Characterization of triatomine bloodmeal sources using direct Sanger sequencing and amplicon deep sequencing methods

Knowledge of host associations of blood-feeding vectors may afford insights into managing disease systems and protecting public health. However, the ability of methods to distinguish bloodmeal sources varies widely. We used two methods—Sanger sequencing and amplicon deep sequencing—to target a 228 b...

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Published in:Scientific Reports
Main Authors: Balasubramanian, Sujata, Curtis-Robles, Rachel, Chirra, Bhagath, Auckland, Lisa D., Mai, Alan, Bocanegra-Garcia, Virgilio, Clark, Patti, Clark, Wilhelmina, Cottingham, Mark, Fleurie, Geraldine, Johnson, Charles D., Metz, Richard P., Wang, Shichen, Hathaway, Nicholas J., Bailey, Jeffrey A., Hamer, Gabriel L., Hamer, Sarah A.
Format: Text
Language:English
Published: Nature Publishing Group UK 2022
Subjects:
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205944/
http://www.ncbi.nlm.nih.gov/pubmed/35715521
https://doi.org/10.1038/s41598-022-14208-8
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spelling ftpubmed:oai:pubmedcentral.nih.gov:9205944 2023-05-15T15:50:40+02:00 Characterization of triatomine bloodmeal sources using direct Sanger sequencing and amplicon deep sequencing methods Balasubramanian, Sujata Curtis-Robles, Rachel Chirra, Bhagath Auckland, Lisa D. Mai, Alan Bocanegra-Garcia, Virgilio Clark, Patti Clark, Wilhelmina Cottingham, Mark Fleurie, Geraldine Johnson, Charles D. Metz, Richard P. Wang, Shichen Hathaway, Nicholas J. Bailey, Jeffrey A. Hamer, Gabriel L. Hamer, Sarah A. 2022-06-17 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205944/ http://www.ncbi.nlm.nih.gov/pubmed/35715521 https://doi.org/10.1038/s41598-022-14208-8 en eng Nature Publishing Group UK http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205944/ http://www.ncbi.nlm.nih.gov/pubmed/35715521 http://dx.doi.org/10.1038/s41598-022-14208-8 © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . CC-BY Sci Rep Article Text 2022 ftpubmed https://doi.org/10.1038/s41598-022-14208-8 2022-06-26T00:32:09Z Knowledge of host associations of blood-feeding vectors may afford insights into managing disease systems and protecting public health. However, the ability of methods to distinguish bloodmeal sources varies widely. We used two methods—Sanger sequencing and amplicon deep sequencing—to target a 228 bp region of the vertebrate Cytochrome b gene and determine hosts fed upon by triatomines (n = 115) collected primarily in Texas, USA. Direct Sanger sequencing of PCR amplicons was successful for 36 samples (31%). Sanger sequencing revealed 15 distinct host species, which included humans, domestic animals (Canis lupus familiaris, Ovis aries, Gallus gallus, Bos taurus, Felis catus, and Capra hircus), wildlife (Rattus rattus, Incilius nebulifer, Sciurus carolinensis, Sciurus niger, and Odocoileus virginianus), and captive animals (Panthera tigris, Colobus spp., and Chelonoidis carbonaria). Samples sequenced by the Sanger method were also subjected to Illumina MiSeq amplicon deep sequencing. The amplicon deep sequencing results (average of 302,080 usable reads per sample) replicated the host community revealed using Sanger sequencing, and detected additional hosts in five triatomines (13.9%), including two additional blood sources (Procyon lotor and Bassariscus astutus). Up to four bloodmeal sources were detected in a single triatomine (I. nebulifer, Homo sapiens, C. lupus familiaris, and S. carolinensis). Enhanced understanding of vector-host-parasite networks may allow for integrated vector management programs focusing on highly-utilized and highly-infected host species. Text Canis lupus Rattus rattus PubMed Central (PMC) Scientific Reports 12 1
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Article
spellingShingle Article
Balasubramanian, Sujata
Curtis-Robles, Rachel
Chirra, Bhagath
Auckland, Lisa D.
Mai, Alan
Bocanegra-Garcia, Virgilio
Clark, Patti
Clark, Wilhelmina
Cottingham, Mark
Fleurie, Geraldine
Johnson, Charles D.
Metz, Richard P.
Wang, Shichen
Hathaway, Nicholas J.
Bailey, Jeffrey A.
Hamer, Gabriel L.
Hamer, Sarah A.
Characterization of triatomine bloodmeal sources using direct Sanger sequencing and amplicon deep sequencing methods
topic_facet Article
description Knowledge of host associations of blood-feeding vectors may afford insights into managing disease systems and protecting public health. However, the ability of methods to distinguish bloodmeal sources varies widely. We used two methods—Sanger sequencing and amplicon deep sequencing—to target a 228 bp region of the vertebrate Cytochrome b gene and determine hosts fed upon by triatomines (n = 115) collected primarily in Texas, USA. Direct Sanger sequencing of PCR amplicons was successful for 36 samples (31%). Sanger sequencing revealed 15 distinct host species, which included humans, domestic animals (Canis lupus familiaris, Ovis aries, Gallus gallus, Bos taurus, Felis catus, and Capra hircus), wildlife (Rattus rattus, Incilius nebulifer, Sciurus carolinensis, Sciurus niger, and Odocoileus virginianus), and captive animals (Panthera tigris, Colobus spp., and Chelonoidis carbonaria). Samples sequenced by the Sanger method were also subjected to Illumina MiSeq amplicon deep sequencing. The amplicon deep sequencing results (average of 302,080 usable reads per sample) replicated the host community revealed using Sanger sequencing, and detected additional hosts in five triatomines (13.9%), including two additional blood sources (Procyon lotor and Bassariscus astutus). Up to four bloodmeal sources were detected in a single triatomine (I. nebulifer, Homo sapiens, C. lupus familiaris, and S. carolinensis). Enhanced understanding of vector-host-parasite networks may allow for integrated vector management programs focusing on highly-utilized and highly-infected host species.
format Text
author Balasubramanian, Sujata
Curtis-Robles, Rachel
Chirra, Bhagath
Auckland, Lisa D.
Mai, Alan
Bocanegra-Garcia, Virgilio
Clark, Patti
Clark, Wilhelmina
Cottingham, Mark
Fleurie, Geraldine
Johnson, Charles D.
Metz, Richard P.
Wang, Shichen
Hathaway, Nicholas J.
Bailey, Jeffrey A.
Hamer, Gabriel L.
Hamer, Sarah A.
author_facet Balasubramanian, Sujata
Curtis-Robles, Rachel
Chirra, Bhagath
Auckland, Lisa D.
Mai, Alan
Bocanegra-Garcia, Virgilio
Clark, Patti
Clark, Wilhelmina
Cottingham, Mark
Fleurie, Geraldine
Johnson, Charles D.
Metz, Richard P.
Wang, Shichen
Hathaway, Nicholas J.
Bailey, Jeffrey A.
Hamer, Gabriel L.
Hamer, Sarah A.
author_sort Balasubramanian, Sujata
title Characterization of triatomine bloodmeal sources using direct Sanger sequencing and amplicon deep sequencing methods
title_short Characterization of triatomine bloodmeal sources using direct Sanger sequencing and amplicon deep sequencing methods
title_full Characterization of triatomine bloodmeal sources using direct Sanger sequencing and amplicon deep sequencing methods
title_fullStr Characterization of triatomine bloodmeal sources using direct Sanger sequencing and amplicon deep sequencing methods
title_full_unstemmed Characterization of triatomine bloodmeal sources using direct Sanger sequencing and amplicon deep sequencing methods
title_sort characterization of triatomine bloodmeal sources using direct sanger sequencing and amplicon deep sequencing methods
publisher Nature Publishing Group UK
publishDate 2022
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205944/
http://www.ncbi.nlm.nih.gov/pubmed/35715521
https://doi.org/10.1038/s41598-022-14208-8
genre Canis lupus
Rattus rattus
genre_facet Canis lupus
Rattus rattus
op_source Sci Rep
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205944/
http://www.ncbi.nlm.nih.gov/pubmed/35715521
http://dx.doi.org/10.1038/s41598-022-14208-8
op_rights © The Author(s) 2022
https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
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container_title Scientific Reports
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