<p>The sensitivity of sublethally injured <i>Escherichia coli</i> O157:H7 caused by dielectric barrier discharge (DBD) plasma to diverse environmental factors was investigated in the work. The sublethally injured <i>E. coli</i> cells were achieved by DBD plasma treatment at 18&#xa0;W for 40&#xa0;s. The cultivability of injured cells decreased progressively with increasing NaCl concentration in trypticase soy agar (TSA). Although both normal and injured cells were sensitive to mild heat, the latter exhibited increased sensitivity. Incubation at pH 3.0 and 4.0 for 40&#xa0;min had no effect on the viable counts of normal cells. However, exposure to pH 4.0 for the same duration reduced the viable counts of injured cells from 6.05 to 3.51 log<sub>10</sub> CFU/mL, whereas a 30-min exposure to pH 3.0 caused a reduction of over 6.0 log<sub>10</sub> CFU/mL. The acids used in this study did not result in the inactivation of normal cells, but all of them inactivated injured <i>E. coli</i> cells, with the reduction ranging from 0.51 to 2.81 log<sub>10</sub> cycles. Moreover, natural preservatives and H<sub>2</sub>O<sub>2</sub> utilized in the work led to an extra reduction of injured cells from 2.05 to 4.45 log<sub>10</sub> cycles, yet the survival of normal cells was not influenced. These findings indicate that DBD plasma-induced injured <i>E. coli</i> O157:H7 cells present a higher sensitivity to high osmotic pressure, mild heat, acids, natural preservatives, as well as H<sub>2</sub>O<sub>2</sub>. These suggest the potential of a synergistic approach combining DBD plasma with other technologies to inactivate microorganisms.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Increased sensitivity of sublethally injured Escherichia coli O157:H7 to environmental factors induced by dielectric barrier discharge plasma

  • Yafei Zhai,
  • Zhaotian Liu,
  • Bohua Wang,
  • Liyuan Niu,
  • Dianbo Zhao

摘要

The sensitivity of sublethally injured Escherichia coli O157:H7 caused by dielectric barrier discharge (DBD) plasma to diverse environmental factors was investigated in the work. The sublethally injured E. coli cells were achieved by DBD plasma treatment at 18 W for 40 s. The cultivability of injured cells decreased progressively with increasing NaCl concentration in trypticase soy agar (TSA). Although both normal and injured cells were sensitive to mild heat, the latter exhibited increased sensitivity. Incubation at pH 3.0 and 4.0 for 40 min had no effect on the viable counts of normal cells. However, exposure to pH 4.0 for the same duration reduced the viable counts of injured cells from 6.05 to 3.51 log10 CFU/mL, whereas a 30-min exposure to pH 3.0 caused a reduction of over 6.0 log10 CFU/mL. The acids used in this study did not result in the inactivation of normal cells, but all of them inactivated injured E. coli cells, with the reduction ranging from 0.51 to 2.81 log10 cycles. Moreover, natural preservatives and H2O2 utilized in the work led to an extra reduction of injured cells from 2.05 to 4.45 log10 cycles, yet the survival of normal cells was not influenced. These findings indicate that DBD plasma-induced injured E. coli O157:H7 cells present a higher sensitivity to high osmotic pressure, mild heat, acids, natural preservatives, as well as H2O2. These suggest the potential of a synergistic approach combining DBD plasma with other technologies to inactivate microorganisms.