ABSTRACT
Different chilling treatments are used before meat storage. The effect of spray chilling (SC) on meat quality appears to vary. Here, we investigated the effects of SC on beef carcass weight loss and meat quality during subsequent storage. The 2-h SC program tested involved 180-s initial spraying, followed by 60-s spray cycles at 540-s intervals. Deboned chuck tender (IMPS 116B) beef cuts were vacuum-packaged and stored for up to 60 d. Purge and cooking losses, Warner-Bratzler shear force, meat colour [CIE L*, a*, b*], and microbiological quality were evaluated. SC reduced carcass weight loss (P<0.001) compared with conventional chilling. However, storage time affected the purge and cooking losses, and Warner-Bratzler shear force. CIE a* and b* values increased (P<0.05) after 30-d aging in both chilling treatments. Pronounced psychrotrophic growth was observed during storage after both treatments. In conclusion, SC can be used to reduce the economic losses associated with meat chilling, without affecting meat quality attributes.
Diferentes tratamentos de resfriamento são utilizados antes da estocagem das carnes. O efeito da aspersão de carcaças (SC) na qualidade da carne parece variar. Neste estudo, investigou-se os efeitos da aspersão de carcaças bovinas na perda de peso e na qualidade da carne durante subsequente estocagem. O programa de aspersão testado foi de um tempo total de 2 h, com uma aspersão inicial de 180 s, seguida por ciclos de aspersão de 60 s em intervalos de 540 s. Os cortes comerciais desossados "Peixinho" (IMPS 116B) foram embalados a vácuo e estocados por até 60 dias. Foram avaliadas as perdas por exsudação e cozimento, força de cisalhamento por Warner-Bratzler, cor da carne (CIE L*, a*, b*) e qualidade microbiológica. SC reduziu a perda de peso da carcaça (P < 0,001) em comparação com o resfriamento convencional. No entanto, o tempo de estocagem influenciou a perda por exsudação, por cozimento e força de cisalhamento. Os valores de CIE a* e b* aumentaram (P < 0,05) após 30 dias de maturação em ambos os tratamentos de resfriamento. O crescimento pronunciado de psicrotróficos foi observado durante a estocagem em ambos os tratamentos. Em conclusão, o SC pode ser usado para reduzir as perdas econômicas associadas ao resfriamento da carne, sem afetar os atributos de qualidade da carne.
Subject(s)
Animals , Cattle , Chemical Phenomena , Red Meat/microbiology , Frozen Foods/microbiology , Identity and Quality Standard for Products and ServicesABSTRACT
INTRODUCTION: Plasmid-mediated resistance to ß-lactam and fluoroquinolone antibiotics was investigated in Enterobacteriaceae isolated from retailed frozen chickens from Brazil, South Africa and Mozambique. METHODOLOGY: Carcass swabs and the liquid thaw of 33 chickens from each of the three countries constituted the total sample size of 198. Isolates were identified by biochemical tests, antibiotic susceptibility was ascertained by the disc diffusion assay and ß-lactamases were detected using the double-disk synergy test. PCR was used to detect the presence of blaCTX-M, blaSHV, blaTEM, blaCMY, blaMOX, blaFOX, blaDHA, qnrB, qnrD, qnrS and qepA genes. A random selection of CTX-M genes was sequenced. RESULTS: The 198 samples yielded 27 (13.6%) putative extended-spectrum ß-lactamase (ESBL)-positive isolates, 15 from carcass swabs and 12 from the liquid thaw from 22 chickens with 19, 5 and 3 isolates from South African, Mozambican and Brazilian chicken, respectively. Isolates exhibited the following resistance: ampicillin 100%, ceftriaxone 89%, trimethoprim-sulfamethoxazole 78%, cefotaxime 74%, ciprofloxacin 70%, ceftazidime 67%, cefoxitin 22% and gentamicin 8%. The predominant putative ESBL gene was blaSHV (85%), followed by blaCTX-M (62.9%) and blaTEM (44.4%) whilst blaMOX and blaDHA were the most common pAmpC genes at 33.3%. The predominant plasmid-mediated fluoroquinolone-resistance gene was qepA (22.2%). DNA sequencing identified blaCTX-M-55/-79/-101/-164. ERIC-PCR profiles did not show strong evidence of clonality. CONCLUSION: The Mozambican population is exposed to a reservoir of plasmid-mediated, and hence mobile ß-lactam and quinolone resistance genes via imported, and to a lesser extent, locally produced poultry. This presents a food safety concern.
Subject(s)
Anti-Bacterial Agents/pharmacology , Enterobacteriaceae/drug effects , Fluoroquinolones/pharmacology , Poultry/microbiology , beta-Lactams/pharmacology , Animals , Brazil , Chickens/microbiology , Communicable Diseases, Imported/microbiology , Drug Resistance, Multiple, Bacterial , Enterobacteriaceae/enzymology , Food Safety , Frozen Foods/microbiology , Mozambique , Plasmids/genetics , South Africa , beta-Lactamases/geneticsABSTRACT
Falhas nas etapas do processamento do açaí afetam a qualidade da polpa. Desta forma, objetivou-se analisar a qualidade microscópica e microbiológica de polpas de açaí congeladas, comercializadas em supermercados de Teresina-PI. As amostras de açaí foram adquiridas em cincos supermercados e em seguidas foram submetidas às análises de sujidades e microbiológicas (Coliformes e Salmonella spp.). Os resultados microbiológicos indicaram que houve ausência de coliformes termotolerantes e Salmonella ssp. nas polpas de açaí analisadas. Todas as polpas analisadas apresentaram matérias estranhas tais como, fragmentos de insetos, pelo animal, filamentos de fungos, fibra sintética, fragmentos de caroço e casca e adulteração por adição de amido. Portanto, as polpas de açaí congeladas necessitam de atenção pelos órgãos fiscalizadores.
Subject(s)
Frozen Foods/microbiology , Food Contamination/analysis , Food Contamination/legislation & jurisprudence , Euterpe/microbiology , Fruit/microbiologyABSTRACT
Falhas nas etapas do processamento do açaí afetam a qualidade da polpa. Desta forma, objetivou-se analisar a qualidade microscópica e microbiológica de polpas de açaí congeladas, comercializadas em supermercados de Teresina-PI. As amostras de açaí foram adquiridas em cincos supermercados e em seguidas foram submetidas às análises de sujidades e microbiológicas (Coliformes e Salmonella spp.). Os resultados microbiológicos indicaram que houve ausência de coliformes termotolerantes e Salmonella ssp. nas polpas de açaí analisadas. Todas as polpas analisadas apresentaram matérias estranhas tais como, fragmentos de insetos, pelo animal, filamentos de fungos, fibra sintética, fragmentos de caroço e casca e adulteração por adição de amido. Portanto, as polpas de açaí congeladas necessitam de atenção pelos órgãos fiscalizadores.(AU)
Subject(s)
Euterpe/microbiology , Food Contamination/analysis , Frozen Foods/microbiology , Food Contamination/legislation & jurisprudence , Fruit/microbiologyABSTRACT
O hambúrguer é um produto industrializado de origem animal, extremamente utilizado pela população principalmente pela sua praticidade no consumo. Esse trabalho teve como objetivo realizar a análise microbiológica de hambúrgueres congelados comercializados em Maceió-AL. Foram selecionadas nove marcas comerciais de hambúrgueres dos tipos: bovino, frango e misto (bovino e frango), foram pesquisados os seguintes micro-organismos: bactérias do grupo coliformes, Estafilococos coagulase positiva e Salmonella sp. As amostras das marcas comerciais B (misto), E (frango), F (misto), H (bovino) apresentaram contaminação por coliformes a 35 ºC e 45 ºC, porém dentro dos padrões da legislação brasileira. Para inibir o crescimento de micro-organismos nos alimentos cárneos é necessário manter a temperatura de armazenamento e distribuição a -18 °C, além da conservação destes em equipamentos adequadamente higienizados, de forma a garantir a qualidade sanitária do produto. De acordo com os resultados encontrados, todos os hambúrgueres congelados industrializados avaliados estavam aptos para consumo.
The burger is a product of animal origin used by the population, highly industrialized mainly for your convenience in consumption. This work aimed to carry out microbiological analysis of frozen hamburgers marketed in enniskillen has been selected nine trademarks of burgers: beef, chicken and mixed (beef and chicken), were searched the following microorganisms: bacteria of the coliform group, coagulase positive and salmonella sp. In trademarks b (mixed), and(chicken), f (mixed), h (veal) samples obtained coliform contamination to 35° c and 45° c, but within the brazilian legislation standards. To inhibit the growth of microorganisms in meat food is necessary to maintain the temperature of storage and distribution, in-18° c, in addition to the conservation of these properly sanitized equipment, to ensure the sanitary quality of the product. According to the results all the frozen processed burgers were able for consumption.
Subject(s)
Animals , Cattle , Food Contamination/analysis , Colimetry/methods , Meat/microbiology , Salmonella/pathogenicity , Prospective Studies , Industrialized Foods , Food Storage/standards , Food Preservation/standards , Frozen Foods/microbiologyABSTRACT
The major contamination sources, biofilm-forming ability and biocide resistance of Staphylococcus aureus in tilapia-processing plants were evaluated. Twenty-five processing control points were analysed twice in two factories, including whole tilapias, frozen fillets, water and food-contact surfaces. No final product was contaminated with S. aureus. However, high concentrations of S. aureus carrying enterotoxin ( se) genes were found in several processing points of both factories due to the application of inadequate hygienic and handling procedures, which generate a high risk of cross-contamination of the tilapia fillets with staphylococcal enterotoxins. Nine S. aureus strains were characterized by RAPD-PCR using primers AP-7, ERIC-2 and S. A wide diversity of se gene profiles was detected, most strains being multi- se-carriers. All S. aureus strains showed high biofilm-forming ability on stainless steel and polystyrene. Biofilm-forming ability was correlated with the presence of fliC H7 and the type of origin surface (metallic or plastic). A marked resistance of S. aureus to peracetic acid and sodium hypochlorite was also observed, required doses being higher than those recommended by manufacturers to be eradicated. Case-by-case approaches are thus recommended to determine the sources and degree of contamination present in each factory, which would allow applying precise responses that avoid, or at least reduce, the presence of bacterial pathogens and the emergence of antimicrobial resistance.
Subject(s)
Biofilms/growth & development , Food Contamination/prevention & control , Food-Processing Industry/instrumentation , Frozen Foods , Seafood , Staphylococcus aureus/physiology , Tilapia , Animals , Aquaculture , Bacterial Load , Biofilms/drug effects , Brazil , Disinfectants/pharmacology , Drug Resistance, Multiple, Bacterial , Enterotoxins/genetics , Enterotoxins/isolation & purification , Enterotoxins/metabolism , Flagellin/genetics , Flagellin/isolation & purification , Flagellin/metabolism , Frozen Foods/microbiology , Microbial Sensitivity Tests , Molecular Typing , Peracetic Acid/pharmacology , Polystyrenes , Seafood/microbiology , Sodium Hypochlorite/pharmacology , Stainless Steel , Staphylococcus aureus/classification , Staphylococcus aureus/drug effects , Staphylococcus aureus/isolation & purification , Tilapia/growth & development , Tilapia/microbiology , Water MicrobiologyABSTRACT
ABSTRACT The aim of this work was to study the prevalence of Listeria monocytogenes in foods obtained in retail shops and food industries located in Montevideo-Uruguay, and to identify the serogroups of the obtained isolates. Three-thousand one-hundred and seventy-five food samples (frozen, deli meats, ready-to-eat and cheese) were analyzed. The obtained isolates were serogrouped by multiplex PCR and serotyped by conventional procedure. Genetic comparisons were performed using pulsed-field gel electrophoresis on a sub-set of isolates belonging to the same serotype successively recovered from the same establishment. L. monocytogenes was isolated from 11.2% of samples. The highest prevalence was observed in frozen foods (38%), followed by cheese (10%). 1/2b and 4b were the most frequently identified serotypes. In six of 236 analyzed establishments we successively recovered L. monocytogenes isolates belonging to the same serotype. Most of them corresponded to serotype 1/2b. Pulsed-field gel electrophoresis profiles suggest that at least 33% of L. monocytogenes 1/2b isolates are genetically related and that may remain viable for prolonged periods. The observed prevalence of L. monocytogenes was lower than reported in neighboring countries. Our findings highlight the role that frozen foods may play in the spread of this pathogen, and the relevance of serotypes 1/2b and 4b.
Subject(s)
Animals , Cheese/microbiology , Fast Foods/microbiology , Frozen Foods/microbiology , Listeria monocytogenes/isolation & purification , Meat/microbiology , Food Contamination/analysis , Food Contamination/statistics & numerical data , Food Microbiology , Listeria monocytogenes/classification , Listeria monocytogenes/genetics , Prevalence , Serogroup , UruguayABSTRACT
The aim of this work was to study the prevalence of Listeria monocytogenes in foods obtained in retail shops and food industries located in Montevideo-Uruguay, and to identify the serogroups of the obtained isolates. Three-thousand one-hundred and seventy-five food samples (frozen, deli meats, ready-to-eat and cheese) were analyzed. The obtained isolates were serogrouped by multiplex PCR and serotyped by conventional procedure. Genetic comparisons were performed using pulsed-field gel electrophoresis on a sub-set of isolates belonging to the same serotype successively recovered from the same establishment. L. monocytogenes was isolated from 11.2% of samples. The highest prevalence was observed in frozen foods (38%), followed by cheese (10%). 1/2b and 4b were the most frequently identified serotypes. In six of 236 analyzed establishments we successively recovered L. monocytogenes isolates belonging to the same serotype. Most of them corresponded to serotype 1/2b. Pulsed-field gel electrophoresis profiles suggest that at least 33% of L. monocytogenes 1/2b isolates are genetically related and that may remain viable for prolonged periods. The observed prevalence of L. monocytogenes was lower than reported in neighboring countries. Our findings highlight the role that frozen foods may play in the spread of this pathogen, and the relevance of serotypes 1/2b and 4b.
Subject(s)
Cheese/microbiology , Fast Foods/microbiology , Frozen Foods/microbiology , Listeria monocytogenes/isolation & purification , Meat/microbiology , Animals , Food Contamination/analysis , Food Contamination/statistics & numerical data , Food Microbiology , Listeria monocytogenes/classification , Listeria monocytogenes/genetics , Prevalence , Serogroup , UruguayABSTRACT
Espécies de Campylobacter spp. termotolerantes são agentes de surtos de campilobacteriose em humanos e os produtos de origem avícola são considerados uma importante fonte de infecção. Foram identificados Campylobacter jejuni e Campylobacter coli em carcaças de frango resfriadas e congeladas coletadas em três abatedouros entre 2014 e 2015. A detecção de Campylobacter spp. foi realizada por microbiologia convencional e a identificação de C. jejuni e C. coli por multiplex-PCR. Dentre as amostras avaliadas verificou-se Campylobacter spp. termotolerante em 63,8%, sendo 72,2% em carcaças resfriadas e 55,5% em carcaças congeladas. Destas, 83,3% foram positivas para C. jejuni e 66,6% para C. coli, enquanto 50% foram positivas para ambas as espécies. A presença de Campylobacter spp. termotolerante em carcaças de frangos de corte prontas para consumo representa uma importante fonte de transmissão destes patógenos para humanos.
Species of thermophilic Campylobacter spp. are agents of campylobacteriosis outbreaks in humans, and poultry products are implicated as major sources of infection. The detection of Campylobacter spp. was performed by conventional microbiology in poultry carcasses collected in slaughterhouses and species were identified by multiplex-PCR. Thermophilic Campylobacter spp. was verified in 63.8% of the samples, being 72.2% in chilled carcasses and 55.5% in frozen carcasses. Of these, 83.3% were positive for C. jejuni and 66.6% to C. coli, while 50% were positive for both. The presence of thermophilic Campylobacter spp. in ready-to-eat poultry products represents a potential source of human campylobacteriosis.
Subject(s)
Animals , Frozen Foods/microbiology , Cooled Foods , Campylobacter/isolation & purification , Meat/microbiology , Campylobacter Infections/veterinary , Chickens/microbiology , Abattoirs , ThermotoleranceABSTRACT
Espécies de Campylobacter spp. termotolerantes são agentes de surtos de campilobacteriose em humanos e os produtos de origem avícola são considerados uma importante fonte de infecção. Foram identificados Campylobacter jejuni e Campylobacter coli em carcaças de frango resfriadas e congeladas coletadas em três abatedouros entre 2014 e 2015. A detecção de Campylobacter spp. foi realizada por microbiologia convencional e a identificação de C. jejuni e C. coli por multiplex-PCR. Dentre as amostras avaliadas verificou-se Campylobacter spp. termotolerante em 63,8%, sendo 72,2% em carcaças resfriadas e 55,5% em carcaças congeladas. Destas, 83,3% foram positivas para C. jejuni e 66,6% para C. coli, enquanto 50% foram positivas para ambas as espécies. A presença de Campylobacter spp. termotolerante em carcaças de frangos de corte prontas para consumo representa uma importante fonte de transmissão destes patógenos para humanos.(AU)
Species of thermophilic Campylobacter spp. are agents of campylobacteriosis outbreaks in humans, and poultry products are implicated as major sources of infection. The detection of Campylobacter spp. was performed by conventional microbiology in poultry carcasses collected in slaughterhouses and species were identified by multiplex-PCR. Thermophilic Campylobacter spp. was verified in 63.8% of the samples, being 72.2% in chilled carcasses and 55.5% in frozen carcasses. Of these, 83.3% were positive for C. jejuni and 66.6% to C. coli, while 50% were positive for both. The presence of thermophilic Campylobacter spp. in ready-to-eat poultry products represents a potential source of human campylobacteriosis.(AU)
Subject(s)
Animals , Campylobacter/isolation & purification , Campylobacter Infections/veterinary , Meat/microbiology , Frozen Foods/microbiology , Cooled Foods , Chickens/microbiology , Abattoirs , ThermotoleranceABSTRACT
Wohlfahrtiimonas chitiniclastica is an emerging zoonotic bacterium commensally living in larvae of particular flies. It has been associated with human and animal infections but never isolated from food. In the present study, a whole chicken carcass was rinsed in buffered peptone water which was then inoculated into BHI and the growth plated onto selective medium. Species identification was performed by MALDI-TOF MS. Those bacteria identified as W. chitiniclastica were subjected to 16S rRNA sequencing for confirmation and MEGA software was used to obtain their phylogenetic position. The findings of this study raise concerns regarding the abattoir, transport and stock practices of frozen meat carcasses and should be of interest with regard to microbiology, entomology and food production.
Subject(s)
Chickens/microbiology , Frozen Foods/microbiology , Meat/microbiology , Xanthomonadaceae/classification , Xanthomonadaceae/isolation & purification , Zoonoses/microbiology , Animals , Brazil , Communicable Diseases, Emerging/microbiology , DNA, Bacterial/genetics , Diptera/microbiology , Food Handling , Food Microbiology , Phylogeny , RNA, Ribosomal, 16S/genetics , Wound Infection/microbiology , Xanthomonadaceae/chemistry , Xanthomonadaceae/geneticsABSTRACT
Extending the shelf-life of bakery products has been an important requirement resulting from the mechanization of this industry and the need to increase the distance for the distribution of final products, caused by the increase in production and consumer demand. Technologies based on the interruption of the breadmaking process represent an alternative to overcome product staling and microbiological deterioration. The production of par-baked breads is one of these technologies. It consists of baking the bread in two stages, and due to the possibility of retarding the second stage, it can be said that the bread can always be offered fresh to the consumer. The technology inserts logistics as part of the production process and creates the "hot point" concept, these being the locations where the bread is finalized, such as in the consumers' homes or sales locations. In this work, a review of the papers published on this subject was carried out, and aspects related to both the formulation and the process were considered. This technology still faces a few challenges, such as solving bread quality problems that appear due to process modifications, and these will also be considered. The market for these breads has grown rapidly and the bakery industry searches innovations related to par-baked bread technology.
Subject(s)
Bread/analysis , Cooking , Food Quality , Bread/economics , Bread/microbiology , Fast Foods/analysis , Fast Foods/economics , Fast Foods/microbiology , Fermentation , Food Packaging/trends , Food Storage , Frozen Foods/analysis , Frozen Foods/economics , Frozen Foods/microbiology , Humans , Quality Control , Refrigeration , Saccharomyces cerevisiae/growth & development , Saccharomyces cerevisiae/metabolism , Social ChangeABSTRACT
The practice of freezing food is one of the main processes used by the industry to prolong the shelf life of foods. Its use has expanded in recent years due to the increased consumption of convenience products, many of which are sold in frozen form. The temperature at which these foods are maintained during marketing in supermarkets or stored in the consumer's home is critical to ensure microbiological stability of products. Temperature abuse can allow microbial growth, especially growth of filamentous psychrophilic fungi. Besides economic losses in the industrial sector due to the return of products and loss of confidence by consumers, the development of fungi in foods is a public health problem due to the possibility of mycotoxin production. The aim of this study was to assess the growth at temperatures of 5, 0, -5 and -18°C for two species of fungi involved in the deterioration of frozen chicken nuggets, Penicillium polonicum (33/12 NGT) and Penicillium glabrum (29/12 NGT), inoculated both in culture medium and in the food. The results demonstrated that P. polonicum was able to form microcolonies on potato dextrose agar plates at 0°C and form visible colonies on the surface of the frozen chicken nuggets kept at -5°C for 120 days, regardless of brand. For P. glabrum the limiting growth temperature was 5°C in the culture medium and 0°C on frozen chicken nuggets, regardless of the brand analyzed. Thus, it is essential to adhere to the storage temperatures recommended to ensure the stability and safety of this food product.
Subject(s)
Food Handling/standards , Food Microbiology , Frozen Foods/microbiology , Meat/microbiology , Penicillium/growth & development , Temperature , Animals , ChickensABSTRACT
BACKGROUND: This study examined the ability of Salmonella enterica serovar Enteritidis and Listeria monocytogenes to grow or survive in mango pulp stored at -20°C, 4°C, 10°C and 25°C, as well as to cross-contaminate mangoes by means of a knife contaminated with different levels of these pathogens. RESULTS: At 25°C lag phase durations of 19 h and 7.2 h and generation times of 0.66 and 1.44 were obtained, respectively, for S. Enteritidis and L. monocytogenes. At 10°C only the growth of L. monocytogenes was observed. At 4°C both bacteria survived for 8 days. At -20°C S. Enteritidis was able to survive for 5 months while L. monocytogenes survived for 8 months. Cross-contamination was observed for knives contaminated with 106, 105 and 104 CFU mL⻹ of S. Enteritidis and 106 and 105 CFU mL⻹ of L. monocytogenes. CONCLUSION: Both microorganisms can grow well in mango pulp at 25°C, thus lower temperatures for the maintenance of the pulps are crucial to avoid growth of these microorganisms. A refrigeration temperature of 10°C will avoid only the growth of S. Enteritidis. Thus good handling practices should be rigidly enforced to avoid any contamination as even at refrigeration and freezing temperatures survival of these pathogens may occur.
Subject(s)
Cooking and Eating Utensils , Equipment Contamination , Food Storage , Fruit/microbiology , Listeria monocytogenes/growth & development , Mangifera/microbiology , Salmonella enteritidis/growth & development , Brazil , Cold Temperature , Colony Count, Microbial , Food Handling , Frozen Foods/microbiology , Listeria monocytogenes/isolation & purification , Microbial Viability , Models, Biological , Refrigeration , Salmonella enteritidis/isolation & purification , Time FactorsABSTRACT
The objective of this study was to determine Salmonella counts, serovars, and antimicrobial-resistant phenotypes on retail raw chicken carcasses in Colombia. A total of 301 chicken carcasses were collected from six departments (one city per department) in Colombia. Samples were analyzed for Salmonella counts using the most-probable-number method as recommended by the U.S. Department of Agriculture, Food Safety Inspection Service protocol. A total of 378 isolates (268 from our previous study) were serotyped and tested for antimicrobial susceptibility. The overall Salmonella count (mean log most probable number per carcass ± 95% confidence interval) and prevalence were 2.1 (2.0 to 2.3) and 37%, respectively. There were significant differences (P < 0.05) by Salmonella levels (i.e., counts and prevalence) by storage temperature (i.e., frozen, chilled, or ambient), retail store type (wet markets, supermarkets, and independent markets), and poultry company (chicken produced by integrated or nonintegrated company). Frozen chicken had the lowest Salmonella levels compared with chicken stored at other temperatures, chickens from wet markets had higher levels than those from other retail store types, and chicken produced by integrated companies had lower levels than nonintegrated companies. Thirty-one Salmonella serovars were identified among 378 isolates, with Salmonella Paratyphi B tartrate-positive (i.e., Salmonella Paratyphi B dT+) the most prevalent (44.7%), followed by Heidelberg (19%), Enteritidis (17.7%), Typhimurium (5.3%), and Anatum (2.1%). Of all the Salmonella isolates, 35.2% were resistant to 1 to 5 antimicrobial agents, 24.6% to 6 to 10, and 33.9% to 11 to 15. Among all the serovars obtained, Salmonella Paratyphi B dT+ and Salmonella Heidelberg were the most antimicrobial resistant. Salmonella prevalence was determined to be high, whereas cell numbers were relatively low. These data can be used in developing risk assessment models for preventing the transmission of Salmonella from chicken to humans in Colombia.
Subject(s)
Commerce/statistics & numerical data , Drug Resistance, Bacterial , Food Contamination/analysis , Meat/microbiology , Salmonella/isolation & purification , Animals , Anti-Bacterial Agents/pharmacology , Chickens , Colombia/epidemiology , Colony Count, Microbial , Drug Resistance, Multiple, Bacterial , Food Contamination/statistics & numerical data , Food Handling/methods , Frozen Foods/microbiology , Humans , Microbial Sensitivity Tests , Phenotype , Prevalence , Salmonella/classification , Salmonella/drug effects , United StatesABSTRACT
O objetivo deste trabalho foi realizar o isolamento e analisar o perfil de resistência antimicrobiana de Enterococcus de carcaças de frango resfriadas e congeladas comercializadas no Distrito Federal, detectando genes de resistência antimicrobiana e identificando as espécies Enterococcus faecalis e Enterococcus faecium por reação polimerase em cadeia. Foram analisadas 100 carcaças de frangos, das quais foram isoladas 50 cepas de Enterococcus spp., sendo 42% de E. faecalis e 2% de E. faecium. O teste de susceptibilidade antimicrobiana demonstrou que todas as cepas isoladas apresentaram resistência a pelo menos um antimicrobiano, dos quais 90,47% das cepas de E. faecalis, 100% das cepas de E. Faecium e 82,14% dos Enterococcus spp. apresentaram resistência à Tetraciclina; 80,95% das cepas de E. faecalis e 35,71% das cepas de Enterococcus spp. foram resistentes à Eritromicina; 39,28% dos Enterococcus spp. e 23,80% dos E. faecalis à Ciprofloxacina e 28,57% dos E. faecalis apresentaram resistência ao Cloranfenicol. Foram detectados os genes de resistência antimicrobiana erm(B), vanC-1, aph(3')-llla, ant(6)-la, vanB, vanA, aac(6')-le-aph(2'')-la, erm(A) e tet(M) - este último mais frequente. Estes resultados sugerem sérios problemas para a Saúde Pública, uma vez que esses microrganismos podem possuir a capacidade de transmitir genes de resistência antimicrobiana para outros microrganismos presentes na microbiota intestinal de humanos e animais, podendo inviabilizar o uso destas drogas para tratamentos clínicos.
The aim of this study was to isolate and analyze the antimicrobial profile resistance of Enterococcus from cooled and frozen poultry carcasses commercialized at the Federal District area, detecting the antimicrobial resistance genes and identifying Enterococcus faecalis and Enterococcus faecium by polymerase chain reaction. One hundred poultry carcasses were analyzed and 50 strains of Enterococcus spp. were isolated, of which 42% were E. faecalis and 2% E. faecium. The antimicrobial susceptibility test showed that all isolates were resistant to at least one antibiotic; 90,47% of E. faecalis, 100% of E. faecium and 82,14% of Enterococcus spp. were resistant to Tetracycline; 80,95% of E. faecalis and 35,71% of Enterococcus spp. strains were resistant to Erythromycin; 39,28% of Enterococcus spp. and 23,80% of E. faecalis to Ciprofloxacin, and 28,57% of E. faecalis were resistant to Chloramphenicol. There were detected erm(B), vanC-1, aph(3')-llla, ant(6)-la, vanB, vanA, aac(6')-le-aph(2'')-la, erm(A) and tet(M) resistance genes, the last one most often verified. The results might suggest problems for public health due the high resistance, since these microorganisms have ability to transmit genes for antimicrobial resistance to others in the intestinal tract of humans and animals. Thus, the use of these drugs for clinical treatment could be hindered.
Subject(s)
Animals , Frozen Foods/microbiology , Drug Resistance, Microbial , Enterococcus faecalis/isolation & purification , Enterococcus faecium/isolation & purification , Chickens/microbiology , Chloramphenicol Resistance , Tetracycline ResistanceABSTRACT
O objetivo deste trabalho foi realizar o isolamento e analisar o perfil de resistência antimicrobiana de Enterococcus de carcaças de frango resfriadas e congeladas comercializadas no Distrito Federal, detectando genes de resistência antimicrobiana e identificando as espécies Enterococcus faecalis e Enterococcus faecium por reação polimerase em cadeia. Foram analisadas 100 carcaças de frangos, das quais foram isoladas 50 cepas de Enterococcus spp., sendo 42% de E. faecalis e 2% de E. faecium. O teste de susceptibilidade antimicrobiana demonstrou que todas as cepas isoladas apresentaram resistência a pelo menos um antimicrobiano, dos quais 90,47% das cepas de E. faecalis, 100% das cepas de E. Faecium e 82,14% dos Enterococcus spp. apresentaram resistência à Tetraciclina; 80,95% das cepas de E. faecalis e 35,71% das cepas de Enterococcus spp. foram resistentes à Eritromicina; 39,28% dos Enterococcus spp. e 23,80% dos E. faecalis à Ciprofloxacina e 28,57% dos E. faecalis apresentaram resistência ao Cloranfenicol. Foram detectados os genes de resistência antimicrobiana erm(B), vanC-1, aph(3')-llla, ant(6)-la, vanB, vanA, aac(6')-le-aph(2'')-la, erm(A) e tet(M) - este último mais frequente. Estes resultados sugerem sérios problemas para a Saúde Pública, uma vez que esses microrganismos podem possuir a capacidade de transmitir genes de resistência antimicrobiana para outros microrganismos presentes na microbiota intestinal de humanos e animais, podendo inviabilizar o uso destas drogas para tratamentos clínicos.(AU)
The aim of this study was to isolate and analyze the antimicrobial profile resistance of Enterococcus from cooled and frozen poultry carcasses commercialized at the Federal District area, detecting the antimicrobial resistance genes and identifying Enterococcus faecalis and Enterococcus faecium by polymerase chain reaction. One hundred poultry carcasses were analyzed and 50 strains of Enterococcus spp. were isolated, of which 42% were E. faecalis and 2% E. faecium. The antimicrobial susceptibility test showed that all isolates were resistant to at least one antibiotic; 90,47% of E. faecalis, 100% of E. faecium and 82,14% of Enterococcus spp. were resistant to Tetracycline; 80,95% of E. faecalis and 35,71% of Enterococcus spp. strains were resistant to Erythromycin; 39,28% of Enterococcus spp. and 23,80% of E. faecalis to Ciprofloxacin, and 28,57% of E. faecalis were resistant to Chloramphenicol. There were detected erm(B), vanC-1, aph(3')-llla, ant(6)-la, vanB, vanA, aac(6')-le-aph(2'')-la, erm(A) and tet(M) resistance genes, the last one most often verified. The results might suggest problems for public health due the high resistance, since these microorganisms have ability to transmit genes for antimicrobial resistance to others in the intestinal tract of humans and animals. Thus, the use of these drugs for clinical treatment could be hindered.(AU)
Subject(s)
Animals , Chickens/microbiology , Frozen Foods/microbiology , Enterococcus faecium/isolation & purification , Enterococcus faecalis/isolation & purification , Drug Resistance, Microbial , Tetracycline Resistance , Chloramphenicol ResistanceABSTRACT
We compared the application of high hydrostatic pressure (HHP) on unfrozen carpaccio (HHP at 20 °C) and on previously-frozen carpaccio (HHP at -30 °C). HHP at 20 °C changed the color. The pressure increase from 400 to 650 MPa and the time increment from 1 to 5 min at 400 MPa increased L* and b*. a* decreased only with 650 MPa for 5 min at 20 °C. The prior freezing of the carpaccio and the HHP at -30 °C minimized the effect of the HHP on the color and did not change the shear force, but increased expressible moisture as compared to the untreated carpaccio. HHP at 20 °C was more effective in reducing the counts of microorganisms (aerobic total count at 30 °C, Enterobacteriaceae, psychrotrophs viable at 6.5 °C and lactic acid bacteria) than HHP at -30 º C. With HHP at 20 °C, we observed a significant effect of pressure and time on the reduction of the counts.
Subject(s)
Fast Foods/analysis , Food Preservation/methods , Food Quality , Meat/analysis , Animals , Argentina , Cattle , Chemical Phenomena , Cold Temperature , Diet/ethnology , Enterobacteriaceae/growth & development , Enterobacteriaceae/isolation & purification , Fast Foods/microbiology , Frozen Foods/analysis , Frozen Foods/microbiology , Hydrostatic Pressure , Lactobacillales/growth & development , Lactobacillales/isolation & purification , Meat/microbiology , Mechanical Phenomena , Microbial Viability , Pigmentation , Shear Strength , Time Factors , Water/analysisABSTRACT
O caranguejo é um produto que participa da culinária maranhense, sendo de fácil aquisição em feiras e mercados. Por ser um alimento normalmente consumido cru ou após leve fervura, torna-se um veículo de disseminação de microorganismos enteropatogênicos. O estudo objetivou avaliar a qualidade microbiológica da carne de caranguejo comercializada em supermercados e feiras da cidade de São Luís, MA. Para avaliar a qualidademicrobiológica do produto foi utilizada a técnica do NMP (Número Mais Provável)e Pesquisa de Salmonella spp. A análise parasitológica foi realizada pelométodo de Hoffman, com alterações. Foi verificada a eficácia do cozimento dasamostras bacterianas que foram submetidas à água fervendo a 50°C por 5,15e 30 minutos. A carne de caranguejo de todos os estabelecimentos apresentouíndices de coliformes termotolerantes acima do permitido pela legislação eapenas três estabelecimentos apresentaram pesquisa de Salmonella spp positiva.Constatou-se a ausência de cistos. Após o aquecimento, a maioria dasamostras cresceu em tempo inferior a 15 minutos, indicando altos níveis decontaminação. As amostras de carne de caranguejo não estão adequadas parao consumo, pois o número de coliformes totais e termotolerantes encontradosestá acima do permitido pela legislação vigente.(AU)
Crabs are important produces inthe cuisine of Maranhão (Brazil),being easily purchased in fairs andmarkets. For the crabmeat is usuallyeaten raw or after quick boiling, itbecomes a contamination sourcefor enteropathogenic microorganisms.The aim of this study was tocarry out a microbiological andparasitological evaluations in thecrabmeat commercialized in supermarketsand fairs in São Luís/MA. .To evaluate microbiological qualitythe multiple tubes technique (NMP)and Salmonella investigation wereused. Parasitological analysis wasperformed by Hoffman techniquewith alterations. It was verifiedthe effectiveness of the cookingof bacterial samples that weresubjected to boiling water at 50ºC for 5, 15 and 30 minutes. Thecrabmeat of all establishmentshad levels of fecal coliform abovethose permitted by law and onlythree establishments were positivefor Salmonella spp. Absence ofcysts. After heating the majorityof samples grown in less than 15minutes indicating high levels ofcontamination. Samples of crabmeat are not suitable for consumptionbecause the alls numbers offecal coliforms are found abovethe permissible current legislation. (AU)
Subject(s)
Brachyura/microbiology , /parasitology , Food Samples , Food Microbiology , Food Contamination , Frozen Foods/microbiology , Coliforms , Salmonella/isolation & purification , BrazilABSTRACT
O caranguejo é um produto que participa da culinária maranhense, sendo de fácil aquisição em feiras e mercados. Por ser um alimento normalmente consumido cru ou após leve fervura, torna-se um veículo de disseminação de microorganismos enteropatogênicos. O estudo objetivou avaliar a qualidade microbiológica da carne de caranguejo comercializada em supermercados e feiras da cidade de São Luís, MA.