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A global genotyping survey of Strongyloides stercoralis and Strongyloides fuelleborni using deep amplicon sequencing.
- Source :
-
PLoS neglected tropical diseases [PLoS Negl Trop Dis] 2019 Sep 16; Vol. 13 (9), pp. e0007609. Date of Electronic Publication: 2019 Sep 16 (Print Publication: 2019). - Publication Year :
- 2019
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Abstract
- Strongyloidiasis is a neglected tropical disease caused by the human infective nematodes Strongyloides stercoralis, Strongyloides fuelleborni fuelleborni and Strongyloides fuelleborni kellyi. Previous large-scale studies exploring the genetic diversity of this important genus have focused on Southeast Asia, with a small number of isolates from the USA, Switzerland, Australia and several African countries having been genotyped. Consequently, little is known about the global distribution of geographic sub-variants of these nematodes and the genetic diversity that exists within the genus Strongyloides generally. We extracted DNA from human, dog and primate feces containing Strongyloides, collected from several countries representing all inhabited continents. Using a genotyping assay adapted for deep amplicon sequencing on the Illumina MiSeq platform, we sequenced the hyper-variable I and hyper-variable IV regions of the Strongyloides 18S rRNA gene and a fragment of the mitochondrial cytochrome c oxidase subunit 1 (cox1) gene from these specimens. We report several novel findings including unique S. stercoralis and S. fuelleborni genotypes, and the first identifications of a previously unknown S. fuelleborni infecting humans within Australia. We expand on an existing Strongyloides genotyping scheme to accommodate S. fuelleborni and these novel genotypes. In doing so, we compare our data to all 18S and cox1 sequences of S. fuelleborni and S. stercoralis available in GenBank (to our knowledge), that overlap with the sequences generated using our approach. As this analysis represents more than 1,000 sequences collected from diverse hosts and locations, representing all inhabited continents, it allows a truly global understanding of the population genetic structure of the Strongyloides species infecting humans, non-human primates, and domestic dogs.<br />Competing Interests: RB is a co-author on the following International Patent: #PCT/US2018/052469. Talundzic E, Bradbury R, Olsen C, Flaherty B. Removing Interfering Host Nucleic Acids for Molecular Parasite Detection. Meredith Lane is employed by Synergy America as a contractor to provide laboratory technical service to the Division of Parasitic Diseases and Malaria at the Centers for Disease Control and Prevention. In this capacity, there are no competing Interests in Ms. Lane's employment at Synergy and her authorship of this paper. Meredith Lane is correctly affiliated to this company (Synergy America). Meredith Lane and Synergy America hold no consultancies or patents and have no products in development or marketed products that are competing interests with this publication.
- Subjects :
- Animals
Cyclooxygenase 1 genetics
Dogs
Feces parasitology
Genotype
High-Throughput Nucleotide Sequencing
Humans
Neglected Diseases
Primates
RNA, Ribosomal, 18S genetics
Sequence Analysis, DNA
Strongyloides classification
Strongyloides stercoralis genetics
Strongyloidiasis epidemiology
Strongyloidiasis veterinary
Genetic Variation
Strongyloides genetics
Strongyloidiasis genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1935-2735
- Volume :
- 13
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- PLoS neglected tropical diseases
- Publication Type :
- Academic Journal
- Accession number :
- 31525192
- Full Text :
- https://doi.org/10.1371/journal.pntd.0007609