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Effects of storage conditions and digestion time on DNA amplification of biting midge (Culicoides) blood meals

BACKGROUND: Molecular analysis of blood meals is increasingly used to identify the hosts of biting insects such as midges and mosquitoes. Successful host identification depends on the availability of sufficient host DNA template for PCR amplification, making it important to understand how amplificat...

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Autores principales: Bellekom, Ben, Bailey, Abigail, England, Marion, Langlands, Zoe, Lewis, Owen T., Hackett, Talya D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837887/
https://www.ncbi.nlm.nih.gov/pubmed/36635709
http://dx.doi.org/10.1186/s13071-022-05607-x
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author Bellekom, Ben
Bailey, Abigail
England, Marion
Langlands, Zoe
Lewis, Owen T.
Hackett, Talya D.
author_facet Bellekom, Ben
Bailey, Abigail
England, Marion
Langlands, Zoe
Lewis, Owen T.
Hackett, Talya D.
author_sort Bellekom, Ben
collection PubMed
description BACKGROUND: Molecular analysis of blood meals is increasingly used to identify the hosts of biting insects such as midges and mosquitoes. Successful host identification depends on the availability of sufficient host DNA template for PCR amplification, making it important to understand how amplification success changes under different storage conditions and with different durations of blood meal digestion within the insect gut before being placed into the storage medium. METHOD: We characterised and compared the digestion profile of two species of Culicoides over a 96-h period using a novel set of general vertebrate primers targeting the 16S rRNA gene. A set number of individuals from each species were killed over 13 time points post-blood feeding and preserved in 95% ethanol. Samples were stored either at ambient room temperature or in a − 20 °C freezer to examine the effect of storage condition on the PCR amplification success of host DNA. RESULTS: We found that amplification success across the 96-h sampling period post-feeding was reduced from 96 to 6% and 96% to 14% for Culicoides nubeculosus and Culicoides sonorensis, respectively. We found no effect of storage condition on PCR amplification success, and storage in 95% ethanol was sufficient to maintain high rates of amplifiable host DNA for at least 9 months, even at room temperature. CONCLUSIONS: These findings highlight the limited time frame during which an individual may contain amplifiable host DNA and demonstrate the importance of timely sample capture and processing post-blood feeding. Moreover, storage in 95% ethanol alone is sufficient to limit host DNA degradation. These results are relevant to the design of studies investigating the biting behaviour and disease transmission potential of Culicoides and other biting Diptera. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13071-022-05607-x.
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spelling pubmed-98378872023-01-14 Effects of storage conditions and digestion time on DNA amplification of biting midge (Culicoides) blood meals Bellekom, Ben Bailey, Abigail England, Marion Langlands, Zoe Lewis, Owen T. Hackett, Talya D. Parasit Vectors Brief Report BACKGROUND: Molecular analysis of blood meals is increasingly used to identify the hosts of biting insects such as midges and mosquitoes. Successful host identification depends on the availability of sufficient host DNA template for PCR amplification, making it important to understand how amplification success changes under different storage conditions and with different durations of blood meal digestion within the insect gut before being placed into the storage medium. METHOD: We characterised and compared the digestion profile of two species of Culicoides over a 96-h period using a novel set of general vertebrate primers targeting the 16S rRNA gene. A set number of individuals from each species were killed over 13 time points post-blood feeding and preserved in 95% ethanol. Samples were stored either at ambient room temperature or in a − 20 °C freezer to examine the effect of storage condition on the PCR amplification success of host DNA. RESULTS: We found that amplification success across the 96-h sampling period post-feeding was reduced from 96 to 6% and 96% to 14% for Culicoides nubeculosus and Culicoides sonorensis, respectively. We found no effect of storage condition on PCR amplification success, and storage in 95% ethanol was sufficient to maintain high rates of amplifiable host DNA for at least 9 months, even at room temperature. CONCLUSIONS: These findings highlight the limited time frame during which an individual may contain amplifiable host DNA and demonstrate the importance of timely sample capture and processing post-blood feeding. Moreover, storage in 95% ethanol alone is sufficient to limit host DNA degradation. These results are relevant to the design of studies investigating the biting behaviour and disease transmission potential of Culicoides and other biting Diptera. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13071-022-05607-x. BioMed Central 2023-01-13 /pmc/articles/PMC9837887/ /pubmed/36635709 http://dx.doi.org/10.1186/s13071-022-05607-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Brief Report
Bellekom, Ben
Bailey, Abigail
England, Marion
Langlands, Zoe
Lewis, Owen T.
Hackett, Talya D.
Effects of storage conditions and digestion time on DNA amplification of biting midge (Culicoides) blood meals
title Effects of storage conditions and digestion time on DNA amplification of biting midge (Culicoides) blood meals
title_full Effects of storage conditions and digestion time on DNA amplification of biting midge (Culicoides) blood meals
title_fullStr Effects of storage conditions and digestion time on DNA amplification of biting midge (Culicoides) blood meals
title_full_unstemmed Effects of storage conditions and digestion time on DNA amplification of biting midge (Culicoides) blood meals
title_short Effects of storage conditions and digestion time on DNA amplification of biting midge (Culicoides) blood meals
title_sort effects of storage conditions and digestion time on dna amplification of biting midge (culicoides) blood meals
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837887/
https://www.ncbi.nlm.nih.gov/pubmed/36635709
http://dx.doi.org/10.1186/s13071-022-05607-x
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