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Int J Food Microbiol ; 216: 91-4, 2016 Jan 04.
Article in English | MEDLINE | ID: mdl-26421832

ABSTRACT

Surveys from different parts of the world have reported that viable Mycobacterium avium subsp. paratuberculosis (MAP) can be cultured from approximately 2% of samples of retail pasteurised milk samples. Pasteurised milk is used for the production of powdered infant formula (PIF) and therefore there is a concern that MAP may also be present in these products. Several studies have previously reported the detection of MAP in PIF using PCR-based assays. However, culture-based surveys of PIF have not detected viable MAP. Here we describe a phage amplification assay coupled with PCR (page-PCR) that can rapidly detect viable MAP in PIF. The results of a small survey showed that the phage-PCR assay detected viable MAP in 13% (4/32) of PIF samples. Culture detected viable MAP in 9% (3/32) PIF samples, all of which were also phage-PCR positive. Direct IS900 PCR detected MAP DNA in 22% (7/32) of PIF samples. The presence of viable MAP in PIF indicates that MAP either survived PIF manufacturing or that post-production contamination occurred. Irrespective of the route of MAP contamination, the presence of viable MAP in PIF is a potential public health concern.


Subject(s)
DNA, Bacterial/genetics , Infant Formula/microbiology , Milk/microbiology , Mycobacterium avium subsp. paratuberculosis/isolation & purification , Animals , Bacteriophages/genetics , Humans , Infant , Infant, Newborn , Mycobacterium avium subsp. paratuberculosis/genetics , Polymerase Chain Reaction/methods
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