Acid resistance of Salmonella Typhimurium ATCC 14028 after desiccation stress during peanut storage / Avaliação da resistência ácida de Salmonella Typhimurium ATCC 14028 após o estresse dessecativo durante o armazenamento de amendoim

ABSTRACT: Salmonella is a relevant pathogen, which causes foodborne outbreaks associated with both high and low moisture foods (LMF). This study evaluated the effect of previous desiccation stress on the acid resistance of S. Typhimurium ATCC 14028 using blanched peanut kernels as an LMF model. Salmonella was recovered from the peanut samples throughout 180 days of blanched peanut kernels storage at 28 ºC. During this period two death rates were verified, 0.04 log cfu/g/day in the first 30 days and 0.007 log cfu/g/day between 30 and180 days.Regarding acid resistance, there was no difference (P > 0.05) in the Salmonella growth/death kinetics between the undesiccated sample (TSB)and the cells recovered from peanut samples over 180 days of storage after 4 h at pHs 3.0, 3.5, 4.5 and 7.2. The average growth rate observed for pH 7.2 was 0.44 log cfu/ml/h. At pH 4.5, the Salmonella counts did not change significantly over 4 h. In contrast, Salmonella populations declined by 0.14 to 0.29 log cfu/ml/h at pH 3.5. At pH 3.0 declines were estimated to be 0.65 log cfu/ml/h for the undesiccated sample and 2.07 log cfu/ml/h for Salmonella recovered from peanuts stored for 120 days. Therefore, our data indicated that desiccation stress caused during the peanut storagedid not influence the Salmonella acid resistance.

RESUMO: Em alimentos de baixa umidade (LMF), o primeiro desafio encontrado por patógenos como a Salmonella é o estresse de dessecação. Neste estudo, o efeito prévio do estresse de dessecação sobre a resistência ácida de S. Typhimurium ATCC 14028 foi avaliado utilizando amendoim blancheado como um modelo de LMF. Salmonella foi recuperada das amostras de amendoim após 180 dias de estocagem a 28 ºC. Durante este período foram verificadas duas taxas de mortalidade, 0,04 log ufc/g/dia nos primeiros 30 dias e 0,007 log ufc/g/dia entre 30 e 180 dias. Com relação à resistência ácida, não houve diferença (P > 0,05) na cinética de crescimento/morte de Salmonella entre a amostra sem estresse dessecativo (TSB) e as amostras de amendoim após 4 h em pHs 3,0, 3,5, 4,5 e 7,2. A taxa média de crescimento observada para o pH 7,2 foi de 0,44 log cfu/ml/h. No pH 4,5, a contagem de Salmonella não mudou significativamente durante 4 h. Em contraste, a população de Salmonella diminuiu de 0,14 a 0,29 log cfu/ml/h no pH 3,5. No pH 3,0, a queda foi estimada em 0,65 log cfu/ml/h para a amostra sem estresse dessecativo e 2,07 log cfu/ml/h para a Salmonella recuperada das amostras de amendoim estocadas por 120 dias. Portanto, nossos dados indicaram que o estresse dessecativo causado durante a estocagem do amendoim não influenciou a resistência ácida de Salmonella.

Acid resistance of Salmonella Typhimurium ATCC 14028 after desiccation stress during peanut storage / Avaliação da resistência ácida de Salmonella Typhimurium ATCC 14028 após o estresse dessecativo durante o armazenamento de amendoim

Salmonella is a relevant pathogen, which causes foodborne outbreaks associated with both high and low moisture foods (LMF). This study evaluated the effect of previous desiccation stress on the acid resistance of S. Typhimurium ATCC 14028 using blanched peanut kernels as an LMF model. Salmonella was recovered from the peanut samples throughout 180 days of blanched peanut kernels storage at 28 ºC. During this period two death rates were verified, 0.04 log cfu/g/day in the first 30 days and 0.007 log cfu/g/day between 30 and180 days.Regarding acid resistance, there was no difference (P > 0.05) in the Salmonella growth/death kinetics between the undesiccated sample (TSB)and the cells recovered from peanut samples over 180 days of storage after 4 h at pHs 3.0, 3.5, 4.5 and 7.2. The average growth rate observed for pH 7.2 was 0.44 log cfu/ml/h. At pH 4.5, the Salmonella counts did not change significantly over 4 h. In contrast, Salmonella populations declined by 0.14 to 0.29 log cfu/ml/h at pH 3.5. At pH 3.0 declines were estimated to be 0.65 log cfu/ml/h for the undesiccated sample and 2.07 log cfu/ml/h for Salmonella recovered from peanuts stored for 120 days. Therefore, our data indicated that desiccation stress caused during the peanut storagedid not influence the Salmonella acid resistance.

Em alimentos de baixa umidade (LMF), o primeiro desafio encontrado por patógenos como a Salmonella é o estresse de dessecação. Neste estudo, o efeito prévio do estresse de dessecação sobre a resistência ácida de S. Typhimurium ATCC 14028 foi avaliado utilizando amendoim blancheado como um modelo de LMF. Salmonella foi recuperada das amostras de amendoim após 180 dias de estocagem a 28 ºC. Durante este período foram verificadas duas taxas de mortalidade, 0,04 log ufc/g/dia nos primeiros 30 dias e 0,007 log ufc/g/dia entre 30 e 180 dias. Com relação à resistência ácida, não houve diferença (P > 0,05) na cinética de crescimento/morte de Salmonella entre a amostra sem estresse dessecativo (TSB) e as amostras de amendoim após 4 h em pHs 3,0, 3,5, 4,5 e 7,2. A taxa média de crescimento observada para o pH 7,2 foi de 0,44 log cfu/ml/h. No pH 4,5, a contagem de Salmonella não mudou significativamente durante 4 h. Em contraste, a população de Salmonella diminuiu de 0,14 a 0,29 log cfu/ml/h no pH 3,5. No pH 3,0, a queda foi estimada em 0,65 log cfu/ml/h para a amostra sem estresse dessecativo e 2,07 log cfu/ml/h para a Salmonella recuperada das amostras de amendoim estocadas por 120 dias. Portanto, nossos dados indicaram que o estresse dessecativo causado durante a estocagem do amendoim não influenciou a resistência ácida de Salmonella.

Pesquisa de enterobactérias em chocolates / in chocolates

O chocolate é um dos produtos responsáveis pelos maiores surtos de salmonelose em humanos, contudo pouco se sabe sobre a presença de agentes enteropatogênicos em chocolate produzido no Brasil. Neste contexto, este trabalho pesquisou a presença de enterobactérias totais, coliformes, Escherichia coli e Salmonella em 65 amostras de chocolate (22 ao leite, 22 branco, 17 meio amargo e 4 em pó) comercializadas em Campinas/SP. As amostras apresentaram valores médios de pH entre 5,8 e 7,5 e atividade de água entre 0,31 e 0,59. Não foram isolados coliformes termotolerantes, E. coli e Salmonella nas amostras analisadas. Porém, enterobactérias totais foram detectadas em 22,7% das amostras de chocolate ao leite e branco e em 11,7% das amostras de chocolate meio amargo. Os coliformes totais foram isolados, respectivamente, em 13,6% e 4,5% das amostras de chocolate ao leite e branco. Enterobactérias totais e coliformes não foram detectados nas amostras de chocolate em pó. A contaminação encontrada reforça a necessidade de implementação de rigoroso programa de boas práticas de fabricação pelas indústrias processadoras de chocolate para garantir a segurança microbiológica dos produtos manufaturados. (AU)

Chocolate is one product responsible for causing major outbreaks of salmonellosis in humans, although little is known about the presence of enteropathogens in chocolate produced in Brazil. In this context, the present study investigated the occurrence of total enterobacteria, coliforms, Escherichia coli and Salmonella in 65 samples of chocolate (22 milk chocolate, 22 white chocolate, 17 dark chocolate and 4 chocolate powder) marketed in Campinas/SP. The samples showed mean values of pH from 5.8 to 7.5 and water activity from 0.31 to 0.59. No fecal coliform, E. coli and Salmonella were isolated from the analyzed samples. Nevertheless, total enterobacteria were detected in 22.7% of milk and white chocolate and in 11.7% of dark chocolate samples. Total coliforms were isolated from 13.6% and 4.5% of milk and white chocolate samples, respectively. Neither total enterobacteria nor total coliforms were detected in chocolate powder samples. These findings reinforce the need for implanting a strict program of good manufacturing practices for chocolate processing to ensure the microbiological safety of these products.(AU)

Enterobacteriaceae in processed cocoa products

Little is known of the presence of Salmonella in Brazilian cocoa, which justifies the present work that had the aim of checking the presence of total Enterobacteriaceae, coliforms, Escherichia coli and Salmonella in semi-processed cocoa products. A total of 150 samples of cocoa products from two different cocoa-processing manufacturers were analyzed (30 samples of nibs, 30 of liquor, 30 of cocoa cake, 30 of cocoa butter and 30 of cocoa powder). The samples of processed cocoa products had pH values between 5.31 and 7.35, and water activity ranging from 0.29 to 0.52. E. coli and Salmonella were not detected in any of the samples analyzed. Regarding the other analyzed microorganisms, 17 of the nibs contained total Enterobacteriaceae, 20 showed total coliforms, while thermotolerant coliforms were detected in one sample (0.6 log MPN/g). Seven percent of liquor and cocoa powder samples showed total coliforms. In cocoa cake, the same percentage in regard to total Enterobacteriaceae was observed. Total Enterobacteriaceae and total coliforms were detected in one sample of cocoa butter. Despite the low contamination observed, these results indicate failure in quality programs of the manufactures studied, since these bacteria are easily inactivated by thermal and sanitizer process.(AU)

Antimicrobial activity of Enterococcus faecium FAIR-E 198 against gram-positive pathogens

This study investigated the antimicrobial activity of Enterococcus faecium FAIR-E 198 against Bacillus cereus, Listeria monocytogenes and Staphylococcus aureus. Using the critical-dilution method, the bacteriocin produced by E. faecium FAIR-E 198 inhibited all L. monocytogenes strains evaluated (1,600 to 19,200 AU mL-1). However, none of the B. cereus and S. aureus strains investigated were inhibited. The maximum activity of this bacteriocin (800 AU mL-1) was observed in MRS broth, while the activity in milk was 100 AU mL-1. In the co-cultivation test in milk, B. cereus K1-B041 was reduced to below the detection limit (1.00 log CFU mL-1) after 48 h. E. faecium reduced the initial L. monocytogenes Scott A population by 1 log CFU mL-1 after 3 h at 35ºC. However, the pathogen regained growth, reaching 3.68 log CFU mL-1 after 48 h. E. faecium did not influence the growth of S. aureus ATCC 27154 during the 48 h of co-cultivation. Therefore, it can be concluded that the effectiveness of the antimicrobial activity of E. faecium FAIR-E 198 is strictly related to the species and strain of the target microorganism and to the culture medium.