P2-228 Growth Assessment of Listeria monocytogenes in Indian Cottage Cheese (Paneer) under Homemade and Industrial Scenario

Tuesday, July 11, 2017
Exhibit Hall (Tampa Convention Center)
Varalakshmi Sudagar , Ghent University , Ghent , Belgium
Sarah Leysen , Ghent University , Ghent , Belgium
An Vermeulen , Ghent University , Gent , Belgium
Frank Devlieghere , Ghent University , Ghent , Belgium
Mieke Uyttendaele , Ghent University (UGent), Faculty of Bioscience Engineering, Department of Food Technology, Safety and Health, Research Unit Food Microbiology and Food Preservation (FMFP-UGent) , Ghent , Belgium
Introduction: Fresh cheese is an at risk product for Listeria monocytogenes and there have been several multistate listeriosis outbreaks and recalls reported in USA and Australia.

Purpose: No data are available on the growth assessment of L. monocytogenes in paneer and the safety of the final product. The goal of this study was to see if paneer acts as a vehicle that supports the growth of L. monocytogenes by conducting the challenge testing experiments in paneer under homemade and industrial scenarios and to compare the results with existing predictive models for validation.

Methods: Growth of L. monocytogenes was assessed by conducting challenge testing with an initial concentration of ca. 500 cfu/g. The paneer was prepared in the laboratory simulating homemade preparation and storage with three different pathogen contamination modes: during coagulum preparation stage, during immersion of the coagulated milk in water, and post-processing surface contamination. For the industrial scenario, using different concentrations of preservatives (2700 ppm and 1350 ppm of potassium sorbate), vacuum packaging without preservatives, and post-vacuum packaging pasteurization treatment. Each trial was conducted using three batches with two replicates each. Results of challenge testing were compared with Combase and FSSP prediction softwares.

Results: The models predicted the growth of L. monocytogenes when contamination occurred during the surface or immersion stage. However, the models were unable to predict the growth if contamination occurred during the coagulum preparation stage. For the homemade scenario, an increase of more than two log CFU L. monocytogenes/g was observed on day 10 when stored at 4°C. For the industrial scenario, a prolonged storage with no or restricted growth of the L. monocytogenes during several weeks was observed.

Significance: This work is the first growth assessment study of L. monocytogenes in paneer under artisanal homemade conditions and industrial conditions where a preservative system was included.