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1.
Food Sci Technol Int ; : 10820132231190103, 2023 Jul 27.
Article in English | MEDLINE | ID: mdl-37499189

ABSTRACT

Owing to concerns about the antimicrobial resistance of agents that can prevent the growth of Listeria monocytogenes in meat, researchers have investigated natural preservatives with antilisterial effects. However, in vivo application of essential oils and plant extracts usually results in reduced antimicrobial activity in meat products when compared to in vitro studies. This study aimed to evaluate the in vivo antimicrobial activity of cinnamon essential oil, pomegranate, and strawberry tree extracts in slices of dry-cured ham and pork loin against L. monocytogenes. Fragments of sterile dry-cured ham were inoculated with 100 µL cinnamon oil 0.5%, pomegranate, or strawberry crude extract. After 10 min, 100 µL of L. monocytogenes serotype 4b (104 colony-forming unit [CFU]/mL) was inoculated, and samples were incubated at 7 °C for 7 d to simulate the processing and storage temperature conditions of dry-cured meat products. L. monocytogenes was detected and quantified. Only strawberry extract presented significant differences (P < 0.05) from the control; thus, it was selected for the assay with 2% and 4% salt-treated pork loin. The strawberry tree extract significantly (P < 0.05) reduced the growth of L. monocytogenes in dry-cured ham. However, it could not reduce L. monocytogenes growth in pork loin, regardless of the salt concentration. This is the first report on the antimicrobial effect of strawberry tree leaf extract against L. monocytogenes in dry-cured ham.

2.
Food Sci Technol Int ; : 10820132221144341, 2022 Dec 18.
Article in English | MEDLINE | ID: mdl-36529875

ABSTRACT

Salmonellosis is one of the most common foodborne diseases worldwide. Surface adherence and biofilm formation are among the main strategies evolved by Salmonella to survive under harsh conditions and are risk factors for its spread through the food chain. Owing to the increase in antimicrobial resistance, there is a growing need to develop other methods to control foodborne pathogens, and bacteriophages have been suggested as a potential alternative for this purpose. The aim of this study was to evaluate bacteriophages as a biological control of Salmonella enterica serotypes to inhibit and remove bacterial biofilms. A total of 12 S. enterica isolates were selected for this study, all of which were biofilm producers. Seven bacteriophages were tested, individually and in a cocktail, for their host range and efficiency of plating (EOP). The phage cocktail was evaluated for its antibiofilm effect against the Salmonella biofilms. Phages UPF_BP1, UPF_BP2, UPF_BP3, UPF_BP6, and 10:2 possessed a broad lytic spectrum and could infect all S. enterica strains. Phages 10:2, UPF_BP6, and UPF_BP3 had high EOP in 10, 9, and 9 out of the 12 S. enterica strains, respectively. The cocktail was able to infect all S. enterica strains and had a high EOP in 10 out of 12 S. enterica isolates, presenting a broader host range than any of the tested single phages. A wide variation of inhibition among strains was observed, ranging from 14.72% to 88.53%. Multidrug-resistant and strong biofilm producer strains showed high biofilm inhibition levels by phage cocktail. Our findings demonstrate the ability of the cocktail to prevent biofilm formation and remove formed biofilms of Salmonella. These results indicate that the phage cocktail is a promising candidate to be used as an alternative for the control of Salmonella biofilms through surface conditioning.

3.
Curr Microbiol ; 80(1): 11, 2022 Dec 02.
Article in English | MEDLINE | ID: mdl-36459239

ABSTRACT

Bovines are carriers of Salmonella spp., a relevant foodborne pathogen, acting as contamination sources in slaughterhouses. Calves are prone to infection, and antimicrobial resistance may occur in such bacteria. This study aimed to determine the prevalence and virulence determinants of Salmonella spp. recovered from calves in the Rio Grande do Sul state, Brazil. Eighty-five calves' carcasses were evaluated (leather and veal meat). Thirteen Salmonella spp. isolates (8%) from 11 animals (13%) were obtained only from leather, indicating that contamination occurred before slaughter and that the meat was safe regarding this aspect. The serotypes S. Minnesota, S. Abony, S. Cerro, and S. Gafsa were identified, and all isolates were multidrug-resistant. The isolates had at least 19 virulence-related genes, and the blaOXA-48 resistance gene was detected in three (23%). The data suggest that treating infections caused by these bacteria may be difficult in animals from these farms and can also be an extended human health problem.


Subject(s)
Abattoirs , Salmonella , Humans , Animals , Cattle , Serogroup , Brazil/epidemiology , Tunisia , Salmonella/genetics
4.
Int J Food Microbiol ; 379: 109863, 2022 Oct 16.
Article in English | MEDLINE | ID: mdl-35940116

ABSTRACT

Salmonella Heidelberg is a clinically-important serovar linked to food-borne illness, and commonly isolated from poultry products. Since 1962, Salmonella Heidelberg has been widely reported from poultry production systems in several countries, including Brazil. The emergence of multidrug-resistant (MDR) Salmonella Heidelberg strains in food animals underscores a significant food safety hazard. In our study, we performed antimicrobial susceptibility testing (AST) and Whole-genome sequencing (WGS) to identify the antimicrobial resistance (AMR) genes, pathogenicity mechanisms and virulence factors (VF) in Salmonella Heidelberg E2 strain recovered from a chicken carcass in Southern Brazil. Salmonella Heidelberg strain belonged to ST15 and showed to be susceptible to colistin (MIC ≤2 µg/mL) and multidrug-resistant to amoxicillin-clavulanic acid, gentamicin, ampicillin, cefaclor, cefazolin, ceftiofur, nalidixic acid, azithromycin, erythromycin, doxycycline, tetracycline and sulfonamide. We identified AMR genes mediating resistance to aminoglycosides (aac(6')-Iaa, aac(3)-VIa, aph(3')-Ia, aadA, 16S rrsD), ß-lactams (blaCTX-M-2), quinolones (parC), macrolides (acrB), tetracyclines (tet(A)), fosfomycin (fosA7) and sulfonamide (sul1). Interestingly, the mutation in parC T255S has never been reported among Salmonella Heidelberg strains. To our knowledge, this is the first report of a Salmonella enterica strain harbouring 16S rrsD 471G > A, acrB F28L and acrB L40P chromosomal point mutations. Three plasmid replicon types, ST2-IncHI2, ST2-IncHI2A and IncX1 were identified. Nine Salmonella Pathogenicity Islands and 98 virulence genes encoding virulence factors were identified associated with cell adhesion, invasion, intracellular survival and resistance to antimicrobial peptides. Although Salmonella Heidelberg E2 strain likely originated from poultry, cross-contamination during meat processing cannot be excluded. This study adds to our understanding of Salmonella Heidelberg transmission along the food-chain and informs ongoing regulatory discussions on Salmonella Heidelberg in poultry.


Subject(s)
Chickens , Salmonella enterica , Animals , Anti-Bacterial Agents/pharmacology , Brazil , Drug Resistance, Multiple, Bacterial/genetics , Genomics , Interleukin-1 Receptor-Like 1 Protein , Microbial Sensitivity Tests , Poultry , Salmonella , Sulfonamides , Virulence Factors
5.
Environ Sci Pollut Res Int ; 28(28): 37843-37850, 2021 Jul.
Article in English | MEDLINE | ID: mdl-33718999

ABSTRACT

Owls are outstanding environmental quality bioindicators due to their position at the top of the food chain and susceptibility to pollutant accumulation. Exposure to chemical contaminants is often a risk for these animals. Moreover, studies addressing the bioaccumulation of trace elements and pesticide residues in tropical nocturnal raptor species are scarce. We analyzed the 26 organs (heart, liver, and kidney) of Tyto furcata (n=3), Megascops spp. (n=5), Pulsatrix koeniswaldiana (n=1), and Asio stygius (n=1) carcasses, collected from June 2018 to May 2019 in the Southern region of Brazil. The original vegetation consisted of areas of Araucaria forests and grassy-woody steppes with gallery forests, which were greatly modified by the introduction of agriculture. In four animals and eight organs, the pesticides abamectin, atrazine, chlorpyrifos-ethyl, and diurom were analyzed through high-performance liquid chromatography coupled with a mass detector. In six animals and eighteen organs, the trace elements cadmium, lead, chromium, and nickel were identified via atomic absorption spectrophotometry. Chlorpyrifos-ethyl was detected in the livers of the genus Megascops. Chromium was found at high concentrations in all matrices analyzed for this trace element. Moreover, P. koeniswaldiana presented lead levels indicative of high exposure. The bioaccumulation of these toxics in owls described here can impact the population levels of these species, impact on its ecological function, and consequently unbalance the ecosystem. Moreover, owls are considered bioindicators; therefore, the occurrence of bioaccumulation indirectly gives us information about the quality of the environment.


Subject(s)
Pesticides , Strigiformes , Trace Elements , Animals , Bioaccumulation , Brazil , Ecosystem , Environmental Monitoring , Lead , Trace Elements/analysis
6.
Sci Rep ; 11(1): 4588, 2021 02 25.
Article in English | MEDLINE | ID: mdl-33633256

ABSTRACT

Campylobacter jejuni is one of the most common causes of foodborne diseases worldwide. There are few reports on Campylobacter strains isolated from Latin-American countries. Here, 140 C. jejuni strains isolated from cloacal and transport boxes swabs, water from chiller tanks, and broiler carcasses of five poultry companies in Southern Brazil were identified using phenotypic and genotypic methods. Polymerase chain reaction (PCR) was used to analyze eight C. jejuni virulence markers: flaA, cadF, and invasion-associated (iam) genes, cdtABC operon (associated with the cytolethal distending toxin), and plasmidial virB11 and wlaN genes were present in 78.5%, 77.8%, 0%, 74.2%, 22.1%, and 10.7% of samples, respectively. There were 25 different virulence profiles: 1 (cdtA, cdtB, cdtC, flaA, and cadF), 2 (cdtA, cdtB, cdtC, flaA, cadF, and virB11), and 3 (cdtA, cdtB, cdtC, flaA, cadF, and wlaN) were the most common (> 60% of strains). We provide insight into factors related to the occurrence of this pathogen and their epidemiology.


Subject(s)
Campylobacter jejuni/genetics , Chickens/microbiology , Genes, Bacterial , Virulence/genetics , Abattoirs , Animals , Biomarkers/metabolism
7.
Trop Anim Health Prod ; 53(1): 87, 2021 Jan 07.
Article in English | MEDLINE | ID: mdl-33415502

ABSTRACT

The search for better zootechnical indexes such as feed conversion, daily weight gain, uniformity, and lower bird mortality has become a priority within the poultry industry. The use of food restriction programs has emerged as an alternative to improve these rates as well as to mitigate the effect of the increased cost of nutrition over the past few years. In this work, the feed conversion (FC), daily weight gain (DWG), uniformity, and mortality of male broilers submitted to two food restriction programs were evaluated; one program reduced food by 10% and the other by 20% in relation to the feeding program suggested by the Cobb500 strain. One hundred and eighty birds aged 10 days old were housed in 12 boxes for 30 days. Fifteen birds were placed in each box, and four replicates per treatment were designed: T1 (control group-feed intake as recommended by the Cobb500 strain), T2 (10% reduction), and T3 (20% reduction). There was no statistical difference in DWG, uniformity, or mortality between the treatment groups. As for FC, a statistical difference was observed with a gain of 100 g in T2 and 252 g in T3 in relation to T1. The results of this work demonstrate that food restriction programs can be used to improve FC in broiler flocks, without interfering with the DWG, uniformity, or mortality of birds.


Subject(s)
Animal Feed/analysis , Caloric Restriction/veterinary , Chickens/growth & development , Weight Gain , Animals , Male
8.
Ciênc. rural (Online) ; 50(2): 20190425, 2020. tab, graf
Article in English | LILACS-Express | LILACS | ID: biblio-1055862

ABSTRACT

ABSTRACT: The preservation of milk samples for microbiological analyses by the Brazilian Network of Milk Quality Control Laboratories requires the addition of preservatives to maintain the microbiota from the time of sample collection to the moment of analysis. The number of microorganisms can change as a result of the active ingredients and concentration of the preservative, as well as due to interactions between the preservatives, incubation time, and packaging temperature. The objective of this research was to evaluate the conservation potential of different concentrations of sodium azide and chloramphenicol on the analytical shelf life of milk samples. Two farms were selected, one with a low bacterial count and one with a high bacterial count. The milk was dispensed into sterile vials and tested after the addition of the usual concentrations of sodium azide and chloramphenicol, doubled concentrations, tripled concentrations, and as a control, without preservatives. The samples were incubated at 3 ± 1 °C, 6 ± 1 °C, and 9 ± 1 °C for 14 days and analyzed daily for their bacterial count by flow cytometry. The tripled preservative concentrations improved conservation, increasing the timespan of the analytical viability of the samples without altering the results.


RESUMO: A conservação das amostras de leite destinadas para análises microbiológicas pela Rede Brasileira de Laboratórios de Controle da Qualidade do Leite requer adição de conservantes para a preservação da microbiota existente desde o momento da coleta até as análises. O número de microrganismos pode apresentar alterações decorrentes do princípio ativo e concentração do conservante, e ainda entre as interações conservante, tempo de incubação e temperatura de acondicionamento. O objetivo deste trabalho foi avaliar o potencial de conservação de diferentes concentrações de azida sódica e cloranfenicol sobre a vida útil analítica de amostras de leite. Foram selecionadas duas fazendas, sendo uma com baixa contagem bacteriana e outra com alta contagem bacteriana. O leite foi fracionado em frascos estéreis e testado nas seguintes condições: pastilhas com a concentração usual de azida sódica e cloranfenicol, com dupla concentração, com tripla concentração e sem a adição do conservante. As amostras foram incubadas por quatorze dias a 3 ± 1 °C, 6 ± 1 °C e 9 ± 1 °C, e analisadas diariamente por citometria de fluxo para a determinação da contagem bacteriana. A tripla concentração do conservante demonstrou maior conservação, possibilitando o aumento da viabilidade analítica das amostras sem alteração nos resultados.

9.
Rev Inst Med Trop Sao Paulo ; 61: e36, 2019 Jul 22.
Article in English | MEDLINE | ID: mdl-31340248

ABSTRACT

During the last years, Brazilian government control programs have detected an increase of Salmonella Heidelberg in poultry slaughterhouses a condition that poses a threat to human health However, the reasons remain unclear. Differences in genetic virulence profiles may be a possible justification. In addition, effective control of Salmonella is related to an efficient epidemiological surveillance system through genotyping techniques. In this context, the aim of this study was the detection of 24 virulence-associated genes in 126 S. Heidelberg isolates. We classified the isolates into 56 different genetic profiles. None of the isolates presented all the virulence genes. The prevalence of these genes was high in all tested samples as the lowest number of genes detected in one isolate was 10/24. The lpfA and csgA (fimbriae), invA and sivH (TTSS), and msgA and tolC (intracellular survival) genes were present in 100% of the isolates analyzed. Genes encoding effector proteins were detected in the majority of SH isolates. No single isolate had the sefA gene. The pefA gene was found in only four isolates. We have also performed a screening of genes associated with iron metabolism: 88.9% of isolates had the iroN geneand 79.4% the sitC gene . Although all the isolates belong to the same serotype, several genotypic profiles were observed. These findings suggest that there is a diversity of S. Heidelberg isolates in poultry products. The fact that a single predominant profile was not found in this study indicates the presence of variable sources of contamination caused by SH. The detection of genetic profiles of Salmonella strains can be used to determine the virulence patterns of SH isolates.


Subject(s)
Poultry Diseases/microbiology , Poultry Products/microbiology , Salmonella Infections, Animal/microbiology , Salmonella/genetics , Salmonella/pathogenicity , Virulence Factors/genetics , Virulence/genetics , Animals , Food Microbiology , Genotype , Polymerase Chain Reaction
10.
Ciênc. rural (Online) ; 49(7): e20181022, 2019. tab, graf
Article in English | LILACS | ID: biblio-1045398

ABSTRACT

ABSTRACT: We evaluated the influence of temperature on the ability of Salmonella Enteritidis (SE) to form biofilms on stainless steel, polyethylene, and polyurethane surfaces under different hygiene procedures. These materials were placed on SE culture and incubated at 42±1 ºC, 36±1 ºC, 25±1 ºC, 9±1 ºC, and 3±1 ºC for 4, 8, 12, and 24 h. Hot water at 45 ºC and 85 ºC, 0.5% peracetic acid solution, and 1% quaternary ammonia were used for hygienization. Biofilm formation occurred at all temperatures evaluated, highlighting at 3 ºC which has not been reported as an ideal temperature for the adhesion of SE to these materials. The SE adhered more often to polyethylene surfaces than to polyurethane and stainless steel surfaces (P<0.05). Peracetic acid and water at 85 ºC had similar hygienization efficiency (P<0.05) followed by quaternary ammonia whereas water at 45 ºC was not effective. SE adhered to these materials under low temperatures which to date have been deemed safe for food preservation.


RESUMO: Avaliou-se o efeito da temperatura na capacidade de Salmonella Enteritidis (SE) formar biofilme em superfícies de aço inoxidável, polietileno e poliuretano e diferentes processos de higienização. Corpos de prova destes materiais foram postos frente a culturas de SE e incubados a 42±1 ºC, 36±1 ºC, 25±1 ºC, 9±1 ºC e 3±1 ºC por 4, 8, 12 e 24 horas. Para a higienização foram testados água aquecida a 45ºC e 85 ºC e soluções de ácido peracético 0,5% e amônia quaternária 1%. Verificou-se a formação de biofilmes em todas as temperaturas avaliadas, ressaltando-se a 3 ºC, ainda não citada como propícia para adesão de SE. Houve maior adesão ao polietileno do que ao poliuretano e ao aço inoxidável (P<0.05). Para higienização, o ácido peracético e a água a 85 ºC tiveram ação semelhante (P<0.05), seguidos por amônia quaternária, enquanto que a água a 45 ºC não foi eficaz. Todos os materiais avaliados propiciaram a aderência de SE, mesmo sob temperaturas baixas, consideradas até então seguras para a conservação dos alimentos.

11.
Braz. j. microbiol ; 47(3): 764-769, July-Sept. 2016. tab
Article in English | LILACS | ID: lil-788981

ABSTRACT

ABSTRACT Campylobacter spp. cause foodborne illnesses in humans primarily through the consumption of contaminated chicken. The aim of this study was to evaluate the United States Department of Agriculture's (USDA) recommended methodology, protocol MLG 41.02, for the isolation, identification and direct plate counting of Campylobacter jejuni and C. coli samples from the broiler slaughtering process. A plating method using both mCCDA and Campy-Cefex agars is recommended to recover Campylobacter cells. It is also possible to use this method in different matrices (cloacal swabs and water samples). Cloacal swabs, samples from pre-chiller and post-chiller carcasses and samples of pre-chiller, chiller and direct supply water were collected each week for four weeks from the same flock at a slaughterhouse located in an abattoir in southern Brazil. Samples were analyzed to directly count Campylobacter spp., and the results showed a high frequency of Campylobacter spp. on Campy-Cefex agar. For the isolated species, 72% were identified as Campylobacter jejuni and 38% as Campylobacter coli. It was possible to count Campylobacter jejuni and Campylobacter coli from different samples, including the water supply samples, using the two-agar method. These results suggest that slaughterhouses can use direct counting methods with both agars and different matrices as a monitoring tool to assess the presence of Campylobacter bacteria in their products.


Subject(s)
Humans , Animals , Campylobacter/isolation & purification , Chickens/microbiology , Bacterial Load/methods , Food Microbiology , Campylobacter/classification , Campylobacter/genetics , Bacterial Typing Techniques/methods , Abattoirs
12.
Braz J Microbiol ; 47(3): 764-9, 2016.
Article in English | MEDLINE | ID: mdl-27237112

ABSTRACT

Campylobacter spp. cause foodborne illnesses in humans primarily through the consumption of contaminated chicken. The aim of this study was to evaluate the United States Department of Agriculture's (USDA) recommended methodology, protocol MLG 41.02, for the isolation, identification and direct plate counting of Campylobacter jejuni and C. coli samples from the broiler slaughtering process. A plating method using both mCCDA and Campy-Cefex agars is recommended to recover Campylobacter cells. It is also possible to use this method in different matrices (cloacal swabs and water samples). Cloacal swabs, samples from pre-chiller and post-chiller carcasses and samples of pre-chiller, chiller and direct supply water were collected each week for four weeks from the same flock at a slaughterhouse located in an abattoir in southern Brazil. Samples were analyzed to directly count Campylobacter spp., and the results showed a high frequency of Campylobacter spp. on Campy-Cefex agar. For the isolated species, 72% were identified as Campylobacter jejuni and 38% as Campylobacter coli. It was possible to count Campylobacter jejuni and Campylobacter coli from different samples, including the water supply samples, using the two-agar method. These results suggest that slaughterhouses can use direct counting methods with both agars and different matrices as a monitoring tool to assess the presence of Campylobacter bacteria in their products.


Subject(s)
Bacterial Load/methods , Campylobacter/isolation & purification , Chickens/microbiology , Food Microbiology , Abattoirs , Animals , Bacterial Typing Techniques/methods , Campylobacter/classification , Campylobacter/genetics , Humans
13.
Article in English | MEDLINE | ID: mdl-27007562

ABSTRACT

Salmonella spp. causes diseases in fowls, when species-specific serovars (Salmonella Pullorum and S.Gallinarum) are present in flocks, and public health problems, when non-typhoid serovars are isolated, as well as possible bacterial resistance induced by the preventive and therapeutic use of antimicrobials in animal production. This study describes the serovars and bacterial resistance of 280 Salmonella spp. strains isolated from turkey and broiler carcasses in Southern Brazil between 2004 and 2006. Salmonella Enteritidis was the most prevalent serovar (55.7%), followed by Heidelberg (5.0%), Agona (4.3%), Bredeney (3.9%), Hadar (3.2%), and Typhimurium (2.9%). Tennessee and S. Enterica subspecies enterica(O: 4.5) were isolated only in turkeys, and Hadar (18.6%) was the most prevalent serovar in this species. Antimicrobial susceptibility tests were performed in 178 isolates (43 from turkeys and 135 from broilers). All isolates were sensitive to amoxicillin + clavulanic acid, polymyxin B, ciprofloxacin, and norfloxacin, and were resistant to bacitracin and penicillin. Broiler carcass isolates showed resistance to nalidixic acid (48.9%), nitrofurantoin (34.3%), neomycin (9.6%), tetracycline (5.2%), and kanamycin (8.9%); and turkey carcass isolates were resistant to nalidixic acid (62.8%), tetracycline (34.9%), and neomycin (30.2%), with a significant difference in turkeys when compared to broiler carcass isolates. These results indicate the need for judicious use of antimicrobials in livestock production, given that the serovars identified are potential causes of food poisoning.


Subject(s)
Anti-Bacterial Agents/pharmacology , Salmonella/drug effects , Animals , Brazil , Chickens , DNA, Bacterial/analysis , Microbial Sensitivity Tests , Poultry Diseases/microbiology , Salmonella/classification , Salmonella/isolation & purification , Salmonella Infections, Animal/microbiology , Turkeys
14.
Pesqui. vet. bras ; 35(3): 223-229, 03/2015. tab
Article in Portuguese | LILACS | ID: lil-751978

ABSTRACT

Os produtos de origem avícola podem ser importantes veículos de transmissão de Salmonella spp. para humanos e, dentre os vários parâmetros que determinam a qualidade de um alimento, destacam-se os que definem suas características microbiológicas. Objetivou-se detectar e quantificar Salmonella spp. na tecnologia de abate de frangos de corte por microbiologia convencional (MC) e número mais provável miniaturizado (mNMP). As coletas foram realizadas em duas visitas a três abatedouros sob Inspeção Federal e em seis pontos de coleta em triplicata, definidos como: recepção das aves (swabs de cloaca e esponjas de gaiolas de transporte antes e após a higienização) e carcaças (após pré resfriamento em chiller, após o gotejamento e antes da embalagem primária e congeladas a -12oC por 24 horas), totalizando 108 amostras...


Poultry products can be important modes of transmission of Salmonella spp. to humans and, among several parameters used to determine food quality, microbiological characteristics play an essential role. The aim of this study was to determine and quantify Salmonella spp. at broiler slaughtering facilities. This was done by conventional microbiology and by the miniaturized most probable number (mMPN) methods. Three federally-inspected slaughterhouses were visited, where samples were collected in triplicate from six sites: reception of live birds (cloacal swabs and sponge samples from transport cages before and after sanitation) and carcass processing (after pre-chiller, after dripping, and before primary packaging and refrigeration at -12oC for 24h), totaling 108 samples...


Subject(s)
Animals , Abattoirs , Poultry/microbiology , Serogroup , Salmonella/isolation & purification , Multiple Tube Method
15.
Pesqui. vet. bras ; 34(4): 320-324, abr. 2014. graf, tab
Article in Portuguese | LILACS | ID: lil-712718

ABSTRACT

Os objetivos do trabalho foram avaliar o perfil de sensibilidade a antimicrobianos e a eficácia de três sanitizantes frente a isolados de Salmonella spp. oriundos de carcaças na tecnologia de abate de suínos. Avaliaram-se 120 amostras, das quais 39 foram positivas para Salmonella spp. Os princípios ativos testados foram penicilina G 10 U, amoxicilina + ácido clavulânico 30mcg, ampicilina 10mcg, cloranfenicol 30mcg, tetraciclina 30mcg, estreptomicina 10mcg, neomicina 30mcg, gentamicina 10mcg, enrofloxacina 5mcg, sulfazotrim 25mcg, sulfonamida 300mcg e trimetropima 5mcg. Nos testes com sanitizantes utilizaram-se clorexidina, amônia quaternária e ácido peracético com tempos de contato de um, cinco, 10 e 15 minutos. Os índices de resistência aos antimicrobianos foram de 100 por cento para penicilina, 94,9 por cento para tetraciclina, 89,7 por cento para trimetropima e 87,2 por cento para ampicilina. Nenhum dos princípios ativos foi 100 por cento eficaz frente aos isolados testados, observando-se melhor ação para amoxicilina+ácido clavulânico (86,7 por cento), neomicina (86,7 por cento) e cloranfenicol (64,1 por cento). Nos testes de eficácia dos sanitizantes, o ácido peracético a 0.5 por cento foi efetivo a partir de 10 minutos (94,6 por cento) e 15 minutos (97,3 por cento) de contato; amônia quaternária a 1 por cento por 10 minutos (89,2 por cento) e 15 minutos (97,3 por cento) e clorexidina a 0.5 por cento por 10 minutos (70,3 por cento) e 15 minutos de contato (72,8 por cento). Todas as amostras testadas apresentaram multirresistência e seis [...] O sanitizante mais efetivo frente aos isolados testados foi o ácido peracético a 0.5 por cento por 15 minutos, reforçando a necessidade de monitorar também a efetividade de produtos sanitizantes frente aos isolados de Salmonella spp.


The aim of this study was to evaluate the antimicrobial sensitivity and efficacy of three sanitizers against Salmonella spp. isolated from carcasses in swine slaughterhouse. Thirty nine of 120 samples were positive for Salmonella spp. The antimicrobials tested included: penicillin G 10 U, amoxicillin + clavulanic acid 30mcg, ampicillin 10mcg, chloramphenicol 30mcg, tetracycline 30mcg, streptomycin 10mcg, gentamicin 10mcg, neomycin 30mcg, enrofloxacin 5mcg, sulfazotrim 25mcg, sulfonamide 300mcg and trimetropim 5mcg. In the tests with sanitizers were used chlorhexidine, quaternary ammonia and peracetic acid, which were put in contact intervals of 1, 5, 10 and 15 minutes. Antimicrobial resistance was observed using penicillin (100 percent), tetracycline (94.9 percent), trimetropim (89.7 percent), and ampicillin (87.2 percent). None of the antimicrobials was 100 percent effective against the samples tested. Amoxicillin + clavulanic acid (86.7 percent), neomycin (86.7 percent) and chloramphenicol (64.1 percent) showed better antimicrobial action. In tests of efficacy of sanitizers, 0.5 percent peracetic acid was effective at 10 minutes (94.6 percent) and 15 minutes (97.3 percent) of contact; 1 percent quaternary ammonia at 10 minutes (89.2 percent) and 15 minutes (97.3 percent) and 0.5 percent chlorhexidine at 10 minutes (70.3 percent) and 15 minutes (72.8 percent). All samples tested were multidrug resistance and six (15.3 percent) showed resistance to ampicillin, chloramphenicol, streptomycin, sulfonamide and tetracycline (ACSSuT group) indicating the need to monitor the spread of antimicrobial resistance of Salmonella spp. isolated from swine. The most effective sanitizing against the bacteria tested was 0.5 percent peracetic acid per 15 minutes, reinforcing the need to monitor the effectiveness of products sanitizers against Salmonella spp.


Subject(s)
Animals , Ampicillin Resistance , Anti-Infective Agents, Local , Penicillin Resistance , Salmonella/isolation & purification , Tetracycline Resistance , Trimethoprim Resistance , Drug Resistance, Bacterial , Swine/microbiology
16.
Arq. ciênc. vet. zool. UNIPAR ; 17(3): 157-160, jul.-set.2014. graf
Article in Portuguese | LILACS | ID: lil-758601

ABSTRACT

A Salmonella pode estar presente em carcaças suínas ao final da tecnologia de abate, sendo que não existem procedimentos de inspeção especificamente direcionados para o controle desta bactéria, consideradas um risco potencial para a saúde pública. O objetivo do trabalho foi verificar a presença de Salmonella em carcaças suínas e caracterizar os pontos críticos de controle (PCCs) da tecnologia de abate como subsídio ao sistema APPCC. Foram realizados swabs de carcaças após a escaldagem/depilação, antes da evisceração, após evisceração e serragem da carcaça e após 24 horas de refrigeração, gerando 120 amostras (30 carcaças de cinco lotes). Isolou-se Salmonella em 53,3% dos PCs analisados, sendo 40% antes da eviscerarão e 30% após a escaldagem/depilação e evisceração/serragem. Nas carcaças resfriadas por 24 horas não foi isolada Salmonella. Os sorovares identificados foram Typhimurium (96,7 %) e Panama (3,22%). O isolamento de Salmonella reforça a necessidade de programas de monitoria da bactéria, desde as granjas até os abatedouros, enquanto o não isolamento nas carcaças resfriadas indica a importância da lavagem final e adequação da cadeia do frio, o que minimiza a contaminação pela intensificação das medidas de higiene e controle de pontos críticos para subsidiar o sistema APPCC...


Salmonella can be present in swine carcasses at the end of slaughtering and there is no specifically guided inspection procedure for the control of this bacterium, considered a potential risk for public health. The objective of this paper is to verify the presence of Salmonella in carcasses and to characterize the critical points of control (CPCs) of the slaughtering technology as a subsidy to the HACCP system. The carcasses were swabbed at different points during the slaughtering process, ant after 24 hours of refrigeration, generating 120 samples (30 carcasses from five different batches). Salmonella was isolated in 53.3% of the CPs analyzed, being 40% before evisceration and 30% after scalding/depilation and evisceration/ sawing. No Salmonella was isolated in the carcasses refrigerated for 24 hours. Typhimurium (96.7%) and Panama (3.22%) were the serovars identified. Salmonella isolation indicates the need of programs to monitor the bacterium from the farms to the slaughterhouse, while the non-isolation in the refrigerated carcasses shows the relevance of the cold chain, which minimizes the contamination by the intensification of hygiene measures and the control of critical points to subsidize the HACCP system...


La Salmonella puede estar presente en carcasas porcinas al final de la matanza, siendo que no existen procedimientos de inspección específicamente direccionados para el control de esta bacteria, consideradas un riesgo potencial a la salud pública. El objetivo del trabajo ha sido verificar la presencia de Salmonella en carcasas porcinas y caracterizar los puntos críticos de control (PCCs) en la tecnología de matanza como subsidio al sistema APPCC. Se han realizado swabs de carcasas tras escaldadura/depilación, antes de evisceración, después de la evisceración y serrín de la carcasa y después de 24 horas de refrigeración, generando 120 muestras (30 carcasas de cinco lotes) Se ha aislado Salmonella en 53,3% de los PCs analizados, siendo 40% antes de evisceración y 30% después de la escaldadura/depilación y evisceración/serrín. En las carcasas enfriadas por 24 horas no se ha aislado Salmonella. Los serovares identificados fueron Typhimurium (96,7%) y Panama (3,22%). El aislamiento de Salmonella refuerza la necesidad de programas de monitoria de la bacteria, desde las granjas hasta los mataderos, el no aislamiento en las carcasas enfriadas indica la importancia del lavado final y adecuación de la cadena del frío, lo que minimiza la contaminación por la intensificación de las medidas de higiene y control de puntos críticos para subsidiar el sistema APPCC...


Subject(s)
Animals , Animal Culling/instrumentation , Animal Culling/methods , Hazard Analysis and Critical Control Points/methods , Salmonella/isolation & purification , Swine/abnormalities , Technology
18.
Braz. j. microbiol ; 42(1): 266-273, Jan.-Mar. 2011. ilus, tab
Article in English | LILACS | ID: lil-571399

ABSTRACT

Over the years, Salmonella Heidelberg (SH) has gained prominence in North America poultry production and in the poultry production of other countries. Salmonella Heidelberg has been isolated and reported from poultry and poultry products in Brazil since 1962, whereas Salmonella Enteritidis (SE) has only emerged as a serious problem in poultry and public health since 1993. These strains of Salmonella can cause intestinal problems in newly hatched chicks, and infection may persist until adulthood. Upon slaughter of chickens, Salmonella can contaminate carcasses, a condition that poses a threat to human health. The aim of this study was to compare the fecal excretion of Salmonella Enteritidis and Salmonella Heidelberg in newly hatched chicks (orally inoculated with 10(5)ufc/mL each) until 20 days of age. In addition, the ratio of cecal villus height:crypt depth (morphometry) and liver and cecum cell counts was analyzed in chicks ranging from 0 to 3 days of age and infected with these two Salmonella strains. One hundred seventeen chicks were separated into one of three experimental groups: a control group, an SE-infected group and an SH-infected group. Eight chicks per group were euthanized at 6, 12 and 72 hours post-inoculation (pi) to allow for Salmonella isolation from the liver and cecum and for the collection of the cecum for villi and crypt analysis. Other birds were allowed to mature to 20 days of age and cloacal swabs were taken at 2, 6, 13 and 20 days pi to compare the fecal excretion of inoculated strains. The Salmonella Enteritidis group had a higher number of cells excreted during the trial. Both strains were isolated from the liver and cecum by 6h pi. At 12h pi the Salmonella Heidelberg group had high cell counts in the cecum. No difference was found in liver cell counts. Both strains showed lower villus height:crypt depth ratio than the control group post-infection.


Subject(s)
Animals , Microscopy, Electron , Poultry , Salmonella Infections, Animal , Salmonella enteritidis/isolation & purification , Colony Count, Microbial , Food Samples , Methods , Serial Passage , Methods
19.
Braz. j. microbiol ; 41(4): 1082-1085, Oct.-Dec. 2010. tab
Article in English | LILACS | ID: lil-595751

ABSTRACT

This study assessed biofilm formation on polystyrene by Staphylococcus aureus, Listeria monocytogenes, L. welshimeri and Escherichia coli, isolated from a slaughtering plant, grown on tryptic soy broth (TSB) using different glucose concentrations. The tested bacteria produced biofilm in at least one of the concentrations used, and some of them were strong biofilm producers.

20.
Braz J Microbiol ; 41(4): 1082-5, 2010 Oct.
Article in English | MEDLINE | ID: mdl-24031590

ABSTRACT

This study assessed biofilm formation on polystyrene by Staphylococcus aureus, Listeria monocytogenes, L. welshimeri and Escherichia coli, isolated from a slaughtering plant, grown on tryptic soy broth (TSB) using different glucose concentrations. The tested bacteria produced biofilm in at least one of the concentrations used, and some of them were strong biofilm producers.

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