National Food Agency, Department of Risk Benefit Assessment, PO Box 622, SE-751 26 Uppsala, Sweden.
National Food Agency, Department of Risk Benefit Assessment, PO Box 622, SE-751 26 Uppsala, Sweden.
Int J Food Microbiol. 2019 Mar 2;292:13-20. doi: 10.1016/j.ijfoodmicro.2018.12.003. Epub 2018 Dec 7.
Estimations of consumer exposure to mycotoxins through surveillance of mycotoxins in the food trade are well described, but the exposure due to mouldy food in private homes is not known, and may result from removing visible mould on food and eating the rest. In this study, we followed the growth of Penicillium expansum on the surface of apple jam and Penicillium verrucosum on crème fraiche, as well as production and distribution of fungal metabolites throughout the sample (approx. 6 cm high divided into three equal layers), using a multianalyte method, over time (up to 28 days) and at 4, 8 and 15 °C. Growth rates and apparent lag times for P. expansum in apple jam at different temperatures were estimated by fitting to the Baranyi model. The growth rates were 1.7, 2.7 and 4.3 mm day for storage at 4, 8 and 15 °C, respectively; apparent lag times decreased with increasing storage temperature and were 10.6, 7.9 and 2.6 days at corresponding temperatures. Patulin and roquefortine C were identified and quantified, among other fungal metabolites. Patulin was detected in all 2-cm layers of the apple jam at 15 °C. Concentrations in the upper two layers of the jar corresponded to exposures exceeding the health based guidance value (HBGV) for a normal serving size. Consequently, removal of the mouldy part is insufficient to avoid unhealthy exposure. In contrast to patulin, roquefortine C was also produced at 4 °C. The growth of P. verrucosum on crème fraiche was very restricted and could not be modelled. Despite the small colony (8 ± 0.5 mm in diameter), ochratoxin A and citrinin were detected after 21 days at 15 °C in the top 2 cm layer (including the fungal colony), and at concentrations in a normal serving corresponding to an exposure above the HBGV established by EFSA for both mycotoxins. Questiomycin A, an antibiotic, was also produced in crème fraiche but in contrast to the two mycotoxins, was detected throughout all layers of the crème fraiche and was produced also at 4 and 8 °C. As a complement to a previous study, we also present production and the distribution of major fungal metabolites in apple jam and crème fraiche for some additional fungal strains (P. crustosum, P. roqueforti and P. verrucosum on apple jam and P. expansum on crème fraiche). A pilot study investigating the effect of inoculation size on toxin production may have implications for the best inoculum to use in experimental studies.
通过监测食品贸易中的霉菌毒素来估计消费者接触霉菌毒素的情况已有很好的描述,但家庭中发霉食物导致的接触情况尚不清楚,这可能是由于去除食物表面可见的霉菌并食用其余部分造成的。在这项研究中,我们使用多分析物方法,随着时间的推移(长达 28 天)以及在 4、8 和 15°C 时,跟踪青霉扩张在苹果果酱表面、粗奶油上的产毒青霉 verrucosum 的生长情况以及整个样本(约 6cm 高,分为三个相等的层)中真菌代谢物的产生和分布情况。通过拟合巴尼模型来估计不同温度下苹果果酱中青霉扩张的生长率和明显的滞后时间。在 4、8 和 15°C 下储存时,青霉扩张的生长率分别为 1.7、2.7 和 4.3mm·天;明显的滞后时间随储存温度的升高而降低,分别为 10.6、7.9 和 2.6 天。鉴定并定量了其他真菌代谢物,包括棒曲霉素和罗库福林 C。在 15°C 下,所有 2cm 层的苹果果酱中均检测到棒曲霉素。罐内上两层的浓度对应于超过健康基准指导值(HBGV)的正常食用量的暴露量。因此,去除发霉部分不足以避免不健康的接触。与棒曲霉素不同,罗库福林 C 也在 4°C 下产生。粗奶油上的产毒青霉 verrucosum 的生长受到严格限制,无法建模。尽管菌落很小(直径 8±0.5mm),但在 15°C 下 21 天后,在顶层 2cm 层(包括真菌菌落)中检测到了赭曲霉毒素 A 和桔青霉素,浓度与 EFSA 为两种霉菌毒素建立的 HBGV 对应的正常食用量的暴露量相同。在粗奶油中也产生了抗生素喹肟 A,但与两种霉菌毒素不同,它在粗奶油的所有层中都有检测到,并且在 4 和 8°C 下也有产生。作为之前研究的补充,我们还展示了苹果果酱和粗奶油中一些其他真菌菌株(产毒青霉 crustosum、青霉 roqueforti 和青霉 verrucosum 及产毒青霉 expansum)的主要真菌代谢物的产生和分布情况。一项关于接种量对毒素产生影响的初步研究可能对实验研究中使用的最佳接种量具有重要意义。