Vázquez-Sánchez Daniel, Galvão Juliana Antunes, Oetterer Marília
Laboratory of Freshwater Fish and Seafood Technology, Department of Agri-Food Industry, Food and Nutrition, "Luiz de Queiroz" College of Agriculture (ESALQ), University of São Paulo (USP), Av. Pádua Dias 11, Piracicaba, São Paulo CEP 13418-900 Brazil.
J Food Sci Technol. 2017 Nov;54(12):3867-3879. doi: 10.1007/s13197-017-2843-x. Epub 2017 Sep 22.
The major contamination sources, serogroups, biofilm-forming ability and biocide resistance of persistent in tilapia-processing facilities were assessed. Twenty-five processing-control points were examined twice in two factories, including whole tilapias, frozen fillets, water and food-contact surfaces. were detected in 4 and 20% of points of Factory A and B respectively, but at low concentrations. Contamination was due to inadequate handling of tilapias in the slaughter room of Factory A and to the application of ineffective sanitizing procedures in Factory B. Seven strains were characterized by RAPD-PCR using primers HLWL85, OPM-01 and DAF4. Genotypic similarity allowed tracing the contamination source of tilapia fillets in Factory B and detecting a prevalent strain in Brazilian tilapia-processing facilities. The serogroup II (including the serotype 1/2c) was the most frequently found, followed by serogroup I (1/2a) and III (1/2b), whereas the serotype 4b was not detected. All strains showed high biofilm-forming ability on stainless steel and polystyrene, but biofilm formation was positively correlated with the type of origin surface. Biofilms were highly resistant to peracetic acid and sodium hypochlorite, being required doses higher than those recommended by manufacturers to be eradicated. Peracetic acid was more effective than sodium hypochlorite, but the use of disinfectants with similar mechanisms of action increases the risk of cross-resistance. Case-by-case approaches are thus recommended to determine the sources and degree of contamination present in each factory, which would allow applying precise responses to control the persistence of bacterial pathogens such as .
对罗非鱼加工设施中持久性污染物的主要污染源、血清群、生物膜形成能力和抗杀菌剂能力进行了评估。在两家工厂对25个加工控制点进行了两次检查,包括整条罗非鱼、冷冻鱼片、水和食品接触表面。在工厂A和B的检测点中,分别有4%和20%检测到污染物,但浓度较低。工厂A的污染是由于屠宰室对罗非鱼处理不当,而工厂B的污染是由于采用了无效的消毒程序。使用引物HLWL85、OPM-01和DAF4通过RAPD-PCR对7株菌株进行了鉴定。基因型相似性有助于追踪工厂B中罗非鱼片的污染源,并检测巴西罗非鱼加工设施中的一种流行菌株。血清群II(包括血清型1/2c)是最常见的,其次是血清群I(1/2a)和III(1/2b),而血清型4b未被检测到。所有菌株在不锈钢和聚苯乙烯上均表现出较高的生物膜形成能力,但生物膜形成与原始表面类型呈正相关。生物膜对过氧乙酸和次氯酸钠具有高度抗性,需要高于制造商推荐的剂量才能将其根除。过氧乙酸比次氯酸钠更有效,但使用作用机制相似的消毒剂会增加交叉耐药的风险。因此,建议采用逐案处理方法来确定每个工厂中存在的污染源和污染程度,这将有助于采取精确措施来控制诸如细菌病原体的持久性。