Comparison of three diagnostic methods for Salmonella enterica serovars detection in chicken rinse
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1590/1678-5150-PVB-5211 http://hdl.handle.net/11449/188246 |
Resumo: | Salmonella detection is a key point in food safety testing, because of the frequent association of this pathogen with food poisoning in humans. The standard bacteriological tests currently used for Salmonella-detection are time-consuming; therefore, there is a need to develop alternative methods to accelerate the detection. In order to accelerate Salmonella diagnosis, we used the immunomagnetic separation assay associated with bacteriophage P22 for the rapid detection of the following Salmonella serovars in chicken rinses of drumsticks, artificially contaminated with 5, 10, and 100 CFU/25mL of bacteria: Salmonella enterica subsp. enterica serovar Heidelberg (S. Heidelberg), Salmonella enterica subsp. enterica serovar Enteritidis (S. Enteritidis) and Salmonella enterica subsp. enterica serovar Typhimurium (S. Typhimurium). The efficiency of the technique, represented by the time required for detection of positive and negative samples, was compared with that of the standard diagnostic tests used for this pathogen, the bacteriological assay and the polymerase chain reaction (PCR)-based test. This study confirmed the ability of the bacteriophage-associated immunomagnetic separation assay to identify 99.6% of Salmonella-positive samples of the three serovars tested. In contrast, the bacteriological assay and PCR-based test detected 95.1% and 98.5% of the Salmonella-positive samples respectively. |
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Comparison of three diagnostic methods for Salmonella enterica serovars detection in chicken rinseChicken rinseDiagnosticImmunomagneticPhage P22Salmonella entericaSalmonella EnteritidisSalmonella HeidelbergSalmonella TyphimuriumSerovarsSalmonella detection is a key point in food safety testing, because of the frequent association of this pathogen with food poisoning in humans. The standard bacteriological tests currently used for Salmonella-detection are time-consuming; therefore, there is a need to develop alternative methods to accelerate the detection. In order to accelerate Salmonella diagnosis, we used the immunomagnetic separation assay associated with bacteriophage P22 for the rapid detection of the following Salmonella serovars in chicken rinses of drumsticks, artificially contaminated with 5, 10, and 100 CFU/25mL of bacteria: Salmonella enterica subsp. enterica serovar Heidelberg (S. Heidelberg), Salmonella enterica subsp. enterica serovar Enteritidis (S. Enteritidis) and Salmonella enterica subsp. enterica serovar Typhimurium (S. Typhimurium). The efficiency of the technique, represented by the time required for detection of positive and negative samples, was compared with that of the standard diagnostic tests used for this pathogen, the bacteriological assay and the polymerase chain reaction (PCR)-based test. This study confirmed the ability of the bacteriophage-associated immunomagnetic separation assay to identify 99.6% of Salmonella-positive samples of the three serovars tested. In contrast, the bacteriological assay and PCR-based test detected 95.1% and 98.5% of the Salmonella-positive samples respectively.Laboratório de Patologia Aviária Departamento de Clínica Veterinária Faculdade de Medicina Veterinária e Zootecnia Universidade Estadual Paulista (Unesp)Laboratório de Patologia Aviária Departamento de Clínica Veterinária Faculdade de Medicina Veterinária e Zootecnia Universidade Estadual Paulista (Unesp)Universidade Estadual Paulista (Unesp)Corrêa, Isadora M.O. [UNESP]Pereira, Larissa Q. [UNESP]Silva, Isabella G.O. [UNESP]Altarugio, Rafaela [UNESP]Smaniotto, Bruna D. [UNESP]Silva, Tarcísio M. [UNESP]Okamoto, Adriano S. [UNESP]Filho, Raphael L. Andreatti [UNESP]2019-10-06T16:01:58Z2019-10-06T16:01:58Z2018-07-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1300-1306application/pdfhttp://dx.doi.org/10.1590/1678-5150-PVB-5211Pesquisa Veterinaria Brasileira, v. 38, n. 7, p. 1300-1306, 2018.1678-51500100-736Xhttp://hdl.handle.net/11449/18824610.1590/1678-5150-PVB-5211S0100-736X20180007013002-s2.0-85055327272S0100-736X2018000701300.pdf85024628735174640000-0003-4939-8024Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPesquisa Veterinaria Brasileirainfo:eu-repo/semantics/openAccess2023-10-15T06:10:49Zoai:repositorio.unesp.br:11449/188246Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:02:47.081406Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Comparison of three diagnostic methods for Salmonella enterica serovars detection in chicken rinse |
title |
Comparison of three diagnostic methods for Salmonella enterica serovars detection in chicken rinse |
spellingShingle |
Comparison of three diagnostic methods for Salmonella enterica serovars detection in chicken rinse Corrêa, Isadora M.O. [UNESP] Chicken rinse Diagnostic Immunomagnetic Phage P22 Salmonella enterica Salmonella Enteritidis Salmonella Heidelberg Salmonella Typhimurium Serovars |
title_short |
Comparison of three diagnostic methods for Salmonella enterica serovars detection in chicken rinse |
title_full |
Comparison of three diagnostic methods for Salmonella enterica serovars detection in chicken rinse |
title_fullStr |
Comparison of three diagnostic methods for Salmonella enterica serovars detection in chicken rinse |
title_full_unstemmed |
Comparison of three diagnostic methods for Salmonella enterica serovars detection in chicken rinse |
title_sort |
Comparison of three diagnostic methods for Salmonella enterica serovars detection in chicken rinse |
author |
Corrêa, Isadora M.O. [UNESP] |
author_facet |
Corrêa, Isadora M.O. [UNESP] Pereira, Larissa Q. [UNESP] Silva, Isabella G.O. [UNESP] Altarugio, Rafaela [UNESP] Smaniotto, Bruna D. [UNESP] Silva, Tarcísio M. [UNESP] Okamoto, Adriano S. [UNESP] Filho, Raphael L. Andreatti [UNESP] |
author_role |
author |
author2 |
Pereira, Larissa Q. [UNESP] Silva, Isabella G.O. [UNESP] Altarugio, Rafaela [UNESP] Smaniotto, Bruna D. [UNESP] Silva, Tarcísio M. [UNESP] Okamoto, Adriano S. [UNESP] Filho, Raphael L. Andreatti [UNESP] |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Corrêa, Isadora M.O. [UNESP] Pereira, Larissa Q. [UNESP] Silva, Isabella G.O. [UNESP] Altarugio, Rafaela [UNESP] Smaniotto, Bruna D. [UNESP] Silva, Tarcísio M. [UNESP] Okamoto, Adriano S. [UNESP] Filho, Raphael L. Andreatti [UNESP] |
dc.subject.por.fl_str_mv |
Chicken rinse Diagnostic Immunomagnetic Phage P22 Salmonella enterica Salmonella Enteritidis Salmonella Heidelberg Salmonella Typhimurium Serovars |
topic |
Chicken rinse Diagnostic Immunomagnetic Phage P22 Salmonella enterica Salmonella Enteritidis Salmonella Heidelberg Salmonella Typhimurium Serovars |
description |
Salmonella detection is a key point in food safety testing, because of the frequent association of this pathogen with food poisoning in humans. The standard bacteriological tests currently used for Salmonella-detection are time-consuming; therefore, there is a need to develop alternative methods to accelerate the detection. In order to accelerate Salmonella diagnosis, we used the immunomagnetic separation assay associated with bacteriophage P22 for the rapid detection of the following Salmonella serovars in chicken rinses of drumsticks, artificially contaminated with 5, 10, and 100 CFU/25mL of bacteria: Salmonella enterica subsp. enterica serovar Heidelberg (S. Heidelberg), Salmonella enterica subsp. enterica serovar Enteritidis (S. Enteritidis) and Salmonella enterica subsp. enterica serovar Typhimurium (S. Typhimurium). The efficiency of the technique, represented by the time required for detection of positive and negative samples, was compared with that of the standard diagnostic tests used for this pathogen, the bacteriological assay and the polymerase chain reaction (PCR)-based test. This study confirmed the ability of the bacteriophage-associated immunomagnetic separation assay to identify 99.6% of Salmonella-positive samples of the three serovars tested. In contrast, the bacteriological assay and PCR-based test detected 95.1% and 98.5% of the Salmonella-positive samples respectively. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-07-01 2019-10-06T16:01:58Z 2019-10-06T16:01:58Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/1678-5150-PVB-5211 Pesquisa Veterinaria Brasileira, v. 38, n. 7, p. 1300-1306, 2018. 1678-5150 0100-736X http://hdl.handle.net/11449/188246 10.1590/1678-5150-PVB-5211 S0100-736X2018000701300 2-s2.0-85055327272 S0100-736X2018000701300.pdf 8502462873517464 0000-0003-4939-8024 |
url |
http://dx.doi.org/10.1590/1678-5150-PVB-5211 http://hdl.handle.net/11449/188246 |
identifier_str_mv |
Pesquisa Veterinaria Brasileira, v. 38, n. 7, p. 1300-1306, 2018. 1678-5150 0100-736X 10.1590/1678-5150-PVB-5211 S0100-736X2018000701300 2-s2.0-85055327272 S0100-736X2018000701300.pdf 8502462873517464 0000-0003-4939-8024 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Pesquisa Veterinaria Brasileira |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1300-1306 application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128451364782080 |