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Survival of Mycobacterium avium subspecies paratuberculosis in retail pasteurised milk
Zara E Gerrard1, Benjamin M C Swift2, George Botsaris3
1University of Nottingham, Sutton Bonington Campus, College Road, Leicestershire LE12 5RD, England; SRUC, West Mains Road, Edinburgh EH9 3JG, Scotland.
Abstract:
A survey of retail purchased semi-skimmed pasteurised milk (n = 368) for Mycobacterium avium subspecies paratuberculosis (MAP) was conducted between May 2014 and June 2015 across the midlands of England using the Phage-PCR assay. Overall, 10.3% of the total samples collected contained viable MAP cells, confirming that pasteurisation is not capable of fully eliminating human exposure to viable MAP through milk. Comparison of the results gained using the Phage-PCR assay with the results of surveys using either culture or direct PCR suggest that the phage-PCR assay is able to detect lower numbers of cells, resulting in an increase in the number of MAP-positive samples detected. Comparison of viable count and levels of MAP detected in bulk milk samples suggest that MAP is not primarily introduced into the milk by faecal contamination but rather are shed directly into the milk within the udder. In addition results detected an asymmetric distribution of MAP exists in the milk matrix prior to somatic cell lysis, indicating that the bacterial cells in naturally contaminated milk are clustered together and may primarily be located within somatic cells. These latter two results lead to the hypothesis that intracellular MAP within the somatic cells may be protected against heat inactivation during pasteurisation, accounting for the presence of low levels of MAP detected in retail milk.
Insights
Pasteurised milk can still contain viable Mycobacterium avium subspecies paratuberculosis (MAP) cells, posing a risk of human exposure. This study highlights MAP
Area of Science:
- Food safety and microbiology
- Veterinary public health
- Bacteriology
Background:
- Mycobacterium avium subspecies paratuberculosis (MAP) is a pathogen of concern in milk.
- Pasteurisation is a key process for eliminating milkborne pathogens.
- Previous surveys have investigated MAP in milk with varying detection methods.
Purpose of the Study:
- To survey retail pasteurised milk for viable MAP using the Phage-PCR assay.
- To compare the efficacy of Phage-PCR with other detection methods for MAP.
- To investigate the source and distribution of MAP in milk.
Main Methods:
- Survey of 368 retail semi-skimmed pasteurised milk samples in England (May 2014 - June 2015).
- Utilisation of the Phage-PCR assay for viable MAP detection.
- Comparison of Phage-PCR results with culture and direct PCR methods.
Main Results:
- 10.3% of surveyed milk samples contained viable MAP cells.
- Phage-PCR detected lower cell numbers and increased MAP-positive samples compared to other methods.
- MAP appears to be shed directly into milk within the udder, not solely from faecal contamination.
- MAP cells were found to be clustered and potentially located within somatic cells prior to lysis.
Conclusions:
- Pasteurisation does not fully eliminate viable MAP in milk.
- The Phage-PCR assay offers enhanced sensitivity for MAP detection in milk.
- MAP's presence within somatic cells may confer protection against heat inactivation during pasteurisation.
- Intracellular MAP within somatic cells is a potential explanation for viable MAP in retail milk.
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