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Successful storage of Trichomonas gallinae on Whatman FTA cards following culture
Logistical constraints concerning parasite sample storage can hinder progress with the discovery of genetic variation on a global scale. New storage methods are being developed to address this, but require testing in order to understand how widely applicable these methods are. Whatman FTA cards have...
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Published in: | Conservation genetics resources 2022-06, Vol.14 (2), p.225-229 |
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container_title | Conservation genetics resources |
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creator | Thomas, Rebecca C. Dunn, Jenny C. Orsman, Chris J. Morris, Antony J. Hipperson, Helen Grice, Philip V. Hamer, Keith C. Goodman, Simon J. |
description | Logistical constraints concerning parasite sample storage can hinder progress with the discovery of genetic variation on a global scale. New storage methods are being developed to address this, but require testing in order to understand how widely applicable these methods are. Whatman FTA cards have been tested previously under laboratory conditions for storing low-concentration
Trichomonas gallinae
isolates with the conclusion that they are not suitable, but have not been tested under field conditions. Here, we conducted a field-test, comparing FTA cards with storage in ethanol for
T. gallinae
samples collected and cultured from wild Columbiformes in Africa using standard field methods, before transportation to the UK. After 6 months storage, both methods resulted in an overall prevalence of 100% following PCR amplification (n = 59), suggesting that FTA cards are suitable for estimation of
T. gallinae
prevalence. However, samples stored in ethanol produced more, and longer, sequences than those stored on FTA cards. These data suggest storage in ethanol is preferable for the acquisition of high quality genetic strain data, but that FTA cards can be used successfully to ascertain infection prevalence and identify parasite strains under field conditions. |
doi_str_mv | 10.1007/s12686-022-01263-6 |
format | article |
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Trichomonas gallinae
isolates with the conclusion that they are not suitable, but have not been tested under field conditions. Here, we conducted a field-test, comparing FTA cards with storage in ethanol for
T. gallinae
samples collected and cultured from wild Columbiformes in Africa using standard field methods, before transportation to the UK. After 6 months storage, both methods resulted in an overall prevalence of 100% following PCR amplification (n = 59), suggesting that FTA cards are suitable for estimation of
T. gallinae
prevalence. However, samples stored in ethanol produced more, and longer, sequences than those stored on FTA cards. These data suggest storage in ethanol is preferable for the acquisition of high quality genetic strain data, but that FTA cards can be used successfully to ascertain infection prevalence and identify parasite strains under field conditions.</description><identifier>ISSN: 1877-7260</identifier><identifier>ISSN: 1877-7252</identifier><identifier>EISSN: 1877-7260</identifier><identifier>DOI: 10.1007/s12686-022-01263-6</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Animal Genetics and Genomics ; Biodiversity ; Biomedical and Life Sciences ; Conservation Biology/Ecology ; Ecology ; Ethanol ; Evolutionary Biology ; Genetic diversity ; Life Sciences ; Methods and Resources Article ; Plant Genetics and Genomics ; Trichomonas gallinae</subject><ispartof>Conservation genetics resources, 2022-06, Vol.14 (2), p.225-229</ispartof><rights>The Author(s) 2022</rights><rights>The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c363t-641a286ccddc149f9b376ff567a2433752c168b9c8650023b8cbc183b0ad46d33</citedby><cites>FETCH-LOGICAL-c363t-641a286ccddc149f9b376ff567a2433752c168b9c8650023b8cbc183b0ad46d33</cites><orcidid>0000-0002-6277-2781</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Thomas, Rebecca C.</creatorcontrib><creatorcontrib>Dunn, Jenny C.</creatorcontrib><creatorcontrib>Orsman, Chris J.</creatorcontrib><creatorcontrib>Morris, Antony J.</creatorcontrib><creatorcontrib>Hipperson, Helen</creatorcontrib><creatorcontrib>Grice, Philip V.</creatorcontrib><creatorcontrib>Hamer, Keith C.</creatorcontrib><creatorcontrib>Goodman, Simon J.</creatorcontrib><title>Successful storage of Trichomonas gallinae on Whatman FTA cards following culture</title><title>Conservation genetics resources</title><addtitle>Conservation Genet Resour</addtitle><description>Logistical constraints concerning parasite sample storage can hinder progress with the discovery of genetic variation on a global scale. New storage methods are being developed to address this, but require testing in order to understand how widely applicable these methods are. Whatman FTA cards have been tested previously under laboratory conditions for storing low-concentration
Trichomonas gallinae
isolates with the conclusion that they are not suitable, but have not been tested under field conditions. Here, we conducted a field-test, comparing FTA cards with storage in ethanol for
T. gallinae
samples collected and cultured from wild Columbiformes in Africa using standard field methods, before transportation to the UK. After 6 months storage, both methods resulted in an overall prevalence of 100% following PCR amplification (n = 59), suggesting that FTA cards are suitable for estimation of
T. gallinae
prevalence. However, samples stored in ethanol produced more, and longer, sequences than those stored on FTA cards. 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New storage methods are being developed to address this, but require testing in order to understand how widely applicable these methods are. Whatman FTA cards have been tested previously under laboratory conditions for storing low-concentration
Trichomonas gallinae
isolates with the conclusion that they are not suitable, but have not been tested under field conditions. Here, we conducted a field-test, comparing FTA cards with storage in ethanol for
T. gallinae
samples collected and cultured from wild Columbiformes in Africa using standard field methods, before transportation to the UK. After 6 months storage, both methods resulted in an overall prevalence of 100% following PCR amplification (n = 59), suggesting that FTA cards are suitable for estimation of
T. gallinae
prevalence. However, samples stored in ethanol produced more, and longer, sequences than those stored on FTA cards. These data suggest storage in ethanol is preferable for the acquisition of high quality genetic strain data, but that FTA cards can be used successfully to ascertain infection prevalence and identify parasite strains under field conditions.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s12686-022-01263-6</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-6277-2781</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animal Genetics and Genomics Biodiversity Biomedical and Life Sciences Conservation Biology/Ecology Ecology Ethanol Evolutionary Biology Genetic diversity Life Sciences Methods and Resources Article Plant Genetics and Genomics Trichomonas gallinae |
title | Successful storage of Trichomonas gallinae on Whatman FTA cards following culture |
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