Antimicrobial activity of enterocins against Listeria sp. and other food spoilage bacteria.

OBJECTIVE: To determine bacteriocin producers and the prevalence of structural enterocin genes and to detect the spectrum of activity against foodborne pathogens, from isolates of Enterococcus faecium and Enterococcus faecalis that were isolated from food and the environment. RESULTS: The entA, entB, entP, ent1071 and entX genes, which encode enterocins were the most frequently observed. Enterocins were thermostable, proteinaceous, and resistant to catalase. None of the isolates produced hemolysin, and inhibition resulting from bacteriophage lysis was excluded. The bactericidal effect of enterocins against L. innocua 12612 was determined by optical density and colony forming units. For the activity spectrum, elimination of mainly Listeria strains, Bacillus sp. and clinical enterococci, was observed. Imaging with scanning electron microscopy after treatment with enterocin Efm22 showed irregular rod-shaped cells and loss of cellular integrity. CONCLUSIONS: The isolates evaluated in this study are candidates for the production of enterocins that will be used as food biopreservatives, because they have high anti-listerial activity even after 24 h of experimentation, and used in the pharmaceutical area because they inhibit clinical microorganisms.

Inhibitory effect of bacteriocins from enterococci on developing and preformed biofilms of Listeria monocytogenes, Listeria ivanovii and Listeria innocua.

The biofilm-forming ability of Listeria spp. is a concern to the food industry and health sectors. The aim of this study was to verify the inhibitory activity of bacteriocins produced by enterococci (Enterococcus faecium 20, 22 and 24 and Enterococcus faecalis 27) on developing biofilm and preformed biofilm of Listeria species. Bacteriocins were partially purified from cell free supernatant (CFS). L. monocytogenes 2032, L. innocua 2050 and L. ivanovii 2056 were selected to analyse the inhibitory effect of bacteriocins on biofilm biomass (crystal violet staining) and biofilm viability (XTT-reduction). The biomass of the developing and preformed biofilms of Listeria species were reduced (p < 0.05) in the presence of all bacteriocins tested. Overall, the reduction in biofilm biomass of developing biofilms was up to 87.4% for bacteriocin produced by E. faecium 22 (CFS22) against L. ivanovii and up to 87.1% for CFS22 against L. monocytogenes. These findings are in accordance with those observed in confocal microscopy analysis. Most of the CFS-containing bacteriocin (CFS22, CFS24, CFS27) were effective at decreasing the viability of biofilm cells from all Listeria species. The highest reduction in viability was observed for L. monocytogenes preformed biofilm cells (up to 98.7%), evidenced by fluorescence microscopy of propidium iodide-labelled cells. Scanning electron microscopy showed that cells of biofilm-treated bacteriocins displayed degenerative changes that may be indicative of cellular leakages. This study suggests that bacteriocins produced by enterococci have prospective applications to prevent biofilm formation and/or to reduce cell viability of formed biofilms of distinct Listeria species.

Atividade de nucleação de gelo e densidade populacional do patógeno podem ser fatores que contribuem para o progresso da doença mancha branca do milho / Ice nucleation activity and density of the pathogen population may be factors that contribute to the progression of maize white spot disease / La actividad de nucleación de hielo y la densidad de población del patógeno pueden ser factores que contribuyen al progreso de la enfermedad mancha blanca del maíz

A Mancha Branca do Milho (MBM) é uma doença foliar que tem causado perdas apreciáveis, tanto qualitativas como quantitativas para a produção de milho. Seu agente etiológico, a Pantoea ananatis, é uma bactéria epifítica, Gram-negativa formadora de colônia amarela, capaz de formar gelo, mesmo em ambiente tropical (ice nucleation activity - INA). Este estudo teve por objetivo caracterizar isolados de P. ananatis quanto à atividade INA e avaliar o efeito da densidade bacteriana na expressão do fenótipo INA e no processo de desenvolvimento da doença. O agente patogênico foi isolado de lesões iniciais da doença, as anasarcas, e avaliado quanto à expressão do fenótipo INA em diferentes concentrações bacterianas. O mesmo foi feito com isolados epifíticos obtidos da superfície foliar de plantas de milho sadias. Dos 24 isolados bacterianos estudados, apenas 13 apresentaram o fenótipo INA+. A expressão deste fenótipo foi dependente da densidade celular. Isolados INA+ e INA­ foram inoculados em folhas destacadas e em plantas da cultivar HS200 a campo, em diferentes concentrações do inóculo. Nenhum isolado INA­ reproduziu sintomas em laboratório. Dos cinco isolados INA+ somente um deles reproduziu sintomas em laboratório. Em campo o isolado INA+ foi capaz de promover lesões em todas as concentrações avaliadas. Conclui-se que a atividade de nucleação de gelo pela bactéria P. ananatis é dependente da linhagem e da densidade bacteriana e este fenômeno pode estar envolvido no desenvolvimento dos sintomas da MBM.(AU)

Maize White Spot Disease is a leaf disease that has caused considerable losses, both qualitative and quantitative for corn production. Its etiologic agent, Pantoea ananatis, is an epiphytic, Gram-negative, yellow colony-forming bacterium, capable of forming ice, even in tropical environments at temperatures where this normally does not occur (Ice Nucleation Activity - INA). This study aimed at characterizing P. ananatis isolates in terms of INA activity and evaluating the effect of bacterial density on the expression of the INA phenotype and on the disease development process. The pathogen was isolated from the initial lesions of the disease, the anasarcas, and were evaluated for the expression of the INA phenotype in different bacterial concentrations. The same procedure was performed on epiphytic isolates obtained from the leaf surface of healthy maize plants. From the 24 bacterial isolates studied, only 13 presented the INA+ phenotype. The expression of this phenotype is dependent on cell density. INA+ and INA­ isolates were inoculated on detached leaves and on plants of cultivar HS200 in the field, in different concentrations of the inoculum. No INA­ isolates reproduced symptoms in the laboratory. From the five INA+ isolates, only one of them reproduced symptoms in the laboratory. In the field, the INA+ isolate was able to promote lesions in all concentrations evaluated. It can be concluded that the ice nucleation activity by P. ananatis is dependent on the strain and bacterial density and this phenomenon may be involved in the development of Maize White Spot Disease symptoms.(AU)

La mancha blanca del maíz es una enfermedad de la hoja que ha causado pérdidas considerables, tanto cualitativas como cuantitativas para la producción de maíz. Su agente etiológico, Pantoea ananatis, es una bacteria epífita, Gram-negativa, formadora de colonias amarillas, capaz de causar hielo, incluso en ambientes tropicales a temperaturas donde esto normalmente no ocurre (actividad de nucleación de hielo - INA). Este estudio tuvo como objetivo caracterizar los aislados de P. ananatis en términos de actividad de INA y evaluar el efecto de la densidad bacteriana en la expresión del fenotipo de INA y en el proceso de desarrollo de la enfermedad. El patógeno se aisló de las lesiones iniciales de la enfermedad, las anasarcas, y se evaluó la expresión del fenotipo INA en diferentes concentraciones bacterianas. Lo mismo se hizo con aislamientos epifitos obtenidos de la superficie de la hoja de plantas de maíz sanas. De los 24 aislados bacterianos estudiados, solo 13 presentaron el fenotipo INA+. La expresión de este fenotipo depende de la densidad celular. Se inocularon aislamientos INA+ e INA- en hojas desprendidas y en plantas del cultivar HS200 en el campo, en diferentes concentraciones del inóculo. Ninguno aislado INA- reprodujo síntomas en el laboratorio. De los cinco aislamientos de INA+, solo uno de ellos reprodujo síntomas en el laboratorio. En el campo, el aislado INA+ pudo promover lesiones en todas las concentraciones evaluadas. Se concluye que la nucleación de hielo por P. ananatis depende de la cepa y la densidad bacteriana, y este fenómeno puede estar involucrado en el desarrollo de los síntomas de la enfermedad de la mancha blanca del maíz.(AU)

Screening of the Enterocin-Encoding Genes and Antimicrobial Activity in Enterococcus Species.

In the current study, a total of 135 enterococci strains from different sources were screened for the presence of the enterocin-encoding genes entA, entP, entB, entL50A, and entL50B. The enterocin genes were present at different frequencies, with entA occurring the most frequently, followed by entP and entB; entL50A and L50B were not detected. The occurrence of single enterocin genes was higher than the occurrence of multiple enterocin gene combinations. The 80 isolates that harbor at least one enterocin-encoding gene (denoted "Gene(+) strains") were screened for antimicrobial activity. A total of 82.5% of the Gene(+) strains inhibited at least one of the indicator strains, and the isolates harboring multiple enterocin-encoding genes inhibited a larger number of indicator strains than isolates harboring a single gene. The indicator strains that exhibited growth inhibition included Listeria innocua strain CLIP 12612 (ATCC BAA-680), Listeria monocytogenes strain CDC 4555, Enterococcus faecalis ATCC 29212, Staphylococcus aureus ATCC 25923, S. aureus ATCC 29213, S. aureus ATCC 6538, Salmonella enteritidis ATCC 13076, Salmonella typhimurium strain UK-1 (ATCC 68169), and Escherichia coli BAC 49LT ETEC. Inhibition due to either bacteriophage lysis or cytolysin activity was excluded. The growth inhibition of antilisterial Gene+ strains was further tested under different culture conditions. Among the culture media formulations, the MRS agar medium supplemented with 2% (w/v) yeast extract was the best solidified medium for enterocin production. Our findings extend the current knowledge of enterocin-producing enterococci, which may have potential applications as biopreservatives in the food industry due to their capability of controlling food spoilage pathogens.

COMPARISON BETWEEN AUTOMATED SYSTEM AND PCR-BASED METHOD FOR IDENTIFICATION AND ANTIMICROBIAL SUSCEPTIBILITY PROFILE OF CLINICAL Enterococcus spp / Comparação entre o sistema automatizado e PCR na identificação e susceptibilidade de isolados clínicos de Enterococcus spp

Enterococci are increasingly responsible for nosocomial infections worldwide. This study was undertaken to compare the identification and susceptibility profile using an automated MicrosScan system, PCR-based assay and disk diffusion assay of Enterococcus spp. We evaluated 30 clinical isolates of Enterococcus spp. Isolates were identified by MicrosScan system and PCR-based assay. The detection of antibiotic resistance genes (vancomycin, gentamicin, tetracycline and erythromycin) was also determined by PCR. Antimicrobial susceptibilities to vancomycin (30 µg), gentamicin (120 µg), tetracycline (30 µg) and erythromycin (15 µg) were tested by the automated system and disk diffusion method, and were interpreted according to the criteria recommended in CLSI guidelines. Concerning Enterococcus identification the general agreement between data obtained by the PCR method and by the automatic system was 90.0% (27/30). For all isolates of E. faecium and E. faecalis we observed 100% agreement. Resistance frequencies were higher in E. faecium than E. faecalis. The resistance rates obtained were higher for erythromycin (86.7%), vancomycin (80.0%), tetracycline (43.35) and gentamicin (33.3%). The correlation between disk diffusion and automation revealed an agreement for the majority of the antibiotics with category agreement rates of > 80%. The PCR-based assay, the van(A) gene was detected in 100% of vancomycin resistant enterococci. This assay is simple to conduct and reliable in the identification of clinically relevant enterococci. The data obtained reinforced the need for an improvement of the automated system to identify some enterococci.

Os enterococos são cada vez mais responsáveis por infecções hospitalares em todo o mundo. Este estudo foi realizado para comparar a identificação e perfil de suscetibilidade entre o sistema automatizado MicrosScan e a técnica molecular de PCR em espécies de Enterococcus spp. Foram avaliados 30 isolados clínicos de Enterococcus spp. Os isolados foram identificados pelo sistema MicrosScan® e pela técnica de PCR. A detecção de genes de resistência a antibióticos (vancomicina, gentamicina, tetraciclina e eritromicina) foi determinada por PCR. Suscetibilidades antimicrobianas à vancomicina (30 µg), gentamicina (120 µg), tetraciclina (30 µg) e eritromicina (15 µg), foram testados pelos métodos automatizados e pelo disco difusão, de acordo com as orientações do CLSI. No que diz respeito à identificação de Enterococcus em geral entre os dados obtidos pelo método de PCR e pelo sistema automático foi de 90,0% (27/30). Para todos os isolados de E. faecium e E. faecalis observamos concordância de 100%. Freqüências de resistência foi maior em E. faecium do que em E. faecalis. As taxas de resistência obtidas foi maior para eritromicina (86,7%), vancomicina (80,0%), tetraciclina (43,35%) e gentamicina (33,3%). A correlação entre a técnica de disco difusão e automação revelou-se de acordo para maioria dos antibióticos com taxas > 80%. O gene van(A) foi detectado em 100% dos Enterococcus resistentes á vancomicina. O ensaio baseado em PCR é de simples realização e de confiança para identificação de enterococos clinicamente relevantes. Os dados obtidos reforçam a necessidade de melhoria no sistema automatizado para identificar alguns enterococos.

Comparison between automated system and PCR-based method for identification and antimicrobial susceptibility profile of clinical Enterococcus spp.

Enterococci are increasingly responsible for nosocomial infections worldwide. This study was undertaken to compare the identification and susceptibility profile using an automated MicrosScan system, PCR-based assay and disk diffusion assay of Enterococcus spp. We evaluated 30 clinical isolates of Enterococcus spp. Isolates were identified by MicrosScan system and PCR-based assay. The detection of antibiotic resistance genes (vancomycin, gentamicin, tetracycline and erythromycin) was also determined by PCR. Antimicrobial susceptibilities to vancomycin (30 µg), gentamicin (120 µg), tetracycline (30 µg) and erythromycin (15 µg) were tested by the automated system and disk diffusion method, and were interpreted according to the criteria recommended in CLSI guidelines. Concerning Enterococcus identification the general agreement between data obtained by the PCR method and by the automatic system was 90.0% (27/30). For all isolates of E. faecium and E. faecalis we observed 100% agreement. Resistance frequencies were higher in E. faecium than E. faecalis. The resistance rates obtained were higher for erythromycin (86.7%), vancomycin (80.0%), tetracycline (43.35) and gentamicin (33.3%). The correlation between disk diffusion and automation revealed an agreement for the majority of the antibiotics with category agreement rates of > 80%. The PCR-based assay, the van(A) gene was detected in 100% of vancomycin resistant enterococci. This assay is simple to conduct and reliable in the identification of clinically relevant enterococci. The data obtained reinforced the need for an improvement of the automated system to identify some enterococci.