Please use this identifier to cite or link to this item: https://ktisis.cut.ac.cy/handle/10488/14647
Title: Rapid detection methods for viable Mycobacterium avium subspecies paratuberculosis in milk and cheese
Authors: Botsaris, George 
Slana, Iva 
Liapi, Maria 
Dodd, Christine E R 
Economides, Constantinos 
Rees, Catherine 
Pavlik, Ivo 
Keywords: Culture;Decontamination;Food safety;Milk;PCR;Real time PCR
Category: Biological Sciences;AGRICULTURAL SCIENCES;Other Agricultural Sciences
Field: Agricultural Sciences
Issue Date: 31-Jul-2010
Source: International Journal of Food Microbiology, Volume 141, Issue SUPPL., July 2010, Pages S87-S90
Journal: International journal of food microbiology 
Abstract: Mycobacterium avium subsp. paratuberculosis (MAP) may have a role in the development of Crohn's disease in humans via the consumption of contaminated milk and milk products. Detection of MAP from milk and dairy products has been reported from countries on the European continent, Argentina, the UK and Australia. In this study three different methods (quantitative real time PCR, combined phage IS900 PCR and conventional cultivation) were used to detect the presence of MAP in bulk tank milk (BTM) and cheese originating from sheep, goat and mixed milks from farms and products in Cyprus. During the first survey the presence of MAP was detected in 63 (28.6%) of cows' BTM samples by quantitative real time PCR. A second survey of BTM used a new combined phage IS900 PCR assay, and in this case MAP was detected in 50 (22.2%) samples showing a good level of agreement by both methods. None of the herds tested were known to be affected by Johne's disease and the presence of viable MAP was confirmed by conventional culture in only two cases of cows BTM. This suggests that either rapid method used is more sensitive than the conventional culture when testing raw milk samples for MAP. The two isolates recovered from BTM were identified by IS1311 PCR REA as cattle and sheep strains, respectively. In contrast when cheese samples were tested, MAP DNA was detected by quantitative real time PCR in seven (25.0%) samples (n=28). However no viable MAP was detected when either the combined phage IS900 PCR or conventional culture methods were used.
URI: https://ktisis.cut.ac.cy/handle/10488/14647
ISSN: 01681605
DOI: 10.1016/j.ijfoodmicro.2010.03.016
Type: Article
Appears in Collections:Άρθρα/Articles

Show full item record

SCOPUSTM   
Citations

47
checked on Sep 12, 2019

WEB OF SCIENCETM
Citations

40
checked on Sep 16, 2019

Page view(s)

5
Last Week
0
Last month
1
checked on Sep 18, 2019

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.