A global genotyping survey of Strongyloides stercoralis and Strongyloides fuelleborni using deep amplicon sequencing.

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 Southea...

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Main Authors: Joel L N Barratt, Meredith Lane, Emir Talundzic, Travis Richins, Gemma Robertson, Fabio Formenti, Bobbi Pritt, Guilherme Verocai, Joelma Nascimento de Souza, Neci Mato Soares, Rebecca Traub, Dora Buonfrate, Richard S Bradbury
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-09-01
Series:PLoS Neglected Tropical Diseases
Online Access:https://doi.org/10.1371/journal.pntd.0007609
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spelling doaj-0032f649681644ca9c8b4194f2bc2a972021-06-20T04:31:56ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352019-09-01139e000760910.1371/journal.pntd.0007609A global genotyping survey of Strongyloides stercoralis and Strongyloides fuelleborni using deep amplicon sequencing.Joel L N BarrattMeredith LaneEmir TalundzicTravis RichinsGemma RobertsonFabio FormentiBobbi PrittGuilherme VerocaiJoelma Nascimento de SouzaNeci Mato SoaresRebecca TraubDora BuonfrateRichard S BradburyStrongyloidiasis 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.https://doi.org/10.1371/journal.pntd.0007609
collection DOAJ
language English
format Article
sources DOAJ
author Joel L N Barratt
Meredith Lane
Emir Talundzic
Travis Richins
Gemma Robertson
Fabio Formenti
Bobbi Pritt
Guilherme Verocai
Joelma Nascimento de Souza
Neci Mato Soares
Rebecca Traub
Dora Buonfrate
Richard S Bradbury
spellingShingle Joel L N Barratt
Meredith Lane
Emir Talundzic
Travis Richins
Gemma Robertson
Fabio Formenti
Bobbi Pritt
Guilherme Verocai
Joelma Nascimento de Souza
Neci Mato Soares
Rebecca Traub
Dora Buonfrate
Richard S Bradbury
A global genotyping survey of Strongyloides stercoralis and Strongyloides fuelleborni using deep amplicon sequencing.
PLoS Neglected Tropical Diseases
author_facet Joel L N Barratt
Meredith Lane
Emir Talundzic
Travis Richins
Gemma Robertson
Fabio Formenti
Bobbi Pritt
Guilherme Verocai
Joelma Nascimento de Souza
Neci Mato Soares
Rebecca Traub
Dora Buonfrate
Richard S Bradbury
author_sort Joel L N Barratt
title A global genotyping survey of Strongyloides stercoralis and Strongyloides fuelleborni using deep amplicon sequencing.
title_short A global genotyping survey of Strongyloides stercoralis and Strongyloides fuelleborni using deep amplicon sequencing.
title_full A global genotyping survey of Strongyloides stercoralis and Strongyloides fuelleborni using deep amplicon sequencing.
title_fullStr A global genotyping survey of Strongyloides stercoralis and Strongyloides fuelleborni using deep amplicon sequencing.
title_full_unstemmed A global genotyping survey of Strongyloides stercoralis and Strongyloides fuelleborni using deep amplicon sequencing.
title_sort global genotyping survey of strongyloides stercoralis and strongyloides fuelleborni using deep amplicon sequencing.
publisher Public Library of Science (PLoS)
series PLoS Neglected Tropical Diseases
issn 1935-2727
1935-2735
publishDate 2019-09-01
description 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.
url https://doi.org/10.1371/journal.pntd.0007609
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