Detection of native interferon-γ in nyala (Tragelaphus angasii) : towards diagnosing tuberculosis
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Date
Authors
Roux, Lezaan
McCall, Alicia J.
Michel, Anita Luise
Journal Title
Journal ISSN
Volume Title
Publisher
OASIS
Abstract
Mycobacterium bovis is the main cause of tuberculosis in wildlife. In South Africa, African
buffaloes (Syncerus caffer) are a wildlife maintenance host while a number of other species are
considered spillover hosts. Nyala (Tragelaphus angasii), a large antelope species from Southern
Africa, is frequently traded and can be infected with M. bovis. Interferon gamma (IFN-γ) release
assays that detect cell-mediated immune (CMI) responses to M. bovis infection have shown
promise in elephants, rhinoceroses and buffaloes. The BOVIGAM® assay is a commercial
IFN-γ release assay designed to detect tuberculosis in cattle and has been validated in buffaloes.
We tested the suitability of the BOVIGAM® assay to detect native IFN-γ release in nyala. Blood
samples collected from 17 nyalas were stimulated with different mitogens and IFN-γ release
measured. We found that incubating whole blood with phorbol 12-myristate 13-acetate and
calcium ionophore (PMA/CaI) resulted in the highest levels of IFN-y release. Samples
stimulated with tuberculin purified protein derivatives of M. bovis (PPDb) and M. avium
(PPDa) did not show significant IFN-γ production. An intradermal tuberculin test (IDT) and
culture of tissues from 15 of the 17 culled nyala were also performed, which supported the
findings of the BOVIGAM® assay, suggesting the potential value of this assay for the diagnosis
of tuberculosis in nyala.
Description
Keywords
Mycobacterium bovis, Tuberculosis (TB), Nyala (Tragelaphus angasii), Interferon gamma (IFN-γ), Cell-mediated immune (CMI)
Sustainable Development Goals
Citation
Roux, L., McCall, A.J. &
Michel, A.L., 2019, ‘Detection
of native interferon-γ in nyala
(Tragelaphus angasii):
Towards diagnosing
tuberculosis’, Onderstepoort
Journal of Veterinary
Research 86(1), a1796.
https://doi.org/10.4102/ojvr.
v86i1.1796.
