The prevalence and risk factors associated with Leptospira in donkeys in Ngaka Modiri Molema District, North West Province, South Africa.
Abstract: Leptospirosis is one of the major emerging global economic and health problems affecting donkeys, thereby reducing their work output. Furthermore, the disease has public health importance because of its zoonotic nature. Despite the significant contribution donkeys make to the national economy, less attention is given to diseases that afflict donkeys and reduce their productivity and performance. A cross-sectional study was conducted to investigate the seroprevalence of Leptospira and identify risk factors associated with the occurrence of the disease among donkeys in the study area. Methods: A questionnaire survey was used to collect the following data: Demographic, environmental, management, and health-related factors. Blood samples were aseptically collected from 365 randomly selected donkeys from 19 villages. The sera were tested using the microscopic agglutination test. Categorical variables were summarized and presented as proportions and their 95% confidence interval (CI). A binary logistic regression model was fitted to the data to identify risk factors associated with Leptospira seroprevalence in donkeys within the study areas. Results: The majority of the donkeys (29.6%; n=108/365) were from Mafikeng local municipality, and the rest (19.7%; n=72/365) were from Ratlou. Just over half (58.1%; n=212/365) of the donkeys tested were female, and the remaining (41.9%; n=153/365) were males. In addition, most donkeys (42.7%; n=156/365) were between 6 and 12 years old, followed by those between 0 and 5 years (37%; n=135/365), and only 20.3% (n=74/365) were above 12 years. Out of the donkeys tested, 11.5% (95% CI: 4.86-18.14) donkeys tested positive for Leptospira antibodies. The most common serovar was Bratislava (81%; n=34/42), followed by Tarassovi (19.04%; n=8/42). While gender was positively associated with seroprevalence of the disease (Adjusted Odds Ratio [AOR]=4.88; p=0.0001), the presence of horses (AOR=0.226; p=0.002) and agricultural activities (AOR=0.093; p=0.0001) in the vicinity of the dwellings of the donkeys were negatively associated with Leptospira seropositivity in the study area. Conclusions: Findings reported here show that donkeys in the study area are reservoirs for the predominant serovar Bratislava and the less dominant serovar Tarassovi. The gender of the donkey was a risk factor for Leptospira seroprevalence. Further studies are needed to investigate the role of agricultural activities in the vicinity of the dwellings of donkeys on the occurrence of Leptospira in the study area.
Copyright: © Daddy, et al.
Publication Date: 2020-09-28 PubMed ID: 33132620PubMed Central: PMC7566248DOI: 10.14202/vetworld.2020.2020-2027Google Scholar: Lookup
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Summary
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The article presents a study on the occurrence and risk factors of Leptospira, a bacterial disease, in donkeys from Ngaka Modiri Molema District, South Africa, to understand its impact on the animals’ health and productivity, and its potential zoonotic nature.
Objective and Methodology
- The primary goal of this research was to investigate the seroprevalence, which is the level of a pathogen in a population as measured in blood serum, of Leptospira in donkeys in the Ngaka Modiri Molema District, North West Province, South Africa.
- The research team also sought to identify risk factors associated with the disease’s prevalence among these animals.
- The researchers used a cross-sectional study design, a type of observational study that analyzes data from a population, or a representative subset, at a specific point in time.
- As part of the study, a questionnaire survey was conducted to gather information related to demographic, environmental, management, and health-associated factors.
- Blood samples were collected from 365 randomly selected donkeys inhabiting 19 different villages, and these samples were tested using a diagnostic tool, the microscopic agglutination test.
- The data collected was used to fit a binary logistic regression model, a statistical model that predicts the probability of occurrence of an event by fitting data to a logistic curve, to identify risk factors associated with the seroprevalence of Leptospira.
Results
- This study found that 29.6% of the tested donkeys were from the Mafikeng local municipality and 19.7% were from Ratlou.
- In terms of the gender of the donkeys, 58.1% were female, and 41.9% were males.
- The majority of the donkeys (42.7%) were between 6 and 12 years old.
- Out of all the tested donkeys, 11.5% were found to be positive for Leptospira antibodies, indicating exposure to the bacterial disease.
- The most common strain of Leptospira found was Bratislava (81%), followed by Tarassovi (19.04%).
- Gender appeared to be a risk factor associated with the presence of the disease with males at higher risk. In contrast, the presence of horses and agricultural activities near the donkeys’ dwellings were negatively associated with the occurrence of Leptospira.
Conclusions
- The study findings suggest that donkeys within the studied geographical area are carriers for the predominant Leptospira serovar, Bratislava, and the less prominent, Tarassovi.
- Gender was found to be a significant risk factor for the disease’s seroprevalence with males being more susceptible.
- The researchers recommend further studies to investigate the role of agricultural activities in the vicinity of the donkeys’ dwellings on the occurrence of Leptospira.
Cite This Article
APA
Daddy KK, Mwanza M, Oguttu JW, Ngoma L.
(2020).
The prevalence and risk factors associated with Leptospira in donkeys in Ngaka Modiri Molema District, North West Province, South Africa.
Vet World, 13(9), 2020-2027.
https://doi.org/10.14202/vetworld.2020.2020-2027 Publication
Researcher Affiliations
- Department of Animal Health, School of Agriculture, Faculty of Natural and Agriculture Sciences, North West University, Private Bag X2046, Mmabatho 2735, South Africa.
- Department of Animal Health, School of Agriculture, Faculty of Natural and Agriculture Sciences, North West University, Private Bag X2046, Mmabatho 2735, South Africa.
- Department of Agriculture and Animal Health, College of Agriculture and Environmental Sciences, University of South Africa, Florida Science Campus, Johannesburg, South Africa.
- Department of Animal Health, School of Agriculture, Faculty of Natural and Agriculture Sciences, North West University, Private Bag X2046, Mmabatho 2735, South Africa.
References
This article includes 31 references
- Faostat F. Food and Agriculture Organization Statistical Database. 2014. Available from: http://www.fao.org/corp/statistics/access online . Retrieved on 19-02-2018.
- Marufu M. Socio-Economic Importance, Health and Welfare Aspects of Donkeys (Equus asinus) Used for Carting in a Peri-Urban Area of South Africa. University of Fort Hare, Alice, Eastern Cape, South Africa. 2014.
- Bharti AR, Nally JE, Ricaldi JN, Matthias MA, Diaz MM, Lovett MA, Levett PN, Gilman RH, Willig MR, Gotuzzo E, Vinetz JM. Leptospirosis: a zoonotic disease of global importance.. Lancet Infect Dis 2003 Dec;3(12):757-71.
- Burriel A.R. Leptospirosis:An important zoonotic diseases. Current Research, Technology and Education Topics in Applied Microbiology and Microbial Biotechnology Spain: Formatex; 2010; pp. 687–693.
- Derne BT, Fearnley EJ, Lau CL, Paynter S, Weinstein P. Biodiversity and leptospirosis risk: a case of pathogen regulation?. Med Hypotheses 2011 Sep;77(3):339-44.
- Loureiro A.P, Martins G, Thomé S, Lilenbaum W. Laboratorial diagnosis of animal leptospirosis. Rev. Bras. Ciênc. Vet. 2013;20(3):119–126.
- Haake D.A. Spirochetes. Encyclopedia of Microbiology 3rd ed. Oxford: Academic Press; 2009; pp. 278–292.
- Martins G, Lilenbaum W. Control of bovine leptospirosis: Aspects for consideration in a tropical environment.. Res Vet Sci 2017 Jun;112:156-160.
- Utzinger J, Becker SL, Knopp S, Blum J, Neumayr AL, Keiser J, Hatz CF. Neglected tropical diseases: diagnosis, clinical management, treatment and control.. Swiss Med Wkly 2012;142:w13727.
- Adler B, de la Peña Moctezuma A. Leptospira and leptospirosis.. Vet Microbiol 2010 Jan 27;140(3-4):287-96.
- Hesterberg UW, Bagnall R, Bosch B, Perrett K, Horner R, Gummow B. A serological survey of leptospirosis in cattle of rural communities in the province of KwaZulu-Natal, South Africa.. J S Afr Vet Assoc 2009 Mar;80(1):45-9.
- Potts AD, Lötter C, Robinson JT. Serological prevalence of leptospiral antibodies in pigs in South Africa.. Onderstepoort J Vet Res 1995 Dec;62(4):281-4.
- Roach JM, van Vuuren M, Picard JA. A serological survey of antibodies to Leptospira species in dogs in South Africa.. J S Afr Vet Assoc 2010 Sep;81(3):156-9.
- Simbizi V, Saulez MN, Potts A, Lötter C, Gummow B. A study of leptospirosis in South African horses and associated risk factors.. Prev Vet Med 2016 Nov 1;134:6-15.
- Mucina L, Rutherford M.C. The vegetation of South Africa, Lesotho and Swaziland. South African National Biodiversity Institute, South African. 2006.
- South African Weather Services. Average of the Daily Temperatures (°c) and Total of the Monthly Daily Rain (mm) form 2008-2017 in Different Station in the North-West Province. South African Weather Services, Pretoria, 2017.
- de Vries SG, Visser BJ, Nagel IM, Goris MG, Hartskeerl RA, Grobusch MP. Leptospirosis in Sub-Saharan Africa: a systematic review.. Int J Infect Dis 2014 Nov;28:47-64.
- Alvarado-Esquivel C, Cruz-Romero A, Romero-Salas D, Alvarado-Félix ÁO, Aguilar-Domínguez M, Ochoa-Valencia JL, Alvarado-Esquivel D, Hernández-Tinoco J, Zamarripa-Barboza JA, Sánchez-Anguiano LF. Apparently high Leptospira antibody seropositivity in donkeys for slaughter in three municipalities in Durango, Mexico.. J Vet Diagn Invest 2018 Nov;30(6):929-932.
- Benkirane A, Noury S, Hartskeerl RA, Goris MG, Ahmed A, Nally JE. Preliminary Investigations on the Distribution of Leptospira Serovars in Domestic Animals in North-west Morocco.. Transbound Emerg Dis 2016 Apr;63(2):e178-84.
- Grubišic M, Milas Z, Cvetnic Z, Habuš J, Perko V.M, Majetic Z. Š, Turk N. Serological research of the distribution of leptospirosis in donkeys in the Republic of Croatia. Vet. Stanica 2011;42(4):307–315.
- Barragan V, Nieto N, Keim P, Pearson T. Meta-analysis to estimate the load of Leptospira excreted in urine: beyond rats as important sources of transmission in low-income rural communities.. BMC Res Notes 2017 Jan 28;10(1):71.
- Hajikolaei M.R.H, Haidari M, Abdollapour G. Comparison of leptospiral infection in the horse and donkey. Bull. Vet. Inst. Pulawy 2005;49:175–178.
- Barsoum IS, Botros BA, Morcos MB. Equine leptospirosis with some clinical observations.. Ann Rech Vet 1978;9(1):115-8.
- Gummow B, Myburgh JG, Thompson PN, van der Lugt JJ, Spencer BT. Three case studies involving Leptospira interrogans serovar pomona infection in mixed farming units.. J S Afr Vet Assoc 1999 Mar;70(1):29-34.
- Azócar-Aedo L, Monti G, Jara R. Leptospira spp. in Domestic Cats from Different Environments: Prevalence of Antibodies and Risk Factors Associated with the Seropositivity.. Animals (Basel) 2014 Sep 29;4(4):612-26.
- Alavi SM, Khoshkho MM. Seroprevalence study of leptospirosis among rice farmers in khuzestan province, South west iran, 2012.. Jundishapur J Microbiol 2014 Jul;7(7):e11536.
- Kikuti M, Langoni H, Nobrega D, Corrêa A, Ullmann L. Occurrence and risk factors associated with canine leptospirosis. J. Venom. Anim. Toxins Incl. Trop. Dis. 2012;18(1):124–127.
- Meeyam T, Tablerk P, Petchanok B, Pichpol D, Padungtod P. Seroprevalence and risk factors associated with leptospirosis in dogs.. Southeast Asian J Trop Med Public Health 2006 Jan;37(1):148-53.
- Dias JP, Teixeira MG, Costa MC, Mendes CM, Guimarães P, Reis MG, Ko A, Barreto ML. Factors associated with Leptospira sp infection in a large urban center in northeastern Brazil.. Rev Soc Bras Med Trop 2007 Sep-Oct;40(5):499-504.
- Hamond C, Martins G, Bremont S, Medeiros MA, Bourhy P, Lilenbaum W. Predominance of Leptospira interrogans serovar Bratislava DNA in vaginal fluid of mares suggests sexual transmission of leptospirosis.. Anim Reprod Sci 2014 Dec 30;151(3-4):275-9.
- Schoonman L, Swai ES. Herd- and animal-level risk factors for bovine leptospirosis in Tanga region of Tanzania.. Trop Anim Health Prod 2010 Oct;42(7):1565-72.
Citations
This article has been cited 2 times.- de Andrade Morais D, Nunes BC, Soares RR, de Oliveira MD, da Costa DF, de Araújo HG, Júnior JPA, Malossi CD, Silva MLCR, de Azevedo SS, Alves CJ. Strong Evidence of the Role of Donkeys in the Epidemiology of Leptospira spp. in Semiarid Conditions.. Microorganisms 2023 Jul 22;11(7).
- Hassan ZM, Manyelo TG, Nemukondeni N, Sebola AN, Selaledi L, Mabelebele M. The Possibility of Including Donkey Meat and Milk in the Food Chain: A Southern African Scenario.. Animals (Basel) 2022 Apr 21;12(9).
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