Moisture content of bacterial cells determines thermal resistance of Salmonella Enteritidis PT 30
Salmonella spp. are resilient bacterial pathogens in low-moisture foods. There has been a general lack of understanding of critical factors contributing to the enhanced thermal tolerance of Salmonella spp, in dry environments. In this study, we hypothesized that the moisture content (XW) of bacterial cells is a critical intrinsic factor influencing the resistance of Salmonella spp. against thermal inactivation. We selected Salmonella Enteritidis PT 30 to test this hypothesis. We first produced viable freeze-dried S. Enteritidis PT 30, conditioned the bacterial cells to different XW (7.7, 9.2, 12.4 and 15.7 g water/100g dry solids), and determined thermal inactivation kinetics of those cells at 80 °C. The results show that D-value (time required to achieve one-log reduction) decreased exponentially with increasing XW. We further measured water activities (aw) of the freeze-dried S. Enteritidis PT 30 as influenced by temperature between 20 and 80 °C. By using those data, we estimated the XW of S. Enteritidis PT 30 from the published papers that related D-values of the same bacteria strain at 80 °C with aw of five different food and silicon dioxide matrices. We discovered that the logarithmic D-values of S. Enteritidis PT 30 in all those matrices also decreased linearly with increasing XW of the bacterial cells. The findings suggest that the amount of moisture in S. Enteritidis PT 30 is a determinant factor on their ability to resist thermal inactivation. Our results may help future research into fundamental mechanisms for thermal inactivation of bacterial pathogens in dry environments. IMPORTANCE This paper established a logarithmic relationship between the thermal death time (D-value) of S. Enteritidis PT 30 and the moisture content (XW) of the bacterial cells by conducting thermal inactivation tests on freeze-dried S. Enteritidis PT 30. We further verified this relationship using literature data for S. Enteritidis PT 30 in five low moisture matrices. The findings suggest that XW of S. Enteritidis PT 30, which is rapidly adjusted by microenvironmental aw, or relative humidity, during heat treatments, is the key intrinsic factor determining thermal resistance of the bacterium. The quantitative relationships reported in this study may help guide future designs of industrial thermal processes for control of S. Enteritidis PT 30 or other Salmonella stains in low-moisture foods. Our findings highlight a need for further fundamental investigation into the role of water in protein denaturation and accumulation of compatible solutes during thermal inactivation of bacterial pathogens in dry environments.