2007
DOI: 10.1016/j.ijfoodmicro.2006.12.035
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Occurrence and persistence of Listeria spp. in the environment of ewe and cow's milk cheese dairies in Portugal unveiled by an integrated analysis of identification, typing and spatial–temporal mapping along production cycle

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Cited by 69 publications
(42 citation statements)
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“…Pulsed-Field Gel Electrophoresis (PFGE) and Random Amplification of Polymorphic DNA (RAPD) subtyping showed that the clinical isolate was indistinguishable from those collected from the processing plant and that closely related isolates persisted for five months in the dairy (Gianfranceschi et al, 2006). Different subtyping methods proved that specific isolates of L. monocytogenes are able to establish persistent contaminations in dairy premises for months and sometimes even years (Chambel et al, 2007;Leite et al, 2006;Rückerl et al, 2014). The mechanisms leading to the persistence are poorly understood.…”
Section: Introductionmentioning
confidence: 99%
“…Pulsed-Field Gel Electrophoresis (PFGE) and Random Amplification of Polymorphic DNA (RAPD) subtyping showed that the clinical isolate was indistinguishable from those collected from the processing plant and that closely related isolates persisted for five months in the dairy (Gianfranceschi et al, 2006). Different subtyping methods proved that specific isolates of L. monocytogenes are able to establish persistent contaminations in dairy premises for months and sometimes even years (Chambel et al, 2007;Leite et al, 2006;Rückerl et al, 2014). The mechanisms leading to the persistence are poorly understood.…”
Section: Introductionmentioning
confidence: 99%
“…Researches on the presence of L. monocytogenes on the surface of equipment and utensils, report its occurrence in meat and dairy processing industries (11,15,27). According to Chae et al.…”
mentioning
confidence: 99%
“…Therefore, three oligomer primers which had been successfully applied in other studies were used simultaneously. The primers were M13 (5′-GAG GGT GGC GGT TCT-3′) [57], Eric2 (5′-AAG TAA GTG ACT GGG GTG AGC G-3′) [58] and inlA.F (5′-CAG GCA GCT ACA ATT ACA CA-3′) [25]. These primers address different genomic regions: M13 is directed to sections containing micro-or mini-satellites, Eric.2 focuses repeated regions and inlA.F targets internalin genes [25].…”
Section: Rapd Typing Of Listeria Sppmentioning
confidence: 99%
“…The primers were M13 (5′-GAG GGT GGC GGT TCT-3′) [57], Eric2 (5′-AAG TAA GTG ACT GGG GTG AGC G-3′) [58] and inlA.F (5′-CAG GCA GCT ACA ATT ACA CA-3′) [25]. These primers address different genomic regions: M13 is directed to sections containing micro-or mini-satellites, Eric.2 focuses repeated regions and inlA.F targets internalin genes [25]. RAPD PCR reactions were performed in a final volume of 25 µl containing 50-100 ng of template DNA, 3 µl of 10 × PCR Buffer IV (Thermo Fisher Scientific, Dreieich, Germany), 1 mM dNTP Mix (Thermo Fisher Scientific), 3.5 mM MgCl 2 , 6.25 pmol/µl of each primer and 0.5 U of Thermoprime Plus Taq Polymerase (Thermo Fisher Scientific).…”
Section: Rapd Typing Of Listeria Sppmentioning
confidence: 99%
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