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定量测定生菜叶片结构在保护大肠杆菌O157:H7免受氯消毒方面的作用。

Quantitative determination of the role of lettuce leaf structures in protecting Escherichia coli O157:H7 from chlorine disinfection.

作者信息

Takeuchi K, Frank J F

机构信息

Center for Food Safety and Quality Enhancement, Department of Food Science and Technology, University of Georgia, Athens 30602-2106, USA.

出版信息

J Food Prot. 2001 Feb;64(2):147-51. doi: 10.4315/0362-028x-64.2.147.

Abstract

Viability of Escherichia coli O157:H7 cells on lettuce leaves after 200 mg/liter (200 ppm) chlorine treatment and the role of lettuce leaf structures in protecting cells from chlorine inactivation were evaluated by confocal scanning microscopy (CSLM). Lettuce samples (2 by 2 cm) were inoculated by immersing in a suspension containing 10(9) CFU/ml of E. coli O157: H7 for 24+/-1 h at 4 degrees C. Rinsed samples were treated with 200 mg/liter (200 ppm) chlorine for 5 min at 22 degrees C. Viability of E. coli O157:H7 cells was evaluated by CSLM observation of samples stained with Sytox green (dead cell stain) and Alexa 594 conjugated antibody against E. coli O157:H7. Quantitative microscopic observations of viability were made at intact leaf surface, stomata, and damaged tissue. Most E. coli O157:H7 cells (68.3+/-16.2%) that had penetrated 30 to 40 microm from the damaged tissue surface remained viable after chlorine treatment. Cells on the surface survived least (25.2+/-15.8% survival), while cells that penetrated 0 to 10 microm from the damaged tissue surface or entered stomata showed intermediate survival (50.8 +/-13.5 and 45.6+/-9.7% survival, respectively). Viability was associated with the depth at which E. coli O157:H7 cells were in the stomata. Although cells on the leaf surface were mostly inactivated, some viable cells were observed in cracks of cuticle and on the trichome. These results demonstrate the importance of lettuce leaf structures in the protection of E. coli O157:H7 cells from chlorine inactivation.

摘要

通过共聚焦扫描显微镜(CSLM)评估了200毫克/升(200 ppm)氯处理后生菜叶片上大肠杆菌O157:H7细胞的活力,以及生菜叶片结构在保护细胞免受氯灭活方面的作用。将生菜样品(2×2厘米)浸入含有10⁹CFU/ml大肠杆菌O157:H7的悬浮液中,在4℃下培养24±1小时进行接种。冲洗后的样品在22℃下用200毫克/升(200 ppm)氯处理5分钟。通过CSLM观察用Sytox green(死细胞染色剂)和抗大肠杆菌O157:H7的Alexa 594共轭抗体染色的样品,评估大肠杆菌O157:H7细胞的活力。在完整叶片表面、气孔和受损组织处进行了活力的定量显微镜观察。大多数从受损组织表面穿透30至40微米的大肠杆菌O157:H7细胞(68.3±16.2%)在氯处理后仍保持活力。表面的细胞存活最少(存活率为25.2±15.8%),而从受损组织表面穿透0至10微米或进入气孔的细胞存活率居中(分别为50.8±13.5%和45.6±9.7%)。活力与大肠杆菌O157:H7细胞在气孔中的深度有关。尽管叶片表面的细胞大多被灭活,但在角质层裂缝和毛状体上观察到了一些活细胞。这些结果证明了生菜叶片结构在保护大肠杆菌O157:H7细胞免受氯灭活方面的重要性。

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