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Giardia duodenalis multi-locus genotypes in dogs with different levels of synanthropism and clinical signs
BACKGROUND: In dogs, infections with Giardia duodenalis are mainly caused by assemblages C and D, but also by the potentially zoonotic assemblages A and B. The aims of this study were to assess differences in assemblages (i) between dogs living mainly in close proximity to humans (synanthropic dogs)...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709413/ https://www.ncbi.nlm.nih.gov/pubmed/33267878 http://dx.doi.org/10.1186/s13071-020-04496-2 |
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author | Uiterwijk, Mathilde Mughini-Gras, Lapo Nijsse, Rolf Wagenaar, Jaap A. Ploeger, Harm W. Kooyman, Frans N. J. |
author_facet | Uiterwijk, Mathilde Mughini-Gras, Lapo Nijsse, Rolf Wagenaar, Jaap A. Ploeger, Harm W. Kooyman, Frans N. J. |
author_sort | Uiterwijk, Mathilde |
collection | PubMed |
description | BACKGROUND: In dogs, infections with Giardia duodenalis are mainly caused by assemblages C and D, but also by the potentially zoonotic assemblages A and B. The aims of this study were to assess differences in assemblages (i) between dogs living mainly in close proximity to humans (synanthropic dogs) versus dogs living mainly among other dogs, (ii) between samples of dogs with or without loose stool, and (iii) related to the amount of cysts shedding. METHODS: One hundred eighty-nine qPCR Giardia positive fecal samples of dogs originating from four groups (household, sheltered, hunting, and dogs for which a veterinarian sent a fecal sample to a diagnostic laboratory) were used for genotyping. For this, multi-locus genotyping of beta-giardin, triose phosphate isomerase, and glutamate dehydrogenase and genotyping of SSU rDNA gene fragments were performed. Fecal consistency was scored (loose or non-loose stool), and cysts per gram of feces were determined with qPCR. RESULTS: Assemblage D was the most prevalent in all groups, followed by the other canid assemblage C. Also, mixed C/D was common. In two (synanthropic) household dogs, the potentially zoonotic assemblage AI was present. Although occurrence of assemblage AI in household dogs was not significantly different from dogs living among other dogs (sheltered and hunting dogs), it was significantly higher compared to dogs for which a sample was sent to a diagnostic laboratory. Dogs with assemblage D shed significantly more cysts than dogs with other assemblages (except for mixed C/D results) or dogs in which no assemblage could be determined. None of the assemblages was significantly associated with loose stool. CONCLUSION: Not only do dogs mainly shed the canid Giardia duodenalis assemblages D and/or C, the numbers of cysts per gram for the canid assemblage D were also higher than for the potential zoonotic assemblage AI. Based on the assemblages shed by dogs, the risk to public health posed by dogs is estimated to be low, even though the dogs that shed AI were synanthropic household dogs. Loose stool in infected dogs was not associated with any particular Giardia assemblage. |
format | Online Article Text |
id | pubmed-7709413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77094132020-12-03 Giardia duodenalis multi-locus genotypes in dogs with different levels of synanthropism and clinical signs Uiterwijk, Mathilde Mughini-Gras, Lapo Nijsse, Rolf Wagenaar, Jaap A. Ploeger, Harm W. Kooyman, Frans N. J. Parasit Vectors Short Report BACKGROUND: In dogs, infections with Giardia duodenalis are mainly caused by assemblages C and D, but also by the potentially zoonotic assemblages A and B. The aims of this study were to assess differences in assemblages (i) between dogs living mainly in close proximity to humans (synanthropic dogs) versus dogs living mainly among other dogs, (ii) between samples of dogs with or without loose stool, and (iii) related to the amount of cysts shedding. METHODS: One hundred eighty-nine qPCR Giardia positive fecal samples of dogs originating from four groups (household, sheltered, hunting, and dogs for which a veterinarian sent a fecal sample to a diagnostic laboratory) were used for genotyping. For this, multi-locus genotyping of beta-giardin, triose phosphate isomerase, and glutamate dehydrogenase and genotyping of SSU rDNA gene fragments were performed. Fecal consistency was scored (loose or non-loose stool), and cysts per gram of feces were determined with qPCR. RESULTS: Assemblage D was the most prevalent in all groups, followed by the other canid assemblage C. Also, mixed C/D was common. In two (synanthropic) household dogs, the potentially zoonotic assemblage AI was present. Although occurrence of assemblage AI in household dogs was not significantly different from dogs living among other dogs (sheltered and hunting dogs), it was significantly higher compared to dogs for which a sample was sent to a diagnostic laboratory. Dogs with assemblage D shed significantly more cysts than dogs with other assemblages (except for mixed C/D results) or dogs in which no assemblage could be determined. None of the assemblages was significantly associated with loose stool. CONCLUSION: Not only do dogs mainly shed the canid Giardia duodenalis assemblages D and/or C, the numbers of cysts per gram for the canid assemblage D were also higher than for the potential zoonotic assemblage AI. Based on the assemblages shed by dogs, the risk to public health posed by dogs is estimated to be low, even though the dogs that shed AI were synanthropic household dogs. Loose stool in infected dogs was not associated with any particular Giardia assemblage. BioMed Central 2020-12-02 /pmc/articles/PMC7709413/ /pubmed/33267878 http://dx.doi.org/10.1186/s13071-020-04496-2 Text en © The Author(s) 2020 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 | Short Report Uiterwijk, Mathilde Mughini-Gras, Lapo Nijsse, Rolf Wagenaar, Jaap A. Ploeger, Harm W. Kooyman, Frans N. J. Giardia duodenalis multi-locus genotypes in dogs with different levels of synanthropism and clinical signs |
title | Giardia duodenalis multi-locus genotypes in dogs with different levels of synanthropism and clinical signs |
title_full | Giardia duodenalis multi-locus genotypes in dogs with different levels of synanthropism and clinical signs |
title_fullStr | Giardia duodenalis multi-locus genotypes in dogs with different levels of synanthropism and clinical signs |
title_full_unstemmed | Giardia duodenalis multi-locus genotypes in dogs with different levels of synanthropism and clinical signs |
title_short | Giardia duodenalis multi-locus genotypes in dogs with different levels of synanthropism and clinical signs |
title_sort | giardia duodenalis multi-locus genotypes in dogs with different levels of synanthropism and clinical signs |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709413/ https://www.ncbi.nlm.nih.gov/pubmed/33267878 http://dx.doi.org/10.1186/s13071-020-04496-2 |
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