Microbial load can be controlled using either synthetic or natural preservatives. Particular interest has been focused on the potential application of plant essential oils as safer additives for meat. However, there is no published research on the use of essential oils during the meat drying process. This study was focused on enhancing the meat drying process. At first a value-added dried meat product by using oregano essential oil (OEO) to inhibit the growth of bacteria, and the sensorial response from assessors is presented. It was found that the application of the OEO in meat is effective in inhibiting Salmonella enteritidis and Escherichia coli. After 6 hours of drying at 55°C, 2 ml (0.038 ml l-1 air) and 1.5 ml (0.028 ml l-1 air) of OEO were considered the minimal inhibitory concentrations (MICs) against S. enteritidis and E. coli, respectively. Samples treated with 0.75 ml of OEO were more attractive for consumption compared with the control; at a higher concentration of OEO, the sensory quality of the food was affected. Next, the effect of modified blanching treatments on the drying behaviour of beef meat was evaluated by determining moisture ratio versus time curves and the influence on sensory quality of the resulted product. The 3 treatments under investigation were (1) oil treatment (2) steam blanching and (3) hot air blanching with 3 doses of oregano essential oil (1) 1.5 ml (2) 3 ml and (3) 6 ml. Each treatment had an effect on the drying time of the beef samples, however, the dose of oregano essential oil applied did not affect the drying process. The results showed that steam blanching was very effective reducing the drying time. Meanwhile, 1.5 ml and 3 ml hot air blanching samples and 1.5 ml oil treatment samples were judged as better from sensory point of view and the respondents considered that adding oregano essential oil enriched the pleasantness of the smell. In conclusion, a value-added dried meat product obtained by using oregano essential oil to enhance food safety received an acceptable sensorial response from consumers. Additionally, each modified blanching treatment tested influences the drying kinetics process, but the dose of oregano applied did not affect the drying process. In this sense, hot air blanching and oil treatment with the lowest dose had an acceptable sensorial response from consumers.

<p>Two experimentswere  conducted  using  pigs  at different  life stages to  determine  the  effects  of dietary  tryptophan  and  water  delivered  oregano  essential  oil  on growth performance, rectal temperature, water use,intestinal integrity and gene expression of biomarkers in the face heat or transport stress. In the first experiment, 192 grow-finish pigs were used to investigate the effects of  water  supplementation  of  oregano  essential  oil  (OEO)  on  growth  performance,  water  intake, rectal temperature, intestinal integrity, and expression of genetic biomarkers during an acute heat challenge. Pigs were randomly allotted to 2 X 2 factorial arrangement of treatments with pigs being heat  stressed  or  not  and  being  supplemented  with  OEO  or  not with 8  replicate  pens  of  each treatment  with  6  pigs/pen  (4  barrows,  2  gilts  per  pen).  Water  treatments  were administered immediately, with  dosing at  47 μL/L of OEO. One-half  of  the  pigs  on  each  water  treatment remained under thermoneutral conditions (TN; 21.1C), while the other half was subjected to a 3 d diurnal, acute heat stress (HS) with 12 hours at 33.3 oC (7AM-7PM) and 12 hours at 26.7oC (7PM-7AM). Three days post-HS, temperatures were reduced back to TN for the rest of the study, and pigs remained on their water treatments. Rectal temperatures were collected in the morning and evening  of  the  heat  stress  period  on  one  barrow  and  one  gilt  in  each  pen. Jejunal  tissue was collected for subsequent histological examination and determination of gene expression. All data were  analyzed  using  the  GLM  procedure  of  SAS  (ver.  9.4).  Pigs  subjected  to  heat  stress  had reduced ADG (P < 0.003) and G:F (P < 0.008) during the 3d heat stress compared to pigs reared under thermoneutral conditions. However, post-heatstress, heat stressed pigs had compensatory gain resulting in increased ADG (P < 0.001) and G:F (P < 0.001) compared to thermoneutral reared pigs.   Overall,  there  was an  interaction  (P  <  0.006)  observed  between  water  and  heat  treatment with  OEO  increasing  ADG  in  thermoneutral  pigs  but  not  in  heat  stressed  pigs.  Similarly, interactions  between  water  and  heat  treatment  were  observed  for  ADFI  during  heat  stress  (P  < 0.004),  post  heat  stress  (P  <  0.01),  and  overall  (P  <  0.004)  from  increasing  OEO  intake  in thermoneutral pigs but not in heat stressed pigs. Rectal temperatures were higher (P < 0.001) for heat stressed pigs at the end of d 1 and 2 of the acute heat challenge compared to TN housed pigs. Pigs exposed to HS also used more water than pigs housed in a thermoneutral environment (P < 0.002). There were no differences between villi height, crypt depth or VH:CD between treatment groups  (P  >0.05).  There  was  also  no  difference  in  TP53  and  CDKNA1  gene  expression  among treatments (P > 0.10). In the second experiment, 36 barrows were used in an 18d experiment to investigate the effects of pre-weaning tryptophan supplementation on performance and intestinal integrity following  weaning  with  or  without  transport  stress  at  weaning.  Pigs  were  randomly allotted to 2 X 2 factorial arrangement of treatments of pre-weaning tryptophan supplementation or not and weaning transport or not. Pigs on the tryptophan treatment received 0.35, 0.45, and 0.55 g Trp/d in 5 day intervals, beginning 15 d prior to weaning.Tryptophan was dissolved in chocolate milk and administered by oral gavage with control pigs receiving milk only. At weaning, 4 pigs from each pre-weaning treatmentwere euthanized for collection of jejunal tissue.  Of the remaining pigs, half the pigs oneach treatment were transported for 12 h, and half were moved into individual pens  with  no  transport.  Following  transport,  all  pigs  were  individually  housed  and  provided  ad libitum  access  towater  andfeed  from  a  common  diet.  On  d  3  post-weaning,  all  pigswere euthanized for collection of jejunal tissue. Jejunal tissue was used for histological examination and for determination of gene expression. All data were analyzed using the GLM procedure of SAS (9.4).  No  effects  of  Trp  supplementation  were  observed  on  pre-weaning  (P  >  0.10)  growth. Pig BW and ADFI were unaffected (P > 0.10) by Trp supplementation and transport at weaning. Post-weaning, there was a tendency (P < 0.06) for an effect of transport on ADG as transported pigs lost weight in the 3 d post-weaning period while non-transported pigs gained slightly. Gain:Feed post-weaning  was  lower  (P  <  0.04)  for  transported  pigs  compared  to  non-transported  pigs.  No differences  were  observed  for villus base  and  mid  width,  villus  height,  crypt  depth  or  villus height:crypt   depth.   There   was   a   tendency   for   an   interaction   of   transportation   and   Trp supplementation  (P  <  0.06)  on  villi  base  width  driven  by  an  increased  villus  width  in  non-transported pigs given supplemental Trp but a decrease in villus width in transported pigs given supplemental Trp.These results conclude that these alleviating agents had minimal effects when pigs  were  stressed, however TN grow-finish pigs  benefitted  from  OEO  water  supplementation among growth performance.</p>

Este trabalho de Mestrado teve por objetivo avaliar a atividade antifúngica in vitro e em queijo Minas Padrão de duas formulações (A e B) de nanoemulsões encapsulando óleo essencial de orégano (Origanum vulgare) produzidas pelo método da temperatura de inversão de fases (método PIT). Cladosporium sp., Fusarium sp. e Penicillium sp. foram os fungos identificados nas amostras de queijo Minas Padrão deteriorados. Tais cepas foram utilizadas na avaliação da atividade antifúngica in vitro e em queijo Minas Padrão do óleo de orégano nanoemulsionado. Nos testes in vitro foram determinadas as concentrações mínimas inibitórias (CMI) do óleo essencial de orégano puro e nanoemulsionado sobre o Cladosporium sp., Fusarium sp. e Penicillium sp. Foram utilizadas fatias de queijo Minas Padrão para avaliar o efeito inibitório das nanoemulsões contendo óleo essencial de orégano. Por último foi avaliado o efeito inibitório das nanoemulsões durante o processo de maturação de queijos Minas Padrão. Determinaram-se valores de CMI para óleo essencial puro de 0,2; 0,3 µg/ml para Fusarium sp. e Penicillium sp., respectivamente. Enquanto para as duas formulações de nanoemulsão; os valores de CMI dependeram da quantidade de óleo essencial de orégano que estava contido nelas, obtendo-se valores de 0,26; 0,11 e 1,62 µg/ml para a formulação A de óleo de orégano nanoemulsionado sobre Cladosporium sp., Fusarium sp. e Penicillium sp., respectivamente, e CMIs de 0,32; 0,1 e 0,8 µg/ml para a formulação B de nanoemulsão sobre os mesmos gêneros de fungos. Os ensaios nas fatias de queijo evidenciaram que o efeito das CMIs, quando aplicadas na matriz alimentícia, foi nulo, permitindo o desenvolvimento normal dos fungos avaliados, da mesma forma se determinou a importância da atividade de água no crescimento fúngico. Já nos queijos em ambiente de maturação o efeito inibitório do óleo de orégano foi pouco satisfatório, o que indicou a importância do controle dos demais parâmetros ambientais no ambiente de maturação. Pode-se concluir que o óleo essencial de orégano nanoemulsionado apresentou efeito inibitório contra os gêneros de fungos avaliados. Quando controlados parâmetros ambientais como temperatura de armazenamento e atividade de água, seu efeito inibitório pode ser amplamente melhorado, apresentando-o como potencial alternativa na conservação dos alimentos. / This Master Thesis aimed to evaluate the in vitro antifungal activity and in Minas Padrão cheese of two formulations (A and B) of nanoemulsions encapsulating essential oil of oregano (Origanum vulgare) produced by the method of phase inversion temperature (PIT method). Cladosporium sp., Fusarium sp. and Penicillium sp. fungi were identified in deteriorated cheese samples. These strains were used in the evaluation of antifungal activity of oregano essential oil nanoemulsions, both in vitro and in cheese. Minimum inhibitory concentrations (MIC) of essential oil of pure oregano oil and nanoemulsions were determined. Cheese slices were used to evaluate the inhibitory effect of nanoemulsions containing essential oil of oregano. Finally the inhibitory effect of encapsulated oregano oil was tested during cheese ripening. MIC values determined for pure essential oil were 0.20 and 0.3 µg/ml for Fusarium sp. and Penicillium sp., respectively. As for the two nanoemulsion formulations, MIC values depended on the amount of essential oil of oregano which was contained therein, and the values for formulation A were 0.26, 0.11 and 1.62 µg/ml for Cladosporium sp., Fusarium sp. and Penicillium sp, respectively. For formulation B, the values of MIC were 0.32, 0.10 and 0.80 µg/ml. The tests on the cheese slices showed that the effect of MIC when applied in the food matrix was null, as the fungi growth was not avoided. As for the tests during cheese ripening, the inhibitory effect of oregano oil in nanoemulsions was unsatisfactory, which indicated the importance of controlling other environmental parameters in the maturation chamber. It can be concluded that the nanoemulsions of essential oil presented inhibitory effect against the genera of fungi evaluated. Controlled environmental parameters such as storage temperature and water activity, its inhibitory effect can be highly improved, and the nanoemulsions of oregano oil can be seen as a potential system for food preservation.

Este trabalho de Mestrado teve por objetivo avaliar a atividade antifúngica in vitro e em queijo Minas Padrão de duas formulações (A e B) de nanoemulsões encapsulando óleo essencial de orégano (Origanum vulgare) produzidas pelo método da temperatura de inversão de fases (método PIT). Cladosporium sp., Fusarium sp. e Penicillium sp. foram os fungos identificados nas amostras de queijo Minas Padrão deteriorados. Tais cepas foram utilizadas na avaliação da atividade antifúngica in vitro e em queijo Minas Padrão do óleo de orégano nanoemulsionado. Nos testes in vitro foram determinadas as concentrações mínimas inibitórias (CMI) do óleo essencial de orégano puro e nanoemulsionado sobre o Cladosporium sp., Fusarium sp. e Penicillium sp. Foram utilizadas fatias de queijo Minas Padrão para avaliar o efeito inibitório das nanoemulsões contendo óleo essencial de orégano. Por último foi avaliado o efeito inibitório das nanoemulsões durante o processo de maturação de queijos Minas Padrão. Determinaram-se valores de CMI para óleo essencial puro de 0,2; 0,3 µg/ml para Fusarium sp. e Penicillium sp., respectivamente. Enquanto para as duas formulações de nanoemulsão; os valores de CMI dependeram da quantidade de óleo essencial de orégano que estava contido nelas, obtendo-se valores de 0,26; 0,11 e 1,62 µg/ml para a formulação A de óleo de orégano nanoemulsionado sobre Cladosporium sp., Fusarium sp. e Penicillium sp., respectivamente, e CMIs de 0,32; 0,1 e 0,8 µg/ml para a formulação B de nanoemulsão sobre os mesmos gêneros de fungos. Os ensaios nas fatias de queijo evidenciaram que o efeito das CMIs, quando aplicadas na matriz alimentícia, foi nulo, permitindo o desenvolvimento normal dos fungos avaliados, da mesma forma se determinou a importância da atividade de água no crescimento fúngico. Já nos queijos em ambiente de maturação o efeito inibitório do óleo de orégano foi pouco satisfatório, o que indicou a importância do controle dos demais parâmetros ambientais no ambiente de maturação. Pode-se concluir que o óleo essencial de orégano nanoemulsionado apresentou efeito inibitório contra os gêneros de fungos avaliados. Quando controlados parâmetros ambientais como temperatura de armazenamento e atividade de água, seu efeito inibitório pode ser amplamente melhorado, apresentando-o como potencial alternativa na conservação dos alimentos. / This Master Thesis aimed to evaluate the in vitro antifungal activity and in Minas Padrão cheese of two formulations (A and B) of nanoemulsions encapsulating essential oil of oregano (Origanum vulgare) produced by the method of phase inversion temperature (PIT method). Cladosporium sp., Fusarium sp. and Penicillium sp. fungi were identified in deteriorated cheese samples. These strains were used in the evaluation of antifungal activity of oregano essential oil nanoemulsions, both in vitro and in cheese. Minimum inhibitory concentrations (MIC) of essential oil of pure oregano oil and nanoemulsions were determined. Cheese slices were used to evaluate the inhibitory effect of nanoemulsions containing essential oil of oregano. Finally the inhibitory effect of encapsulated oregano oil was tested during cheese ripening. MIC values determined for pure essential oil were 0.20 and 0.3 µg/ml for Fusarium sp. and Penicillium sp., respectively. As for the two nanoemulsion formulations, MIC values depended on the amount of essential oil of oregano which was contained therein, and the values for formulation A were 0.26, 0.11 and 1.62 µg/ml for Cladosporium sp., Fusarium sp. and Penicillium sp, respectively. For formulation B, the values of MIC were 0.32, 0.10 and 0.80 µg/ml. The tests on the cheese slices showed that the effect of MIC when applied in the food matrix was null, as the fungi growth was not avoided. As for the tests during cheese ripening, the inhibitory effect of oregano oil in nanoemulsions was unsatisfactory, which indicated the importance of controlling other environmental parameters in the maturation chamber. It can be concluded that the nanoemulsions of essential oil presented inhibitory effect against the genera of fungi evaluated. Controlled environmental parameters such as storage temperature and water activity, its inhibitory effect can be highly improved, and the nanoemulsions of oregano oil can be seen as a potential system for food preservation.

Listeria monocytogenes é conhecida como um importante patógeno causador de doenças transmitidas por alimentos na última década. Apesar do número de casos por ano ser relativamente baixo, a infecção pode ser grave, com mortalidades acima de 30%. Pesquisas realizadas no Brasil relataram uma incidência de 32% em amostras de produtos cárneos, e o microrganismo foi encontrado em 80% das amostras lingüiças frescal de carne suína. Apesar dos recentes avanços nas tecnologias de controle de patógenos em alimentos, os consumidores têm procurado alimentos \"naturais\", isto é, submetidos a tratamentos menos agressivos e isentos de conservadores químicos. Antimicrobianos naturais são uma opção interessante, mas sua aplicação requer uma melhor compreensão de sua funcionalidade nos alimentos. Os óleos essenciais e seus compostos fenólicos estão se tornando agentes antimicrobianos naturais bastante populares, assim como a nisina, uma bacteriocina produzida por Lactococcus lactis subsp. lactis. Esta pesquisa foi desenvolvida para avaliar o efeito de óleo essencial de orégano (O.E.O.) e de nisina, individualmente ou em combinação, na inibição da multiplicação de Listeria monocytogenes Scott A in vitro (meio de cultura) e in situ -(lingüiça frescal suína). A atividade inibitória foi testada pela metodologia de difusão em poços, e os halos de inibição foram medidos 24 horas após a incubação à 37ºC. Foram testadas as concentrações 0,05%, 0,1%, 0,2%, 0,3%, 0,4% e 0,5% (v/v) de O.E.O. e 0, 100, 200, 400, 600, 800, 1000, 1200, 1400, 1600, 1800 e 2000 ppm de nisina. Quando o óleo essencial foi usado em combinação com a nisina foi observado um efeito sinérgico na inibição de L. monocytogenes. As concentrações que apresentaram o maior efeito contra o patógeno nos testes in vitro, ou seja 0,5% (v/v) O.E.O. com 200 ppm de nisina, foram utilizadas nos experimentos com três formulações diferentes lingüiça frescal, contendo pernil de porco, sal (2%), nitrito (0,015%), condimentos, emulsificantes e antioxidantes, experimentalmente contaminadas com L. monocytogenes Scott A (106 UFC/g). A multiplicação do patógeno foi monitorada no produto refrigerado a 5oC por até 10 dias, através da contagem em placas. Controles sem antimicrobianos também foram estudados. Os resultados indicaram que o O.E.O., usado isoladamente, não conferiu proteção ao alimento. A nisina causou uma redução de 2 log imediatamente após o contato com o microrganismo, mas durante o armazenamento, as células sobreviventes apresentaram a mesma taxa de multiplicação que na lingüiça controle (??0,05), mantendo as contagens 2 log inferiores as do controle por até 9 dias. Quando os dois antimicrobianos foram usados em combinação, a redução imediata após o contato foi de 4 log, e, quando comparado ao controle, a taxa de multiplicação durante o armazenamento a 5oC foi significativamente mais altas que no controle (??0,05). Entretanto, as amostras de lingüiça contendo esses antimicrobianos nas concentrações testadas não foram aprovadas nos testes sensoriais de aceitação (??0,05). Esses resultados indicam que a combinação desses antimicrobianos pode ser utilizada como uma barreira adicional para a multiplicação de L.monocytogenes em lingüiça frescal suína, mas os atributos sensoriais que conferem ao produto podem limitar sua aplicação. / Listeria monocytogenes has been recognized as an important foodborne pathogen for the past decade. Although the number of cases per annum is relatively low, the infections can be acute, with mortality up to 30%. In Brazil, some works reported that 32% of dairy meat products were contaminated with L. monocytogenes, and this organism was found in 80% of fresh pork sausage. In spite of modern improvements in food production techniques, the consumers are seeking for \"natural\" food products, i.e., not submitted to aggressive treatments or added of chemical preservatives. Natural antimicrobials are a promising option, but their application requires a better understanding of their functionality in foods. Naturally occurring antimicrobial agents, such as essential oils and their phenolic components, are becoming increasingly popular as preservation agents. Other compound with increased application in foods is nisin, a bacteriocin produced by Lactococcus lactis subsp. lactis. This study aimed to evaluate the antimicrobial effect of oregano essential oil (O.E.O.) and nisin, individually or in combination, on the inhibition of growth of Listeria monocytogenes Scott A in vitro (agar culture medium) and in situ (fresh pork sausage). The inhibitory activity was tested by the well diffusion method, measuring the inhibition halos after 24hours incubation at 37ºC. The concentrations tested were 0.05%, 0.1%, 0.2%, 0.3%, 0.4%, 0.5% (v/v) for OEO and 0, 100, 200, 400, 600, 800, 1000, 1200, 1400, 1600, 1800 and 2000 ppm for nisin. When the essential oil was used in combination with nisin, a synergistic effect was observed for L. monocytogenes, i.e., the oil enhanced the activity of the bacteriocin. The combination 0.5% (v/v) O.E.O. with 200 ppm nisin presented the best results and was used to test the functionality in fresh pork sausage prepared with three different formulations, containing deboned minced pork meat, 2% salt and 0.015% nitrite, plus spices, emulsifier and antioxidant, and experimentally contaminated with L. monocytogenes Scott A (106 CFU/g). The growth of the pathogen was monitored in the refrigerated product (5oC) up to 10 days, by means of plate counting. Controls without antimicrobials were included in the experiments. Results indicated that O.E.O., used alone, was not effective. Nisin alone caused a 2-log reduction immediately after contact, but during storage the surviving cells presented the same multiplication rate as in the control (? ? 0.5), keeping the counts 2 log lower up to 9 days. When used in combination, the two antimicrobials caused a 4-log count reduction immediately after addition and, when compared to the control, the multiplication rate of the surviving cells during storage under refrigeration up to 10 days was significantly higher (? ? 0.5). However, samples containing these antimicrobials in the tested concentrations failed the sensorial acceptance tests (? ? 0.5). These results indicate that the combination of these antimicrobials can be an additional hurdle for the control of L. monocytogenes in fresh pork sausages, but the final sensorial attributes of the product may hamper their application.

Listeria monocytogenes é conhecida como um importante patógeno causador de doenças transmitidas por alimentos na última década. Apesar do número de casos por ano ser relativamente baixo, a infecção pode ser grave, com mortalidades acima de 30%. Pesquisas realizadas no Brasil relataram uma incidência de 32% em amostras de produtos cárneos, e o microrganismo foi encontrado em 80% das amostras lingüiças frescal de carne suína. Apesar dos recentes avanços nas tecnologias de controle de patógenos em alimentos, os consumidores têm procurado alimentos \"naturais\", isto é, submetidos a tratamentos menos agressivos e isentos de conservadores químicos. Antimicrobianos naturais são uma opção interessante, mas sua aplicação requer uma melhor compreensão de sua funcionalidade nos alimentos. Os óleos essenciais e seus compostos fenólicos estão se tornando agentes antimicrobianos naturais bastante populares, assim como a nisina, uma bacteriocina produzida por Lactococcus lactis subsp. lactis. Esta pesquisa foi desenvolvida para avaliar o efeito de óleo essencial de orégano (O.E.O.) e de nisina, individualmente ou em combinação, na inibição da multiplicação de Listeria monocytogenes Scott A in vitro (meio de cultura) e in situ -(lingüiça frescal suína). A atividade inibitória foi testada pela metodologia de difusão em poços, e os halos de inibição foram medidos 24 horas após a incubação à 37ºC. Foram testadas as concentrações 0,05%, 0,1%, 0,2%, 0,3%, 0,4% e 0,5% (v/v) de O.E.O. e 0, 100, 200, 400, 600, 800, 1000, 1200, 1400, 1600, 1800 e 2000 ppm de nisina. Quando o óleo essencial foi usado em combinação com a nisina foi observado um efeito sinérgico na inibição de L. monocytogenes. As concentrações que apresentaram o maior efeito contra o patógeno nos testes in vitro, ou seja 0,5% (v/v) O.E.O. com 200 ppm de nisina, foram utilizadas nos experimentos com três formulações diferentes lingüiça frescal, contendo pernil de porco, sal (2%), nitrito (0,015%), condimentos, emulsificantes e antioxidantes, experimentalmente contaminadas com L. monocytogenes Scott A (106 UFC/g). A multiplicação do patógeno foi monitorada no produto refrigerado a 5oC por até 10 dias, através da contagem em placas. Controles sem antimicrobianos também foram estudados. Os resultados indicaram que o O.E.O., usado isoladamente, não conferiu proteção ao alimento. A nisina causou uma redução de 2 log imediatamente após o contato com o microrganismo, mas durante o armazenamento, as células sobreviventes apresentaram a mesma taxa de multiplicação que na lingüiça controle (??0,05), mantendo as contagens 2 log inferiores as do controle por até 9 dias. Quando os dois antimicrobianos foram usados em combinação, a redução imediata após o contato foi de 4 log, e, quando comparado ao controle, a taxa de multiplicação durante o armazenamento a 5oC foi significativamente mais altas que no controle (??0,05). Entretanto, as amostras de lingüiça contendo esses antimicrobianos nas concentrações testadas não foram aprovadas nos testes sensoriais de aceitação (??0,05). Esses resultados indicam que a combinação desses antimicrobianos pode ser utilizada como uma barreira adicional para a multiplicação de L.monocytogenes em lingüiça frescal suína, mas os atributos sensoriais que conferem ao produto podem limitar sua aplicação. / Listeria monocytogenes has been recognized as an important foodborne pathogen for the past decade. Although the number of cases per annum is relatively low, the infections can be acute, with mortality up to 30%. In Brazil, some works reported that 32% of dairy meat products were contaminated with L. monocytogenes, and this organism was found in 80% of fresh pork sausage. In spite of modern improvements in food production techniques, the consumers are seeking for \"natural\" food products, i.e., not submitted to aggressive treatments or added of chemical preservatives. Natural antimicrobials are a promising option, but their application requires a better understanding of their functionality in foods. Naturally occurring antimicrobial agents, such as essential oils and their phenolic components, are becoming increasingly popular as preservation agents. Other compound with increased application in foods is nisin, a bacteriocin produced by Lactococcus lactis subsp. lactis. This study aimed to evaluate the antimicrobial effect of oregano essential oil (O.E.O.) and nisin, individually or in combination, on the inhibition of growth of Listeria monocytogenes Scott A in vitro (agar culture medium) and in situ (fresh pork sausage). The inhibitory activity was tested by the well diffusion method, measuring the inhibition halos after 24hours incubation at 37ºC. The concentrations tested were 0.05%, 0.1%, 0.2%, 0.3%, 0.4%, 0.5% (v/v) for OEO and 0, 100, 200, 400, 600, 800, 1000, 1200, 1400, 1600, 1800 and 2000 ppm for nisin. When the essential oil was used in combination with nisin, a synergistic effect was observed for L. monocytogenes, i.e., the oil enhanced the activity of the bacteriocin. The combination 0.5% (v/v) O.E.O. with 200 ppm nisin presented the best results and was used to test the functionality in fresh pork sausage prepared with three different formulations, containing deboned minced pork meat, 2% salt and 0.015% nitrite, plus spices, emulsifier and antioxidant, and experimentally contaminated with L. monocytogenes Scott A (106 CFU/g). The growth of the pathogen was monitored in the refrigerated product (5oC) up to 10 days, by means of plate counting. Controls without antimicrobials were included in the experiments. Results indicated that O.E.O., used alone, was not effective. Nisin alone caused a 2-log reduction immediately after contact, but during storage the surviving cells presented the same multiplication rate as in the control (? ? 0.5), keeping the counts 2 log lower up to 9 days. When used in combination, the two antimicrobials caused a 4-log count reduction immediately after addition and, when compared to the control, the multiplication rate of the surviving cells during storage under refrigeration up to 10 days was significantly higher (? ? 0.5). However, samples containing these antimicrobials in the tested concentrations failed the sensorial acceptance tests (? ? 0.5). These results indicate that the combination of these antimicrobials can be an additional hurdle for the control of L. monocytogenes in fresh pork sausages, but the final sensorial attributes of the product may hamper their application.