Giardia duodenalis in a clinically healthy population of captive zoo chimpanzees: Rapid antigen testing, diagnostic real-time PCR and faecal microbiota profiling

0556445 - ÚBO 2023 RIV AU eng J - Článek v odborném periodiku
Willenborg, C. M. - Červená, Barbora - Thompson, P. - Rosario, E. - Ruaux, C. - Vogelnest, L. - Šlapeta, J.
Giardia duodenalis in a clinically healthy population of captive zoo chimpanzees: Rapid antigen testing, diagnostic real-time PCR and faecal microbiota profiling.
International Journal for Parasitology: Parasites and Wildlife. Roč. 17, April (2022), s. 308-318. ISSN 2213-2244. E-ISSN 2213-2244
Grant CEP: GA MŠMT(CZ) EF16_027/0008027
Institucionální podpora: RVO:68081766
Klíčová slova: Giardiasis * Diagnostics * Zoonosis * Zoo animals * Parasite * Commensal * Microbiome
Obor OECD: Veterinary science
Impakt faktor: 1.8, rok: 2022
Způsob publikování: Open access
https://www.sciencedirect.com/science/article/pii/S2213224422000268?via%3Dihub

Giardia duodenalis is one of the most common intestinal parasites of humans, with a worldwide distribution. Giardia duodenalis has been reported in both wild and captive populations of non-human primates, namely chimpanzees. In this study we investigated an entire troop of clinically healthy chimpanzees (n = 21) for the presence of G. duodenalis and its association with faecal microbiota profile. Faecal samples (n = 26) were collected from the chimpanzee exhibit from a zoo in Sydney, Australia. Diagnosis of G. duodenalis was made using a Rapid Antigen Test (RAT) as a point-of-care-test and compared to a reference standard real-time PCR test. Approximately half of the chimpanzee faecal samples tested positive for G. duodenalis by both RAT (13/26, 50%) and real-time PCR (14/26, 53.85%). The RAT sensitivity was 85.7% (95% CI: 63.8%–96%) and specificity was 91.7% (95% CI: 68.3%–99%) when compared to the in-house real-time PCR. Genotyping of the samples revealed the presence of zoonotic assemblage B. Microscopic analysis revealed the presence of Troglodytella spp. (14/26), Balantioides sp. (syn. Balantidium sp.) (8/26) as well as Entamoeba spp. (3/26). Microbiota profile based on 16S rRNA gene sequencing revealed that the community was significantly different between G. duodenalis positive and negative samples if RAT results were taken into an account, but not real-time PCR diagnostics results. Proteobacteria and Chloroflexi were the significant features in the dataset that separated G. duodenalis positive and negative samples using LEfSe analysis. Being able to rapidly test for G. duodenalis in captive populations of primates assists in point-of-care diagnostics and may better identify animals with subclinical disease. Under the investigated conditions of the zoo setting, however, presence of G. duodenalis either detected by RAT or real-time PCR was not associated with clinically apparent disease in captive chimpanzees.
Trvalý link: http://hdl.handle.net/11104/0330662