Short Communication · Volume 53, Issue 1, 31 December 2020 · Open Access
Bovine and Caprine Brucellosis Detected by Milk Indirect ELISA and Milk Ring Test in Islamabad Capital Territory, Pakistan
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Affiliations & Notes ⌄
- 1Department of Clinical Studies, Faculty of Veterinary and Animal Sciences, Pir Mehr Ali Shah Arid Agriculture University, Rawalpindi, Pakistan 2Section of Epidemiology and Public Health, Department of Clinical Sciences, University of Veterinary and Animal Sciences, Lahore Sub-Campus Jhang, Pakistan 3Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China 4University College of Veterinary and Animal Sciences, The Islamia Univeristy of Bahawalpur, Bahawalpur, Pakistan 5Department of
Article Info ⌄
- Journal:
- Pakistan Journal of Zoology
- Published:
- 31 December 2020

From the article
- Milk ring test (MRT) and milk indirect ELISA are used to screen anti-Brucella antibodies in buffaloes and goat milk.
- It can be speculated that relevant number of abortions in buffaloes or goats were caused by brucellosis.
- In conclusion, the overall prevalence of brucellosis was 4.97% and 1.9% in goats and 5.6% and 16.1% in buffaloes through MRT and i-ELISA respectively in Islamabad Capital Territory.
- Goats older than 6 months, buffaloes older than 2 years and animals kept for business purpose were at high risk for brucellosis.
Selected from the article's own text.
Abstract
Materials and methods
The present study was carried out in the peri-urban area of ICT, Pakistan during the period February-May, 2017. Islamabad lies in a hilly area having a great diversity of fauna and flora. The area is located in north-eastern Pakistan with an elevation of 575 m between the northern part of the Punjab and the western part of Azad Kashmir.
A total of 341 milk samples (5 ml) were collected from buffaloes (Nili-Ravi) and goats (Teddy, Beetal and crossbred) according to standard procedures (OIE, 2009). Initial milk streams were discarded before the actual milk samples were collected. The samples were transported to and stored at 4°C at Veterinary Research Laboratory, Pir Mehr Ali Shah Arid Agriculture University Rawalpindi. Samples were analyzed within 6 hours by Milk Ring Test (MRT). All screened animals were reported to be unvaccinated.
In the present study, parameters like education level and main occupation of the farmer, type of husbandry, vaccination and deworming status were also documented. The samples were taken during routine visits and the owners were informed and asked for participation in the study.
For Milk Ring Test the MRT antigen was purchased from Veterinary Research Institute (VRI), Lahore, Pakistan. Milk samples were analyzed as per manufacturer’s recommendations. Briefly, 30-50µl of homogenized MRT antigen was mixed with 1ml milk sample in a test tube at room temperature and was well shaken. This antigen-milk mixture was incubated at 37 °C for 1 hour and observed for presence of a violet/bluish colored ring over the milk fraction. Presence of ring indicated positive reaction of anti-Brucella antibodies.
For Milk Indirect ELISA the milk i-ELISA kit (ID Vet, France) was used for detection of anti-Brucella antibodies as per manufacturer’s instructions. Briefly, all milk samples were centrifuged at 5,000 g for 5 mins. A volume of 100 µl skimmed milk was collected under the cream and transferred to a well of the iELISA plate and incubated at 21 °C for 45 mins. After washing a (3×2) volume of 100 µl of conjugate was added and incubated again at 21 ºC for 30mins. After (3×2) washing 100 µl of substrate was added and incubated at 21ºC for 15mins. Finally, 100 µl of stop solution was added to each well and optical density was measured at 450 nm.
Results
A total of 4.97% (8/161) goat samples and 5.6% (10/180) of buffalo milk samples were found positive by MRT. iELISA showed 1.9% (3/161) and 16.1% (29/180) positive results for goat and buffalo samples, respectively.
Table I. Comparative seroprevalence of MRT and milk iELISA in buffaloes and goats.
| Animal species | No. | MRT | Milk iELISA |
| Goats | 161 | 4.97% (8/161) | 1.9% (3/161) |
| Buffalos | 180 | 5.6% (10/180) | 16.1% (29/180) |
| Total | 341 | 5.27% (18/341) | 9.38% (32/341) |
History of abortion was found to be significantly associated with a seropositive to MRT and iELISA results (Table II). Still birth was not found significantly associated with positive results (Table III).
Table II. Association of abortion with brucellosis.
| Category | No. | Positive | %age | Chi-square | P-value |
| MRT +ve | |||||
| Non-aborted | 332 | 6 | 1.8 | 33.892 | 0.001** |
| Aborted | 9 | 3 | 33.3 | ||
| ELISA +ve | |||||
| Non-aborted | 332 | 4 | 1.2 | 10.731 | 0.000** |
| Aborted | 9 | 5 | 55.6 | ||
P-value<0.05 was considered significantly associate; P-value <0.01 was considered highly significant; P-value >0.01 was consider non-significant.
Table III. Association of still birth with brucellosis.
| Category | No. | Positive | %age | Chi-square | P-value |
| MRT +ve | |||||
| Normal birth | 149 | 11 | 7.4 | 0.15 | 0.619NS |
| Stillbirth | 12 | 1 | 8.3 | ||
| ELISA +ve | |||||
| Stillbirth absent | 149 | 10 | 6.7 | 1.596 | 0.221 NS |
| Present | 12 | 2 | 16.7 |
P-value <0.05 was considered significantly associate. P-value <0.01 was considered highly significant. P-value >0.01 was consider non-significant.
Age [Young stock (goats<6months and buffaloes<24months) compared to old stock (goats>6months and buffaloes>24months)] and purpose of rearing (domestic use or business purpose) of animals showed significant association with seropositivity by iELISA. Old stock was more prone to be seropositive than young stock. The animals kept for business purpose were more often seropositive as compared to the domestic purpose animals. Farm type (home vicinity and away from home) and unit of animals/farm (1-8, 9-15 and >15) did not show apparent influence on prevalence of anti-Brucella antibodies (Table IV).
Table IV. Relationship of different factors with positive results of the milk iELISA.
| Factor | Category | Positive samples | Chi-square | P-value |
| Age | Young stock | 5 | 6.084 | 0.009 |
| Old stock | 27 | |||
| Farm type | House vicinity | 6 | 0.471 | 0.321 |
| Away from house | 26 | |||
| Animal unit | 1 to 8 | 8 | 1.201 | 0.549 |
| 9 to 15 | 14 | |||
| >15 | 10 | |||
| Rearing purpose | Domestic | 1 | 3.502 | 0.041 |
| Business | 31 |
P-value<0.05 was considered significantly associated.
Discussion
Milk ring test (MRT) and milk indirect ELISA are used to screen anti-Brucella antibodies in buffaloes and goat milk. Higher prevalence was reported for buffaloes compared to goats with both the tests. Milk iELISA was found to be highly sensitive for the diagnosis of bovine brucellosis (98.2%) . Milk iELISA could be an effective screening test because it can detect lower titers of anti-Brucella antibodies especially during early infection . A previous report describes similar prevalence of anti-Brucella antibodies in cattle and buffaloes using MRT and milk iELISA .
Several studies reported that milk ELISA is more sensitive than MRT for the diagnosis of brucellosis in farm animals ; ; . Variation of sensitivity and specificity of serological tests may be influenced by external environment (season or temperature), disease endemicity, vaccination status of animal and herd and presence of any other gram-negative bacterium that might cross-react due to similar epitopes with Brucella ; ; ; .
Abortion and Brucella seropositivity showed significant association. It can be speculated that relevant number of abortions in buffaloes or goats were caused by brucellosis. Thus brucellosis is to be considered a threat for other animals as well as humans. Another study conducted in the same area also reported that abortion is risk factor for brucellosis. Relationship of stillbirth was recorded only in goats; however, there is no available data in buffaloes. Results showed non-significant association between brucella seropositivity and stillbirth in goats.
In the present study, age and rearing purpose of animals were found to be the main risk factors for brucellosis. Similar findings were recorded earlier where association of age with presence of brucella infection was observed ; ; ; . Higher seroprevalence of brucellosis in animals kept for commercial purposes might be due to frequent selling and buying events, exposure of purchased to infected animals in markets, no screening before sale or purchase time because of fear of business loss among people in peri-urban areas.
Conclusion
In conclusion, the overall prevalence of brucellosis was 4.97% and 1.9% in goats and 5.6% and 16.1% in buffaloes through MRT and i-ELISA respectively in Islamabad Capital Territory. Goats older than 6 months, buffaloes older than 2 years and animals kept for business purpose were at high risk for brucellosis.
Acknowledgments
Financial support from German Federal Foreign Office through Friedrich-Loeffler-Institute (FLI), Jena, Germany, via Project # je-0113, titled “Brucellosis in Pakistan” is highly appreciated.
Statement of conflict of interest
The authors have declared no conflict of interests regarding the publication of this article.
References
- Abubakar, M., Arshed, M.J., Hussain, M., Ehtisham, U.H. and Ali, Q., 2010. Trans. Emerg. Dis., 57: 443-447. https://doi.org/10.1111/j.1865-1682.2010.01171.x[CrossRef]
- Abubakar, M., Mansoor, M. and Arshed, M.J., 2012. Pak.Vet. J., 32: 147-155.
- Ali, S., Akhter, S., Neubauer, H., Melzer, F., Khan, I., Abatih, E.N., Adawy, H. E., Irfan, M., Muhammad, A., Akbar, M. W., Umar, S., Ali, Q., Iqbal, M. N., Mahmood, A. and Haroon, A., 2017. BMC Res. Notes, 10: 73. https://doi.org/10.1186/s13104-017-2394-2[CrossRef]
- Alton, G.G., Jones, L.M., Angus, R.D. and Verjer,G.M., 1988. Techniques for the brucellosis laboratory. INRA, Paris, France.
- Aulakh, H.K., Patil, P.K., Sharma, S., Kumar, H., Mahajan, V. and Sandhu, K.S., 2008. Acta Vet. Brno, 77: 393-399. https://doi.org/10.2754/avb200877030393[CrossRef]
- Blasco, J.M. and Molina-Flores, B., 2011. Vet. Clin. Fd. Anim. Pract., 27: 95-104. https://doi.org/10.1016/j.cvfa.2010.10.003[CrossRef]
- Godfroid, J., Scholz, C.H., Barbier, T., Nicolas, C., Wattiau, P., Frettin, D., Whatmore, M.A., Cloeckaert, A., Blasco, M.J. and Moriyon, I., 2011. Pre. Vet. Med., 102: 118-131. https://doi.org/10.1016/j.prevetmed.2011.04.007[CrossRef]
- Greiner, M. and Gardner, I., 2000. Pre. Vet. Med., 45: 3-22. https://doi.org/10.1016/S0167-5877(00)00114-8[CrossRef]
- Guarino, A., Fusco, G., Di-Matteo, A., Urbani, G., Condoleo, R., Serpe, L., Tittarelli, M., Di-Ventura, M. and Gallo, P., 2001. Vet. Rec., 149: 88-90. https://doi.org/10.1136/vr.149.3.88[CrossRef]
- Sukumar, K., Tamilselvan, P. and Dorairajan, N., 2012. Tamil. J. Vet. Anim. Sci., 8: 235-237.
- Kang’ethe, E.K., Arimi, S.M., Omore, A.O., McDermott, J.J., Nduhiu, J.G., Macharia, J.K. and Githua, A., 2000. The prevalence of antibodies to Brucella abortus in marketed milk in Kenya and its public health implications. Paper presented in 3rd All Africa Conference on Animal Agriculture (AACAA), Alexendria, Egypt. Nairobi (Kenya): ILRI.
- Kattar, M.M., Zalloua, P.A., Araj, G.F., Samaha-Kfoury, J., Shbaklo, H., Kanj, S.S. and Deeb, M., 2007. Diagn. Microbiol. Infect. Dis., 59: 23-32. https://doi.org/10.1016/j.diagmicrobio.2007.04.002[CrossRef]
- Kerkhofs, P., Botton, Y., Thiange, P., Dekeyser, P. and Limet, J.N., 1990. Vet. microbiol., 24: 73-80. https://doi.org/10.1016/0378-1135(90)90052-W[CrossRef]
- Khan, T.I., Ehtisham-ul-Haque, S., Waheed, U., Khan, I., Younas, M. and Ali, S., 2018. Pak. Vet. J., 38:105-108.
- Kolar, J., 1984. Pre. Vet. Med., 2: 215-225. https://doi.org/10.1016/0167-5877(84)90065-5[CrossRef]
- Mainar-Jaime, R.C., Munoz, P.M., de-Miguel, M.J., Grillo, M.J., Marin, C.M., Moriyon, I. and Blasco, J.M., 2005. Can. Vet. J., 46: 913-916.
- Matope, G., Bhebhe, E., Muma, J.B., Lund, A. and Skjerve, E., 2011. Epi. Inf., 139: 157-164. https://doi.org/10.1017/S0950268810000968[CrossRef]
- Mohamand, N., Gunaseelan, L., Sukumar, B. and Porteen, K., 2014. J. Adv. Vet. Anim. Res. 1: 70-72. https://doi.org/10.5455/javar.2014.a8[CrossRef]
- Mohammed, F.U., Ibrahim, S., Ajogi, I. and Olaniyi, B.J., 2011. ISRN Vet. Sci., 2011:132897. https://doi.org/10.5402/2011/132897[CrossRef]
- Nicoletti, P., 2010. Sec. Biol. Med. Sci., 31: 21-32.
- Nielsen, K., 2002. Vet. Microbiol., 90: 447-459. https://doi.org/10.1016/S0378-1135(02)00229-8[CrossRef]
- OIE. 2009. Bovine Brucellosis, In: OIE Terrestrial Manual: Manual of standard for diagnostic test.
- Samartino, L., Gall, D., Gregoret, R. and Nielsen, K., 1999. Vet. Microbiol., 70: 193-200. https://doi.org/10.1016/S0378-1135(99)00122-4[CrossRef]
- Shafee, M., Rabbani, M., Sheikh, A.A., Ahmad, M.D. and razzaq, A., 2011. Vet. Med. Int., 2011: 358950. https://doi.org/10.4061/2011/358950[CrossRef]
- Vanzini, V.R., Aguirre, N.P., Valentini, B.S., Toreoni de Echaide, S., Lugaresi, C.I., Marchesino, M.D. and Nielsen, K., 2001. Vet. Microbiol., 82: 55-60. https://doi.org/10.1016/S0378-1135(01)00370-4[CrossRef]
- Kumar, V.N., Bharathi, M.V., Proteen, K. and Sekar, M., 2016. Adv. Dairy Res., 4: 4.
- Wadood, F., Ahmad, M., Khan, A., Gul. S.T. and Rehman. N., 2009. Pak. Vet. J., 29: 196-198.
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