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Development of a novel carbohydrate-based method for the detection of norovirus from ready-to-eat foods.

机译:开发了一种基于碳水化合物的新型方法,用于从即食食品中检测诺如病毒。

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摘要

Norovirus is an enteric pathogen transmitted via the fecal-oral route. It is a leading cause of outbreaks and sporadic cases of gastroenteritis worldwide. Outbreaks of norovirus are often linked to contaminated food or water. Ready-to-eat foods are particularly prone to contamination, since they often require handling during preparation and are not usually heated before serving.;Magnetic beads were coated with multiple types of HBGA [A, B, H(type 2) and H(type 3)]. These beads were added to a 250 mL volume sample and concentrated using either the Pathatrix(TM) or iCropTheBug. Both systems were able to concentrate the beads from a 250 mL sample to 140 muL, using the magnetic properties of the beads. The RNA was then extracted from the sample and the presence of norovirus. was determined using realtime Reverse Transcription-PCR.;This method was successful at detecting norovirus from artificially-spiked and naturally-contaminated food samples. It was also able to detect multiple strains from norovirus genogroup I and II within the infectious dose range (10-100 particles). These results demonstrate that carbohydrate-conjugated beads can be successfully used to detect norovirus contamination of food products. This method can provide rapid and effective food testing for use in the investigation of suspected norovirus outbreaks.;Norovirus capsids have been shown to interact specifically with histo-blood group antigens (HBGAs). HBGAs are carbohydrates present on the surface of red blood cells, on mucosal epithelial cells and in bodily fluids. The work in this thesis used the interaction between norovirus and HBGAs to develop a method to detect norovirus in food samples.
机译:诺如病毒是通过粪-口途径传播的肠道病原体。它是全球胃肠炎暴发和零星病例的主要原因。诺如病毒的暴发通常与受污染的食物或水有关。即食食品特别容易受到污染,因为它们在制备过程中经常需要处理,并且通常在食用前不加热。;磁珠上涂有多种类型的HBGA [A,B,H(2型)和H(类型3)]。将这些珠粒添加至250 mL体积的样品中,并使用PathatrixTM或iCropTheBug进行浓缩。两种系统都能利用磁珠的磁性将250 mL样品中的磁珠浓缩至140μL。然后从样品中提取RNA,并检测诺如病毒的存在。用实时逆转录-PCR测定。该方法成功地从人工加标和自然污染的食物样品中检测诺如病毒。它还能够在感染剂量范围内(10-100个颗粒)检测诺如病毒基因组I和II的多种毒株。这些结果证明,缀合有碳水化合物的珠可以成功地用于检测食品的诺如病毒污染。该方法可提供快速有效的食品检测,用于调查可疑的诺如病毒暴发。;已证明诺如病毒衣壳与组织血型抗原(HBGA)特异性相互作用。 HBGA是存在于红细胞表面,粘膜上皮细胞和体液中的碳水化合物。本文的工作是利用诺如病毒与HBGA之间的相互作用来开发一种检测食品样本中诺如病毒的方法。

著录项

  • 作者

    Morton, Vanessa Karen.;

  • 作者单位

    University of Ottawa (Canada).;

  • 授予单位 University of Ottawa (Canada).;
  • 学科 Agriculture Food Science and Technology.;Biology Microbiology.
  • 学位 M.Sc.
  • 年度 2010
  • 页码 116 p.
  • 总页数 116
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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