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Culture-free genome-wide locus sequence typing (GLST) provides new perspectives on Trypanosoma cruzi dispersal and infection complexity

Analysis of genetic polymorphism is a powerful tool for epidemiological surveillance and research. Powerful inference from pathogen genetic variation, however, is often restrained by limited access to representative target DNA, especially in the study of obligate parasitic species for which ex vivo...

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Autores principales: Schwabl, Philipp, Maiguashca Sánchez, Jalil, Costales, Jaime A., Ocaña-Mayorga, Sofía, Segovia, Maikell, Carrasco, Hernán J., Hernández, Carolina, Ramírez, Juan David, Lewis, Michael D., Grijalva, Mario J., Llewellyn, Martin S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7743988/
https://www.ncbi.nlm.nih.gov/pubmed/33326438
http://dx.doi.org/10.1371/journal.pgen.1009170
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author Schwabl, Philipp
Maiguashca Sánchez, Jalil
Costales, Jaime A.
Ocaña-Mayorga, Sofía
Segovia, Maikell
Carrasco, Hernán J.
Hernández, Carolina
Ramírez, Juan David
Lewis, Michael D.
Grijalva, Mario J.
Llewellyn, Martin S.
author_facet Schwabl, Philipp
Maiguashca Sánchez, Jalil
Costales, Jaime A.
Ocaña-Mayorga, Sofía
Segovia, Maikell
Carrasco, Hernán J.
Hernández, Carolina
Ramírez, Juan David
Lewis, Michael D.
Grijalva, Mario J.
Llewellyn, Martin S.
author_sort Schwabl, Philipp
collection PubMed
description Analysis of genetic polymorphism is a powerful tool for epidemiological surveillance and research. Powerful inference from pathogen genetic variation, however, is often restrained by limited access to representative target DNA, especially in the study of obligate parasitic species for which ex vivo culture is resource-intensive or bias-prone. Modern sequence capture methods enable pathogen genetic variation to be analyzed directly from host/vector material but are often too complex and expensive for resource-poor settings where infectious diseases prevail. This study proposes a simple, cost-effective ‘genome-wide locus sequence typing’ (GLST) tool based on massive parallel amplification of information hotspots throughout the target pathogen genome. The multiplexed polymerase chain reaction amplifies hundreds of different, user-defined genetic targets in a single reaction tube, and subsequent agarose gel-based clean-up and barcoding completes library preparation at under 4 USD per sample. Our study generates a flexible GLST primer panel design workflow for Trypanosoma cruzi, the parasitic agent of Chagas disease. We successfully apply our 203-target GLST panel to direct, culture-free metagenomic extracts from triatomine vectors containing a minimum of 3.69 pg/μl T. cruzi DNA and further elaborate on method performance by sequencing GLST libraries from T. cruzi reference clones representing discrete typing units (DTUs) TcI, TcIII, TcIV, TcV and TcVI. The 780 SNP sites we identify in the sample set repeatably distinguish parasites infecting sympatric vectors and detect correlations between genetic and geographic distances at regional (< 150 km) as well as continental scales. The markers also clearly separate TcI, TcIII, TcIV and TcV + TcVI and appear to distinguish multiclonal infections within TcI. We discuss the advantages, limitations and prospects of our method across a spectrum of epidemiological research.
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spelling pubmed-77439882020-12-31 Culture-free genome-wide locus sequence typing (GLST) provides new perspectives on Trypanosoma cruzi dispersal and infection complexity Schwabl, Philipp Maiguashca Sánchez, Jalil Costales, Jaime A. Ocaña-Mayorga, Sofía Segovia, Maikell Carrasco, Hernán J. Hernández, Carolina Ramírez, Juan David Lewis, Michael D. Grijalva, Mario J. Llewellyn, Martin S. PLoS Genet Research Article Analysis of genetic polymorphism is a powerful tool for epidemiological surveillance and research. Powerful inference from pathogen genetic variation, however, is often restrained by limited access to representative target DNA, especially in the study of obligate parasitic species for which ex vivo culture is resource-intensive or bias-prone. Modern sequence capture methods enable pathogen genetic variation to be analyzed directly from host/vector material but are often too complex and expensive for resource-poor settings where infectious diseases prevail. This study proposes a simple, cost-effective ‘genome-wide locus sequence typing’ (GLST) tool based on massive parallel amplification of information hotspots throughout the target pathogen genome. The multiplexed polymerase chain reaction amplifies hundreds of different, user-defined genetic targets in a single reaction tube, and subsequent agarose gel-based clean-up and barcoding completes library preparation at under 4 USD per sample. Our study generates a flexible GLST primer panel design workflow for Trypanosoma cruzi, the parasitic agent of Chagas disease. We successfully apply our 203-target GLST panel to direct, culture-free metagenomic extracts from triatomine vectors containing a minimum of 3.69 pg/μl T. cruzi DNA and further elaborate on method performance by sequencing GLST libraries from T. cruzi reference clones representing discrete typing units (DTUs) TcI, TcIII, TcIV, TcV and TcVI. The 780 SNP sites we identify in the sample set repeatably distinguish parasites infecting sympatric vectors and detect correlations between genetic and geographic distances at regional (< 150 km) as well as continental scales. The markers also clearly separate TcI, TcIII, TcIV and TcV + TcVI and appear to distinguish multiclonal infections within TcI. We discuss the advantages, limitations and prospects of our method across a spectrum of epidemiological research. Public Library of Science 2020-12-16 /pmc/articles/PMC7743988/ /pubmed/33326438 http://dx.doi.org/10.1371/journal.pgen.1009170 Text en © 2020 Schwabl et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Schwabl, Philipp
Maiguashca Sánchez, Jalil
Costales, Jaime A.
Ocaña-Mayorga, Sofía
Segovia, Maikell
Carrasco, Hernán J.
Hernández, Carolina
Ramírez, Juan David
Lewis, Michael D.
Grijalva, Mario J.
Llewellyn, Martin S.
Culture-free genome-wide locus sequence typing (GLST) provides new perspectives on Trypanosoma cruzi dispersal and infection complexity
title Culture-free genome-wide locus sequence typing (GLST) provides new perspectives on Trypanosoma cruzi dispersal and infection complexity
title_full Culture-free genome-wide locus sequence typing (GLST) provides new perspectives on Trypanosoma cruzi dispersal and infection complexity
title_fullStr Culture-free genome-wide locus sequence typing (GLST) provides new perspectives on Trypanosoma cruzi dispersal and infection complexity
title_full_unstemmed Culture-free genome-wide locus sequence typing (GLST) provides new perspectives on Trypanosoma cruzi dispersal and infection complexity
title_short Culture-free genome-wide locus sequence typing (GLST) provides new perspectives on Trypanosoma cruzi dispersal and infection complexity
title_sort culture-free genome-wide locus sequence typing (glst) provides new perspectives on trypanosoma cruzi dispersal and infection complexity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7743988/
https://www.ncbi.nlm.nih.gov/pubmed/33326438
http://dx.doi.org/10.1371/journal.pgen.1009170
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