Data from: Non-invasive methods unveil the trophic transmission of the tapeworm Ligula intestinalis in Gull-billed Terns
Data files
Nov 15, 2024 version files 822.49 KB
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Appendix.docx
448.60 KB
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Capasso-et-al._-2024.pdf
330.44 KB
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df.xlsx
17.65 KB
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README.md
2.55 KB
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Table_A1.xlsx
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Abstract
Recent developments in microscopic and molecular tools have allowed the implementation of new approaches for assessing parasitic infections in wildlife populations. This is particularly important for the noninvasive detection and quantification of endoparasites in live animals. Here, we combined copromicroscopic (Mini-FLOTAC) and molecular (qPCR) techniques to detect the infection of the macroparasite Ligula intestinalis (Cestoda, Pseudophyllidea) in fresh droppings of Gull-billed Terns Gelochelidon nilotica (Charadriiformes, Laridae) breeding in southwestern Spain. Additionally, we sequenced the cytochrome b gene in parasite isolates from Gull-billed Terns (definitive host) and Common Bleak Alburnus alburnus (second intermediate host) sampled around tern colonies to explore potential genetic differences between the isolates. The qPCR test showed a higher prevalence (18%; in 13/73 samples) than Mini-FLOTAC (9%; in 8/88 samples), indicating that qPCR was more sensitive for diagnostic purposes than fecal flotation alone. Although the agreement between both techniques was substantial (84.2%) mainly due to the large number of uninfected samples, only Mini-FLOTAC allowed us to quantify parasite shedding. When combining techniques, prevalence of infection did not differ between adults and chicks, suggesting frequent trophic transmission from parents to their offspring via food provisioning. Phylogenetic analyses identified four haplotypes in the isolates from Gull-billed Terns and Bleak, all of which were placed within a European clade composed of tapeworms recovered exclusively from phylogenetically derived cyprinid fish. This, combined with the short lifespan of mature tapeworms, suggests that Gull-billed Terns became infected after consuming infected fish around their breeding colonies rather than on their West African wintering grounds. Altogether, our results represent the first record of L. intestinalis in Gull-billed Terns and the first molecular characterization of the parasite in the Iberian Peninsula. This integrative copro-diagnostic protocol can be applied to other host–parasite systems, allowing researchers to study helminth infections in wild populations using a noninvasive approach.
https://doi.org/10.5061/dryad.h70rxwdv0
Description of the data and file structure
Data analyses presented in this article (https://doi.org/10.1002/ece3.70564) can be reproduced using the dataset and R code provided here.
Files and variables
File: df.xlsx
Description: This dataset contains all sampled individuals and their parasitised state analysed in the article.
Sheet 1: dataset
Variables:
- id: Bird ring identifier
- Species: species to which the id belongs
- Year: sampling year
- Date: sampling date
- Site: sampling site
- Nest: id of nest where the bird was captured
- Sex: female or male
- Age: chick or adult
- days of life: data for chicks only. Days since hatching
- weight_faeces_gr: faeces sample weight
- positive_Lintestinalis_molecular: if positive by qPCR
- positive_Lintestinalis_morphology: if positive by Mini-FLOTAC
- parasitised.Ligula: Whether or not he was parasitised by L. intestinalis
- EPG_Ligula: L. intestinalis eggs per gram of faeces
- Par_NoPar: whether or not the bird was parasitised by L. intestinalis
NA represents not available
Sheet 2: Eggs Ligula
Variables
- id: Bird ring identifier
- long: Egg length of L. intestinalis
- wide: Egg width of L. intestinalis
File: Capasso-et-al._-2024.pdf
Description: R code to replicate the analyses carried out in the article.
File: Appendix.docx
Description: Appendix for the article containing Figure A1 and A2.
Figure A1: Eggs with polar cap observed after Mini-Flotac analysis.
Figure A2: Relationship between sample weight and egg detectability during Mini-FLOTAC performance.
File: Table A1
Description: Taxa included in the phylogenetic tree reconstruction (Figure 4) of mitochondrial cytochrome b gene lineages of L. intestinalis, representing a broad geographic area from 27 countries.
Bold: New L. intestinalis sequences resulting from this study
- id: Haplotype name
- Cytb GenBank accession numbers: Sequence accession number in GenBank
- Parasite: parasitic species of the haplotype
- Host: host species of the parasitic species of the haplotype
- Family: host family of the parasitic species of the haplotype
- Country: Country where the parasite was found
- locality: Locality where the parasite was found
- reference: Article where the sequence is published