Kolling G L, Matthews K R
Department of Food Science, Rutgers University, New Brunswick, New Jersey 08901, USA.
Appl Environ Microbiol. 2001 Sep;67(9):3928-33. doi: 10.1128/AEM.67.9.3928-3933.2001.
Escherichia coli O157:H7 (strains ATCC 43895 and FO46) became nonculturable in sterile, distilled, deionized water or after exposure to chlorine. Recovery of nonculturable E. coli O157:H7 was examined by in vitro and in vivo methods. The decline in culturability of starved E. coli O157:H7 was measured by plate count on rich medium. Recovery in vitro of nonculturable cells was conducted with media amended with catalase or sodium pyruvate; however, there was no apparent increase over culturable cell counts on amended versus nonamended media. Although nonculturable E. coli O157:H7 did not recover under in vitro conditions, a mouse model was used to determine if in vivo conditions would provide sufficient conditions for recovery of nonculturable E. coli O157:H7. In separate studies, mice were orally challenged with starvation-induced nonculturable cells (FO46) or chlorine-induced nonculturable cells (43895 and FO46). Passage through the mouse gastrointestinal tract had no effect on recovery of nonculturable (starvation or chlorine induced) E. coli O157:H7 (43895 or FO46), based on analysis of fecal samples. Mouse kidneys were assayed for the presence of Shiga toxin using the Vero cell assay. Differences in cytotoxicity towards Vero cells from kidney samples of mice receiving nonculturable cells and control mice were not significant, suggesting a loss of virulence.
大肠杆菌O157:H7(菌株ATCC 43895和FO46)在无菌蒸馏水、去离子水中或暴露于氯后变得不可培养。通过体外和体内方法检测不可培养的大肠杆菌O157:H7的复苏情况。通过在丰富培养基上进行平板计数来测量饥饿的大肠杆菌O157:H7可培养性的下降。用添加了过氧化氢酶或丙酮酸钠的培养基进行不可培养细胞的体外复苏;然而,与未添加培养基相比,添加培养基上的可培养细胞计数没有明显增加。尽管不可培养的大肠杆菌O157:H7在体外条件下没有复苏,但使用小鼠模型来确定体内条件是否能为不可培养的大肠杆菌O157:H7的复苏提供足够的条件。在单独的研究中,给小鼠口服接种饥饿诱导的不可培养细胞(FO46)或氯诱导的不可培养细胞(43895和FO46)。基于粪便样本分析,通过小鼠胃肠道对不可培养的(饥饿或氯诱导的)大肠杆菌O157:H7(43895或FO46)的复苏没有影响。使用Vero细胞试验检测小鼠肾脏中志贺毒素的存在。接受不可培养细胞的小鼠肾脏样本与对照小鼠的肾脏样本对Vero细胞的细胞毒性差异不显著,表明毒力丧失。