Article Information

Authors:
Anita L. Michel1
Roy G. Bengis2

Affiliations:
1Department of Veterinary Tropical Diseases, University of Pretoria, South Africa

2Directorate Veterinary Services, Skukuza, South Africa

Correspondence to:
Anita Michel

Postal address:
Private Bag X04, Onderstepoort 0110, South Africa

How to cite this proceeding:
 Michel, A.L. & Bengis, R.G., 2012, ‘The African buffalo: A villain for inter-species spread of infectious diseases in southern Africa’, Onderstepoort Journal of Veterinary Research 79(2), Art. #453, 5 pages. http://dx.doi.org/10.4102/
ojvr.v79i2.453

Note:
Proceedings of the Conference of the Southern African Centre for Infectious Disease Surveillance ‘One Health’ held at the National Institute for Communicable Diseases, Johannesburg, July 2011.

Copyright Notice:
© 2012. The Authors. Licensee: AOSIS OpenJournals.

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 work is properly cited.
The African buffalo: A villain for inter-species spread of infectious diseases in southern Africa
In This Proceeding...
Open Access
• Abstract
• Introduction
   • Status of African buffaloes
   • Infectious diseases transmitted by African buffaloes
   • Factors related to African buffaloes in disease transmission
   • Factors related to the pathogen
   • Factors related to the environment
   • Impact of infectious diseases on African buffaloes and their environment
   • Diagnosis and control of infectious diseases in African buffaloes
• Conclusion
• References
Abstract

The African buffalo (Syncerus caffer) is a large wild bovid which until recently ranged across all but the driest parts of sub-Saharan Africa, and their local range being limited to about 20 km from surface water. They are of high ecological value due to their important role as bulk feeders in the grazing hierarchy. They also have high economic value, because they are one of the sought after ‘Big Five’ in the eco-tourism industry. In Africa, buffaloes have been recognised for some time as an important role player in the maintenance and transmission of a variety of economically important livestock diseases at the wildlife and/or livestock interface. These include African strains of foot-and-mouth disease (FMD), Corridor disease (theileriosis), bovine tuberculosis and bovine brucellosis. For a number of other diseases of veterinary importance, African buffaloes may also serve as amplifier or incidental host, whereby infection with the causative pathogens may cause severe clinical signs such as death or abortion as in the case of anthrax and Rift Valley fever, or remain mild or subclinical for example heartwater. The long term health implications of most of those infections on the buffalo at a population level is usually limited, and they do not pose a threat on the population’s survival. Because of their ability to harbour and transmit important diseases to livestock, their sustainable future in ecotourism, trade and transfrontier conservation projects become complex and costly and reliable diagnostic tools are required to monitor these infections in buffalo populations.

Introduction

The transmission and spread of infectious diseases amongst and between domestic and wild animals can occur directly through contact (foot-and-mouth disease [FMD], bovine tuberculosis and brucellosis), or indirectly through the agency of haematophagous arthropod vectors such as mosquitoes, tsetse flies and Ixodid ticks (Kock 2005). In addition, environmental contamination with infected ticks (theileriosis) or fomites (anthrax) can infect livestock even when the habitat is not shared at the same time. Some of these diseases can affect a variety of wildlife hosts, but only very few species play a decisive role in disease maintenance and transmission at the wildlife and/or livestock interface. The increasing competition for land available for livestock – based agriculture or wildlife ranching and conservation has highlighted the need for an integrated approach to sustainable livestock and wildlife health, use and management. In this debate the African buffalo features as a villain to those who wish to protect livestock populations from devastating diseases, as they undermine national and international disease eradication schemes, which have been implemented and executed with significant success, and at great cost in the past (Munag’andu et al. 2006). On the other hand, conservationists and wildlife ranchers take on a distinctly different attitude towards controlling livestock diseases transmitted by wildlife (Bengis, Kock & Fischer 2002).

In this overview the role of the African buffalo, both as a victim and asymptomatic carrier in the transmission of the most important livestock diseases at the wildlife and/or livestock interface, is reviewed. Links between disease ecology and buffaloes’ ecology are examined in an attempt to reveal why buffaloes are successful maintenance hosts for several of those diseases.

Status of African buffaloes
Since the early days of European settlement in southern and eastern Africa, African buffaloes have attracted the admiration of hunters and have consequently been a highly sought after trophy animal for the past three centuries (Prins 1996). In addition, they gained extraordinary value for other ecotourism related purposes during the past decades (Van der Merwe, Saayman & Krugell 2004). The African buffalo (Syncerus caffer) is one of the most ubiquitous large herbivores which can tolerate a wide range of climatic conditions and habitats as long as it is provided with access to an abundant supply of water (Grimsdell 1969; Sinclair 1977). Ecologically, the African buffalo is a bulk grazer and occupies an important niche through opening up habitats that are preferred by short-grass grazers (De Vos & Bengis 1994). Currently the conservation status of the African buffalo is satisfactory with no immediate threat of extinction (Friedmann & Daly 2004).

Infectious diseases transmitted by African buffaloes
African buffaloes have been recognised for some time for various roles in disease transmission amongst wildlife species and at the interface with livestock. Amongst the best known diseases are foot-and-mouth disease, caused by the African strains SAT 1, 2 and 3 (FMD viruses) and Corridor disease (theileriosis, caused by Theileria parva), owing to the disastrous, large scale clinical outbreaks they may cause in livestock (Anonymous 2007; Norval, Perry & Young 1992). However, African buffaloes have been implicated in a number of other epidemiological roles involving both indigenous and alien livestock diseases.

Diseases which originated in Africa and co-evolved with African wildlife species including African buffaloes are defined as indigenous. They generally do not pose a threat on the survival of their hosts’ populations because of the evolutionary development of unique coping mechanisms. Well known indigenous diseases maintained by African buffaloes include FMD caused by the SAT strain viruses (Thomson 1995), Corridor disease and African trypanosomosis (Anonymous 2007, 2009; De Vos & Bengis 1994; Norval et al. 1992).

In contrast, foreign, so-called alien livestock diseases, such as bovine tuberculosis (Mycobacterium bovis) and bovine brucellosis (Brucella abortus), have been introduced and successfully established themselves in buffaloes which serve as wildlife maintenance host (De Vos et al. 2001). Rinderpest falls within the same grouping of alien diseases but its extreme pathogenicity and high mortality precluded the development of a wildlife reservoir (De Vos & Bengis 1994). The devastating effect of rinderpest on many cloven hoofed African ungulate species and African buffaloes (as an epidemic end host) in particular at a local or regional population level was more important ecologically and epidemiologically than their potential role in transmission of the disease to livestock. In 2011, rinderpest was officially eradicated from the world (Morens et al. 2011) and therefore its significance for interspecies transmission no longer exists.

Due to their wide geographical range and distribution, African buffaloes have been furthermore implicated as amplifiers or incidental hosts in the epidemiology of a number of other indigenous infectious agents, including those confined to specific localised geographic areas, for example trypanosomes is limited to certain savannah and forested areas endemic for tsetse flies, and buffalo are one of the preferred hosts for these flies and develop a symptomatic carrier state for this parasite (Molooa et al. 1999).

Anthrax, caused by Brucella anthracis is limited to certain anthrax endemic areas of the African continent (Anonymous 2009). For Rift Valley fever little is known about the precise mechanisms of virus maintenance and transmission. However, buffaloes have been associated with a possible sentinel role during epidemics and a possible maintenance role during interepidemic periods, respectively (Bengis et al. 2010; LaBeaud et al. 2011).

Factors related to African buffaloes in disease transmission
The epidemiology of infectious diseases is determined by factors related to the host, the environment and the causative pathogen. In the case of African buffaloes a number of intrinsic behavioural characteristics are instrumental to its role in hosting and transmitting livestock diseases. They are a highly social species living in large herds of up to 1000 animals, whose gregarious behaviour provides ideal conditions for direct pathogen transmission via aerosol and body secretions (Grimsdell 1969; Michel et al. 2006). Individual or small groups of buffaloes have also been shown to migrate over large distances within short periods of time, either in response to drought or as a result of the dispersal strategies for heifers or bachelor bulls. These events, like fission and fusion events driven by changes in the seasonal availability of grazing, take place on a regular basis and constitute a powerful vehicle for pathogen dispersal across herds (Cross, Lloyd-Smith & Getz 2005; Halley, Vandewalle & Taolo 2002).

Factors related to the pathogen
As regards the chronic, slow alien livestock diseases, such as bovine tuberculosis and bovine brucellosis, the lack of coping mechanisms in naïve African buffaloes may result in deleterious long term effect on certain buffalo populations.

Some pathogens exhibit a very strict and narrow host range, for example T. parva, whilst M. bovis is capable of causing disease in a very broad spectrum of domestic and wild animal species. Amongst its wildlife hosts, maintenance host potential has been confirmed for African buffaloes and is suspected for greater kudu and possibly others (Michel et al. 2006). Indirect transmission of pathogens via environmental contamination is more effective if the organism can survive for significant periods of time outside of its host(s). Whilst the survival of most viruses outside the host is very short, M. bovis has been shown to survive for between five days and four weeks in the environment (Tanner & Michel 1999) and the spore forming Bacillus anthracis bacterium is ideally equipped for long term (years) survival outside of a host (De Vos 2004).

Factors related to the environment
African buffaloes occur in many different habitats including woodlands, grasslands, swamps, floodplains and thickets, at a range of altitudes, provided they have access to an abundant supply of water and good quality grazing. This species’ ability to survive in all but the more arid habitats, allows it to host a variety of pathogens under diverse environmental conditions. For example, the abundance of the Aedine mosquitoes, the endemic vector of the Rift Valley fever virus, is influenced by wet climatic shifts which are frequently associated with increased virus transmission to domestic and wild ruminants (Bengis et al. 2010). In addition, African buffaloes spend a considerable percentage of their time in and near water (Ryan, Knechtel & Getz 2006) which further increases their risk of exposure to vectors. In addition, African buffaloes are a preferred host for certain ixodid tick species, the vectors of various protozoal and rickettsial parasites of bovids.

The modern wildlife industry grows at an average annual rate of 5.6% in terms of area exempted for game ranching and is mainly based on ecotourism, hunting and live game trade (Cloete, Taljaard & Grove 2007). This rapid growth rate in conjunction with the historical iconic role of the African buffalo as a member of the ‘Big Five’ for viewing, photographing and hunting has lead to an increase in the numbers and distribution of buffaloes on private land. In certain parts of South Africa the number of game farms registered for keeping buffaloes has equalled or exceeded that of livestock, resulting in an expansion of the wildlife and/or live stock interface and hence a risk in bi-directional disease transmission. High population densities and frequent translocation of African buffaloes between private game properties for commercial gain are contributing to cumulative risk of African buffalo to contract or transmit livestock diseases. For this reason, in South Africa buffaloes and cattle may not be kept together on shared rangeland. However, pathogens do not generally respect fences.

Against the background of the establishment of large wildlife conservation areas and transfrontier parks in southern Africa, the potential role of buffaloes in the transmission of infectious diseases at the wildlife and/or livestock interface cannot be ignored. High expectations have been linked to the creation of large conservation areas in terms of improved and sustainable livelihoods for the communities in and around those wildlife areas. However, increased numbers of livestock and buffaloes, in the absence of game deterrent fences and often a lack of effective livestock vaccines, will inevitably increase the risk of disease transmission, and make disease eradication from livestock virtually impossible (Kock 2005).

Impact of infectious diseases on African buffaloes and their environment
Amongst the infectious diseases, FMD and Corridor disease and African trypanosomosis are truly asymptomatic in African buffaloes, which act as biological reservoirs of infection in an endemic cycle. The FMD infection occasionally escapes into other sympatric wild cloven-hoofed species, and where livestock are in contact with African buffaloes, they may become infected resulting in devastating outbreaks with a high socio-economic impact (Vosloo et al. 2005).

Rift Valley fever, is a seasonal vector born disease and viremia and abortions have been reported in African buffaloes (Evans et al. 2008). Their exact role in the epidemiology of Rift Valley fever is however, still unknown but results of serological investigations in Kenya and South Africa indicated that African buffaloes become infected with the virus (Evans et al. 2008; LaBeaud et al. 2011).

Bovine tuberculosis in African buffaloes has been well documented and can be described as a chronic, progressively debilitating condition (De Vos et al. 2001). It has spread throughout the buffalo population of the Kruger National Park and spilled into more than a dozen other wildlife species. There is a continuous risk for spillback into livestock and an associated zoonotic risk for animal owners, which is undetermined (Berg et al. 2011; Michel, Müller & Van Helden 2010).

Anthrax is a sporadic, usually fatal disease affecting buffaloes in numerous endemic areas in sub-Saharan Africa (De Vos 1990; Mohan & Gotts 1970). Herbivores are known to be more susceptible to anthrax than omnivores and carnivores, and losses in African buffaloes, greater kudu, nyala and waterbuck have been significant in outbreaks of this disease in southern and eastern Africa (De Vos 2004). When buffaloes are affected by anthrax, they serve as highly effective multipliers of B. anthracis, which can contaminate the soil and run-off water, and carcasses become amplifiers for blowflies. Anthrax may be transmitted to neighbouring livestock farms and initiate an outbreak amongst cattle, and the converse has also been experienced when an outbreak in cattle spilled over into wildlife in an adjoining conservation area (Malilangwe – Zimbabwe) (De Vos 1990).

It has been speculated that African buffaloes are the species with the highest susceptibility to rinderpest, which decimated the buffalo populations all over Africa during the rinderpest epidemic between 1888 and 1899 (De Vos & Bengis 1994).

Diagnosis and control of infectious diseases in African buffaloes
Availability of diagnostic tests for wildlife species is very often the biggest limitation in diagnosing infectious diseases in target wildlife species which are taxonomically far removed from the closest livestock counterparts. The African buffalo falls into the subfamily Bovinae together with domestic cattle, which is helpful and provides a basis for adapting and developing diagnostic tests for relevant infections in buffaloes. However, it needs to be emphasised that all tests applied in buffaloes still require validation to prove fitness for purpose as stated by the World Organisation for Animal Health (OIE) (OIE 2009). The question whether infectious diseases in buffaloes require controlling is a contentious one and is best discussed per disease grouping. Since the causative agents of certain indigenous diseases, namely FMD viruses, trypanosomes and theilerias, are widely maintained by African buffaloes and generally do not pose a threat to these population’s existence, diagnostic testing is usually applied for monitoring and surveillance activities at population level. For movement purposes and international trade, the same tests (including direct pathogen detection for Corridor disease and trypanosomosis) are applied at individual animal level in conjunction with herd testing records. It is accepted that FMD can at best be contained in wildlife areas that have buffaloes, but eradication will not be achievable (Vosloo et al. 2005).

The situation is essentially the same for indigenous diseases detected less frequently in African buffaloes, such as Rift Valley fever and anthrax, where outbreaks are monitored strictly for epidemiological information and analyses.

A very different scenario is presented in the cases of bovine tuberculosis and bovine brucellosis, which are both alien diseases introduced into the buffalo population most likely through contact with infected cattle. Following their successful establishment in African buffaloes as their wildlife reservoir or maintenance host, the state veterinary and conservation authorities have been faced with a set of previously unknown challenges. Apart from the need to prevent spillover of the diseases to neighbouring livestock, these diseases may spread uncontrolled within infected conservation areas. Although our current knowledge on the impact of bovine tuberculosis and bovine brucellosis does not indicate an immediate threat on buffalo survival at the population level, it would be premature to make any prediction about the long term impact at this point in time. As no effective vaccine exists for bovine tuberculosis in animals and given the extremely broad host spectrum of the causative organism, the real threat goes beyond buffalo conservation but concerns severely affected sympatric species such as lions and kudus (Michel et al. 2009). It is fair to speculate that African buffaloes will not remain the only maintenance host in an endemically infected ecosystem such as the Kruger National Park and disease management and control strategies are urgently called for. Two effective vaccines are registered for the control of bovine brucellosis in cattle, but their efficacy and safety in African buffaloes has not been tested, as the disease is currently considered to have little effect on African buffaloes and the ecosystem (Godfroid 2004). Pre-movement testing of buffaloes for both bovine tuberculosis and brucellosis is an absolute requirement to minimise the risk of disease transmission to uninfected populations. In the case of bovine tuberculosis serological tests are not useful to detect infection and the intradermal tuberculin test (skin test) is applied in conjunction with the interferon gamma assay (Michel et al. 2011; Michel & Simoes 2009).

Conclusion

It is clear that disease transmission at the interface is bi-directional and African buffaloes are culprits or villains in respect of some diseases, whilst they have fallen victim to alien diseases transmitted from cattle. As the wildlife and/or livestock and/or human interface is rapidly expanding and gaining in intensity and complexity, there should be no room for a blaming game, but it must be appreciated that African buffaloes form an integral part of the indigenous fauna of Africa and are inseparable from their indigenous pathogens. A strictly separate approach is needed for the alien diseases which may directly affect the health of buffaloes or indirectly the conservation of wildlife by turning infected areas into ‘conservation islands’ and making them unavailable for conservation in the bigger sense.

To enable ecologists, veterinary researchers and conservation biologists to correctly assess and predict the long term dynamics of significant livestock diseases at this growing and intensifying disease interface, an understanding of the host-parasite interactions at population level in cattle and African buffaloes is crucial to finding solutions and to attempt achieve compatibility between traditional livestock farming and wildlife conservation-based ecotourism. It should also be emphasised that host-parasite interactions are not limited to the processes guiding infection and immunopathogenesis, but they must include the external determinants of the environment, including climate change, human interventions and other ecosystem drivers.

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10. Disease mortality in domesticated animals is predicted by host evolutionary relationships
Maxwell J. Farrell, T. Jonathan Davies
Proceedings of the National Academy of Sciences  vol: 116  issue: 16  first page: 7911  year: 2019  
doi: 10.1073/pnas.1817323116

11. Brucellosis in wildlife in Africa: a systematic review and meta-analysis
Gregory Simpson, Peter N. Thompson, Claude Saegerman, Tanguy Marcotty, Jean-Jacques Letesson, Xavier de Bolle, Jacques Godfroid
Scientific Reports  vol: 11  issue: 1  year: 2021  
doi: 10.1038/s41598-021-85441-w

12. The complete genome sequence of the African buffalo (Syncerus caffer)
Brigitte Glanzmann, Marlo Möller, Nikki le Roex, Gerard Tromp, Eileen G. Hoal, Paul D. van Helden
BMC Genomics  vol: 17  issue: 1  year: 2016  
doi: 10.1186/s12864-016-3364-0

13. Improved detection of Mycobacterium tuberculosis and M. bovis in African wildlife samples using cationic peptide decontamination and mycobacterial culture supplementation
Wynand J. Goosen, Léanie Kleynhans, Tanya J. Kerr, Paul D. van Helden, Peter Buss, Robin M. Warren, Michele A. Miller
Journal of Veterinary Diagnostic Investigation  vol: 34  issue: 1  first page: 61  year: 2022  
doi: 10.1177/10406387211044192

14. A review of bovine tuberculosis at the wildlife–livestock–human interface in sub-Saharan Africa
M. De GARINE-WICHATITSKY, A. CARON, R. KOCK, R. TSCHOPP, M. MUNYEME, M. HOFMEYR, A. MICHEL
Epidemiology and Infection  vol: 141  issue: 7  first page: 1342  year: 2013  
doi: 10.1017/S0950268813000708

15. Modeling the spatial distribution of African buffalo (Syncerus caffer) in the Kruger National Park, South Africa
Kristen Hughes, Geoffrey T. Fosgate, Christine M. Budke, Michael P. Ward, Ruth Kerry, Ben Ingram, Arda Yildirim
PLOS ONE  vol: 12  issue: 9  first page: e0182903  year: 2017  
doi: 10.1371/journal.pone.0182903

16. Culture-independent detection of Mycobacterium tuberculosis complex DNA using targeted next generation sequencing in African buffalo (Syncerus caffer) oronasal swabs in South Africa
Sinegugu Kholeka Mhlophe, Charlene Clarke, Giovanni Ghielmetti, Megan Matthews, Tanya Jane Kerr, Michele Ann Miller, Wynand Johan Goosen
Frontiers in Veterinary Science  vol: 12  year: 2025  
doi: 10.3389/fvets.2025.1523628

17. Theileria parva: a parasite of African buffalo, which has adapted to infect and undergo transmission in cattle
W Ivan Morrison, Johanneke D. Hemmink, Philip G. Toye
International Journal for Parasitology  vol: 50  issue: 5  first page: 403  year: 2020  
doi: 10.1016/j.ijpara.2019.12.006

18. Coexisting with wildlife in transfrontier conservation areas in Zimbabwe: Cattle owners’ awareness of disease risks and perceptions of the role played by wildlife
M. de Garine-Wichatitsky, E. Miguel, B. Mukamuri, E. Garine-Wichatitsky, J. Wencelius, D.M. Pfukenyi, A. Caron
Comparative Immunology, Microbiology and Infectious Diseases  vol: 36  issue: 3  first page: 321  year: 2013  
doi: 10.1016/j.cimid.2012.10.007

19. Evaluation of the Discriminatory Power of Variable Number of Tandem Repeat Typing ofMycobacterium bovisIsolates from Southern Africa
T. M. Hlokwe, P. van Helden, A. Michel
Transboundary and Emerging Diseases  vol: 60  first page: 111  year: 2013  
doi: 10.1111/tbed.12096

20. Evidence of increasing intra and inter-species transmission of Mycobacterium bovis in South Africa: Are we losing the battle?
T.M. Hlokwe, P. van Helden, A.L. Michel
Preventive Veterinary Medicine  vol: 115  issue: 1-2  first page: 10  year: 2014  
doi: 10.1016/j.prevetmed.2014.03.011

21. Antimicrobial resistance (AMR) as a form of human–wildlife conflict: Why and how nondomesticated species should be incorporated into AMR guidance
Jessica Mitchell
Ecology and Evolution  vol: 13  issue: 9  year: 2023  
doi: 10.1002/ece3.10421

22. Review of Diagnostic Tests for Detection of Mycobacterium bovis Infection in South African Wildlife
Netanya Bernitz, Tanya J. Kerr, Wynand J. Goosen, Josephine Chileshe, Roxanne L. Higgitt, Eduard O. Roos, Christina Meiring, Rachiel Gumbo, Candice de Waal, Charlene Clarke, Katrin Smith, Samantha Goldswain, Taschnica T. Sylvester, Léanie Kleynhans, Anzaan Dippenaar, Peter E. Buss, David V. Cooper, Konstantin P. Lyashchenko, Robin M. Warren, Paul D. van Helden, Sven D. C. Parsons, Michele A. Miller
Frontiers in Veterinary Science  vol: 8  year: 2021  
doi: 10.3389/fvets.2021.588697

23. The bison–human–environment dynamics of brucellosis infection with prevention and control studies
Adison Thongtha, Chairat Modnak
International Journal of Dynamics and Control  vol: 12  issue: 2  first page: 551  year: 2024  
doi: 10.1007/s40435-023-01194-6

24. Mixed-host aggregations and helminth parasite sharing in an East African wildlife–livestock system
Kimberly VanderWaal, George Paul Omondi, Vincent Obanda
Veterinary Parasitology  vol: 205  issue: 1-2  first page: 224  year: 2014  
doi: 10.1016/j.vetpar.2014.07.015

25. Wild Animal Tuberculosis: Stakeholder Value Systems and Management of Disease
Eamonn Gormley, Leigh A. L. Corner
Frontiers in Veterinary Science  vol: 5  year: 2018  
doi: 10.3389/fvets.2018.00327

26. The evaluation of candidate biomarkers of cell-mediated immunity for the diagnosis of Mycobacterium bovis infection in African buffaloes (Syncerus caffer)
Wynand J. Goosen, David Cooper, Robin M. Warren, Michele A. Miller, Paul D. van Helden, Sven D.C. Parsons
Veterinary Immunology and Immunopathology  vol: 162  issue: 3-4  first page: 198  year: 2014  
doi: 10.1016/j.vetimm.2014.10.008

27. Global Foot-and-Mouth Disease Research Update and Gap Analysis: 2 - Epidemiology, Wildlife and Economics
T. J. D. Knight-Jones, L. Robinson, B. Charleston, L. L. Rodriguez, C. G. Gay, K. J. Sumption, W. Vosloo
Transboundary and Emerging Diseases  vol: 63  first page: 14  year: 2016  
doi: 10.1111/tbed.12522

28. First detection ofMycobacterium bovisinfection in Giraffe (Giraffa camelopardalis) in the Greater Kruger National Park Complex: Role and implications
Tiny M. Hlokwe, Anita L. Michel, Emily Mitchel, Nomakorinte Gcebe, Bjorn Reininghaus
Transboundary and Emerging Diseases  vol: 66  issue: 6  first page: 2264  year: 2019  
doi: 10.1111/tbed.13275

29. Use of blood matrices and alternative biological fluids for antibody detection in animal tuberculosis
Konstantin P. Lyashchenko, Alina Sikar-Gang, Archana A. Sridhara, Ashley Johnathan-Lee, Rubyat Elahi, Rena Greenwald, Paul Lambotte, Javan Esfandiari, Eduard O. Roos, Tanya J. Kerr, Michele A. Miller, Tyler C. Thacker, Mitchell V. Palmer, W. Ray Waters
Veterinary Immunology and Immunopathology  vol: 239  first page: 110303  year: 2021  
doi: 10.1016/j.vetimm.2021.110303

30. Genomic Profiling for Piroplasms in Feeding Ixodid Ticks in the Eastern Cape, South Africa
Olusesan Adeyemi Adelabu, Benson Chuks Iweriebor, Anthony Ifeanyi Okoh, Larry Chikwelu Obi
Pathogens  vol: 9  issue: 12  first page: 1061  year: 2020  
doi: 10.3390/pathogens9121061

31. Combatting African Animal Trypanosomiasis (AAT) in livestock: The potential role of trypanotolerance
M. Yaro, K.A. Munyard, M.J. Stear, D.M. Groth
Veterinary Parasitology  vol: 225  first page: 43  year: 2016  
doi: 10.1016/j.vetpar.2016.05.003

32. BCG vaccination for bovine tuberculosis; conclusions from the Jerusalem One Health workshop
Ben J. Marais, Bryce M. Buddle, Lin‐Mari Klerk‐Lorist, Patrick Nguipdop‐Djomo, Frederick Quinn, Charles Greenblatt
Transboundary and Emerging Diseases  vol: 66  issue: 2  first page: 1037  year: 2019  
doi: 10.1111/tbed.13089

33. Phylogeographical and cross‐species transmission dynamics of SAT1 and SAT2 foot‐and‐mouth disease virus in Eastern Africa
George Omondi, Moh A. Alkhamis, Vincent Obanda, Francis Gakuya, Abraham Sangula, Steven Pauszek, Andres Perez, Stephen Ngulu, Richard van Aardt, Jonathan Arzt, Kim VanderWaal
Molecular Ecology  vol: 28  issue: 11  first page: 2903  year: 2019  
doi: 10.1111/mec.15125

34. Range contraction and expansion of the African buffalo under climate change scenarios
Eric Adjei Lawer, Esther Love Darkoh, Christopher Akasere
Biodiversity  vol: 26  issue: 1  first page: 47  year: 2025  
doi: 10.1080/14888386.2024.2426505

35. The Xpert MTB/RIF Ultra assay detects Mycobacterium tuberculosis complex DNA in white rhinoceros (Ceratotherium simum) and African elephants (Loxodonta africana)
Wynand J. Goosen, Tanya J. Kerr, Léanie Kleynhans, Robin M. Warren, Paul D. van Helden, David H. Persing, Sven D. C. Parsons, Peter Buss, Michele A. Miller
Scientific Reports  vol: 10  issue: 1  year: 2020  
doi: 10.1038/s41598-020-71568-9

36. An Overview of Disease-Free Buffalo Breeding Projects with Reference to the Different Systems Used in South Africa
Liesel Laubscher, Louwrens Hoffman
Sustainability  vol: 4  issue: 11  first page: 3124  year: 2012  
doi: 10.3390/su4113124

37. State-shifts of lion prey selection in the Kruger National Park
N. T. Maruping-Mzileni, P. J. Funston, S. M. Ferreira
Wildlife Research  vol: 44  issue: 1  first page: 28  year: 2017  
doi: 10.1071/WR16090

38. The Bacterial and pathogenic landscape of African buffalo (Syncerus caffer) whole blood and serum from Kenya
Richard Nyamota, Earl A. Middlebrook, Hussein M. Abkallo, James Akoko, Francis Gakuya, Lillian Wambua, Bernard Ronoh, Isaac Lekolool, Athman Mwatondo, Mathew Muturi, Bernard Bett, Jeanne M. Fair, Andrew W. Bartlow
Animal Microbiome  vol: 7  issue: 1  year: 2025  
doi: 10.1186/s42523-024-00374-9

39. Serum biochemistry panels in African buffalo: Defining reference intervals and assessing variability across season, age and sex
Claire E. Couch, Morgan A. Movius, Anna E. Jolles, M. Elena Gorman, Johanna D. Rigas, Brianna R. Beechler, Emmanuel Serrano Ferron
PLOS ONE  vol: 12  issue: 5  first page: e0176830  year: 2017  
doi: 10.1371/journal.pone.0176830

40. Pathological findings in African buffaloes (Syncerus caffer) in South Africa
Daniel B. Woodburn, Johan Steyl, Elizabeth C. du Plessis, Rick D. Last, Bjorn Reininghaus, Emily P. Mitchell
Journal of the South African Veterinary Association  vol: 92  year: 2021  
doi: 10.4102/jsava.v92i0.2117

41. Brucella seroprevalence in cattle near a wildlife reserve in Kenya
Sofie Enström, Daniel Nthiwa, Bernard Bett, Amanda Karlsson, Silvia Alonso, Johanna F. Lindahl
BMC Research Notes  vol: 10  issue: 1  year: 2017  
doi: 10.1186/s13104-017-2941-x

42. Facts and dilemmas in diagnosis of tuberculosis in wildlife
M. Maas, A.L. Michel, V.P.M.G. Rutten
Comparative Immunology, Microbiology and Infectious Diseases  vol: 36  issue: 3  first page: 269  year: 2013  
doi: 10.1016/j.cimid.2012.10.010

43. Tolerance factors in human-wildlife conflicts in protected areas: the case of Cross River National Park, Cross River State Nigeria
Oghenetejiri Digun-Aweto, Peet Van Der Merwe, Melville Saayman
GeoJournal  vol: 87  issue: 1  first page: 349  year: 2022  
doi: 10.1007/s10708-020-10254-9

44. Strategic management of livestock to improve biodiversity conservation in African savannahs: a conceptual basis for wildlife–livestock coexistence
Richard W. S. Fynn, David J. Augustine, Michael J. S. Peel, Michel de Garine‐Wichatitsky, Sarah Durant
Journal of Applied Ecology  vol: 53  issue: 2  first page: 388  year: 2016  
doi: 10.1111/1365-2664.12591

45. WILDLIFE ON THE MOVE: A HIDDEN TUBERCULOSIS THREAT TO CONSERVATION AREAS AND GAME FARMS THROUGH INTRODUCTION OF UNTESTED ANIMALS
Tiny Motlatso Hlokwe, Lin-Mari De Klerk-Lorist, Anita Luise Michel
Journal of Wildlife Diseases  vol: 52  issue: 4  first page: 837  year: 2016  
doi: 10.7589/2015-10-281

46. Molecular Characterization of the Emerging Sublineage IND2001E of Foot-and-Mouth Disease Virus Serotype O in Buffalo in Manikganj, Bangladesh
Md Zulfekar Ali, Naima Tasnim, Md Ataur Rahman, Md Hafizur Rahman, Mirza Mienur Meher, Md Giasuddin
Macedonian Veterinary Review  vol: 48  issue: 2  first page: 229  year: 2025  
doi: 10.2478/macvetrev-2025-0028

47. Context‐dependent survival, fecundity and predicted population‐level consequences of brucellosis inAfrican buffalo
Erin E. Gorsich, Vanessa O. Ezenwa, Paul C. Cross, Roy G. Bengis, Anna E. Jolles, Andrew Fenton
Journal of Animal Ecology  vol: 84  issue: 4  first page: 999  year: 2015  
doi: 10.1111/1365-2656.12356