First Report on the Molecular Detection and Genetic Characterization of Toxoplasma gondii From Donkeys in Kenya.

Toxoplasma gondii Donkeys Genotypes Haplotypes ITS-1 gene Kenya

Journal

Acta parasitologica
ISSN: 1896-1851
Titre abrégé: Acta Parasitol
Pays: Switzerland
ID NLM: 9301947

Informations de publication

Date de publication:
19 Aug 2024
Historique:
received: 23 06 2024
accepted: 05 08 2024
medline: 20 8 2024
pubmed: 20 8 2024
entrez: 19 8 2024
Statut: aheadofprint

Résumé

The present study was conducted to determine the presence of Toxoplasma gondii in donkeys by molecular tests and genetic diversity analysis of the obtained DNA samples from central Kenya. A total of 363 blood samples were collected from donkeys in Meru and Kirinyaga Counties, and 96 samples that were previously seropositive for T. gondii using indirect ELISA were subjected to nested PCR based on the amplification of the internal transcribed spacer 1 (ITS-1) gene followed by DNA sequencing and phylogenetic analysis. Genotyping was performed on 15 selected positive samples using multilocus nested polymerase chain reaction restriction fragment length polymorphism (Mn-PCR-RFLP) with eight genetic markers ('SAG 2, 5'SAG 2, Alt. SAG 2, SAG 3, GRA 6, C29-2, BTUB and L358). Toxoplasma gondii DNA was detected in 36.5% (35/96) of the blood samples. The sequences obtained exhibited 98.2-99.5% homology with those deposited in GenBank. Phylogenetic analysis demonstrated that the obtained sequences are conserved and clustered with those of infecting animals from other regions of the world. Eighteen distinct T. gondii haplotypes were identified to be circulating in donkeys from central Kenya. The T. gondii DNA samples exhibited high haplotype diversity (Hd: 0.915) and limited genetic diversity (π = 0.01027). PCR-RFLP of T. gondii DNA-positive samples revealed three different genetic combinations that consisted of alleles I, II and III, indicating the dissemination of atypical genotypes. This study demonstrated that T. gondii is widespread in donkeys from Kenya and could be a possible source of infection in humans. These findings are important for designing control strategies for this parasite to improve the livestock sector, which is one of the main sources of livelihood for farmers in Kenya.

Identifiants

pubmed: 39160342
doi: 10.1007/s11686-024-00905-z
pii: 10.1007/s11686-024-00905-z
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

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Auteurs

Fredrick O Obonyo (FO)

Department of Veterinary Pathology, Microbiology and Parasitology, University of Nairobi, P.O. Box 29053, Kangemi, 00625, Kenya. fobonyo@must.ac.ke.
Department of Animal Science, Meru University of Science and Technology, P.O. Box 972, Meru, 60200, Kenya. fobonyo@must.ac.ke.

Ndichu Maingi (N)

Department of Veterinary Pathology, Microbiology and Parasitology, University of Nairobi, P.O. Box 29053, Kangemi, 00625, Kenya.

Samuel M Githigia (SM)

Department of Veterinary Pathology, Microbiology and Parasitology, University of Nairobi, P.O. Box 29053, Kangemi, 00625, Kenya.

Kevin O Ochwedo (KO)

Department of Entomology, Plant Pathology and Nematology, University of Idaho, 492 W Taylor Ave, Apt 6, Moscow, Russian Federation.

Anne A Owiti (AA)

Department of Biochemistry, University of Nairobi, P.O. Box 30197, Nairobi, 00100, Kenya.

Evans N Nyaboga (EN)

Department of Biochemistry, University of Nairobi, P.O. Box 30197, Nairobi, 00100, Kenya.

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