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Cryptosporidium Oocyst Contamination in Drinking Water: A Case Study in Italy
The aim of this study was to evaluate the occurrence of Cryptosporidium oocysts in a drinking water treatment plant (DWTP) located in a rural area of northern Italy. Influent and effluent samples were collected at the DWTP over three years (2013–2016). In parallel, tap water samples from a public dr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604028/ https://www.ncbi.nlm.nih.gov/pubmed/31185673 http://dx.doi.org/10.3390/ijerph16112055 |
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author | Pignata, Cristina Bonetta, Silvia Bonetta, Sara Cacciò, Simone M. Sannella, Anna R. Gilli, Giorgio Carraro, Elisabetta |
author_facet | Pignata, Cristina Bonetta, Silvia Bonetta, Sara Cacciò, Simone M. Sannella, Anna R. Gilli, Giorgio Carraro, Elisabetta |
author_sort | Pignata, Cristina |
collection | PubMed |
description | The aim of this study was to evaluate the occurrence of Cryptosporidium oocysts in a drinking water treatment plant (DWTP) located in a rural area of northern Italy. Influent and effluent samples were collected at the DWTP over three years (2013–2016). In parallel, tap water samples from a public drinking fountain were collected as well. All samples were analyzed for the presence of Cryptosporidium spp. oocysts by a common method based on an immunomagnetic separation (IMS)/immunofluorescence assay (IFA), complemented by 4,6-diamidino-2-phenylindole (DAPI) staining. A reverse transcriptase-PCR (RT-PCR) protocol was added to evaluate oocyst viability. The results highlighted a high variability of oocyst concentrations across all samples (mean 4.3 ± 5.8/100 L) and a high variability in the percentage of DAPI-positive specimens (mean 48.2% ± 40.3%). Conversely, RT-PCR did not reveal the presence of viable C. parvum and C. hominis oocysts. A nested PCR targeting Cryptosporidium 18S ribosomal DNA, carried out in two water samples, confirmed the presence of a Cryptosporidium genotype associated with wild animals in the river and in tap water. The results obtained underline the vulnerability of the investigated surface water to Cryptosporidium spp. contamination. Although the recovered Cryptosporidium genotype is not a human pathogen, its presence demonstrates the existence of a potential pathogen Cryptosporidium spp. contamination risk. Moreover, these results underline the importance of also considering unconventional (not bacterial) biological contaminations (protozoa) in water resources in rural areas, including those of developed countries. |
format | Online Article Text |
id | pubmed-6604028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66040282019-07-19 Cryptosporidium Oocyst Contamination in Drinking Water: A Case Study in Italy Pignata, Cristina Bonetta, Silvia Bonetta, Sara Cacciò, Simone M. Sannella, Anna R. Gilli, Giorgio Carraro, Elisabetta Int J Environ Res Public Health Communication The aim of this study was to evaluate the occurrence of Cryptosporidium oocysts in a drinking water treatment plant (DWTP) located in a rural area of northern Italy. Influent and effluent samples were collected at the DWTP over three years (2013–2016). In parallel, tap water samples from a public drinking fountain were collected as well. All samples were analyzed for the presence of Cryptosporidium spp. oocysts by a common method based on an immunomagnetic separation (IMS)/immunofluorescence assay (IFA), complemented by 4,6-diamidino-2-phenylindole (DAPI) staining. A reverse transcriptase-PCR (RT-PCR) protocol was added to evaluate oocyst viability. The results highlighted a high variability of oocyst concentrations across all samples (mean 4.3 ± 5.8/100 L) and a high variability in the percentage of DAPI-positive specimens (mean 48.2% ± 40.3%). Conversely, RT-PCR did not reveal the presence of viable C. parvum and C. hominis oocysts. A nested PCR targeting Cryptosporidium 18S ribosomal DNA, carried out in two water samples, confirmed the presence of a Cryptosporidium genotype associated with wild animals in the river and in tap water. The results obtained underline the vulnerability of the investigated surface water to Cryptosporidium spp. contamination. Although the recovered Cryptosporidium genotype is not a human pathogen, its presence demonstrates the existence of a potential pathogen Cryptosporidium spp. contamination risk. Moreover, these results underline the importance of also considering unconventional (not bacterial) biological contaminations (protozoa) in water resources in rural areas, including those of developed countries. MDPI 2019-06-10 2019-06 /pmc/articles/PMC6604028/ /pubmed/31185673 http://dx.doi.org/10.3390/ijerph16112055 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Pignata, Cristina Bonetta, Silvia Bonetta, Sara Cacciò, Simone M. Sannella, Anna R. Gilli, Giorgio Carraro, Elisabetta Cryptosporidium Oocyst Contamination in Drinking Water: A Case Study in Italy |
title | Cryptosporidium Oocyst Contamination in Drinking Water: A Case Study in Italy |
title_full | Cryptosporidium Oocyst Contamination in Drinking Water: A Case Study in Italy |
title_fullStr | Cryptosporidium Oocyst Contamination in Drinking Water: A Case Study in Italy |
title_full_unstemmed | Cryptosporidium Oocyst Contamination in Drinking Water: A Case Study in Italy |
title_short | Cryptosporidium Oocyst Contamination in Drinking Water: A Case Study in Italy |
title_sort | cryptosporidium oocyst contamination in drinking water: a case study in italy |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604028/ https://www.ncbi.nlm.nih.gov/pubmed/31185673 http://dx.doi.org/10.3390/ijerph16112055 |
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