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Short communication: Exploring gastrointestinal tract nemabiomes in captive ungulates at the SANBI National Zoological Gardens: A next-generation sequencing baseline approach

Published online by Cambridge University Press:  06 January 2025

V. Phetla*
Affiliation:
Foundational Research and Services, South African National Biodiversity Institute, P.O. Box 754, Pretoria 0001, South Africa
K. Masenya
Affiliation:
Foundational Research and Services, South African National Biodiversity Institute, P.O. Box 754, Pretoria 0001, South Africa
M. Chaisi
Affiliation:
Foundational Research and Services, South African National Biodiversity Institute, P.O. Box 754, Pretoria 0001, South Africa Department of Veterinary Tropical Diseases, University of Pretoria, Onderstepoort 0110, South Africa
*
Corresponding author: V. Phetla; Email: [email protected]

Abstract

Gastrointestinal tract (GIT) nematode infections have a significant negative impact on the well-being and productivity of animals. While it is common for a host to be co-infected with multiple species of nematode parasites simultaneously, there is a lack of effective tools to study the composition of these complex parasite communities. We describe the application of the “nemabiome” amplicon sequencing to study parasitic GIT nematode communities in captive wildlife at the National Zoological Garden, South African National Biodiversity Institute. A total of 13 samples from Roan antelope (n=1), Eland (n=1), Sable antelope (n=9), Arabian oryx (n=1), and Blue duiker (n=1) were analysed for the presence of GIT nematode infections. A total of 256 operational taxonomical units (OTUs) were generated and compared to a curated database with ≥99% identity to sequences in the NCBI database. The OTUs found represented nematode species which are commonly associated with wild ruminants. These belonged to members of the genera Haemonchus, Trichostrongylus, and Cooperia, with a few OTUs classified as unidentified genera detected. These were further classified to species level, with Haemonchus contortus and Trichostrongylus colubriformis having high relative abundance across all captive ungulate species. Utilizing amplicon sequencing to examine the nemabiome holds great potential for enhancing our basic knowledge of the biology of gastrointestinal nematodes and monitoring infections. This improved understanding could guide the development of more efficacious preventive and control measures against these significant parasites, which negatively impact animal health and productivity on a global scale.

Type
Short Communication
Copyright
© The Author(s), 2025. Published by Cambridge University Press

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References

Abuessailla, AA, Ismail, AA and Agab, H (2013) The prevalence of gastrointestinal parasites in wild and domestic animals in Radom National Park; South Darfur state, Sudan. Assiut Veterinary Medical Journal 59, 138.Google Scholar
Avramenko, RW, Redman, EM, Lewis, R, Yazwinski, TA, Wasmuth, JD and Gilleard, JS (2015) Exploring the gastrointestinal “nemabiome”: deep amplicon sequencing to quantify the species composition of parasitic nematode communities. PLoS ONE 10(12), e0143559.CrossRefGoogle ScholarPubMed
Avramenko, RW, Redman, EM, Lewis, R, Bichuette, MA, Palmeira, BM, Yazwinski, TA and Gilleard, JS (2017) The use of nemabiome metabarcoding to explore gastro-intestinal nematode species diversity and anthelmintic treatment effectiveness in beef calves. International Journal for Parasitology 47(13), 893902.CrossRefGoogle ScholarPubMed
Beaumelle, C, Redman, EM, de Rijke, J, Wit, J, Benabed, S, Debias, F, Duhayer, J, Pardonnet, S, Poirel, MT, Capron, G and Chabot, S (2021) Metabarcoding in two isolated populations of wild roe deer (Capreolus capreolus) reveals variation in gastrointestinal nematode community composition between regions and among age classes. Parasites & Vectors 14, 113.CrossRefGoogle ScholarPubMed
Boomker, J, Booyse, DG, Watermeyer, R, De Villiers, IL, Horak, IG and Flamand, JR (1996) Parasites of South African wildlife. XIV. Helminths of nyalas (Tragelaphus angasii) in the Mkuzi Game Reserve, KwaZulu-Natal. Onderstepoort Journal of Veterinary Research 63, 265271.Google ScholarPubMed
Caporaso, JG, Kuczynski, J, Stombaugh, J, Bittinger, K, Bushman, FD, Costello, EK, Fierer, N, Peña, AG, Goodrich, JK, Gordon, JI and Huttley, GA (2010) QIIME allows analysis of high-throughput community sequencing data. Nature Methods 7(5), 335336.CrossRefGoogle ScholarPubMed
Chaudhari, PR, Madke, MB and Ambore, BN (2022) Prevalence of gastrointestinal helminths in domestic ungulates from a semi-arid region of Maharashtra, India. Journal of Parasitic Diseases 46(1), 95100.Google Scholar
Gasser, RB, Chilton, NB, Hoste, H and Beveridge, I (1993) Rapid sequencing of rDNA from single worms and eggs of parasitic helminths. Nucleic Acids Research 21(10), 2525.CrossRefGoogle ScholarPubMed
Gentleman, RC, Carey, VJ, Bates, DM, Bolstad, B, Dettling, M, Dudoit, S, Ellis, B, Gautier, L, Ge, Y, Gentry, J and Hornik, K (2004) Bioconductor: open software development for computational biology and bioinformatics. Genome Biology 5, 116.CrossRefGoogle ScholarPubMed
Halvarsson, P, Baltrušis, P, Kjellander, P and Höglund, J (2022) Parasitic strongyle nemabiome communities in wild ruminants in Sweden. Parasites & Vectors 15, 115.CrossRefGoogle ScholarPubMed
Hoberg, EP, Lichtenfels, JR and Pilitt, PA (2015) Synoptic review of Nematoda (Trichocephalida, Enoplida, Trichinellida) in captive and feral ungulates from the Americas. Revista Mexicana de Biodiversidad 86(1), 130164.Google Scholar
Hoberg, EP and Brooks, DR (2015) Evolution in action: climate change, biodiversity dynamics and emerging infectious disease. Philosophical Transactions of the Royal Society B: Biological Sciences 370(1665), 20130553.CrossRefGoogle ScholarPubMed
Mosala, PP (2017) Gastrointestinal parasites infecting ungulates, felids and avian species at National Zoological Gardens of South Africa. Doctoral dissertation, North-West University (South Africa), Potchefstroom Campus. http://hdl.handle.net/10394/28759Google Scholar
Naz, S, Arooj, S, Ali, Z and Farooq, Z (2021) Potential consequences of captivity and environmental pollution in endoparasitic prevalence in different antelopes kept at wildlife parks. Environmental Science and Pollution Research 28, 1630816313.CrossRefGoogle ScholarPubMed
Phetla, V, Chaisi, M and Malatji, PM (2024) Epidemiology and diversity of gastrointestinal tract helminths of wild ruminants in sub-Saharan Africa: a review. Journal of Helminthology 98, 117.CrossRefGoogle ScholarPubMed
Pittman, JS, Shepherd, G, Thacker, BJ and Myers, GW (2020) Pest or guest: a ruminant nemabiome interactome through the application of trait-based ecology. Frontiers in Cellular and Infection Microbiology 10, 337.Google Scholar
Queiroz, C, Levy, M, Avramenko, R, Redman, E, Kearns, K, Swain, L, Silas, H, Uehlinger, F and Gilleard, JS (2020) The use of ITS-2 rDNA nemabiome metabarcoding to enhance anthelmintic resistance diagnosis and surveillance of ovine gastrointestinal nematodes. International Journal for Parasitology: Drugs and Drug Resistance 14, 105117.Google ScholarPubMed
Rognes, T, Flouri, T, Nichols, B, Quince, C and Mahé, F (2016) VSEARCH: a versatile open source tool for metagenomics. Peer Journal 4, e2584.CrossRefGoogle ScholarPubMed
Roos, MH and Grant, WN (1993) Species-specific PCR for the parasitic nematodes Haemonchus contortus and Trichostrongylus colubriformis. International Journal for Parasitology 23(3), 419421.CrossRefGoogle ScholarPubMed
Sulliotti, V (2023) Protostrongylids nematodes as a tool to study the biogeography of wild mammals. The University of Bologna. PhD dissertation. Accessed 05 April 2024.Google Scholar
Zieger, U, Boomker, J, Cauldwell, AE and Horak, IG (1998) Helminths and botfly larvae of wild ungulates on a game ranch in Central Province, Zambia. Onderspoort Journal of Veterinary Research 65, 137141.Google Scholar
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