2011
DOI: 10.1016/j.meatsci.2011.03.011
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Development of PCR assays for detection of Escherichia coli O157:H7 in meat products

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Cited by 21 publications
(12 citation statements)
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“…Molecular approaches based on PCR assays have also been explored in order to develop sensitive, specific and rapid methods for confirming the presence/absence of E. coli O157: H7. In this context, although a lot of efforts have been made by different investigators to develop PCR-based assays targeted against different genes for detection of E. coli O157:H7 (Cadirci et al, 2010;Cocolin et al, 2000;Gooding and Choudary, 1997;Gordillo et al, 2011;Kawasaki et al, 2010;Park et al, 2011;Paton and Paton, 1998;Rice, 2009), the efficacy of these techniques has been tested with food samples artificially spiked with the target organism. Application of such PCR-based techniques has not yet been efficiently and extensively investigated for detection of E. coli O157:H7 in naturally contaminated dairy foods.…”
Section: Introductionmentioning
confidence: 99%
“…Molecular approaches based on PCR assays have also been explored in order to develop sensitive, specific and rapid methods for confirming the presence/absence of E. coli O157: H7. In this context, although a lot of efforts have been made by different investigators to develop PCR-based assays targeted against different genes for detection of E. coli O157:H7 (Cadirci et al, 2010;Cocolin et al, 2000;Gooding and Choudary, 1997;Gordillo et al, 2011;Kawasaki et al, 2010;Park et al, 2011;Paton and Paton, 1998;Rice, 2009), the efficacy of these techniques has been tested with food samples artificially spiked with the target organism. Application of such PCR-based techniques has not yet been efficiently and extensively investigated for detection of E. coli O157:H7 in naturally contaminated dairy foods.…”
Section: Introductionmentioning
confidence: 99%
“…All of these primers were commercially synthesized by TaKaRa Biotechnology Co., Ltd. (Dalian, China). The PCR reagent system was used as described by Gordillo, C ordoba, Andrade, Luque, and Rodríguez (2011), with a total volume of 50 mL containing 3 mL of template DNA, 0.2 mM of each primer, 6 U of Taq enzyme, 5 mL of PCR buffer, 3 mM of MgCl 2 , and 0.2 mM each of the dNTPs. A positive control was used during the detection procedure.…”
Section: Detection Of the Flic H7 And Rfbe Genesmentioning
confidence: 99%
“…HUS is considered as the primary reason for acute renal insufficiency among children. The treatment of the disease includesf hemodialysis and supportive care only (7,8).…”
Section: Introductionmentioning
confidence: 99%