Made available in DSpace on 2014-08-20T14:30:13Z (GMT). No. of bitstreams: 1 Tese_Gloria_Beatriz_Azevedo_Cubas.pdf: 1660996 bytes, checksum: 8bb44113acc263526d63d6f5e7e47e2b (MD5) Previous issue date: 2012-12-07 / The aims of this randomised controlled trial were to evaluate the influence of a preprocedural 0.12% chlorhexidine mouthrinse on the microbial contamination of dental impressions, subsequently disinfected with sodium hypoclorite or water (control). The second objective was to evaluate if aqueous solution of 0.12% chlorhexidine mixed with irreversible hydrocolloid powder would decrease microbial contamination of dental impressions. Forty subjects underwent maxillary dental impressions with irreversible hydrocolloid and were randomly divided into two groups (n=20) according to the preprocedural mouthrinse (0.12% chlorhexidine or placebo).The dental impressions were then divided into two subgroups and disinfected with sodium hypochlorite or water (control). In the second part, 20 subjects underwent maxillary dental impressions with irreversible hydrocolloid and randomly assigned into two groups according to the mixed agent used (0.12% chlorhexidine or water). Saliva and alginate samples were assessed for microbiological counts of total micro-organisms, total streptococci and Candida species. Surface roughness of the impressions and dimensional stability of the casts were also evaluated. Chlorhexidine preprocedural mouthrinse significantly reduced (p<0.05) microbial contamination. Small but significant alterations were produced on dimensional stability and surface quality when sodium hypochlorite was used as disinfectant after the impression (p=0.005). The results also showed that the use of aqueous 0.12% chlorhexidine mixed with the powder of irreversible hydrocolloid decreased the percentage of total micro-organisms and total Streptococci counts (p<0.001), without producing alterations in surface quality and dimensional stability. It can be concluded that 0.12% chlorhexidine used as preprocedural mouthrinse, or mixed with irreversible hydrocolloid powder, are effective methods in reducing microbial contamination of alginate impressions, without causing damage to the physical and mechanical properties of the material / Os objetivos deste ensaio clínico randomizado foram (I) avaliar a influência de um bochecho, com solução de clorexidina 0,12% e placebo, previamente a realização de moldagens bucais, posteriormente desinfetadas com hipoclorito de sódio ou água (controle) na contaminação de moldagens de alginato; e (II) avaliar se solução aquosa de clorexidina 0,12% misturada com o pó de hidrocolóide irreversível reduziria a contaminação microbiana de moldagens bucais.Quarenta voluntários foram submetidos a moldagens bucais com hidrocolóide irreversível e foram divididos de forma randomizada em 2 grupos (n=20) de acordo com a solução bucal (0,12% clorexidina ou placebo). As moldagens bucais foram divididas em 2 grupos e desinfetadas com hipoclorito de sódio ou água (controle). Na segunda parte do ensaio clinico, 20 voluntários foram submetidos a moldagens bucais com hidrocolóide irreversível e foram divididos em 2 grupos de acordo com a solução usada no preparo do alginato (0,12% clorexidina ou água).Amostras de saliva e alginato foram avaliados quanto a contagem microbiana de microrganismos totais, estreptococos totais e espécies de Candida. Rugosidade de superfície e estabilidade dimensional de modelos de gesso também foram avaliados. Bochecho com solução bucal de clorexidina reduziu de forma significativamente (p<0,005) a contaminação microbiana. Pequenas mais significativas alterações dimensionais e de rugosidade de superfície foram produzidas quando hipoclorito de sódio foi utilizado como agente desinfetante pós-moldagem (p=0,005). Os resultados também demonstraram que o uso de solução de clorexidina 0,12% misturada ao pó de hidrocolóide irreversível reduziu a percentagem de microrganismos totais e estreptococos (p<0.001), sem causar alterações de rugosidade de superfície e estabilidade dimensional. Pode ser concluído que o uso de solução de clorexidina 0,12% usada como bochecho bucal ou misturada ao pó de hidrocolóide irreversível são métodos eficientes na redução microbiana de moldagens de alginato, sem causarem danos as propriedades físicas e mecânicas do material

Dans de nombreux pays, l’aquaculture de pectinidés dépend aujourd’hui du succès de la production contrôlée de juvéniles. Néanmoins, les fortes variations des taux d’éclosion des oeufs et de la survie larvaire, enregistrées à ce jour, rendent cette production imprévisible. Les élevages larvaires en flux ouvert de coquilles Saint-Jacques (Pecten maximus) ont été développés en Norvège et présentent des résultats prometteurs. Malheureusement, les rendements de production encore faibles et l’impossibilité de travailler à fortes densités restent un frein majeur au développement de cette technique. En France, une technique en flux-ouvert, en petit volume (5 L), et à forte densité (≤ 300 larves mL-1) a été développée pour les ostréidés. Des expériences préliminaires visant à décliner ce système d’élevage aux larves de P. maximus se sont avérées infructueuses : retard de croissance et forte mortalité en quelques jours. Il est reconnu que les larves de pectinidés doivent faire face à des contraintes diverses en écloserie : bactériologiques, physiologiques et environnementales. Elles sont également plus sensibles que les larves des autres espèces de bivalves comme par exemple l’huître japonaise (Crassostrea gigas). Il apparait donc nécessaire aujourd’hui d’identifier plus clairement l’origine des phénomènes perturbant le bon développement des larves en flux ouvert afin d’améliorer la qualité des élevages et les rendements larvaires. Grâce à l’étude et à la compréhension des mécanismes physiologiques impliqués dans la lutte contre le stress des larves de P. maximus en flux ouvert, ce projet de doctorat donne des clés permettant d’améliorer cette technique d’élevage tout en limitant l’utilisation de produits chimiques en milieu contrôlé. / In many countries, aquaculture of pectinids depends on the success of artificial spat production in hatchery. This production is always unpredictable due to the variability of hatching rate and larval survival. Flow-through larval rearing systems were developed in Norway for the King scallop Pecten maximus and showed promising results. Unfortunately the system needs to be optimized since the larval yields and the densities used are still relatively low. In France, a small-scale (5 L) and high-density (≤ 300 larva mL-1) flow-through larval rearing system was successfully developed for oysters. First trials in such system and in similar conditions with P.maximus failed as we registered slower growth and high mortality rate in only a few days. It is known that pectinids larvae are more sensitive to environmental conditions than the oyster Crassostrea gigas, for example.Nowadays, it is important to identify and to understand the phenomena disturbing larval development in flowthrough system to improve larval quality and production yields. This doctoral project provided some indications how improving P. maximus flowthrough rearing system while limiting the use of antibiotic through a better understanding the physiological mechanisms involved in the larval response to a stressful environment

A produção de etanol nas destilarias brasileiras é baseada na atividade fermentativa da levedura Saccharomyces cerevisiae que utiliza o caldo da cana-de-açúcar e/ou o melaço como substrato. Bactérias contaminantes da fermentação alcoólica competem com as leveduras pelos açúcares, afetando o rendimento do sistema produtivo e, consequentemente, causando perdas econômicas significativas às usinas. Biofilmes formados nos tanques de fermentação alcoólica agem como reservatórios de bactérias, contribuindo para contaminações persistentes e de difícil controle. Os biofilmes proporcionam aos seus habitantes certo grau de proteção contra diversas ameaças do meio, incluindo a ação dos antibióticos. Desta forma, o conhecimento da comunidade bacteriana dos biofilmes é fundamental para as medidas que visam o controle das contaminações na produção do bioetanol. No primeiro estudo, a composição e dinâmica da comunidade bacteriana foram determinadas pela análise de sequências do gene 16S rRNA de biofilmes com diferentes períodos de crescimento, correspondentes aos estágios iniciais de estabelecimento destes biofilmes dentro dos tanques de fermentação alcóolica Os resultados mostraram que estas comunidades foram compostas predominantemente pelas bactérias ácido-lácticas (LAB), com destaque para o gênero Lactobacillus. A visualização da estrutura dos biofilmes por microscopia eletrônica de varredura evidenciou que estes são formados por bactérias e leveduras (biofilmes mistos). No segundo estudo, a suscetibilidade aos antimicrobianos (monensina, virginiamicina e beta-ácido derivado do lúpulo) e a capacidade de formação de biofilmes em culturas puras foram avaliadas para isolados de Lactobacillus spp. provenientes de biofilmes (células sésseis) e de vinho bruto (células planctônicas) coletados dos tanques de fermentação. A partir dos resultados foi possível observar que as diferenças na suscetibilidade aos antimicrobianos e na habilidade de formar biofilmes foram estirpe-dependentes e que, em alguns casos, o perfil apresentado para algumas espécies mostrou-se relacionado à fonte de isolamento. Este foi o primeiro estudo sobre biofilmes contaminantes da fermentação alcoólica, em escala industrial, para a produção de etanol a partir da cana-de-açúcar / Bioethanol production in Brazilian distilleries is based on fermentative activity of the yeast Saccharomyces cerevisiae which uses sugarcane juice and/or molasses as a substrate. Bacterial contaminants of alcoholic fermentation compete with yeasts for sugars, affecting ethanol yield and consequently causing relevant economic losses to the fuel ethanol industry. Biofilms formed into fermentors act as bacterial reservoirs, contributing to persistent contaminations that are difficult to control. Biofilms provide a certain degree of protection for their inhabitants against some environmental threats, including antibiotics. Thus, understanding bacterial community within biofilms is essential for actions to control contaminations in bioethanol production. In the first study, composition and dynamic of bacterial community were determined by 16S rRNA gene sequences analysis of biofilms with different growth periods, corresponding to initial stages of biofilm establishment in fermentation tanks. Results showed that these communities were dominated by lactic acid bacteria (LAB), mainly of the genus Lactobacillus. Visualization of biofilm structure by scanning electron microscopy revealed a mixed-species biofilm composed by bacteria and yeasts. In the second study, susceptibility to antimicrobials (monensina, virginiamicina and beta-acids from hops) and capacity to form biofilm in pure culture were evaluated for Lactobacillus spp. isolated from biofilms (sessile cells) and wine (planktonic cells) collected from fermentors. The results showed that differences in the susceptibility to antimicrobials and the ability to form biofilms were strain-specific and, in certain cases, the response of some species was related to the isolation source. This was the first investigation of contaminant biofilms from sugarcane-based alcoholic fermentation on an industrial scale

A produção de etanol nas destilarias brasileiras é baseada na atividade fermentativa da levedura Saccharomyces cerevisiae que utiliza o caldo da cana-de-açúcar e/ou o melaço como substrato. Bactérias contaminantes da fermentação alcoólica competem com as leveduras pelos açúcares, afetando o rendimento do sistema produtivo e, consequentemente, causando perdas econômicas significativas às usinas. Biofilmes formados nos tanques de fermentação alcoólica agem como reservatórios de bactérias, contribuindo para contaminações persistentes e de difícil controle. Os biofilmes proporcionam aos seus habitantes certo grau de proteção contra diversas ameaças do meio, incluindo a ação dos antibióticos. Desta forma, o conhecimento da comunidade bacteriana dos biofilmes é fundamental para as medidas que visam o controle das contaminações na produção do bioetanol. No primeiro estudo, a composição e dinâmica da comunidade bacteriana foram determinadas pela análise de sequências do gene 16S rRNA de biofilmes com diferentes períodos de crescimento, correspondentes aos estágios iniciais de estabelecimento destes biofilmes dentro dos tanques de fermentação alcóolica Os resultados mostraram que estas comunidades foram compostas predominantemente pelas bactérias ácido-lácticas (LAB), com destaque para o gênero Lactobacillus. A visualização da estrutura dos biofilmes por microscopia eletrônica de varredura evidenciou que estes são formados por bactérias e leveduras (biofilmes mistos). No segundo estudo, a suscetibilidade aos antimicrobianos (monensina, virginiamicina e beta-ácido derivado do lúpulo) e a capacidade de formação de biofilmes em culturas puras foram avaliadas para isolados de Lactobacillus spp. provenientes de biofilmes (células sésseis) e de vinho bruto (células planctônicas) coletados dos tanques de fermentação. A partir dos resultados foi possível observar que as diferenças na suscetibilidade aos antimicrobianos e na habilidade de formar biofilmes foram estirpe-dependentes e que, em alguns casos, o perfil apresentado para algumas espécies mostrou-se relacionado à fonte de isolamento. Este foi o primeiro estudo sobre biofilmes contaminantes da fermentação alcoólica, em escala industrial, para a produção de etanol a partir da cana-de-açúcar / Bioethanol production in Brazilian distilleries is based on fermentative activity of the yeast Saccharomyces cerevisiae which uses sugarcane juice and/or molasses as a substrate. Bacterial contaminants of alcoholic fermentation compete with yeasts for sugars, affecting ethanol yield and consequently causing relevant economic losses to the fuel ethanol industry. Biofilms formed into fermentors act as bacterial reservoirs, contributing to persistent contaminations that are difficult to control. Biofilms provide a certain degree of protection for their inhabitants against some environmental threats, including antibiotics. Thus, understanding bacterial community within biofilms is essential for actions to control contaminations in bioethanol production. In the first study, composition and dynamic of bacterial community were determined by 16S rRNA gene sequences analysis of biofilms with different growth periods, corresponding to initial stages of biofilm establishment in fermentation tanks. Results showed that these communities were dominated by lactic acid bacteria (LAB), mainly of the genus Lactobacillus. Visualization of biofilm structure by scanning electron microscopy revealed a mixed-species biofilm composed by bacteria and yeasts. In the second study, susceptibility to antimicrobials (monensina, virginiamicina and beta-acids from hops) and capacity to form biofilm in pure culture were evaluated for Lactobacillus spp. isolated from biofilms (sessile cells) and wine (planktonic cells) collected from fermentors. The results showed that differences in the susceptibility to antimicrobials and the ability to form biofilms were strain-specific and, in certain cases, the response of some species was related to the isolation source. This was the first investigation of contaminant biofilms from sugarcane-based alcoholic fermentation on an industrial scale

Made available in DSpace on 2014-07-29T15:13:39Z (GMT). No. of bitstreams: 1 Claudia peixoto bueno.pdf: 2154558 bytes, checksum: e3212e2f2e948a89b381b38c7ab473b7 (MD5) Previous issue date: 2009-02-20 / The deterioration of vacuum packed refrigerated meat accompanied by large gas production - a phenomenon called blown pack - is considered a major cause of economic losses of the meat industry in several regions of Brazil and the world. Several psychrophilic and psychrotrophic microorganisms may be involved, especially species of Clostridium. The objective of the present study was to perform the molecular characterization, through the use of the PCR technique, and the molecular isolation by conventional bacteriology, of the main microorganisms that cause blown pack in refrigerated meat from Brazil, New Zealand and the United Kingdom. Thus, typing techniques were used to differentiate the species and subspecies involved in this type of deterioration. Tirty-six samples of Brazilian blown pack meat, 6 samples from the UK and 12 experimental blown pack samples of venison from the North Island of New Zealand were analyzed. Three pairs of primers, the RFP / RRP, the 16SEF/16SER and the pair EISRF / EISRR were used for C. estertheticum estertheticum and Clostridium estertheticum like, and one for C. gasigenes (16DBF/16DBR). The samples with the PCR results were sent to a microbiology laboratory for conventional isolation of Clostridium estertheticum. It was concluded that Clostridium estertheticum estertheticum is responsible for the deterioration of meat and hence the blown pack in the UK. Samples of blown pack Brazilian meat have Clostridium estertheticum like as primary causal agent. The typing was carried out in isolates and strains - donated by Mirinz Center / Ruakura Agresearch / Hamilton / New Zealand - together with two isolates from Brazil, involved in this type of deterioration. The selected techniques AFLP and RFLP - PCR were able to distinguish species and subspecies of psychrophilic and psychrotrophic clostridia. However, the AFLP showed the highest discriminatory power, being able to distinguish 100% of the species - C. estertheticum, C. frigoris, C. bowmani, C. lacusfryxellense and C. psychrophylum - and also the subspecies C. estertheticum estertheticum, C. estertheticum laramiense, C. estertheticum like k21 and k24. Through the technique of RFLP, it was possible to differentiate the species of clostridia psychrotrophic, psichrophilic and also the subspecies C. estertheticum estertheticum and Clostridium estertheticum like, along with the use of four restriction endonucleases - AluI, CfoI, TaqI and HaeIII. The HaeIII provided greater variety of fragments and the ability to differentiate the species of clostridia psychrophilic and psychrotrophic, whereas TaqI was the only enzyme capable of differentiating the subspecies of C. estertheticum estertheticum and C. estertheticum laramiense of C. estertheticum like. The Brazilian samples isolated fit into the group of Clostridium estertheticum like, although there is no confirmation of the absence of Clostridium estertheticum estertheticum in the country. / A deterioração de carnes refrigeradas embaladas a vácuo acompanhada de grande produção de gás - fenômeno denominado tufamento de embalagens - é considerada uma das principais causas de perdas econômicas da indústria cárnea, em várias regiões do Brasil e do mundo. Diversos microrganismos psicrofílicos e psicrotróficos podem estar envolvidos, destacando-se espécies do gênero Clostridium. Objetivou-se com o presente estudo a caracterização molecular, por meio do emprego da técnica de PCR e o isolamento pela bacteriologia convencional, dos principais microrganismos causadores do tufamento de embalagens de carnes refrigeradas procedentes do Brasil, Nova Zelândia e Reino Unido. Para tanto, foram empregadas técnicas de tipagem visando a diferenciação das espécies e subespécies envolvidas neste tipo de deterioração. Foram analisadas 36 amostras tufadas de carnes brasileiras, 6 amostras tufadas oriundas do Reino Unido e 12 amostras experimentais tufadas de carne de cervo provenientes da Ilha Norte da Nova Zelândia. Foram utilizados três pares de primers, o RFP/RRP, o 16SEF/16SER e o par EISRF/EISRR para C. estertheticum estertheticum e Clostridium estertheticum like e um para C. gasigenes (16DBF/16DBR). As amostras com os resultados positivos ao PCR foram enviadas para a microbiologia convencional para isolamento do Clostridium estertheticum. Concluiu-se que o Clostridium estertheticum estertheticum é responsável pela deterioração das carnes e, consequentemente, pelo tufamento das embalagens no Reino Unido. As amostras tufadas de embalagens de carnes brasileiras têm como principal agente causador o Clostridium estertheticum like. A tipagem foi relizada em cepas e isolados doados pelo Mirinz Centre/ Ruakura AgResearch/ Hamilton/NZ - juntamente a dois isolados brasileiros, envolvidos nesse tipo de deterioração . As técnicas eleitas AFLP e RFLP PCR foram capazes de distinguir as espécies e subespécies de clostrídios psicrofílicos e psicrotróficos, porém, o AFLP apresentou maior poder discriminatório, sendo capaz de diferenciar 100% das espécies C. estertheticum, C. frigoris, C. bowmani, C. lacusfryxellense e C psychrophylum - e também as subespécies - Clostridium estertheticum estertheticum, Clostridium estertheticum laramiense, o Clostridium estertheticum like K21 e Clostridium estertheticum like K24. Por meio da técnica de RFLP foi possível diferenciar as espécies do clostrídio psicrofílicos e psicrotróficos e também as subespécies C. estertheticum estertheticum e Clostridium estertheticum like, utilizando em conjunto as quatro endonucleases de restrição AluI, CfoI, TaqI e HaeIII. A HaeIII proporciona maior variedade de fragmentos e capacidade de diferenciar as espécies de clostrídios psicrofílicos e psicrotróficos. Já a TaqI foi a única enzima capaz de diferenciar as subespécies C. estertheticum estertheticum e C. estertheticum laramiense do C. estertheticum like. As amostras brasileiras isoladas se enquadraram no grupo do Clostridium estertheticum like.

Une recherche de souches bactériennes lactiques productrices de bactériocine a été entreprise à partir daliments traditionnels dorigine sénégalaise et les souches les plus actives ont été mises en uvre comme barrière en supplément du sel (NaCl) contre la croissance de la flore contaminante de différents poissons maigre [sompat (Pomadasys jubelini)], moyennement gras [capitaine (Polydactylus quadrifilis)], et gras [mâchoiron (Arius heudeloti)] de production artisanale au Sénégal. La prévalence des bactéries lactiques a été déterminée à 109 UFC/(g ou ml) dans les produits fermentés traditionnels à base de céréale et de lait, et 103 UFC/g dans les produits de la pêche fermentés. Douze souches bactériennes à activité inhibitrice de type bactériocine ont été détectées au sein de 220 souches de bactéries lactiques isolées de 32 échantillons de ces différents types de produits. Les 11 souches ont été caractérisées (API 50 CH, 16S rDNA) comme étant des souches de Lactococcus lactis subsp. lactis qui portent le gène codant pour la nisine, la souche restante est une souche dEnterococcus faecium et possède le gène codant pour lEntérocine B. Les deux souches, Lactococcus lactis subsp. lactis CWBI-B1410, isolée de farine de mil fermentée et productrice de nisine, et la souche Lactobacillus curvatus CWBI-B28 provenant de la collection du CWBI de la FUSAGx, produisant trois bactériocines de type curvalicine 28a, b et c, ont été mises en uvre en combinaison avec du sel comme barrière contre la croissance de la flore contaminante dans les poissons. La flore totale dans les poissons de production artisanale atteingnait 5,70 log UFC/g. La transformation des poissons par fermentation naturelle à 30°C (sans traitement préalable : procédé traditionnel), entraîne une prolifération de bactéries Gram-négatives comme Proteus sp, Shewanella putrefaciens et des souches de Bacillus sp qui atteignent 109-10 UFC/g en moins de 24 h dans les produits. Lutilisation de CWBI-B1410 (107 UFC/g) comme ferment avec ajout de glucose (1% m/m) dans les filets, entraîne une production in situ de substances antagonistes (acides organiques et bactériocine). Il en résulte une réduction du niveau de la flore contaminante entérique de 2 (P. quadrifilis) et de 4 (P. jubelini) log UFC/g par rapport aux poissons préparés traditionnellement. Lajout de sel dans des produits ainsi fermentés réduit la flore entérique. Laddition des surnageants de culture neutralisés (pH 6) bactéricides issus de CWBI-B1410 ou de CWBI-B28 en combinaison avec du chlorure de sodium (0,14 g/ml) sur les filets crus (100 ml/100 g) incubés à 10°C réduit le niveau de la contamination bactérienne de 1,5 log UFC/g et retarde laugmentation de la flore qui reste à un niveau < 106 UFC/g pendant 13 à 18 jours dincubation à 10°C selon le type de poisson, alors que pour les filets contrôles, traités avec des surnageants de culture neutralisés de souches non productrices de bactériocines (Lactobacillus curvatus LMG 21688 et Lactococcus lactis LMG 6890) salés (NaCl 0,14 g/ml), la flore contaminante dépasse 106 UFC/g au bout de 3 à 7 jours. Les effets antibactériens des surnageants de cultures neutralisés bactéricides et salés (NaCl 0,14 g/ml), sont par ailleurs, plus importants que ceux dune solution salée (NaCl 0,14 g/ml) supplémentée de sels de benzoate et de sorbate en concentration de 0,5 mg/ml chacun sur les poissons riches en lipides. Ces résultats suggèrent que, la combinaison des effets antibactériens des bactéries lactiques productrices de bactériocines et du sel, plus particulièrement lutilisation de SCN salés, comme préservatifs, peut constituer un moyen approprié damélioration de la conservation et de la qualité microbiologique des produits de la pêche artisanale au Sénégal. Le traitement des poissons selon lune ou lautre des stratégies décrites précédemment, combiné à un système de séchage devrait permettre de produire des produits halieutiques traditionnels de meilleures qualités microbiologiques et de durée de conservation plus longue, justifiant limportance de continuer cette étude sur lamélioration de la productivité de bactériocine par CWBI-B1410, et les impacts des nouveaux traitements sur les qualités organoleptiques et nutritionelles des produits. A screening of bacteriocin-producing lactic acid bacteria from Senegalese traditional food products was undertaken and the most active strains were tested in combination with sodium chloride as barrier to control spoilage bacteria growth on different artisanal fish products [lean sumpat grunt (Pomadasys jubelini), moderarely fat giant African threadfin (Polydactylus quadrifilis) and fat smoothmouth sea catfish (Arius heudeloti)] in Senegal. The prevalence of lactic acid bacteria was determined at 109 CFU/(g or ml) in traditional fermented cereals and fermented milk products, and 103 CFU/g in fermented seafood products. Twelve bacteriocin-producing strains were detected of 220 lactic acid bacteria strains randomly selected from such products. The eleven were characterized (API 50CH and 16S rDNA) as Lactococcus lactis subsp lactis strains and contain gene encoding nisin, and the remaining one an Enterococcus faecium strain which contains gene encoding Enterocin B. Two strains, Lactococcus lactis subsp. lactis CWBI-B1410, a nisin producer isolated from fermented millet flour from Senegal, and Lactobacillus curvatus CWBI B28 which produces three bacteriocins (Curvalicin 28a, b et c) from CWBI collection, were tested in combination with sodium chloride as barrier to control spoilage bacteria growth on fish from artisanal production. The total bacterial counts of fishes reached 5.7 log CFU/g. The processing of such products by natural fermentation at 30°C (without any preliminary treatment as in traditional process) result in proliferation of Gram-negative bacteria such as Proteus sp and Shewanella putrefaciens, and some Bacillus sp strains, which reached 109-10 CFU/g in products within less than 24 h of incubation. When using CWBI-B1410 living culture (107 CFU/g) with glucose (1% wt/wt) supplementation as barrier against bacterial growth in fishes, a depression of the pH as well as a bacteriocin-like activity were noted, resulting in a decrease of the Gram negative strains counts of 4 log CFU/g (P. jubelini) and 2 log CFU/g (P. quadrifilis) in comparison to fishes prepared in using traditional process. The addition of salt in such fermented products reinforced the antimicrobial effect by CWBI-B1410 strain. The addition of neutralized (pH 6) culture supernatants of CWBI-B1410 or CWBI-B28 strains in combination with sodium chloride (0.14 g/ml) as preservatives on fishes (100 ml/100 g) incubated at 10°C, declined the level of total bacterial counts of 1.5 log CFU/g within 48 h, and delayed the increase of bacteria number in fishes: bacterial counts remained under 106 CFU/g for 13 to 18 days of storage at 10°C following the fish, whereas they were over 106 CFU/g after 3 to 7 days fish storage at 10°C in controls, treated with salted (NaCl 0.14 g/ml) neutralized (pH 6) culture supernatants of non-bacteriocin producers (Lactococcus lactis LMG 6890 and Lactobacillus curvatus LMG 216888). The antimicrobial effects by salted neutralized culture supernatants of the bacteriocin producers were higher to those of salted solution (NaCl 0.14 g/ml) supplemented with benzoate and sorbate acid salts each at concentration of 0.5 mg/ml on the moderate and fat fishes. These data suggest that the use of bacteriocin-producing lactic acid bacteria in combination with sodium chloride as described above, particularly the use of salted bactericidal culture supernatant, as preservatives, can be a suitable strategy to enhance the storage and the bacterial quality of traditional fish products in Senegal. The treatment of fishes in using one of the strategies as described above combined with a drying process could permit production of seafood commodities with higher bacterial quality and time of storage, justifying to continue this investigation on the enhancement of the bacteriocin-productivity by CWBI-B1410, and the evaluation of the effects of the new treatments on the organaoleptic and nutritional quality of products.

Made available in DSpace on 2014-07-29T15:07:57Z (GMT). No. of bitstreams: 1 Dissertacao Fernanda Rodrigues Mendes.pdf: 596557 bytes, checksum: 356192df70d17abe993a9b9d4fc158ba (MD5) Previous issue date: 2010-03-02 / The objective of this study to verify the physical, chemical and bacteriological egg-washed and not washed undergoing experimental infection with Pseudomonas aeruginosa and stored at 5 oC and 25 oC during the 30 days. We used 768 eggs without cracks and classified as large, hens line Dekalb White, 30 to 40 weeks of age, and 384 for physical and chemical quality and 384 for bacteriological quality. The experimental design was in blocks of two stages and in factorial 2 x 2 x 2 (contamination, washing and storage temperature) with six repetitions for variables of physical, chemical and bacteriological. Eggs were contaminated by handling, with 1.5 x 105 units forming colonies (CFU) of Pseudomonas aeruginosa / mL and remained 5c and stored at 25oC for 30 days. Every 10 days were analyzed physical quality of eggs (egg weight, specific gravity, thickness shell, yolk percentage, albumen and shell, Haugh unit, yolk index and albumen), chemistry (pH of albumen and yolk) and bacteriological (count bacteria on the shell and contents of the egg). To analyze the weight loss of eggs at 30 days were used 96 eggs weighed every three days. The experimental design was randomized blocks in factorial 2 x 2 x 2 (Contamination washing x x storage temperature), with six replicates and one egg per experimental unit. It was observed that the cooling maintained the internal egg quality even when there was contamination in shell with inoculum of Pseudomonas aeruginosa (p <0.05). It was concluded that the Refrigeration slows weight loss and provides better internal quality, physics, and chemistry of eggs during the 30 days of storage (p> 0.05), independent of the contamination and the washing process. Best values internal quality were obtained in chilled eggs (p <0.05), eggs stored at 5 ° C had lower bacterial counts (p <0.05). It was concluded that the cooling provides better quality of bacteriological eggs during 30 days of storage and that there was more growth bacterial washed eggs and especially the content of the eggs. / Objetivou-se com este estudo verificar a qualidade física, química e bacteriológica de ovos lavados e não-lavados submetidos à contaminação experimental com Pseudomonas aeruginosa e armazenados a 5oC e 25oC durante o período de 30 dias. Foram utilizados 768 ovos sem trincas e classificados como grandes, de poedeiras leves da linhagem Dekalb White, com 30 a 40 semanas de idade, sendo 384 para qualidade física e química e 384 para qualidade bacteriológica. O delineamento empregado foi em blocos com duas etapas e em esquema fatorial 2 x 2 x 2 (contaminação, lavagem e temperatura de armazenamento) com seis repetições para variáveis de qualidade física, química e bacteriológica. Os ovos foram contaminados, pelo manuseio, com 1,5 x 105 unidades formadoras de colônias (UFCs) de Pseudomonas aeruginosa/mL de solução e permaneceram armazenados a 5oC e 25oC por 30 dias. A cada 10 dias foram realizadas análises de qualidade física dos ovos (peso do ovo, gravidade específica, espessura de casca, porcentagem de gema, albume e casca, unidade Haugh, índices de gema e albume), química (pH do albume e da gema) e bacteriológica (contagem de bactérias na casca e no conteúdo do ovo). Para analisar a perda de peso dos ovos ao final de 30 dias foram utilizados 96 ovos pesados a cada três dias. O delineamento utilizado foi em blocos casualizados em esquema fatorial 2 x 2 x 2 (contaminação x lavagem x temperatura de armazenamento), com seis repetições e um ovo a unidade experimental. Observou-se que a refrigeração manteve a qualidade interna dos ovos mesmo quando houve contaminação na casca com inóculo de Pseudomonas aeruginosa (p<0,05). Concluiu-se que a refrigeração retarda a perda de peso e proporciona melhor qualidade interna, física, e química de ovos durante os 30 dias de armazenamento (p>0,05), independente da contaminação e do processo de lavagem. Melhores valores de qualidade interna foram obtidos nos ovos refrigerados (p<0,05), Os ovos armazenados a 5ºC apresentaram menor contagem bacteriana (p<0,05). Concluiu-se que a refrigeração proporciona melhor qualidade bacteriologica dos ovos durante 30 dias de armazenamento e que houve maior crescimento bacteriano nos ovos lavados e principalmente no conteúdo dos ovos.

Si la sueur fraîchement émise par le corps humain est inodore, la dégradation de celle-ci par la flore bactérienne cutanée produit des composés volatils malodorants, responsables des odeurs de transpiration. Les odeurs de transpiration apparaissent également sur les vêtements au cours de leur utilisation, particulièrement sur les textiles réalisés en fibres synthétiques. Ce travail a pour but d’améliorer la compréhension du phénomène d’émanation d’odeurs en étudiant l’effet du sujet testé, l’effet de la flore bactérienne et l’effet du textile sur les émissions de composés volatils malodorants.L’intérêt de ce travail réside dans l’approche globale de la problématique des odeurs de transpiration et dans la diversité des méthodes de mesure mises en place, tant dans l’étude de la flore microbiologique que dans les méthodes de mesures des composés odorants émis.Dans un premier temps, le dénombrement simultané de la flore bactérienne sur la peau et sur le vêtement a été réalisé sur un échantillon de 15 sujets à l’issue d’un exercice physique. Cette expérimentation a permis d’évaluer le taux de transfert bactérien moyen lors d’une activité sportive et d’étudier son rôle dans l’émission d’odeurs. Ensuite, afin d’affiner ces résultats, une méthode basée sur la biologie moléculaire a été mise en place pour réaliser le suivi qualitatif de la stabilité de la flore commensale axillaire d’un sujet pendant 3 mois. Le transfert bactérien spécifique entre la peau du testeur et le vêtement a été étudié pour 4 matières textiles sélectionnées (dont le coton et le PET). Ceci a permis de déterminer le rôle du transfert bactérien spécifique dans l’émission des odeurs à partir de textile.Enfin, le dernier chapitre est consacré à l’étude de l’émission de composés volatils et odorants à l’aide de mesures olfactives et d’un nez électronique au cours du temps par 8 composants textiles sélectionnés. Après traitement statistique par analyse en composante principale et étude détaillée des mesures, 9 composés chimiques ont été identifiés comme indicateurs d’un comportement textile malodorant. Ces derniers pourraient être utilisés dans la mise en place d’une méthode ciblée de mesure physico-chimique des mauvaises odeurs.Ce travail a permis de déterminer l’impact de chacun des facteurs sujet, flore bactérienne et textile dans l’émission d’odeurs. En outre, ce travail ouvre des perspectives sur l’étude des contaminations bactériennes par contact, mais également dans l’étude des odeurs, sur les phénomènes de désorption de molécules volatiles à partir de différentes matrices textiles et sur les solutions pouvant être envisagées pour limiter les émissions odorantes à partir de textiles. / Fresh human sweat is odorless. Odoriferous volatile compounds are produced by the metabolism of bacteria living on the skin, generating strong malodor. Sweaty body odors do also appear on clothes during use, and especially on synthetic fabrics. The aim of this document is to improve understanding of odor emission by investigating subject effect, microbiota effect and fabric effect on the emission of odoriferous volatile compounds.Odors of perspiration are hereby globally approached with a wide use of methods and experimental devices, for microbial flora study as well as for odoriferous volatile compounds emission study.First, microflora enumeration has been simultaneously processed on the skin and on the fabric after exercise for 15 subjects. This experiment allowed an evaluation of the average bacterial transfer yield during physical activity and the beginning of the investigation of its effect on odor emission.A molecular biology methodology has then been developed in order to refine these results. Monitoring of qualitative composition of the microbiota has been performed to study the stability of the armpit’s ecosystem on a subject during 3 months. Specific microbial transfer from subject’s skin to clothe has been performed for 4 textile fabrics (including cotton and PET). This leaded to characterize the effect of specific bacterial transfer on odor emission from fabric.The last chapter is dedicated to the study of the emission of odoriferous volatile compounds over time using olfactory measurements and electronic nose for 8 selected fabrics. Principal component analysis targeted 9 chemical compounds that have been selected as malodorous behavior indicators for a given fabric. Those 9 compounds could be used for setting up a fitted physicochemical method of malodor.To conclude, this study helped to understand the effect of 3 factors in odor perception from a fabric after sport : subject, microbial flora and fabric. Perspectives have been charted on contact microbial contamination, but also on odor, and especially on desorption of odoriferous volatile molecules from a textile or knitted matrix. The solutions that could be used to limit malodorous emission from fabrics have also been discussed.