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Reliability of molecular host-identification methods for ticks: an experimental in vitro study with Ixodes ricinus

BACKGROUND: Reliable information on host use by arthropod vectors is required to study pathogen transmission ecology and to predict disease risk. Direct observation of host use is often difficult or impossible and indirect methods are therefore necessary. However, the reliability of currently availa...

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Autores principales: Léger, Elsa, Liu, Xiangye, Masseglia, Sébastien, Noël, Valérie, Vourc’h, Gwenaël, Bonnet, Sarah, McCoy, Karen D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546307/
https://www.ncbi.nlm.nih.gov/pubmed/26296344
http://dx.doi.org/10.1186/s13071-015-1043-7
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author Léger, Elsa
Liu, Xiangye
Masseglia, Sébastien
Noël, Valérie
Vourc’h, Gwenaël
Bonnet, Sarah
McCoy, Karen D.
author_facet Léger, Elsa
Liu, Xiangye
Masseglia, Sébastien
Noël, Valérie
Vourc’h, Gwenaël
Bonnet, Sarah
McCoy, Karen D.
author_sort Léger, Elsa
collection PubMed
description BACKGROUND: Reliable information on host use by arthropod vectors is required to study pathogen transmission ecology and to predict disease risk. Direct observation of host use is often difficult or impossible and indirect methods are therefore necessary. However, the reliability of currently available methods to identify the last host of blood-feeding arthropods has not been evaluated, and may be particularly problematic for ticks because host blood has been digested at capture. Biases in host detection may lead to erroneous conclusions on both vector ecology and pathogen circulation. METHODS: Here, we experimentally tested for biases in host detection using the generalist three-host tick Ixodes ricinus as a model system. We fed ticks using an artificial feeding system and amplified blood meal traces post-moult (i.e., in the succeeding unfed life stage) via both a quantitative real-time polymerase chain reaction assay and a reverse line blotting method. We then experimentally tested for three types of biases in host detection: 1) time post-moult, 2) tick life stage and 3) host type (non-nucleated mammal blood versus nucleated avian blood), and compared these biases between the two molecular methods. RESULTS: Our results show that all three factors can influence host detection in ticks but not necessarily in the expected way. Although host detection rates decreased with time post-moult, mammal blood tended to be more readily detected than bird blood. Tick life stage was also an important factor; detection was higher in nymphs than in adults and, in some cases, remnants from both larval and nymphal blood meals could be detected in the adult stage. These biases were similar for the two detection techniques. CONCLUSIONS: We show that different factors associated with questing ticks may influence our ability to correctly infer previous host use and that these factors may bias inferences from field-based studies. As these biases may be common to other vector-borne disease systems, their implications for our understanding of vector ecology and disease transmission require more explicit consideration. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-015-1043-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-45463072015-08-23 Reliability of molecular host-identification methods for ticks: an experimental in vitro study with Ixodes ricinus Léger, Elsa Liu, Xiangye Masseglia, Sébastien Noël, Valérie Vourc’h, Gwenaël Bonnet, Sarah McCoy, Karen D. Parasit Vectors Research BACKGROUND: Reliable information on host use by arthropod vectors is required to study pathogen transmission ecology and to predict disease risk. Direct observation of host use is often difficult or impossible and indirect methods are therefore necessary. However, the reliability of currently available methods to identify the last host of blood-feeding arthropods has not been evaluated, and may be particularly problematic for ticks because host blood has been digested at capture. Biases in host detection may lead to erroneous conclusions on both vector ecology and pathogen circulation. METHODS: Here, we experimentally tested for biases in host detection using the generalist three-host tick Ixodes ricinus as a model system. We fed ticks using an artificial feeding system and amplified blood meal traces post-moult (i.e., in the succeeding unfed life stage) via both a quantitative real-time polymerase chain reaction assay and a reverse line blotting method. We then experimentally tested for three types of biases in host detection: 1) time post-moult, 2) tick life stage and 3) host type (non-nucleated mammal blood versus nucleated avian blood), and compared these biases between the two molecular methods. RESULTS: Our results show that all three factors can influence host detection in ticks but not necessarily in the expected way. Although host detection rates decreased with time post-moult, mammal blood tended to be more readily detected than bird blood. Tick life stage was also an important factor; detection was higher in nymphs than in adults and, in some cases, remnants from both larval and nymphal blood meals could be detected in the adult stage. These biases were similar for the two detection techniques. CONCLUSIONS: We show that different factors associated with questing ticks may influence our ability to correctly infer previous host use and that these factors may bias inferences from field-based studies. As these biases may be common to other vector-borne disease systems, their implications for our understanding of vector ecology and disease transmission require more explicit consideration. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-015-1043-7) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-22 /pmc/articles/PMC4546307/ /pubmed/26296344 http://dx.doi.org/10.1186/s13071-015-1043-7 Text en © Léger et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Léger, Elsa
Liu, Xiangye
Masseglia, Sébastien
Noël, Valérie
Vourc’h, Gwenaël
Bonnet, Sarah
McCoy, Karen D.
Reliability of molecular host-identification methods for ticks: an experimental in vitro study with Ixodes ricinus
title Reliability of molecular host-identification methods for ticks: an experimental in vitro study with Ixodes ricinus
title_full Reliability of molecular host-identification methods for ticks: an experimental in vitro study with Ixodes ricinus
title_fullStr Reliability of molecular host-identification methods for ticks: an experimental in vitro study with Ixodes ricinus
title_full_unstemmed Reliability of molecular host-identification methods for ticks: an experimental in vitro study with Ixodes ricinus
title_short Reliability of molecular host-identification methods for ticks: an experimental in vitro study with Ixodes ricinus
title_sort reliability of molecular host-identification methods for ticks: an experimental in vitro study with ixodes ricinus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546307/
https://www.ncbi.nlm.nih.gov/pubmed/26296344
http://dx.doi.org/10.1186/s13071-015-1043-7
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