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Optimization of an adsorption-elution method with a negatively charged membrane to recover norovirus from lettuce.

机译:优化带有负电荷膜的吸附-洗脱方法以从生菜中回收诺如病毒。

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摘要

Viral pathogens, such as norovirus (NoV), are frequently associated with foodborne gastroenteritis worldwide, and the detection of NoV in food requires appropriate methods and the use of process controls. In this study, an adsorption-elution concentration method using negatively charged membranes was optimized to recover NoV from lettuce, using murine norovirus 1 (MNV-1) as a human NoV (HuNoV) surrogate. Initially, three elution buffers were evaluated by direct elution using a StomacherReg. apparatus with a filter bag and different concentrations of MNV-1 genomic copies. The eluates were filtered in a StericupReg. and concentrated by a Centriprep ConcentratorReg., and the viral RNA was quantified by real-time PCR that was preceded by reverse transcription. The MNV-1 recovery efficiency varied based on the buffers used, ranging from 5.2 to 9.8% for PBS pH 7.2, 0.2-18% for glycine NaCl pH 9.5 and 10.8-33.3% for glycine Tris-HCl pH 9.5. Further analysis of the glycine Tris-HCl pH 9.5 buffer revealed that gentle-shaking, direct elution could replace the use of a StomacherReg., with recovery rates reaching 66 and 32% for MNV-1 and HuNoV, respectively, all of which suggested that this procedure is a quick and efficient method for recovering NoV from lettuce.CAS Registry Numbers 56-40-6 7647-14-5 63231-63-0
机译:病毒病原体,例如诺如病毒(NoV),在世界范围内通常与食源性胃肠炎有关,而食品中NoV的检测需要适当的方法和过程控制的使用。在这项研究中,使用带负电荷的膜的吸附-洗脱浓缩方法经过优化,可以使用鼠诺如病毒1(MNV-1)作为人类NoV(HuNoV)替代品从莴苣中回收NoV。最初,使用StomacherReg通过直接洗脱评估了三种洗脱缓冲液。带有滤袋和不同浓度的MNV-1基因组拷贝的仪器。洗脱液在StericupReg中过滤。并通过Centriprep ConcentratorReg。浓缩,然后通过实时PCR定量病毒RNA,然后进行逆转录。 MNV-1的回收效率根据使用的缓冲液而异,PBS pH 7.2的范围为5.2至9.8%,甘氨酸NaCl pH 9.5的范围为0.2-18%,甘氨酸Tris-HCl pH 9.5的范围为10.8-33.3%。对甘氨酸Tris-HCl pH 9.5缓冲液的进一步分析表明,轻轻摇动,直接洗脱可以代替StomacherReg。的使用,MNV-1和HuNoV的回收率分别达到66%和32%,所有这些都表明该程序是一种从生菜中回收NoV的快速有效方法.CAS注册号56-40-6 7647-14-5 63231-63-0

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