Silva Elaine Nóbrega Gibson, Figueiredo Ana Cláudia Leite, Miranda Fernanda Araújo, de Castro Almeida Rogeria Comastri
Departamento de Análises Bromatológicas Faculdade de Farmácia Universidade Federal da Bahia SalvadorBA Brazil.
Departamento de Ciência dos Alimentos Escola de Nutrição Universidade Federal da Bahia SalvadorBA Brazil.
Braz J Microbiol. 2014 May 19;45(1):11-6. doi: 10.1590/s1517-83822014000100003. eCollection 2014.
The purpose of this study was to determine the effect of bacteriophage P100 on strains of Listeria monocytogenes in artificially inoculated soft cheeses. A mix of L. monocytogenes 1/2a and Scott A was inoculated in Minas Frescal and Coalho cheeses (approximately 10(5) cfu/g) with the bacteriophage added thereafter (8.3 × 10(7) PFU/g). Samples were analyzed immediately, and then stored at 10 °C for seven days. At time zero, 30 min post-infection, the bacteriophage P100 reduced L. monocytogenes counts by 2.3 log units in Minas Frescal cheese and by 2.1 log units in Coalho cheese, compared to controls without bacteriophage. However, in samples stored under refrigeration for seven days, the bacteriophage P100 was only weakly antilisterial, with the lowest decimal reduction (DR) for the cheeses: 1.0 log unit for Minas Frescal and 0.8 log units for Coalho cheese. The treatment produced a statistically significant decrease in the counts of viable cells (p < 0.05) and in all assays performed, we observed an increase of approximately one log cycle in the number of viable cells of L. monocytogenes in the samples under refrigeration for seven days. Moreover, a smaller effect of phages was observed. These results, along with other published data, indicate that the effectiveness of the phage treatment depends on the initial concentration of L. monocytogenes, and that a high concentration of phages per unit area is required to ensure sustained inactivation of target pathogens on food surfaces.
本研究的目的是确定噬菌体P100对人工接种软奶酪中单核细胞增生李斯特氏菌菌株的影响。将单核细胞增生李斯特氏菌1/2a和斯科特A的混合物接种到米纳斯弗雷斯科奶酪和科尔霍奶酪中(约10⁵ cfu/g),随后添加噬菌体(8.3×10⁷ PFU/g)。立即对样品进行分析,然后在10℃下储存7天。在零时间点、感染后30分钟时,与未添加噬菌体的对照相比,噬菌体P100使米纳斯弗雷斯科奶酪中的单核细胞增生李斯特氏菌数量减少了2.3个对数单位,使科尔霍奶酪中的该菌数量减少了2.1个对数单位。然而,在冷藏储存7天的样品中,噬菌体P100的抗李斯特氏菌作用较弱,奶酪的最低十进制减少量(DR)为:米纳斯弗雷斯科奶酪为1.0个对数单位,科尔霍奶酪为0.8个对数单位。该处理使活菌数有统计学意义的下降(p<0.05),并且在所有进行的试验中,我们观察到在冷藏7天的样品中,单核细胞增生李斯特氏菌的活菌数增加了约一个对数周期。此外,观察到噬菌体的作用较小。这些结果与其他已发表的数据表明,噬菌体处理的有效性取决于单核细胞增生李斯特氏菌的初始浓度,并且需要每单位面积有高浓度的噬菌体以确保食品表面目标病原体的持续失活。