2019
DOI: 10.1590/1806-9061-2018-0776
| View full text |Cite
|
Sign up to set email alerts
|

Abstract: The incidence of foodborne diseases caused by the genus Salmonella spp. in industrialized countries is often high in epidemiological surveys. Obtaining a rapid diagnostic test for identification of bacteria is crucial in order to rapidly implement control measures to contain bacterial spread, to reduce losses in animal production and to avoid risks from food-borne infections to human health. The aim of this study was to standardize duplex real-time PCR using SYBr Green I for differential and quantitative diagn… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2021
2021
2023
2023

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(1 citation statement)
references
References 23 publications
0
1
0
Order By: Relevance
“…(Haddad et al, 2001) due to its rapidness, consistency, reliability and reproducibility (Baratto et al, 2012). PCR methods have been used for the identification of many Salmonella enterica serovars, as Typhimurium, Enteritidis, Gallinarum and Pullorum (Rubio et al, 2019;Lee et al, 2009;Burgarel et al, 2011;Xiong et al, 2017). Although PCR has been successfully used for molecular typing (Liu et al, 2003;Borah et al, 2017;Salehi et al, 2011), its success can be challenged by the type of sample and quality of the DNA extraction method (Wilson, 1997).…”
Section: Introductionmentioning
confidence: 99%
“…(Haddad et al, 2001) due to its rapidness, consistency, reliability and reproducibility (Baratto et al, 2012). PCR methods have been used for the identification of many Salmonella enterica serovars, as Typhimurium, Enteritidis, Gallinarum and Pullorum (Rubio et al, 2019;Lee et al, 2009;Burgarel et al, 2011;Xiong et al, 2017). Although PCR has been successfully used for molecular typing (Liu et al, 2003;Borah et al, 2017;Salehi et al, 2011), its success can be challenged by the type of sample and quality of the DNA extraction method (Wilson, 1997).…”
Section: Introductionmentioning
confidence: 99%