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清洗溶液从罗勒中回收卡耶塔环孢子球虫、微小隐孢子虫和刚地弓形虫的效果。

Efficacy of wash solutions in recovering Cyclospora cayetanensis, Cryptosporidium parvum, and Toxoplasma gondii from basil.

作者信息

Chandra Venessa, Torres Maria, Ortega Ynés R

机构信息

Center for Food Safety, University of Georgia, 1109 Experiment Street, Griffin, Georgia 30223-1797, USA.

出版信息

J Food Prot. 2014 Aug;77(8):1348-54. doi: 10.4315/0362-028X.JFP-13-381.

Abstract

Parasitic diseases can be acquired by ingestion of contaminated raw or minimally processed fresh produce (herbs and fruits). The sensitivity of methods used to detect parasites on fresh produce depends in part on the efficacy of wash solutions in removing them from suspect samples. In this study, six wash solutions (sterile E-Pure water, 3% levulinic acid-3% sodium dodecyl sulfate, 1 M glycine, 0.1 M phosphate-buffered saline, 0.1% Alconox, and 1% HCl-pepsin) were evaluated for their effectiveness in removing Cyclospora cayetanensis, Cryptosporidium parvum, and Toxoplasma gondii from basil. One hundred or 1,000 oocysts of these parasites were inoculated onto the adaxial surfaces of 25 g of basil leaves, placed in stomacher bags, and stored for 1 h at 21°C or 24 h at 4°C. Leaves were hand washed in each wash solution for 1 min. DNA was extracted from the wash solutions and amplified using PCR for the detection of all parasites. Oocysts inoculated at a concentration of 1,000 oocysts per 25 g of basil were detected in all wash solutions. At an inoculum concentration of 100 oocysts per 25 g, oocysts were detected in 18.5 to 92.6% of the wash solutions. The lowest variability in recovering oocysts from basil inoculated with 100 oocysts was observed in 1% HCl-pepsin wash solution. Oocyst recovery rates were higher at 1 h than at 24 h postinoculation. Unlike most bacteria, parasites cannot be enriched; therefore, an optimal recovery process for oocysts from suspected foods is critical. The observations in this study provide guidance concerning the selection of wash solutions giving the highest retrieval of parasite oocysts.

摘要

寄生虫病可通过摄入受污染的生的或最少加工的新鲜农产品(草药和水果)而感染。用于检测新鲜农产品上寄生虫的方法的灵敏度部分取决于清洗液从可疑样本中去除寄生虫的效果。在本研究中,评估了六种清洗液(无菌E-纯水、3%乙酰丙酸-3%十二烷基硫酸钠、1M甘氨酸、0.1M磷酸盐缓冲盐水、0.1%爱尔康诺克斯和1%盐酸-胃蛋白酶)从罗勒中去除卡耶塔环孢子虫、微小隐孢子虫和刚地弓形虫的有效性。将这些寄生虫的100个或1000个卵囊接种到25克罗勒叶的正面,放入均质袋中,在21°C下储存1小时或在4°C下储存24小时。将叶子在每种清洗液中手工清洗1分钟。从清洗液中提取DNA,并使用PCR进行扩增以检测所有寄生虫。在所有清洗液中均检测到每25克罗勒接种1000个卵囊浓度的卵囊。在每25克接种100个卵囊的接种浓度下,在18.5%至92.6%的清洗液中检测到卵囊。在1%盐酸-胃蛋白酶清洗液中观察到从接种100个卵囊的罗勒中回收卵囊的变异性最低。接种后1小时的卵囊回收率高于24小时。与大多数细菌不同,寄生虫无法富集;因此,从可疑食物中最佳回收卵囊的过程至关重要。本研究中的观察结果为选择能最高效回收寄生虫卵囊的清洗液提供了指导。

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