Doukaki Angeliki, Papadopoulou Olga S, Tzavara Chrysavgi, Mantzara Aikaterini-Malevi, Michopoulou Konstantina, Tassou Chrysoula, Skandamis Panagiotis, Nychas George-John, Chorianopoulos Nikos
Laboratory of Microbiology and Biotechnology of Foods, Department of Food Science and Human Nutrition, School of Food and Nutritional Sciences, Agricultural University of Athens, Iera Odos 75, 11855 Athens, Greece.
Institute of Technology of Agricultural Products, Hellenic Agricultural Organization-DIMITRA, S. Venizelou 1, Lycovrissi, 14123 Athens, Greece.
Pathogens. 2024 Jul 2;13(7):557. doi: 10.3390/pathogens13070557.
Globally, fresh vegetables or minimally processed salads have been implicated in several foodborne disease outbreaks. This work studied the effect of FMCC-B281 cells (F) and its supernatant (S) on spoilage and on the fate of and O157:H7 on fresh-cut ready-to-eat (RTE) salads during storage. Also, Fourier transform infrared (FTIR) and multispectral imaging (MSI) analysis were used as rapid and non-destructive techniques to estimate the microbiological status of the samples. Fresh romaine lettuce, rocket cabbage, and white cabbage were used in the present study and were inoculated with and the two pathogens. The strains were grown at 37 °C for 24 h in MRS and BHI broths, respectively, and then were centrifuged to collect the supernatant and the pellet (cells). Cells (F, ~5 log CFU/g), the supernatant (S), and a control (C, broth) were used to spray the leaves of each fresh vegetable that had been previously contaminated (sprayed) with the pathogen (3 log CFU/g). Subsequently, the salads were packed under modified atmosphere packaging (10%CO/10%O/80%N) and stored at 4 and 10 °C until spoilage. During storage, microbiological counts and pH were monitored in parallel with FTIR and MSI analyses. The results showed that during storage, the population of the pathogens increased for lettuce and rocket independent of the treatment. For cabbage, pathogen populations remained stable throughout storage. Regarding the spoilage microbiota, the population was lower in the F samples, while no differences in the populations of and yeasts/molds were observed for the C, F, and S samples stored at 4 °C. According to sensory evaluation, the shelf-life was shorter for the control samples in contrast to the S and F samples, where their shelf-life was elongated by 1-2 days. Initial pH values were ca. 6.0 for the three leafy vegetables. An increase in the pH of ca. 0.5 values was recorded until the end of storage at both temperatures for all cases of leafy vegetables. FTIR and MSI analyses did not satisfactorily lead to the estimation of the microbiological quality of salads. In conclusion, the applied bioprotective strain () can elongate the shelf-life of the RTE salads without an effect on pathogen growth.
在全球范围内,新鲜蔬菜或轻度加工的沙拉已与多起食源性疾病暴发有关。这项研究考察了FMCC-B281细胞(F)及其上清液(S)对即食(RTE)鲜切沙拉在储存期间的腐败情况以及大肠杆菌O157:H7存活情况的影响。此外,傅里叶变换红外光谱(FTIR)和多光谱成像(MSI)分析被用作快速无损技术来评估样品的微生物状况。本研究使用了新鲜的长叶生菜、芝麻菜和白菜,并接种了大肠杆菌和这两种病原体。这些菌株分别在MRS肉汤和BHI肉汤中于37°C培养24小时,然后离心收集上清液和沉淀(细胞)。用细胞(F,约5 log CFU/g)、上清液(S)和对照(C,肉汤)喷洒预先已被病原体污染(喷洒)的(3 log CFU/g)每种新鲜蔬菜的叶片。随后,将沙拉包装在气调包装(10%CO₂/10%O₂/80%N₂)下,在4°C和10°C储存直至腐败。在储存期间,对微生物计数和pH值进行监测,并同时进行FTIR和MSI分析。结果表明,在储存期间,生菜和芝麻菜中病原体的数量增加,与处理方式无关。对于白菜,病原体数量在整个储存过程中保持稳定。关于腐败微生物群,F样品中的大肠杆菌数量较低,而在4°C储存的C、F和S样品中,嗜温菌和酵母/霉菌的数量没有差异。根据感官评价,对照样品的货架期较短,而S和F样品的货架期延长了1 - 2天。三种叶菜类蔬菜的初始pH值约为6.0。在两种温度下储存至结束时,所有叶菜类蔬菜的pH值均升高约0.5。FTIR和MSI分析未能令人满意地评估沙拉的微生物质量。总之,所应用的生物保护菌株(FMCC-B281)可以延长即食沙拉的货架期,而不影响病原体的生长。