Loading…
Emerging zooanthroponotic risks: Detection of the human norovirus GII.4 SydneyP31 strain in a domestic dog in Brazil
Recent increases in zoonotic diseases underscore the integration of companion animals into urban environments, posing complex transmission risks and highlighting the necessity of One Health approaches. Respiratory and enteric viruses have been consistently linked to interspecies transmission between...
Saved in:
Published in: | Acta tropica 2024-12, Vol.260, p.107449 |
---|---|
Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | |
container_issue | |
container_start_page | 107449 |
container_title | Acta tropica |
container_volume | 260 |
creator | Azevedo, Lais Sampaio de Silva, Vanessa Cristina Martins Guiducci, Raquel Guadagnucci, Simone Costa, Fernanda Faria Ghani, Monique Beerens Abdul Lopes, Ricardo Duarte da Costa, Antonio Charlys Cunha, Lia Lemos, Marcilio Figueredo Parise, Adriana Moreira, Regina Célia Luchs, Adriana |
description | Recent increases in zoonotic diseases underscore the integration of companion animals into urban environments, posing complex transmission risks and highlighting the necessity of One Health approaches. Respiratory and enteric viruses have been consistently linked to interspecies transmission between humans and animals. This study aimed to assess the circulation of human noroviruses (NoV), human adenoviruses (HAdV), enteroviruses (EV), parechoviruses (PeV-A), human bocaviruses (HBoV), hepatitis A (HAV) and E viruses (HEV), Influenza A and B viruses (Flu A/B), respiratory syncytial virus (RSV), and SARS-CoV-2 in domestic dogs and cats in Brazil to understand potential zooanthroponosis risks. Between 2012 and 2021, 600 fecal samples from dogs and cats (516 and 84, respectively) were collected at small animal clinics in São Paulo state, Brazil. The specimens underwent in-house qPCR screening for HBoV and HAdV, while EV, PeV-A, NoV, and HEV were tested using in-house RT-qPCR. SARS-CoV-2, Flu A/B, and RSV were investigated with a commercial RT-qPCR kit assay. HAV detection utilized conventional nested (RT)-PCR. Positive samples were sequenced for molecular characterization and phylogenetic analysis. NoV was detected in 0.2 % (1/600) of the animals, while all other investigated viruses tested negative. The NoV-positive sample, collected in 2012 from a pet dog, was identified as genotype GII.4_Sydney[P31]. The Dog/BRA/2012/GII.4_Sydney[P31]/IAL-M21 strain exhibited a close genetic relationship to Brazilian human and environmental NoV GII.4_Sydney[P31] strains, with 98.1-99.2 % nucleotide similarity in ORF1 and 99.2-99.6 % in ORF2 sequences, suggesting interspecies transmission. Pet dogs are frequently exposed to human fecal-borne viruses, highlighting the potential for zooanthroponotic transmission due to their close interaction with humans in shared environments. There is an urgent need to enhance surveillance studies in companion animals to better understand the implications of detecting human NoV strains in pets, as NoV could potentially act as a reverse zoonotic disease in households, animal hospitals, or shelters worldwide.Recent increases in zoonotic diseases underscore the integration of companion animals into urban environments, posing complex transmission risks and highlighting the necessity of One Health approaches. Respiratory and enteric viruses have been consistently linked to interspecies transmission between humans and animals. This study aimed to a |
doi_str_mv | 10.1016/j.actatropica.2024.107449 |
format | article |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_3123073091</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3123073091</sourcerecordid><originalsourceid>FETCH-proquest_miscellaneous_31230730913</originalsourceid><addsrcrecordid>eNqVjE9Lw0AUxBdRsFa_w_PmpXH_tbEe1VZ7K-i9PDbbZGuyr-7bCO2nNwUPXoWBGX7MjBC3ShZKqtn9rkCXMSfaB4eFltoOvLR2fiZG6qE0k5me2vM_-VJcMe-kVLqc6pHIi86nOsQajkQYczM8UaQcHKTAn_wILz57lwNFoC3kxkPTdxghUqLvkHqG19WqsPB-qKI_rI0CzglDhEEIFXWeT2cV1SfylPAY2mtxscWW_c2vj8XdcvHx_DbZJ_rqh8GmC-x822L01PPGKG1kaeRcmX9UfwA_EVnz</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3123073091</pqid></control><display><type>article</type><title>Emerging zooanthroponotic risks: Detection of the human norovirus GII.4 SydneyP31 strain in a domestic dog in Brazil</title><source>Elsevier</source><creator>Azevedo, Lais Sampaio de ; Silva, Vanessa Cristina Martins ; Guiducci, Raquel ; Guadagnucci, Simone ; Costa, Fernanda Faria ; Ghani, Monique Beerens Abdul ; Lopes, Ricardo Duarte ; da Costa, Antonio Charlys ; Cunha, Lia ; Lemos, Marcilio Figueredo ; Parise, Adriana ; Moreira, Regina Célia ; Luchs, Adriana</creator><creatorcontrib>Azevedo, Lais Sampaio de ; Silva, Vanessa Cristina Martins ; Guiducci, Raquel ; Guadagnucci, Simone ; Costa, Fernanda Faria ; Ghani, Monique Beerens Abdul ; Lopes, Ricardo Duarte ; da Costa, Antonio Charlys ; Cunha, Lia ; Lemos, Marcilio Figueredo ; Parise, Adriana ; Moreira, Regina Célia ; Luchs, Adriana</creatorcontrib><description>Recent increases in zoonotic diseases underscore the integration of companion animals into urban environments, posing complex transmission risks and highlighting the necessity of One Health approaches. Respiratory and enteric viruses have been consistently linked to interspecies transmission between humans and animals. This study aimed to assess the circulation of human noroviruses (NoV), human adenoviruses (HAdV), enteroviruses (EV), parechoviruses (PeV-A), human bocaviruses (HBoV), hepatitis A (HAV) and E viruses (HEV), Influenza A and B viruses (Flu A/B), respiratory syncytial virus (RSV), and SARS-CoV-2 in domestic dogs and cats in Brazil to understand potential zooanthroponosis risks. Between 2012 and 2021, 600 fecal samples from dogs and cats (516 and 84, respectively) were collected at small animal clinics in São Paulo state, Brazil. The specimens underwent in-house qPCR screening for HBoV and HAdV, while EV, PeV-A, NoV, and HEV were tested using in-house RT-qPCR. SARS-CoV-2, Flu A/B, and RSV were investigated with a commercial RT-qPCR kit assay. HAV detection utilized conventional nested (RT)-PCR. Positive samples were sequenced for molecular characterization and phylogenetic analysis. NoV was detected in 0.2 % (1/600) of the animals, while all other investigated viruses tested negative. The NoV-positive sample, collected in 2012 from a pet dog, was identified as genotype GII.4_Sydney[P31]. The Dog/BRA/2012/GII.4_Sydney[P31]/IAL-M21 strain exhibited a close genetic relationship to Brazilian human and environmental NoV GII.4_Sydney[P31] strains, with 98.1-99.2 % nucleotide similarity in ORF1 and 99.2-99.6 % in ORF2 sequences, suggesting interspecies transmission. Pet dogs are frequently exposed to human fecal-borne viruses, highlighting the potential for zooanthroponotic transmission due to their close interaction with humans in shared environments. There is an urgent need to enhance surveillance studies in companion animals to better understand the implications of detecting human NoV strains in pets, as NoV could potentially act as a reverse zoonotic disease in households, animal hospitals, or shelters worldwide.Recent increases in zoonotic diseases underscore the integration of companion animals into urban environments, posing complex transmission risks and highlighting the necessity of One Health approaches. Respiratory and enteric viruses have been consistently linked to interspecies transmission between humans and animals. This study aimed to assess the circulation of human noroviruses (NoV), human adenoviruses (HAdV), enteroviruses (EV), parechoviruses (PeV-A), human bocaviruses (HBoV), hepatitis A (HAV) and E viruses (HEV), Influenza A and B viruses (Flu A/B), respiratory syncytial virus (RSV), and SARS-CoV-2 in domestic dogs and cats in Brazil to understand potential zooanthroponosis risks. Between 2012 and 2021, 600 fecal samples from dogs and cats (516 and 84, respectively) were collected at small animal clinics in São Paulo state, Brazil. The specimens underwent in-house qPCR screening for HBoV and HAdV, while EV, PeV-A, NoV, and HEV were tested using in-house RT-qPCR. SARS-CoV-2, Flu A/B, and RSV were investigated with a commercial RT-qPCR kit assay. HAV detection utilized conventional nested (RT)-PCR. Positive samples were sequenced for molecular characterization and phylogenetic analysis. NoV was detected in 0.2 % (1/600) of the animals, while all other investigated viruses tested negative. The NoV-positive sample, collected in 2012 from a pet dog, was identified as genotype GII.4_Sydney[P31]. The Dog/BRA/2012/GII.4_Sydney[P31]/IAL-M21 strain exhibited a close genetic relationship to Brazilian human and environmental NoV GII.4_Sydney[P31] strains, with 98.1-99.2 % nucleotide similarity in ORF1 and 99.2-99.6 % in ORF2 sequences, suggesting interspecies transmission. Pet dogs are frequently exposed to human fecal-borne viruses, highlighting the potential for zooanthroponotic transmission due to their close interaction with humans in shared environments. There is an urgent need to enhance surveillance studies in companion animals to better understand the implications of detecting human NoV strains in pets, as NoV could potentially act as a reverse zoonotic disease in households, animal hospitals, or shelters worldwide.</description><identifier>ISSN: 1873-6254</identifier><identifier>EISSN: 1873-6254</identifier><identifier>DOI: 10.1016/j.actatropica.2024.107449</identifier><language>eng</language><ispartof>Acta tropica, 2024-12, Vol.260, p.107449</ispartof><rights>Copyright © 2024 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Azevedo, Lais Sampaio de</creatorcontrib><creatorcontrib>Silva, Vanessa Cristina Martins</creatorcontrib><creatorcontrib>Guiducci, Raquel</creatorcontrib><creatorcontrib>Guadagnucci, Simone</creatorcontrib><creatorcontrib>Costa, Fernanda Faria</creatorcontrib><creatorcontrib>Ghani, Monique Beerens Abdul</creatorcontrib><creatorcontrib>Lopes, Ricardo Duarte</creatorcontrib><creatorcontrib>da Costa, Antonio Charlys</creatorcontrib><creatorcontrib>Cunha, Lia</creatorcontrib><creatorcontrib>Lemos, Marcilio Figueredo</creatorcontrib><creatorcontrib>Parise, Adriana</creatorcontrib><creatorcontrib>Moreira, Regina Célia</creatorcontrib><creatorcontrib>Luchs, Adriana</creatorcontrib><title>Emerging zooanthroponotic risks: Detection of the human norovirus GII.4 SydneyP31 strain in a domestic dog in Brazil</title><title>Acta tropica</title><description>Recent increases in zoonotic diseases underscore the integration of companion animals into urban environments, posing complex transmission risks and highlighting the necessity of One Health approaches. Respiratory and enteric viruses have been consistently linked to interspecies transmission between humans and animals. This study aimed to assess the circulation of human noroviruses (NoV), human adenoviruses (HAdV), enteroviruses (EV), parechoviruses (PeV-A), human bocaviruses (HBoV), hepatitis A (HAV) and E viruses (HEV), Influenza A and B viruses (Flu A/B), respiratory syncytial virus (RSV), and SARS-CoV-2 in domestic dogs and cats in Brazil to understand potential zooanthroponosis risks. Between 2012 and 2021, 600 fecal samples from dogs and cats (516 and 84, respectively) were collected at small animal clinics in São Paulo state, Brazil. The specimens underwent in-house qPCR screening for HBoV and HAdV, while EV, PeV-A, NoV, and HEV were tested using in-house RT-qPCR. SARS-CoV-2, Flu A/B, and RSV were investigated with a commercial RT-qPCR kit assay. HAV detection utilized conventional nested (RT)-PCR. Positive samples were sequenced for molecular characterization and phylogenetic analysis. NoV was detected in 0.2 % (1/600) of the animals, while all other investigated viruses tested negative. The NoV-positive sample, collected in 2012 from a pet dog, was identified as genotype GII.4_Sydney[P31]. The Dog/BRA/2012/GII.4_Sydney[P31]/IAL-M21 strain exhibited a close genetic relationship to Brazilian human and environmental NoV GII.4_Sydney[P31] strains, with 98.1-99.2 % nucleotide similarity in ORF1 and 99.2-99.6 % in ORF2 sequences, suggesting interspecies transmission. Pet dogs are frequently exposed to human fecal-borne viruses, highlighting the potential for zooanthroponotic transmission due to their close interaction with humans in shared environments. There is an urgent need to enhance surveillance studies in companion animals to better understand the implications of detecting human NoV strains in pets, as NoV could potentially act as a reverse zoonotic disease in households, animal hospitals, or shelters worldwide.Recent increases in zoonotic diseases underscore the integration of companion animals into urban environments, posing complex transmission risks and highlighting the necessity of One Health approaches. Respiratory and enteric viruses have been consistently linked to interspecies transmission between humans and animals. This study aimed to assess the circulation of human noroviruses (NoV), human adenoviruses (HAdV), enteroviruses (EV), parechoviruses (PeV-A), human bocaviruses (HBoV), hepatitis A (HAV) and E viruses (HEV), Influenza A and B viruses (Flu A/B), respiratory syncytial virus (RSV), and SARS-CoV-2 in domestic dogs and cats in Brazil to understand potential zooanthroponosis risks. Between 2012 and 2021, 600 fecal samples from dogs and cats (516 and 84, respectively) were collected at small animal clinics in São Paulo state, Brazil. The specimens underwent in-house qPCR screening for HBoV and HAdV, while EV, PeV-A, NoV, and HEV were tested using in-house RT-qPCR. SARS-CoV-2, Flu A/B, and RSV were investigated with a commercial RT-qPCR kit assay. HAV detection utilized conventional nested (RT)-PCR. Positive samples were sequenced for molecular characterization and phylogenetic analysis. NoV was detected in 0.2 % (1/600) of the animals, while all other investigated viruses tested negative. The NoV-positive sample, collected in 2012 from a pet dog, was identified as genotype GII.4_Sydney[P31]. The Dog/BRA/2012/GII.4_Sydney[P31]/IAL-M21 strain exhibited a close genetic relationship to Brazilian human and environmental NoV GII.4_Sydney[P31] strains, with 98.1-99.2 % nucleotide similarity in ORF1 and 99.2-99.6 % in ORF2 sequences, suggesting interspecies transmission. Pet dogs are frequently exposed to human fecal-borne viruses, highlighting the potential for zooanthroponotic transmission due to their close interaction with humans in shared environments. There is an urgent need to enhance surveillance studies in companion animals to better understand the implications of detecting human NoV strains in pets, as NoV could potentially act as a reverse zoonotic disease in households, animal hospitals, or shelters worldwide.</description><issn>1873-6254</issn><issn>1873-6254</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqVjE9Lw0AUxBdRsFa_w_PmpXH_tbEe1VZ7K-i9PDbbZGuyr-7bCO2nNwUPXoWBGX7MjBC3ShZKqtn9rkCXMSfaB4eFltoOvLR2fiZG6qE0k5me2vM_-VJcMe-kVLqc6pHIi86nOsQajkQYczM8UaQcHKTAn_wILz57lwNFoC3kxkPTdxghUqLvkHqG19WqsPB-qKI_rI0CzglDhEEIFXWeT2cV1SfylPAY2mtxscWW_c2vj8XdcvHx_DbZJ_rqh8GmC-x822L01PPGKG1kaeRcmX9UfwA_EVnz</recordid><startdate>20241201</startdate><enddate>20241201</enddate><creator>Azevedo, Lais Sampaio de</creator><creator>Silva, Vanessa Cristina Martins</creator><creator>Guiducci, Raquel</creator><creator>Guadagnucci, Simone</creator><creator>Costa, Fernanda Faria</creator><creator>Ghani, Monique Beerens Abdul</creator><creator>Lopes, Ricardo Duarte</creator><creator>da Costa, Antonio Charlys</creator><creator>Cunha, Lia</creator><creator>Lemos, Marcilio Figueredo</creator><creator>Parise, Adriana</creator><creator>Moreira, Regina Célia</creator><creator>Luchs, Adriana</creator><scope>7X8</scope></search><sort><creationdate>20241201</creationdate><title>Emerging zooanthroponotic risks: Detection of the human norovirus GII.4 SydneyP31 strain in a domestic dog in Brazil</title><author>Azevedo, Lais Sampaio de ; Silva, Vanessa Cristina Martins ; Guiducci, Raquel ; Guadagnucci, Simone ; Costa, Fernanda Faria ; Ghani, Monique Beerens Abdul ; Lopes, Ricardo Duarte ; da Costa, Antonio Charlys ; Cunha, Lia ; Lemos, Marcilio Figueredo ; Parise, Adriana ; Moreira, Regina Célia ; Luchs, Adriana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_31230730913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Azevedo, Lais Sampaio de</creatorcontrib><creatorcontrib>Silva, Vanessa Cristina Martins</creatorcontrib><creatorcontrib>Guiducci, Raquel</creatorcontrib><creatorcontrib>Guadagnucci, Simone</creatorcontrib><creatorcontrib>Costa, Fernanda Faria</creatorcontrib><creatorcontrib>Ghani, Monique Beerens Abdul</creatorcontrib><creatorcontrib>Lopes, Ricardo Duarte</creatorcontrib><creatorcontrib>da Costa, Antonio Charlys</creatorcontrib><creatorcontrib>Cunha, Lia</creatorcontrib><creatorcontrib>Lemos, Marcilio Figueredo</creatorcontrib><creatorcontrib>Parise, Adriana</creatorcontrib><creatorcontrib>Moreira, Regina Célia</creatorcontrib><creatorcontrib>Luchs, Adriana</creatorcontrib><collection>MEDLINE - Academic</collection><jtitle>Acta tropica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Azevedo, Lais Sampaio de</au><au>Silva, Vanessa Cristina Martins</au><au>Guiducci, Raquel</au><au>Guadagnucci, Simone</au><au>Costa, Fernanda Faria</au><au>Ghani, Monique Beerens Abdul</au><au>Lopes, Ricardo Duarte</au><au>da Costa, Antonio Charlys</au><au>Cunha, Lia</au><au>Lemos, Marcilio Figueredo</au><au>Parise, Adriana</au><au>Moreira, Regina Célia</au><au>Luchs, Adriana</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Emerging zooanthroponotic risks: Detection of the human norovirus GII.4 SydneyP31 strain in a domestic dog in Brazil</atitle><jtitle>Acta tropica</jtitle><date>2024-12-01</date><risdate>2024</risdate><volume>260</volume><spage>107449</spage><pages>107449-</pages><issn>1873-6254</issn><eissn>1873-6254</eissn><abstract>Recent increases in zoonotic diseases underscore the integration of companion animals into urban environments, posing complex transmission risks and highlighting the necessity of One Health approaches. Respiratory and enteric viruses have been consistently linked to interspecies transmission between humans and animals. This study aimed to assess the circulation of human noroviruses (NoV), human adenoviruses (HAdV), enteroviruses (EV), parechoviruses (PeV-A), human bocaviruses (HBoV), hepatitis A (HAV) and E viruses (HEV), Influenza A and B viruses (Flu A/B), respiratory syncytial virus (RSV), and SARS-CoV-2 in domestic dogs and cats in Brazil to understand potential zooanthroponosis risks. Between 2012 and 2021, 600 fecal samples from dogs and cats (516 and 84, respectively) were collected at small animal clinics in São Paulo state, Brazil. The specimens underwent in-house qPCR screening for HBoV and HAdV, while EV, PeV-A, NoV, and HEV were tested using in-house RT-qPCR. SARS-CoV-2, Flu A/B, and RSV were investigated with a commercial RT-qPCR kit assay. HAV detection utilized conventional nested (RT)-PCR. Positive samples were sequenced for molecular characterization and phylogenetic analysis. NoV was detected in 0.2 % (1/600) of the animals, while all other investigated viruses tested negative. The NoV-positive sample, collected in 2012 from a pet dog, was identified as genotype GII.4_Sydney[P31]. The Dog/BRA/2012/GII.4_Sydney[P31]/IAL-M21 strain exhibited a close genetic relationship to Brazilian human and environmental NoV GII.4_Sydney[P31] strains, with 98.1-99.2 % nucleotide similarity in ORF1 and 99.2-99.6 % in ORF2 sequences, suggesting interspecies transmission. Pet dogs are frequently exposed to human fecal-borne viruses, highlighting the potential for zooanthroponotic transmission due to their close interaction with humans in shared environments. There is an urgent need to enhance surveillance studies in companion animals to better understand the implications of detecting human NoV strains in pets, as NoV could potentially act as a reverse zoonotic disease in households, animal hospitals, or shelters worldwide.Recent increases in zoonotic diseases underscore the integration of companion animals into urban environments, posing complex transmission risks and highlighting the necessity of One Health approaches. Respiratory and enteric viruses have been consistently linked to interspecies transmission between humans and animals. This study aimed to assess the circulation of human noroviruses (NoV), human adenoviruses (HAdV), enteroviruses (EV), parechoviruses (PeV-A), human bocaviruses (HBoV), hepatitis A (HAV) and E viruses (HEV), Influenza A and B viruses (Flu A/B), respiratory syncytial virus (RSV), and SARS-CoV-2 in domestic dogs and cats in Brazil to understand potential zooanthroponosis risks. Between 2012 and 2021, 600 fecal samples from dogs and cats (516 and 84, respectively) were collected at small animal clinics in São Paulo state, Brazil. The specimens underwent in-house qPCR screening for HBoV and HAdV, while EV, PeV-A, NoV, and HEV were tested using in-house RT-qPCR. SARS-CoV-2, Flu A/B, and RSV were investigated with a commercial RT-qPCR kit assay. HAV detection utilized conventional nested (RT)-PCR. Positive samples were sequenced for molecular characterization and phylogenetic analysis. NoV was detected in 0.2 % (1/600) of the animals, while all other investigated viruses tested negative. The NoV-positive sample, collected in 2012 from a pet dog, was identified as genotype GII.4_Sydney[P31]. The Dog/BRA/2012/GII.4_Sydney[P31]/IAL-M21 strain exhibited a close genetic relationship to Brazilian human and environmental NoV GII.4_Sydney[P31] strains, with 98.1-99.2 % nucleotide similarity in ORF1 and 99.2-99.6 % in ORF2 sequences, suggesting interspecies transmission. Pet dogs are frequently exposed to human fecal-borne viruses, highlighting the potential for zooanthroponotic transmission due to their close interaction with humans in shared environments. There is an urgent need to enhance surveillance studies in companion animals to better understand the implications of detecting human NoV strains in pets, as NoV could potentially act as a reverse zoonotic disease in households, animal hospitals, or shelters worldwide.</abstract><doi>10.1016/j.actatropica.2024.107449</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1873-6254 |
ispartof | Acta tropica, 2024-12, Vol.260, p.107449 |
issn | 1873-6254 1873-6254 |
language | eng |
recordid | cdi_proquest_miscellaneous_3123073091 |
source | Elsevier |
title | Emerging zooanthroponotic risks: Detection of the human norovirus GII.4 SydneyP31 strain in a domestic dog in Brazil |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T05%3A13%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Emerging%20zooanthroponotic%20risks:%20Detection%20of%20the%20human%20norovirus%20GII.4%20SydneyP31%20strain%20in%20a%20domestic%20dog%20in%20Brazil&rft.jtitle=Acta%20tropica&rft.au=Azevedo,%20Lais%20Sampaio%20de&rft.date=2024-12-01&rft.volume=260&rft.spage=107449&rft.pages=107449-&rft.issn=1873-6254&rft.eissn=1873-6254&rft_id=info:doi/10.1016/j.actatropica.2024.107449&rft_dat=%3Cproquest%3E3123073091%3C/proquest%3E%3Cgrp_id%3Ecdi_FETCH-proquest_miscellaneous_31230730913%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3123073091&rft_id=info:pmid/&rfr_iscdi=true |