risk factors.
Results and Discussion
Bovinebrucellosis is considered as one of the most significant bacterial zoonosis hindering the development of the dairy industry in Nigeria. The disease is endemic in many African countries, Asia, Middle East, Central and South America. It is prevalent in areas where effective control programs have not yielded much progress. To this effect, a cross-sectional study was conducted to determine the seroprevalence of bovinebrucellosis in three municipal abattoirs in Gombe state. To achieve this, three serological test, namely RBPT, SAT, and MAT were used to screen for cattle sera. The result obtained showed that 7 (3.5%), 10 (5.0%) and 18 (9.0%) of the cattle sera analyzed were positive by RBPT, SAT and MAT, respectively (Table-1). Statistically, no significant difference was observed between the seropositivity of the disease and the use of RBPT and SAT as a diagnostic tool in screening for bovinebrucellosis. However, a statistically significant difference was observed between the seropositivity of the disease and the sensitivity of MAT in detecting antibodies to B. abortus in the sera screened for bovinebrucellosisThe seroprevalence of bovinebrucellosis as reported in this study was lower than the seroprevalence of bovinebrucellosis reported in Yobe (34.0%), Adamawa (36.6%), and Bauchi state (5.4% and 3.9%) respectively [7]. Similarly, in southern Nigeria, Cadmus et al. [18] reported a seroprevalence of 6% in 2004, 6.17% in 2005 and 5.31% in 2006, which was higher than the seroprevalence of bovinebrucellosis reported in this study. Furthermore, in another study, Cadmus et al. [19] reported a seroprevalence of 8.6% in three cattle production system in southwestern Nigeria. This difference in the seroprevalence of the disease could be attributed to the difference in breeds, sensitivity of test kits, seasonal variation, farming system, and sample size. In addition, lower rates of bovinebrucellosis was reported in this study than those reported in other African countries such as Ethiopia (4.9%) [2], Central African Republic (4.9%) [20], Eritrea (4.2%) [21], Chad (7%) [22], Jordan (6.5%) [23], and Cameroon (8.4%) [24]. In Eastern Sudan, Gumaa et al. [12] reported seroprevalence of 2.15%, after sampling 2500 serum samples collected from sheep. The difference in prevalence could be due to the difference in breeds, geographical location, sample size, serological techniques, and inter-laboratory variation. Similarly, Junaidu et al. [25] also reported a much higher (19.5%) seroprevalence of bovinebrucellosis after sampling 1,547 serum samples in Sokoto, Northwestern Nigeria. In another study, Zubairu et al. [26] reported a seroprevalence of 21.3% in cattle sera collected in Taraba state, North-eastern Nigeria. This disparity in the seroprevalence of bovinebrucellosis in different parts of the country is in congruent with the report of Mai et al. [11]. Where the authors reported that the prevalence of bovinebrucellosis varies between animals in the same agro-pastoral zone. Even though the seroprevalence of brucellosis reported in this study was lower using RPBT and SAT, it was however higher with MAT (Table-2).
Table-2
Seroprevalence of bovine brucellosis among slaughtered cattle in Gombe state, Northeastern Nigeria.
Variables
Number sampled
Number of positive animals (%)
RBPT
MAT
SAT
Sex
Male
19
0 (0)
1 (5.3)
0 (0)
Female
181
7 (3.9)
17 (9.4)
10 (5.5)
Breeds
Sokoto Gudali
50
3 (6.0)
8 (16.0)
4 (8.0)
White Fulani
102
3 (2.9)
9 (8.8)
5 (4.9)
Red Bororo
34
1 (2.9)
1 (2.9)
1 (2.9)
Cross breeds
14
0 (0)
0 (0)
0 (0)
Locations
Billiri
30
2 (6.7)
3 (10.0)
4 (13.3)
Yamaltu Deba
50
2 (4.0)
6 (12.0)
3 (6.0)
Gombe
120
3 (2.5)
9 (7.5)
3 (2.5)
Overall
200
7 (3.5)
18 (9.0)
10 (5.0)
RBPT=Rose bengal plate test, MAT=Microtiter agglutination test, SAT=Serum agglutination test
Seroprevalence of bovinebrucellosis among slaughtered cattle in Gombe state, Northeastern Nigeria.RBPT=Rose bengal plate test, MAT=Microtiter agglutination test, SAT=Serum agglutination testIn this study, the seropositivity of bovinebrucellosis was higher in Sokoto gudali and White fulani as compared with Red bororo and crossbreeds. However, there was no statistically significant association between breeds and occurrence of brucellosis in cattle (p>0.05) (Table-2). This finding is in congruent with the report of Junaidu et al. [24], where the authors reported a higher prevalence of bovinebrucellosis in Sokoto Gudali (29.59%) breeds. In addition, even though the proportion of bovinebrucellosis was higher in females than in males, the difference was not statistically significant (p>0.05) (Table-2). This is because female cows remain the locale of infection, which helps to spread the disease from one animal to another, either through lactation or during mating. Pregnancy and lactation were reported to enhance susceptibility to infection. The growth of virulent strains of Brucella organism was reported to be stimulated more in females because of the presence of higher volume of D-erythritol normally found fetal tissue than in testes and seminal vesicle [24]. These thoughts provide proofs as to the different rates of seroprevalence of bovinebrucellosis observed in this study.The risk of bovinebrucellosis is not only restricted to the animal husbandry alone but also represent significant zoonotic implications characterized by debilitating and severe complications in humans [1]. Serological studies have shown that bovinebrucellosis is a common problem in many grazing zone in Nigeria [7]. From reports, it was observed that there was variation in the prevalence of bovinebrucellosis in many countries, the surveillance strategies adopted for the control and prevention of the disease is generally very poor. Purchase of infected animals as replacement cattle, interaction with wildlife, free movement of animals by nomads, change in climatic conditions, deforestation, and the system of animal production, regulatory issues and demographic factors were considered as likely factors that increase the spread of bovinebrucellosis. Other factors include sharing of bulls between farmers, the practice of free range grazing and movement as a result of trade have greatly increased the risk of exposure to brucellosis in cattle [7].
Conclusion
The presence of Brucella abortus antibodies in the sera of cattle slaughtered in the municipal abattoirs of Gombe state poses a significant public health risk. Therefore, it is imperative to design an effective control and preventive measures aimed at reducing the spread of brucellosis in cattle and subsequent exposure to humans in the study area.
Authors’ Contributions
Authors SMJ and NNA conceived and designed the study. AAB and TMH contributed in literature review and data analysis. AOA conducted sampling from the abattoir. SMJ and AAB drafted the first manuscript. NNA and TMH revised the manuscript. All authors read and approved the final manuscript.
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