Artigo

Detection of human polyomavirus 2 (HPyV2) in oyster samples in northern Brazil

Background: Human polyomavirus 2 (HPyV2 or JCPyV) is persistent in the environment due to its excretion in urine and feces; it is detected in samples of wastewater, surface water and drinking water. A lack of basic sanitation and sewage collection results in the presence of this virus in food, esp...

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Autor principal: Abreu, Isabella Nogueira
Outros Autores: Cortinhas, Jacqueline Monteiro, Santos, Mike Barbosa dos, Queiroz, Maria Alice Freitas, Silva, Andr?a Nazar? Monteiro Rangel da, Cayres-Vallinoto, Izaura Maria Vieira, Vallinoto, Antonio Carlos Ros?rio
Grau: Artigo
Idioma: eng
Publicado em: BMC 2020
Assuntos:
Acesso em linha: http://patua.iec.gov.br//handle/iec/4114
id ir-iec-4114
recordtype dspace
spelling ir-iec-41142020-07-15T13:39:27Z Detection of human polyomavirus 2 (HPyV2) in oyster samples in northern Brazil Abreu, Isabella Nogueira Cortinhas, Jacqueline Monteiro Santos, Mike Barbosa dos Queiroz, Maria Alice Freitas Silva, Andr?a Nazar? Monteiro Rangel da Cayres-Vallinoto, Izaura Maria Vieira Vallinoto, Antonio Carlos Ros?rio Polyomavirus / isolamento & purifica??o V?rus JC / isolamento & purifica??o Ostrea / anatomia & histologia Rea??o em Cadeia da Polimerase em Tempo Real / m?todos Polui??o da ?gua Saneamento B?sico Salin?polis (PA) Augusto Corr?a (PA) S?o Caetano de Odivelas (PA) Curu?? (PA) Bragan?a (PA) Background: Human polyomavirus 2 (HPyV2 or JCPyV) is persistent in the environment due to its excretion in urine and feces; it is detected in samples of wastewater, surface water and drinking water. A lack of basic sanitation and sewage collection results in the presence of this virus in food, especially in oysters, since they are bioaccumulators and are consumed in their natural form, thus posing a risk to human health. Methods: This study investigated the frequency of HPyV2 in samples of oysters marketed in northeastern Par? State, Brazil, and optimized a real-time PCR (qPCR) protocol for the detection of an endogenous oyster control. A total of 217 oysters in 22 pools from five municipalities in the state of Par? were analyzed. Samples underwent dissection and total maceration of oyster tissue using a viral concentration technique, followed by DNA extraction with phenol-chloroform and amplification of the VP1 region for molecular detection via qPCR. Results: HPyV2 was detected in 18.2% (4/22) of the pooled samples, with frequencies of 25, 20, 20 and 16% in the municipalities of Salin?polis, Augusto Corr?a, S?o Caetano de Odivelas and Curu??, respectively. Notably, the sample pool from the municipality of Bragan?a did not have detectable HPyV2 and this was the only sampled location with a water treatment station. In this study, Crassostrea genus-specific primers (AFL52 ribosomal RNA gene) of oyster were developed for use as an endogenous control in the qPCR analysis, which will be useful for future studies. Conclusions: The detection of HPyV2 in oyster samples commercialized in the state of Par? shows the circulation of this virus in the studied municipalities. Thus, it is necessary to implement measures for improving sewage collection and basic sanitation to avoid contamination of water and food with HPyV2 National Council for Scientific and Technological Development (Conselho Nacional de Desenvolvimento Cient?fico and Tecnol?gico - CNPQ) and the Institutional Support Program for Qualified Production (Programa de Apoio a Produ??o Qualificada - PAPQ/2019) of the Universidade Federal do Par?. 2020-07-15T13:03:43Z 2020-07-15T13:03:43Z 2020 Artigo ABREU, Isabella Nogueira et al. Detection of human polyomavirus 2 (HPyV2) in oyster samples in northern Brazil. Virology Journal, v. 17, n. 85, p. 1-6, 2020. 1743-422X http://patua.iec.gov.br//handle/iec/4114 10.1186/s12985-020-01360-8 eng Acesso Aberto application/pdf BMC
institution Instituto Evandro Chagas (IEC)
collection PATUA
language eng
topic Polyomavirus / isolamento & purifica??o
V?rus JC / isolamento & purifica??o
Ostrea / anatomia & histologia
Rea??o em Cadeia da Polimerase em Tempo Real / m?todos
Polui??o da ?gua
Saneamento B?sico
Salin?polis (PA)
Augusto Corr?a (PA)
S?o Caetano de Odivelas (PA)
Curu?? (PA)
Bragan?a (PA)
spellingShingle Polyomavirus / isolamento & purifica??o
V?rus JC / isolamento & purifica??o
Ostrea / anatomia & histologia
Rea??o em Cadeia da Polimerase em Tempo Real / m?todos
Polui??o da ?gua
Saneamento B?sico
Salin?polis (PA)
Augusto Corr?a (PA)
S?o Caetano de Odivelas (PA)
Curu?? (PA)
Bragan?a (PA)
Abreu, Isabella Nogueira
Detection of human polyomavirus 2 (HPyV2) in oyster samples in northern Brazil
topic_facet Polyomavirus / isolamento & purifica??o
V?rus JC / isolamento & purifica??o
Ostrea / anatomia & histologia
Rea??o em Cadeia da Polimerase em Tempo Real / m?todos
Polui??o da ?gua
Saneamento B?sico
Salin?polis (PA)
Augusto Corr?a (PA)
S?o Caetano de Odivelas (PA)
Curu?? (PA)
Bragan?a (PA)
description Background: Human polyomavirus 2 (HPyV2 or JCPyV) is persistent in the environment due to its excretion in urine and feces; it is detected in samples of wastewater, surface water and drinking water. A lack of basic sanitation and sewage collection results in the presence of this virus in food, especially in oysters, since they are bioaccumulators and are consumed in their natural form, thus posing a risk to human health. Methods: This study investigated the frequency of HPyV2 in samples of oysters marketed in northeastern Par? State, Brazil, and optimized a real-time PCR (qPCR) protocol for the detection of an endogenous oyster control. A total of 217 oysters in 22 pools from five municipalities in the state of Par? were analyzed. Samples underwent dissection and total maceration of oyster tissue using a viral concentration technique, followed by DNA extraction with phenol-chloroform and amplification of the VP1 region for molecular detection via qPCR. Results: HPyV2 was detected in 18.2% (4/22) of the pooled samples, with frequencies of 25, 20, 20 and 16% in the municipalities of Salin?polis, Augusto Corr?a, S?o Caetano de Odivelas and Curu??, respectively. Notably, the sample pool from the municipality of Bragan?a did not have detectable HPyV2 and this was the only sampled location with a water treatment station. In this study, Crassostrea genus-specific primers (AFL52 ribosomal RNA gene) of oyster were developed for use as an endogenous control in the qPCR analysis, which will be useful for future studies. Conclusions: The detection of HPyV2 in oyster samples commercialized in the state of Par? shows the circulation of this virus in the studied municipalities. Thus, it is necessary to implement measures for improving sewage collection and basic sanitation to avoid contamination of water and food with HPyV2
format Artigo
author Abreu, Isabella Nogueira
author2 Cortinhas, Jacqueline Monteiro
Santos, Mike Barbosa dos
Queiroz, Maria Alice Freitas
Silva, Andr?a Nazar? Monteiro Rangel da
Cayres-Vallinoto, Izaura Maria Vieira
Vallinoto, Antonio Carlos Ros?rio
author2Str Cortinhas, Jacqueline Monteiro
Santos, Mike Barbosa dos
Queiroz, Maria Alice Freitas
Silva, Andr?a Nazar? Monteiro Rangel da
Cayres-Vallinoto, Izaura Maria Vieira
Vallinoto, Antonio Carlos Ros?rio
title Detection of human polyomavirus 2 (HPyV2) in oyster samples in northern Brazil
title_short Detection of human polyomavirus 2 (HPyV2) in oyster samples in northern Brazil
title_full Detection of human polyomavirus 2 (HPyV2) in oyster samples in northern Brazil
title_fullStr Detection of human polyomavirus 2 (HPyV2) in oyster samples in northern Brazil
title_full_unstemmed Detection of human polyomavirus 2 (HPyV2) in oyster samples in northern Brazil
title_sort detection of human polyomavirus 2 (hpyv2) in oyster samples in northern brazil
publisher BMC
publishDate 2020
url http://patua.iec.gov.br//handle/iec/4114
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score 11.687526