Dipto di Scienze e Tecnologie Alimentari e Microbiologiche, Sezione di Microbiologia Industriale, Univ degli Studi di Milano, Milan, Italy.
J Food Sci. 2012 Feb;77(2):M115-20. doi: 10.1111/j.1750-3841.2011.02535.x. Epub 2012 Jan 17.
Total of 14 filleted yellowfin tuna fish (Thunnus albacares) sold in wholesale fish market and supermarkets in Milan, Italy, were purchased and tested to determine microbial count, histamine level, histamine-forming bacteria, and their ability to produce histamine in culture broth. Although histamine level was less than 10 ppm, many samples showed high total viable bacterial and enterobacterial counts that reached dangerous levels after temperature abuse for short periods of time. A PCR assay targeting a 709-bp fragment of the histidine decarboxylase gene (hdc) revealed that 30.5% of the 141 enteric bacteria isolated from samples were positive and potentially able to produce histamine. The hdc positive strains were mainly isolated from fish bought at wholesale fish market, where we observed several possible risk factors, such as handling in poor and non-refrigerated conditions during fillet preparation. These positive strains were identified as Citrobacter koseri/Enterobacter spp. and Morganella morganii, by 16S/23S rRNA internal transcribed spacer amplification and 16S rRNA sequence analysis. The strains showed a variable ability of histamine production, with Morganella morganii being the most active histamine-producing species. A direct DNA extraction from fish and a PCR targeting the hdc gene showed a high degree of concordance with the results obtained through microbiological and chemical analyses, and could aid in the prompt detection of potentially contaminated fish products, before histamine accumulates.
The use of methods for the early and rapid detection of bacteria producing biogenic amines is important for preventing accumulation of these toxic substances in food products. In this study, we used a molecular approach for the detection of histamine-forming bacteria in fish. PCR-based methods require expensive equipment and a high degree of training for the user, but are fast (< 24 h) and reliable. They now represent the best predictive methods to identify a potential risk factor in fish products during processing, storage, and marketing and can be used in the investigation of risk reduction strategies.
在意大利米兰的批发鱼市场和超市购买并测试了总共 14 条去骨黄鳍金枪鱼,以确定微生物计数、组氨酸水平、组氨酸形成细菌及其在培养肉汤中的产组胺能力。尽管组胺水平低于 10ppm,但许多样本显示出高总活菌和肠杆菌计数,在短时间内温度滥用后达到危险水平。针对组氨酸脱羧酶基因(hdc)的 709bp 片段的 PCR 检测显示,从样本中分离的 141 种肠杆菌中有 30.5%为阳性,并且可能具有产组胺的能力。hdc 阳性菌株主要从批发鱼市场购买的鱼中分离出来,在那里我们观察到了几个可能的危险因素,例如在鱼片准备过程中处理条件差且未冷藏。通过 16S/23S rRNA 内部转录间隔区扩增和 16S rRNA 序列分析,这些阳性菌株被鉴定为柠檬酸杆菌/肠杆菌属和摩氏摩根菌。这些菌株产组胺的能力各不相同,摩氏摩根菌是最活跃的产组胺菌。从鱼中直接提取 DNA 并针对 hdc 基因进行 PCR 检测与通过微生物学和化学分析获得的结果高度一致,并有助于在组胺积累之前快速检测潜在污染的鱼产品。
使用早期和快速检测产生物胺细菌的方法对于防止这些有毒物质在食品中积累非常重要。在这项研究中,我们使用了一种分子方法来检测鱼中的组氨酸形成细菌。基于 PCR 的方法需要昂贵的设备和用户的高度培训,但速度快(<24 小时)且可靠。它们现在是识别加工、储存和销售过程中鱼产品潜在风险因素的最佳预测方法,并可用于调查降低风险策略。