Université de Lyon, VetAgro Sup Campus Vétérinaire de Lyon, Unité de Recherche CALITYSS, F-63280 Marcy l'Etoile, France; CNIEL, F-75314 Paris, France.
Clermont Université, Université d'Auvergne, Centre de Recherche en Nutrition Humaine Auvergne, EA 4678 CIDAM, BP 10448, F-63000 Clermont-Ferrand, France; Clermont Université, Université d'Auvergne, Centre de Recherche en Nutrition Humaine Auvergne, M2iSH, UMR INSERM/Université d'Auvergne U1071 USC-INRA 2018, BP 10448, F-63000 Clermont-Ferrand, France.
Int J Food Microbiol. 2014 Feb 17;172:40-8. doi: 10.1016/j.ijfoodmicro.2013.11.029. Epub 2013 Dec 4.
Shiga toxin producing Escherichia coli (STEC) are an important cause of human foodborne outbreaks. The consumption of raw milk dairy products may be an important route of STEC infection. For successful foodborne transmission, STEC strains must survive stress conditions met during gastrointestinal transit in humans. The aim of this study was to evaluate the survival of two STEC strains of serotypes O157:H7 and O26:H11 during simulated human digestion in the TNO gastro-Intestinal tract Model (TIM) of contaminated uncooked pressed cheeses. The survival of cheese microflora during in vitro gastrointestinal transit was also determined for the first time. The level of STEC increased from 2 log₁₀ CFU/ml to 4 log₁₀ CFU/g during the first 24h of cheese making and remained stable at around 4 log₁₀ CFU/g during cheese ripening and conservation. During transit through the artificial stomach and duodenum, levels of STEC decreased: 0.2% of E. coli O157:H7 and 1.8% of E. coli O26:H11 were recovered at 150 min in the gastric compartment, compared with 14.3% for the transit marker. Bacterial resumption was observed in the jejunum and ileum: 35.8% of E. coli O157:H7 and 663.2% of E. coli O26:H11 were recovered at 360 min in the ileal compartment, compared with 12.6% for the transit marker. The fate of STEC was strain-dependent, the survival of E. coli O26:H11 being 13 times greater than that of E. coli O157:H7 at the end of digestion in the cumulative ileal deliveries. These data provide a better understanding of STEC behavior during gastrointestinal transit in humans after ingestion of contaminated cheese.
产志贺毒素大肠杆菌(STEC)是人类食源性疾病爆发的一个重要原因。食用生乳奶制品可能是 STEC 感染的一个重要途径。为了成功实现食源性传播,STEC 菌株必须能够在人体胃肠道转运过程中存活下来。本研究旨在评估两种血清型 O157:H7 和 O26:H11 的 STEC 菌株在受污染的未煮压奶酪的 TNO 胃肠道模型(TIM)中模拟人体消化过程中的存活情况。首次还确定了奶酪微生物在体外胃肠道转运过程中的存活情况。在奶酪制作的头 24 小时内,STEC 的水平从 2 log₁₀ CFU/ml 增加到 4 log₁₀ CFU/g,在奶酪成熟和保存期间稳定在 4 log₁₀ CFU/g 左右。在通过人工胃和十二指肠的转运过程中,STEC 的水平下降:在胃区 150 分钟时,E. coli O157:H7 回收了 0.2%,E. coli O26:H11 回收了 1.8%,而转运标记物的回收率为 14.3%。在空肠和回肠中观察到细菌恢复:在回肠区 360 分钟时,E. coli O157:H7 回收了 35.8%,E. coli O26:H11 回收了 663.2%,而转运标记物的回收率为 12.6%。STEC 的命运取决于菌株,在回肠累积输送结束时,E. coli O26:H11 的存活能力比 E. coli O157:H7 高 13 倍。这些数据更好地了解了摄入受污染奶酪后 STEC 在人体胃肠道转运过程中的行为。