2. Universidad Cardenal Herrera-CEU

The use of human milk in milk banks requires thermal processing to eliminate microbiological hazards. An evaluation is made of the stability of overall human milk bactericidal capacity following 2 modalities of thermal pasteurization: 63°C/30 minutes and 75°C/15 seconds. Ten milk samples (mature milk) were analyzed. In each sample, the effect of both thermal treatments on bactericidal capacity against Escherichia coli was evaluated in relation to the capacity of fresh milk (control). All the samples analyzed possessed bactericidal capacity. Human milk pasteurization induced a significant loss of this capacity that was more pronounced after high-temperature treatment than after low-temperature processing. Untreated milk, low-pasteurized milk, and high-pasteurized milk yielded a reduction in E. coli growth of 70.10%, 52.27%, and 36.39%, respectively. In conclusion, human milk possesses antimicrobial activity that is lost in part as a result of thermal processing. Such bactericidal capacity is, moreover, better preserved by low-temperature, long-time pasteurization.

The population dynamic of constitutive biota on 84 samples belonging to two different types of French fermented dry sausages during the ripening process in a pilot-scale ripening chamber was investigated. Samples were analyzed in three steps of their production: fresh product, first drying stage, and finished product. In addition, 180 strains of lactic acid bacteria were identified using a miniaturized biochemical procedure of characterization. In general, the number of lactic acid bacteria that evolved during the ripening process of French dry sausages increased during the first days of the process after which the number of these organisms remained constant at approximately 8 log CFU/g. Lactobacillus sakei and Pediococcus pentosaceus, bacteria added as starter, were the dominant species. Pediococcus urinaeequi, Pediococcus acidilactici, and particularly Lactobacillus curvatus were also present. Finally, we have to take into account that the controlled conditions of the pilot plant generally contribute to the homogenization of the behavior of the starter biota.

Samples from 240 carcasses were collected from four animal species (porcine, ovine, bovine and equine). Two samples were taken from each carcass, one using the excision method (EX) and the other the wet–dry swabbing method (SW). Eight areas from each carcass were sampled. Most of the samples obtained by SW revealed total aerobic viable counts (TVC) levels of between 3.1 and 4.0 log CFU cm−2, while most of the values corresponding to excision were located between 4.1 and 5.0 log CFU cm−2. Moreover, Enterobacteriaceae (EC) counts were only detected above 3.0 log CFU cm−2 in 0.85% of the carcasses when the samples were collected by swabbing, while the excision method revealed that 13.75% of the carcasses presented EC greater than 3.0 log CFU cm−2. TVC and EC by EX revealed statistically significant differences compared to SW, while no significant linear relationship was found between carcass surface bacterial counts obtained by SW and EX.

Fifty-five bovine, 50 equine, 60 ovine, and 50 porcine carcasses were sampled in a slaughterhouse in eastern Spain. Two samples were taken from each carcass, one using the excision method and the other using the swabbing method. Four different materials were used for swabbing: cellulose, polyurethane, or viscose sponges, and medical gauze. Samples were collected at the end of the process by four different people before the carcasses were taken to the cooler. The samples were examined for total viable bacteria counts (TVCs) and Enterobacteriaceae counts (ECs). The mean TVC for all species sampled by excision was 4.50 log CFU/cm(2), which was significantly higher than the 3.53 log CFU/cm(2) obtained by swabbing. The TVCs obtained using gauze and the cellulose and polyurethane sponges were significantly higher (P < 0.05) than the corresponding TVCs obtained using viscose sponges. Animal species, the person who collected the samples, and microbiological load also had a significant effect on TVC. ECs were obtained from 82.8% of excision samples, from larger percentages of samples obtained using cellulose or polyurethane sponges or gauze swabs, but from smaller percentages of samples obtained using viscose sponges. The Enterobacteriaceae load significantly influenced the EC. In contrast, animal species and the person who collected the samples had no significant effect. The cellulose sponge, polyurethane sponge, and gauze gave high mean log counts of aerobic bacteria and Enterobacteriaceae, which makes these swab types suitable for use in slaughterhouses for the purpose of assessing production process hygiene.

Mediterranean mussel (Mytilus galloprovincialis) is a species of bivalve mollusk that has a high capacity in filtering the water nearby and concentrate the virus and bacteria present in it. This can constitute a microbiological risk when they are consumed afterwards. Thus, depending on water pollution, mussels suffer a depuration process, usually controlled using Escherichia coli as indicator. The aim of this study was to determine the microbiological quality of mussels from various sources after purifying, and to consider the utility of the use of Clostridium perfringens as quality indicator. For this, microbiological analysis were performed in fifteen lots of mussel samples obtained from Spain and Italy. Aerobic mesophilic microorganisms, Enterobacteriaceae, E. coli, Vibrio spp., Listeria monocytogenes, Cl. perfringens, and the presence Salmonella spp. were measured. The results showed the presence of Salmonella spp. in four batches of mussels from various locations and Cl. perfringrens in thirteen of them. All samples were within the legal limits for E. coli. In conclusion, the results propose that the use of E. coli as an indicator microorganism for the mussels' depuration process is not sufficient to assure the microbiological quality of the product. Thus, it would be appropriate to include of Cl. perfringens, as an additional indicator, in the control carried out during and after the refinement is done. Finally, the results emphasized the necessity to properly cook this food product prior to consumption, as it allows the destruction of any microorganisms present.