Strongyloides genotyping: a review of methods and application in public health and population genetics
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
34757088
DOI
10.1016/j.ijpara.2021.10.001
PII: S0020-7519(21)00297-6
Knihovny.cz E-resources
- Keywords
- Epidemiology, Genome, Genotyping, Strongyloides, Strongyloides fuelleborni, Strongyloides stercoralis, Strongyloidiasis,
- MeSH
- Feces parasitology MeSH
- Phylogeny MeSH
- Genotype MeSH
- Cats MeSH
- Multilocus Sequence Typing MeSH
- Cat Diseases * MeSH
- Dog Diseases * epidemiology parasitology MeSH
- Genetics, Population MeSH
- Primates genetics MeSH
- Dogs MeSH
- Strongyloides stercoralis * genetics MeSH
- Strongyloidiasis * epidemiology parasitology veterinary MeSH
- Public Health MeSH
- Zoonoses parasitology MeSH
- Animals MeSH
- Check Tag
- Cats MeSH
- Dogs MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
Strongyloidiasis represents a major medical and veterinary helminthic disease. Human infection is caused by Strongyloides stercoralis, Strongyloides fuelleborni fuelleborni and Strongyloides fuelleborni kellyi, with S.stercoralis accounting for the majority of cases. Strongyloides f. fuelleborni likely represents a zoonosis acquired from non-human primates (NHPs), while no animal reservoir for S. f. kellyi infection has been found. Whether S. stercoralis represents a zoonosis acquired from dogs and cats remains unanswered. Over the past two decades various tools have been applied to genotype Strongyloides spp. The most commonly sequenced markers have been the hyper-variable regions I and IV of the 18S rRNA gene and selected portions of the cytochrome c oxidase subunit I gene. These markers have been sequenced and compared in Strongyloides from multiple hosts and geographical regions. More recently, a machine learning algorithm multi-locus sequence typing approach has been applied using these markers, while others have applied whole genome sequencing. Genotyping of Strongyloides from dogs, cats, NHPs and humans has identified that S. stercoralis likely originated in dogs and adapted to human hosts. It has also been demonstrated that S. stercoralis is distinct from S. f. fuelleborni and S. f. kellyi. Two distinct genetic clades of S. stercoralis exist, one restricted to dogs and another infecting humans, NHPs, dogs and cats. Genotyping of S. f. fuelleborni has identified two separate clades, one associated with African isolates and another Indochinese peninsular clade. This review summarises the history and development of genotyping tools for Strongyloides spp. It describes the findings of major studies to date in the context of the epidemiology and evolutionary biology of these helminths, with a specific focus on human-infecting species.
Department of Biomedicine Faculty of Medicine Oita University Yufu Oita Japan
Department of Botany and Zoology Faculty of Science Masaryk University Brno Czech Republic
Health Innovation and Transformation Centre Federation University Berwick Victoria Australia
Institute of Vertebrate Biology The Czech Academy of Sciences Brno Czech Republic
References provided by Crossref.org
High-throughput sequencing of Strongyloides stercoralis - a fatal disseminated infection in a dog
Strongyloides in non-human primates: significance for public health control