Exposure and immunity to generalist pathogens differ among host species and vary across spatial scales. Anthrax, caused by a multi-host bacterial pathogen, Bacillus anthracis , is enzootic in Kruger National Park (KNP), South Africa and Etosha National Park (ENP), Namibia. These parks share many of the same potential host species, yet the main anthrax host in one (greater kudu ( Tragelaphus strepsiceros ) in KNP and plains zebra ( Equus quagga ) in ENP) is only a minor host in the other. We investigated species and spatial patterns in anthrax mortalities, B. anthracis exposure, and the ability to neutralize the anthrax lethal toxin to determine if observed host mortality differences between locations could be attributed to population-level variation in pathogen exposure and/or immune response. Using serum collected from zebra and kudu in high and low incidence areas of each park (18- 20 samples/species/area), we estimated pathogen exposure from anti-protective antigen (PA) antibody response using enzyme-linked immunosorbent assay (ELISA) and lethal toxin neutralization with a toxin neutralization assay (TNA). Serological evidence of pathogen exposure followed mortality patterns within each system (kudus: 95% positive in KNP versus 40% in ENP; zebras: 83% positive in ENP versus 63% in KNP). Animals in the high-incidence area of KNP had higher anti-PA responses than those in the low-incidence area, but there were no significant differences in exposure by area within ENP. Toxin neutralizing ability was higher for host populations with lower exposure prevalence, i.e., higher in ENP kudus and KNP zebras than their conspecifics in the other park. These results indicate that host species differ in their exposure to and adaptive immunity against B. anthracis in the two parks. These patterns may be due to environmental differences such as vegetation, rainfall patterns, landscape or forage availability between these systems and their interplay with host behavior (foraging or other risky behaviors), resulting in differences in exposure frequency and dose, and hence immune response.
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Detection of Tick‐Borne Pathogen Coinfections and Coexposures to Foot‐and‐Mouth Disease, Brucellosis, and Q Fever in Selected Wildlife From Kruger National Park, South Africa, and Etosha National Park, Namibia
Background:Although the rate of emerging infectious diseases that originate in wildlife has been increasing globally in recent decades, there is currently a lack of epidemiological data from wild animals. Methodology:We used serology to determine prior exposure to foot‐and‐mouth disease virus (FMDV),Brucellaspp., andCoxiella burnetiiand used genetic testing to detect blood‐borne parasitic infections in the generaEhrlichia,Anaplasma,Theileria, andBabesiafrom wildlife in two national parks, Kruger National Park (KNP), South Africa, and Etosha National Park (ENP), Namibia. Serum and whole blood samples were obtained from free‐roaming plains zebra (Equus quagga), greater kudu (Tragelaphus strepsiceros), impala (Aepyceros melampus), and blue wildebeest (Connochaetes taurinus). Risk factors (host species, sex, and sampling park) for infection with each pathogen were assessed, as well as the prevalence and distribution of co‐occurring infections. Results:In KNP 13/29 (45%; confidence interval [CI]: 26%–64%) kudus tested positive for FMD, but none of these reacted to SAT serotypes. For brucellosis, seropositive results were obtained for 3/29 (10%; CI: 2%–27%) kudu samples. Antibodies againstC. burnetiiwere detected in 6/29 (21%; CI: 8%–40%) kudus, 14/21 (67%; CI: 43%–85%) impalas, and 18/39 (46%; CI: 30%–63%) zebras. A total of 28/28 kudus tested positive forTheileriaspp. (100%; CI: 88%–100%) and 27/28 forAnaplasma/Ehrlichiaspp. (96%; CI: 82%–100%), whereas 12/19 impalas (63%) and 2/39 zebra (5%) tested positive forAnaplasma centrale. In ENP, only 1/29 (3%; CI: 0%–18%) wildebeest samples tested positive for FMD. None of the samples tested positive for brucellosis, whileC. burnetiiantibodies were detected in 26/30 wildebeests (87%; CI: 69%–96%), 16/40 kudus (40%; CI: 25%–57%), and 26/26 plains zebras (100%; CI: 87%–100%). A total of 60%Anaplasma/Ehrlichiaspp. and 35%Theileria/Babesiaspp. in kudu and 37% wildebeest tested positive toTheileriasp. (sable), 30% toBabesia occultans, and 3%–7% toAnaplasmaspp. The seroprevalence of Q fever was significantly higher in ENP, whileBrucellaspp.,Anaplasma,Ehrlichia,Theileria, andBabesiaspecies were significantly higher in KNP. Significant coinfections were also identified. Conclusion:This work provided baseline serological and molecular data on 40+ pathogens in four wildlife species from two national parks in southern Africa.
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- Award ID(s):
- 2106221
- PAR ID:
- 10568159
- Editor(s):
- Chen, Nan-Hua
- Publisher / Repository:
- Transboundary and Emerging Diseases
- Date Published:
- Journal Name:
- Transboundary and Emerging Diseases
- Volume:
- 2024
- Issue:
- 1
- ISSN:
- 1865-1674
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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