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On-line version ISSN 1678-4405
Braz. J. Microbiol. vol.38 no.2 São Paulo Apr./June 2007
Sobrevivência de Listeria monocytogenes em salame tipo italiano de baixa acidez, produzido sob condições brasileiras de fabricação
Roberto Degenhardt; Ernani S Sant'Anna*
Departamento de Ciência e Tecnologia de Alimentos, Centro de Ciências Agrárias, Universidade Federal de Santa Catarina, Florianópolis, SC, Brasil
Dry sausages have been considered readytoeat products with low risk of causing listeriosis due to the hurdles created during the manufacturing process such as low pH and aw, high salt concentration and presence of lactic acid bacteria (LAB). However, several studies have detected survival of Listeria monocytogenes in these products and also shown that process parameters, LAB and L. monocytogenes strains directly influence the results. In this work, survival of the pathogen in sausages prepared with three different formulations (one standard formulation, one formulation added of Lactobacillus plantarum and one added of 2% sodium lactate), using the manufacturing process usually employed in Brazil, was evaluated. Naturally contaminated sausages presented a small increase in the counts of L. monocytogenes in the first days of the process, followed by a gradual decrease until the end of the process. In experimentally contaminated samples containing L. plantarum, the reduction of counts of L. monocytogenes during processing was considerable, but there wasn´t significant differences between the treatments.
Keywords: Listeria monocytogenes, Lactobacillus plantarum, Fermented dry sausage, Survival, Brazilian salami
Salames têm sido considerados produtos prontos para o consumo com baixo risco de provocar listeriose devido aos obstáculos criados no processo de fabricação e suas características de pH e atividade água baixos, alta concentração de sal e presença de bactérias lácticas. Entretanto, a sobrevivência de Listeria monocytogenes nesta classe de produtos é verificada e estudos de processo visando à redução da contaminação por este patógeno, têm demonstrado que particularidades como variação dos parâmetros de processo, cepas de bactérias lácticas e de L. monocytogenes influenciam diretamente os resultados. Neste estudo três formulações foram avaliadas (uma padrão, uma com inoculação da cultura Lactobacillus plantarum e outra com adição 2% de lactato de sódio) empregando parâmetros de processo comumente praticados no Brasil. Os salames naturalmente contaminados apresentaram discreto aumento da população de L. monocytogenes no início do processo, seguidos por redução até o final da maturação. Os salames artificialmente contaminados tiveram redução considerável da contagem de L. monocytogenes não havendo diferenças significativas entre os tratamentos.
Palavraschave: Listeria monocytogenes, Lactobacillus plantarum, embutido seco fermentado, sobrevivência, salame brasileiro
Salamis are dry fermented sausages manufactured with pork, pork fat, salt, ripening adjuvants and spices. This kind of sausage is considered a readytoeat product, because it does not require any thermal treatment befora comsumption (5,10,18,22). The manufacturing process varies according to the production region and regional consumer preferences (1,8,25,28).
Fermented meat products have been considered safe products (23) . During fermentation the acid lactic bacteria (LAB) uptake of the oxygen in the raw matter, decreasing the redox potential and turning nitrite into a more effective tool to prevent the growth of aerobic spoilage and pathogenic bacteria. In addition, low pH causes a decrease in the protein water holding capacity, accelerating sausage dehydration and leading to low aw and high NaCl concentration in the final product (30,31).
Listeria monocytogenes has been considered the most important foodborne pathogen due to the high death rate in risk groups (29). During fermentation and drying, the count of L.monocytogenes in sausages tends to decrease because of a set of hurdles created in the manufacturing process (8,30). However, L. monocytogenes is often isolated from fermented meat products, due to the capability to survive to the adverse conditions of this type of product (2,3,12,33).
Due to the lack of studies on the behavior of L. monocytogenes in Brazilian fermented meat products, the aim of this study was to evaluate the survival of L. monocytogenes in low acid Italian sausages produced under Brazilian conditions and in the presence of intentionally added inhibitory compounds.
MATERIAL AND METHODS
Raw meat, spices and ingredients were obtained in a pork slaughter and industrial plant in VideiraSC, Brazil. The commercial strain of Lactobacillus plantarum (Holbac 100TM) was supplied by Danisco Brasil LTDA.
Preparation of the inoculum
The L. monocytogenes strain ATCC 7644 (OXOID C3970L) was resuspended in Brain Heart Infusion BHI (MERCK 1.10493) and incubated overnight at 36ºC. The culture was transferred to Trypticase Soy Agar TSA (OXOID CM 131) and kept under refrigeration. For usem, the cultures were transfered to BHI broth, incubated overnight at 36ºC, and then submitted ot decimal dilutions in 0.85% sterile saline. The diluted culture containing 104 UFC mL1 was kept under refrigeration until the moment of use.
Preparation of sausages
Three different formulations of sausages were prepared: one standard formulation with no inhibitor additive, one formulation with Lactobacillus plantarum and one with 2% sodium lactate. Each formulation was performed in two batches: one control batch and one added of Listeria monocytogenes ATCC 7644 (Table 1). Assays were performed in duplicates.
The six batches (A1, A2, B1, B2, C1, C2) were prepared with the same raw components: pork meat (74.9%), pork fat (16.0%), salt (2.8%), curing salt (sodium nitrate and nitrite) (0.3%), sodium eritorbate (0.04%), monosodium glutamate (0.25%), maltodextrin (0.5%), dried milk (4.0%), glucono deltalactone (GDL) (1.2%) and Staphylococcus carnosus (BACTOFERM SB 61 Chr. Hansen) (0.025%).
The dry sausages were prepared in two steps. In the first step, a mixture was prepared in a cutter (MADO Granrant®) with pork (15%), salt (10% of the entire content), frozen pork fat, ground with the half graining desired. In the second step, L. monocytogenes inoculum (A2, B2, C2 batches), cultures, spices and additives were added and the cutting continued until the particles were about 5 mm in diameter. Then, the minced mixture was stuffed (stuffer Heinrich Frey Maschinenbau GmmH Henry 20®) in collagen casings (43 mm), making pieces of 350400 g. Sausages were hung in a climatecontrolled chamber for fermentation and drying.
Batches B1 and B2 were added of 0.025% Holbac 100® (DANISCO) dissolved in 50mL of distilled water. Batches C1 and C2 were added of 2.0% sodium lactate (Purasal PURAC).
Fermentation and drying were performed in a climatecontrolled chamber (Reich®). For ripening, the chamber temperature and relative humidity were 2224ºC and 9498%, respectively, during 48 h. The conditions for fermentation and drying up to 28 days are shown in Table 2.
Samples were taken from each batch after 0, 7, 14, 21 and 28 days of production. Portions of 25 g were homogenized with 225 mL of Buffered Peptone Water (OXOID CM 509) using a stomacher (model 400, Seward Medical, England). Further decimal dilutions were prepared with Buffered Peptone Water (OXOID CM 509). The counts of L. monocytogenes were determined by the most probable number dilution technique (MPN), (3 tubes each at 1,0 g, 0,1 g, 0,01 g, 0,001 g e 0,0001 g inocula), using Modified Listeria Enrichment Broth (ACUMEDIA 7409A) for preenrichment (24 h at 30ºC), Fraser broth (ACUMEDIA 7502A) for a second enrichment (48 h at 35ºC) and Listeria selective agar (ALOA BIOLIFE 404605) (2448 h at 35ºC) for isolation (32). Three to five typical colonies of L. monocytogenes were submitted to catalase test, motility by microscopy (32), CAMP test (Tryptic Soy Agar OXOID CM 131 added of sheep blood NEWPROV), acid production from L(+)rhamnose (Phenolred Broth Base MERCK 1.10987, L(+)rhamnose MERCK 1.04736) and Listeria O Antisera Types 1,4 (DIFCO 223021). LAB were counted in MRS Agar (OXOID CM 361) incubated att 30ºC for 48 to 72 h in microaerophilic conditions (26). Typical colonies were confirmed by catalase reaction.
Sausage samples were ground and homogeneized in adequate miller. pH was measured inserting the spear electrode of a pH meter (model 410 060547, ORION) into the samples. Aw was measured calculating water and salt percentages according to Krispien, Rödel and Leinster (15). Moisture was determined by gravimetry at 105ºC until constant weight and chloride was determined by a mercurometric method (4).
Three repetitions of each batch were carried through. The results of Listeria monocytogenes were expressed as log NMP g1 and the counts of LAB were expressed as logCFUg1. The data of pH, Aw, NMP of Listeria monocytogenes and LAB counts were submitted to analysis of variance (ANOVA) using Statistica software version 6.0. Tukey´s Test was applied when the detected difference among the values was significant with 5% of significance (p<0.05).
RESULTS AND DISCUSSION
pH and aw
The differences in pH and Aw for the three formulations (Table 3) were not significant (P>0.05). The decrease of pH until the 14th day, a rise in the 21st day and then a stabilization up to the 28th day in all formulations were considered normal in the Brazilian salamis manufacturing process. The decrease is a consequence of the the activity of naturally occurring LAB and the subsequent rise is caused by proteolysis and lipolysis, probably performed by yeasts, also responsible for the development of the maturation characteristic flavor (19,29,34).
Aw reduction during ripening in all formulations was similar, but from the 14th day on, the Aw decrease in formulations C1 and C2 was more intense than in the other formulations. This fact can be explained by the humectant effect of the sodium lactate, which increases the water retention capacity causing the reduction of Aw (24).
Counts of LAB (Table 3) ranged from 6.0 to 7.0 log CFUg1, with no differences between the batches (p>0.05), except of batch A1. Except for batches B1 and B2, the LAB detected in the other batches originated from the raw material from the production site.
Survival of L. monocytogenes in naturally contaminated samples
As shown in Fig. 1, L. monocytogenes counts in naturally contamined sausages (batches A1, B1 and C1) were very low, as already reported by Peccio (20) and Silva (27). The L. monocytogenes curves for batches A1 e B1 were different from those of the other batches. In batch B1, the initial count was higher than in batches A1 and C1, and the difference between the beginning and the end of the process was 2.42 log. For this batch, a constant decrease until the 14th day was observed, followed by a small increase at the 21st day and a rapid decrease at the 28th day. In batch A1, the difference in counts between the beginning and the end of the process was only 0.04 log. In this batch, the counts increased until the 7th day, and decreased afterwards, with a very small increase at day 28. Campani et al. (6) presented similar results when comparing the effect of two L. plantarum strains, one bacteriocinproducing and another nonbacteriocinproducing, on the survival of L. monocytogenes during the manufacture of Italian sausage. The growth of L. monocytogenes in batch A1 in the first week may be a response to the gradual acidity increase and lack of hurdles, which is expected in strains adapted to environmental stress (21,35).
In batch C1, there ere no L. monocytogenes counts, certainly because raw material contamination was under the detection limit of the analytical method.
Survival of L. monocytogenes in experimentally contaminated samples
The behavior of L. monocytogenes in experimentally contaminated sausages (batches A2, B2 and C2) is presented in Fig. 2. All batches presented a continual decreasing in the count curves with no significant differences between them (p>0.05). The difference between the initial and the final L. monocytogenes counts for batches A2, B2 and C2 were 2.57 log, 3.81 log and 3.3 log, respectively.
Comparing the two batches of standard formulation (A1 naturally contaminated and A2 experimentally contaminated), differences in the two L. monocytogenes count curves were noted. Batch A1, which presented a lower initial count, which increased in the first 7 days and decreased gradually afterwards. On the other hand, batch A2 with higher initial count, presented a constant decrease during the maturation time. This is probably due to the typical trait of the different strains present in each batch. While batch A2 was manufactured with a control strain (ATCC 7644) isolated from humans, batch A1 contained one or more native L. monocytogenes strains from raw meat or processing plants.
Batch B2, manufactured with a L. plantarum strain, presented a L.monocytogenes growth curve that decreased until the 14th day, when the performance was better than in the other batches. At day 21, the L. monocytogenes counts were lower than in batches A2 and C2. Batch B2 presented the best performance if compared to batches A2 and C2, once it had the highest L. monocytogenes initial count and the lowest count at the end of the experiments.
The survival of L. monocytogenes in batch C2 was similar to batches A2 and B2, showing a 3.3 log count reduction during the process.
Several studies have evaluated the efficiency of sausage manufacturing process in controling L. monocytogenes, and their results differ considerably (7,8,17,18,25,29,31). These differences range between the efficacy of the process in decreasing and increasing L. monocytogenes populations and are related to the parameters used in each case (17) and the features of the strains in each experiment (29).
There are hurdles, during the manufacturing process, which could act synergically creating an inhibitory environment for the pathogens (16). In the fermentation stage, the decrease of pH represents an important hurdle to the growth and survival of Listeriae (29). However, in studies where LAB were not used, Chikthimmah et al. (7) and Glass & Doyle (11) reported a growth of Listeriae at this stage. In drying and maturation stages, even at low pH, there was a decrease of Aw and an increase of salt concentration (29). In addition, the presence of bacteriocinproducing and nonbacteriocinproducing LAB cultures is another important hurdle (6).
There are many important reasons to explain L. monocytogenes survival during the manufacturing process and at the final product: its ability in becoming acidresistant (3,22) and, according to several studies, the effect of initial population size on the L. monocytogenes survival under stressful conditions (13,14,17,18). This ability is related to its pathogenicity and it's usually found in strains isolated from fermented food or from meat processing facilities (35).
Under the fermentation and maturation conditions employed in this work, the decrease of L. monocytogenes counts in Italian sausage is less intense than that reported for other European studies (8,18,31), where an expressive decreasing was observed at the beginning of the process. This is probably due to the lowe pH and higher water activity achieved in these processes. When occuring in the first days the increase of L. monocytogenes is higher than that observed in other studies (6).
Although no significant differences were detected among the three artificially contaminated batches (p> 0.05), batch B2 (inoculated with L. plantarum) presented a slightly different reduction in counts of L. monocytogenes when compared to the standard batch (A2). The curve of the C2 treatment (added of sodium lactate) was very similar to the standard curve. Therefore, the use of bioprotective cultures such as Lactobacillus plantarum is highly recommended in commercial production of Italian sausages. However, the use of sodium lactate must be better evaluated, mainly when used with other inhibitory substances.
The authors are thankful to Empresas Perdigão for supporting this work, to Danisco do Brasil for donating Lactobacillus plantarum cultures and to João Degenhardt and Eduardo Degenhardt for technical assistance in sausage manufacturing.
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Submitted: June 19, 2006; Returned to authors for corrections: September 04, 2006; Approved: October 20, 2006.
* Corresponding Author. Mailing address: Departamento de Ciência e Tecnologia de Alimentos Centro de Ciências Agrárias Universidade de Santa Catarina Rod. Ademar Gonzaga, 1346 Itacorubi 88034001 Florianópolis, SC Brasil. Tel.: (48) 3315372 ou (48) 3319943. Email: email@example.com