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ArticleActa parasitologica2024

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

Fredrick O Obonyo, Ndichu Maingi, Samuel M Githigia, Kevin O Ochwedo, Anne A Owiti, Evans N Nyaboga

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Article in Acta parasitologica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2 citing papers in PubMed.

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5 · Who and what money

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6 authors.

Fredrick O ObonyoDepartment of Veterinary Pathology, Microbiology and Parasitology, University of Nairobi, P.O. Box 29053, Kangemi, 00625, Kenya. fobonyo@must.ac.ke.
Ndichu MaingiDepartment of Veterinary Pathology, Microbiology and Parasitology, University of Nairobi, P.O. Box 29053, Kangemi, 00625, Kenya.
Samuel M GithigiaDepartment of Veterinary Pathology, Microbiology and Parasitology, University of Nairobi, P.O. Box 29053, Kangemi, 00625, Kenya.
Kevin O OchwedoDepartment of Entomology, Plant Pathology and Nematology, University of Idaho, 492 W Taylor Ave, Apt 6, Moscow, Russian Federation.
Anne A OwitiDepartment of Biochemistry, University of Nairobi, P.O. Box 30197, Nairobi, 00100, Kenya.
Evans N NyabogaDepartment of Biochemistry, University of Nairobi, P.O. Box 30197, Nairobi, 00100, Kenya.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe 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.

methodA 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).

resultsToxoplasma 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.

conclusionThis 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.

Indexed as

DNA, ProtozoanEquidaeGenetic VariationPhylogenyPolymorphism, Restriction Fragment LengthToxoplasmaToxoplasmosis, AnimalAnimalsGenotypeHaplotypesKenyaPolymerase Chain ReactionSequence Analysis, DNADNA, ProtozoanDonkeysGenotypesHaplotypesITS-1 geneKenyaToxoplasma gondii

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.