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Development of a gp60-subtyping method for Cryptosporidium felis
BACKGROUND: Feline cryptosporidiosis is an increasing problem, especially in catteries. In humans, close contact with cats could be a potential source of infection although the risk of contracting cryptosporidiosis caused by Cryptosporidium felis is considered to be relatively low. Sequencing of the...
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/PMC6979280/ https://www.ncbi.nlm.nih.gov/pubmed/31973771 http://dx.doi.org/10.1186/s13071-020-3906-9 |
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author | Rojas-Lopez, Laura Elwin, Kristin Chalmers, Rachel M. Enemark, Heidi L. Beser, Jessica Troell, Karin |
author_facet | Rojas-Lopez, Laura Elwin, Kristin Chalmers, Rachel M. Enemark, Heidi L. Beser, Jessica Troell, Karin |
author_sort | Rojas-Lopez, Laura |
collection | PubMed |
description | BACKGROUND: Feline cryptosporidiosis is an increasing problem, especially in catteries. In humans, close contact with cats could be a potential source of infection although the risk of contracting cryptosporidiosis caused by Cryptosporidium felis is considered to be relatively low. Sequencing of the 60-kDa glycoprotein gene is a commonly used tool for investigation of the genetic diversity and transmission dynamics of Cryptosporidium species. However, until now the sequence of gp60 from C. felis has not been available and genotyping has been limited to less discriminatory markers, such as 18S rRNA, COWP and HSP70. METHODS: We have identified the gp60 orthologue within the genome sequence of C. felis, and used the sequence to design a nested PCR for subtyping purposes. A total of 128 clinical isolates of both feline and human origin, were used to evaluate the marker. RESULTS: Sequence analysis revealed large variations between the different samples. The C. felis gp60 lack the characteristic serine-tract found in many other cryptosporidian orthologues, instead it has an insertion of variable length (361–742 nt). Also, two cases of suspected zoonotic transmission of C. felis between cats and humans were successfully confirmed. CONCLUSIONS: We have identified the gp60 gene in C. felis and show how this highly variable marker can be used in epidemiological investigations. [Image: see text] |
format | Online Article Text |
id | pubmed-6979280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69792802020-01-29 Development of a gp60-subtyping method for Cryptosporidium felis Rojas-Lopez, Laura Elwin, Kristin Chalmers, Rachel M. Enemark, Heidi L. Beser, Jessica Troell, Karin Parasit Vectors Research BACKGROUND: Feline cryptosporidiosis is an increasing problem, especially in catteries. In humans, close contact with cats could be a potential source of infection although the risk of contracting cryptosporidiosis caused by Cryptosporidium felis is considered to be relatively low. Sequencing of the 60-kDa glycoprotein gene is a commonly used tool for investigation of the genetic diversity and transmission dynamics of Cryptosporidium species. However, until now the sequence of gp60 from C. felis has not been available and genotyping has been limited to less discriminatory markers, such as 18S rRNA, COWP and HSP70. METHODS: We have identified the gp60 orthologue within the genome sequence of C. felis, and used the sequence to design a nested PCR for subtyping purposes. A total of 128 clinical isolates of both feline and human origin, were used to evaluate the marker. RESULTS: Sequence analysis revealed large variations between the different samples. The C. felis gp60 lack the characteristic serine-tract found in many other cryptosporidian orthologues, instead it has an insertion of variable length (361–742 nt). Also, two cases of suspected zoonotic transmission of C. felis between cats and humans were successfully confirmed. CONCLUSIONS: We have identified the gp60 gene in C. felis and show how this highly variable marker can be used in epidemiological investigations. [Image: see text] BioMed Central 2020-01-23 /pmc/articles/PMC6979280/ /pubmed/31973771 http://dx.doi.org/10.1186/s13071-020-3906-9 Text en © The Author(s) 2020 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/. 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 in a credit line to the data. |
spellingShingle | Research Rojas-Lopez, Laura Elwin, Kristin Chalmers, Rachel M. Enemark, Heidi L. Beser, Jessica Troell, Karin Development of a gp60-subtyping method for Cryptosporidium felis |
title | Development of a gp60-subtyping method for Cryptosporidium felis |
title_full | Development of a gp60-subtyping method for Cryptosporidium felis |
title_fullStr | Development of a gp60-subtyping method for Cryptosporidium felis |
title_full_unstemmed | Development of a gp60-subtyping method for Cryptosporidium felis |
title_short | Development of a gp60-subtyping method for Cryptosporidium felis |
title_sort | development of a gp60-subtyping method for cryptosporidium felis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6979280/ https://www.ncbi.nlm.nih.gov/pubmed/31973771 http://dx.doi.org/10.1186/s13071-020-3906-9 |
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