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鲜切农产品加工洗涤水中活的但不可培养(VBNC)细胞的检测与定量方法:工业验证

Detection and Quantification Methods for Viable but Non-culturable (VBNC) Cells in Process Wash Water of Fresh-Cut Produce: Industrial Validation.

作者信息

Truchado Pilar, Gil Maria I, Larrosa Mar, Allende Ana

机构信息

Research Group on Quality, Safety and Bioactivity of Plant Foods, The Centre of Edafology and Applied Biology of Segura, Spanish National Research Council (CEBAS-CSIC), Murcia, Spain.

Faculty of Biomedical and Health Sciences, Nutrition, Microbiota and Health Group, Universidad Europea de Madrid, Villaviciosa de Odón, Madrid, Spain.

出版信息

Front Microbiol. 2020 May 4;11:673. doi: 10.3389/fmicb.2020.00673. eCollection 2020.

Abstract

The significance of viable but non-culturable (VBNC) cells in the food industry is not well known, mainly because of the lack of suitable detection methodologies to distinguish them from dead cells. The study aimed at the selection of the method to differentiate dead and VBNC cells of in process wash water (PWW) from the fruit and vegetable industry. Different methodologies were examined including (i) flow cytometry, (ii) viability quantitative polymerase chain reaction (v-qPCR) using an improved version of the propidium monoazide (PMAxx) dye as DNA amplificatory inhibitor, and (iii) v-qPCR combining ethidium monoazide (EMA) and PMAxx. The results showed that the flow cytometry, although previously recommended, was not a suitable methodology to differentiate between dead and VBNC cells in PWW, probably because of the complex composition of the water, causing interferences and leading to an overestimation of the dead cells. Based on results obtained, the v-qPCR combined with EMA and PMAxx was the most suitable technique for the detection and quantification of VBNC cells in PWW. Concentrations of 10 μM EMA and 75 μM PMAxx incubated at 40°C for 40 min followed by a 15-min light exposure inhibited most of the qPCR amplification from dead cells. For the first time, this methodology was validated in an industrial processing line for shredded lettuce washed with chlorine (10 mg/L). The analysis of PWW samples allowed the differentiation of dead and VBNC cells. Therefore, this method can be considered as a rapid and reliable one recommended for the detection of VBNC cells in complex water matrixes such as those of the food industry. However, the complete discrimination of dead and VBNC cells was not achieved, which led to a slight overestimation of the percentage of VBNC cells in PWW, mostly, due to the complex composition of this type of water. More studies are needed to determine the significance of VBNC cells in case of potential cross-contamination of fresh produce during washing.

摘要

在食品工业中,活的但不可培养(VBNC)细胞的重要性尚不为人所知,主要是因为缺乏合适的检测方法来将它们与死细胞区分开来。该研究旨在选择一种方法,以区分果蔬行业加工用水(PWW)中的死细胞和VBNC细胞。研究考察了不同的方法,包括:(i)流式细胞术;(ii)使用改进版单叠氮碘化丙啶(PMAxx)染料作为DNA扩增抑制剂的活力定量聚合酶链反应(v-qPCR);以及(iii)结合单叠氮溴化乙锭(EMA)和PMAxx的v-qPCR。结果表明,流式细胞术虽然此前被推荐,但并不是区分PWW中死细胞和VBNC细胞的合适方法,这可能是由于水的成分复杂,会产生干扰并导致对死细胞的高估。根据所得结果,结合EMA和PMAxx的v-qPCR是检测和定量PWW中VBNC细胞的最合适技术。10 μM EMA和75 μM PMAxx在40°C孵育40分钟,随后光照15分钟,可抑制大多数来自死细胞的qPCR扩增。该方法首次在使用氯(10 mg/L)清洗的生菜切丝工业加工生产线中得到验证。对PWW样品的分析能够区分死细胞和VBNC细胞。因此,该方法可被视为一种快速可靠的方法,推荐用于检测食品工业等复杂水基质中的VBNC细胞。然而,并未实现对死细胞和VBNC细胞的完全区分,这导致对PWW中VBNC细胞百分比的轻微高估,主要原因是这类水的成分复杂。需要更多研究来确定在新鲜农产品清洗过程中可能发生潜在交叉污染的情况下VBNC细胞的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e48/7214806/1ea83894b9c3/fmicb-11-00673-g001.jpg

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