RESUMO

Background: broilers spend most of their lives in contact with litter; litter quality can affect their health and performance. Objective: the effects of litter treatment on performance and carcass lesions were evaluated in five consecutive flocks with 640 male broilers each. Methods: a completely randomized model was used comprising eight treatments and four replicates. The treatments included (1) untreated litter, (2) litter subjected to in-house composting, (3) litter treated (LT) with aluminum sulfate, (4) LT with gypsum, (5) LT with quicklime, (6) LT with dolomitic limestone, (7) LT with zeolite, and (8) LT with charcoal. Chopped elephant-grass hay was used as poultry litter in all flocks. Results: none of the litter treatments were found to influence the performance and carcass lesions of the male broilers in all five flocks. Furthermore, poultry litter treatments were not economically viable. Conclusion: poultry litter treatments did not affect the performance and scores of carcass lesions of male broilers, but increased the cost of poultry production.

Antecedentes: los pollos de engorde pasan la mayoría de su vida en contacto con la cama; la calidad de la cama puede afectar la salud y desempeño del ave. Objetivo: fueron evaluados los efectos de diferentes tratamientos de la cama sobre el desempeño y lesiones en la canal de pollos de engorde durante cinco lotes consecutivos con 640 aves cada uno. Métodos: se empleó un modelo completamente aleatorizado con ocho tratamientos y cuatro repeticiones. Los tratamientos incluyeron (1) cama no tratada, (2) cama sometida a compostaje en el galpón, (3) cama tratada (CT) con sulfato de aluminio, (4) CT con yeso agrícola, (5) CT con cal, (6) CT con calcáreo dolomítico, (7) CT con zeolita y (8) CT con carbón vegetal. Heno de pasto elefante picado fue usado como cama en todos los lotes. Resultado: los tratamientos no influenciaron el desempeño ni las lesiones en la canal de los pollos en ningún lote. Además, ninguno de los tratamientos de las camas fue económicamente viables. Conclusión: el tratamiento de la cama de pollo no solo no afecta el desempeño ni las lesiones en la canal de los pollos sino que eleva los costos de producción de las aves.

Antecedentes: os frangos de corte passam a maioria de suas vidas em contato com a cama e a qualidade desta pode afetar a saúde e o desempenho produtivo da ave. Objetivo: Avaliou-se os efeitos dos tratamentos da cama de frango sobre o desempenho no crescimento e lesões na carcaça de frangos de corte. Métodos: avaliaram-se 640 aves por lote, durante cinco lotes consecutivos, analisaram-se empregando um modelo completamente casualizado com oito tratamentos e quatro repetições. Os tratamentos consistiram de (1) cama não tratada, (2) cama submetida a compostagem no galpão, (3) cama tratada (CT) com sulfato de alumínio, (4) CT com gesso agrícola, (5) CT com cal virgem, (6) CT com calcário dolomítico, (7) CT com zeolita e (8) CT com carvão vegetal. Feno de capim elefante picado foi usado como cama em todos os lotes. Resultado: os diferentes tratamentos não influenciaram o desempenho na produção e as lesões na carcaça dos frangos em nenhum lote, entretanto, os tratamentos da cama foram economicamente inviáveis. Conclusão: o tratamento da cama de frango não afeta o desempenho produtivo e os escores de lesões na carcaça dos frangos de corte, além, eleva os custos da produção avícola.

RESUMO

Background: Broilers are a reservoir of Campylobacter (C.), an important causal agent of gastroenteritis mostly associated to handling and consumption of broiler meat. The majority of broiler fl ocks are colonized by thermophilic Campylobacter at the slaughter age, and carcasses might be contaminated throughout the processing line. Since surveillance is crucial to evaluate and improve approaches to reduce Campylobacter spread during broiler processing, a cross-sectional study was carried out to detect the level of Campylobacter contamination in a broiler at slaughterMaterials, Methods & Results: Cloacal swabs, caeca and whole carcasses were taken from a broiler fl ock slaughtered in Southern Brazil. Samples were individually inoculated in Bolton Broth (BB) and incubated at 41.5C in a microaerobic atmosphere for 44 h, when the enriched culture was inoculated onto modifi ed Charcoal Cefoperazone Deoxycholate Agar (mCCDA) and Campy-Cefex Agar (CCA) plates. All plates were incubated at 41.5C in the microaerobic atmosphere for 44 h. Aliquots of each enriched BB were collected and submitted to polymerase chain reaction (PCR), while the genetic relatedness of isolates was analyzed by pulsed-fi eld gel electrophoresis (PFGE). A total of 3 (9.4%) cloacal swabs were positive for C. jejuni. No Campylobacter was isolated from any of the caecal contents or broiler carcasses analyzed.

Background: Broilers are a reservoir of Campylobacter (C.), an important causal agent of gastroenteritis mostly associated to handling and consumption of broiler meat. The majority of broiler fl ocks are colonized by thermophilic Campylobacter at the slaughter age, and carcasses might be contaminated throughout the processing line. Since surveillance is crucial to evaluate and improve approaches to reduce Campylobacter spread during broiler processing, a cross-sectional study was carried out to detect the level of Campylobacter contamination in a broiler at slaughter.Materials, Methods & Results: Cloacal swabs, caeca and whole carcasses were taken from a broiler fl ock slaughtered in Southern Brazil. Samples were individually inoculated in Bolton Broth (BB) and incubated at 41.5C in a microaerobic atmosphere for 44 h, when the enriched culture was inoculated onto modifi ed Charcoal Cefoperazone Deoxycholate Agar (mCCDA) and Campy-Cefex Agar (CCA) plates. All plates were incubated at 41.5C in the microaerobic atmosphere for 44 h. Aliquots of each enriched BB were collected and submitted to polymerase chain reaction (PCR), while the genetic relatedness of isolates was analyzed by pulsed-fi eld gel electrophoresis (PFGE). A total of 3 (9.4%) cloacal swabs were positive for C. jejuni. No Campylobacter was isolated from any of the caecal contents or broiler carcasses analyzed.

RESUMO

Background: Broilers are a reservoir of Campylobacter (C.), an important causal agent of gastroenteritis mostly associated to handling and consumption of broiler meat. The majority of broiler flocks are colonized by thermophilic Campylobacter at the slaughter age, and carcasses might be contaminated throughout the processing line. Since surveillance is crucial to evaluate and improve approaches to reduce Campylobacter spread during broiler processing, a cross-sectional study was carried out to detect the level of Campylobacter contamination in a broiler at slaughter. Materials, Methods & Results: Cloacal swabs, caeca and whole carcasses were taken from a broiler flock slaughtered in Southern Brazil. Samples were individually inoculated in Bolton Broth (BB) and incubated at 41.5°C in a microaerobic atmosphere for 44 h, when the enriched culture was inoculated onto modified Charcoal Cefoperazone Deoxycholate Agar (mCCDA) and Campy-Cefex Agar (CCA) plates. All plates were incubated at 41.5°C in the microaerobic atmosphere for 44 h. Aliquots of each enriched BB were collected and submitted to polymerase chain reaction (PCR), while the genetic relatedness of isolates was analyzed by pulsed-field gel electrophoresis (PFGE). A total of 3 (9.4%) cloacal swabs were positive for C. jejuni. No Campylobacter was isolated from any of the caecal contents or broiler carcasses analyzed. In addition, negative mCCDA and CCA plates showed an abundant growth of contaminant cells. The PCR assay detected all thermophilic Campylobacter reference strains tested and also the Arcobacter species. No amplified product was obtained from the non-related bacterial species analyzed. It was possible to identify 29 (90.6%) cloacal swabs, 32 (97.0%) caecal contents and 31 (100%) broiler carcasses Campylobacter-positive by PCR analysis. PFGE typing of the C. jejuni isolated resulted in two clearly distinguished genotypes which were grouped into different clusters. Discussion: The detection of C. jejuni in only few cloacal swabs sampled contrasts with higher frequencies of Campylobacter previously described in broilers. However, the enrichment culture of fecal samples might be compromised by the many competing non-target bacteria present, which may have prevented the detection of Campylobacter-positive samples. In addition, the BB and selective media containing cefoperazone might have allowed the growth of cefoperazone-resistant contaminant cells from fecal and carcasses samples, which masked Campylobacter cells onto mCCDA and CCA. To improve the detection of Campylobacter in broiler samples, alternative antimicrobial supplements or reduction of the time of enrichment has already been suggested. PCR showed a higher number of positive samples, which might reflect the increased ability of the PCR assay to detect either injured cells in conventional enrichment culture or Campylobacter that were masked by the proliferation of competing cells onto selective media used. The PCR assay was able to detect all the reference strains of thermophilic Campylobacter, but also the related Arcobacter species. However, the temperature of incubation of the enriched cultures associated to the selective pressure of the antimicrobials present in the BB restricts the growth of Arcobacter and the false-positive results observed using PCR. The subtypes of the C. jejuni strains isolated showed that the target broiler flock was simultaneously colonized by more than one C. jejuni strain which might be the result of introduction of Campylobacter from different sources at farm. PCR analysis showed high Campylobacter contamination level of the target flock at slaughter, pointing to the need for additional studies to investigate Campylobacter sources at broiler processing.

Assuntos

RESUMO

Background: Broilers are a reservoir of Campylobacter (C.), an important causal agent of gastroenteritis mostly associated to handling and consumption of broiler meat. The majority of broiler fl ocks are colonized by thermophilic Campylobacter at the slaughter age, and carcasses might be contaminated throughout the processing line. Since surveillance is crucial to evaluate and improve approaches to reduce Campylobacter spread during broiler processing, a cross-sectional study was carried out to detect the level of Campylobacter contamination in a broiler at slaughterMaterials, Methods & Results: Cloacal swabs, caeca and whole carcasses were taken from a broiler fl ock slaughtered in Southern Brazil. Samples were individually inoculated in Bolton Broth (BB) and incubated at 41.5C in a microaerobic atmosphere for 44 h, when the enriched culture was inoculated onto modifi ed Charcoal Cefoperazone Deoxycholate Agar (mCCDA) and Campy-Cefex Agar (CCA) plates. All plates were incubated at 41.5C in the microaerobic atmosphere for 44 h. Aliquots of each enriched BB were collected and submitted to polymerase chain reaction (PCR), while the genetic relatedness of isolates was analyzed by pulsed-fi eld gel electrophoresis (PFGE). A total of 3 (9.4%) cloacal swabs were positive for C. jejuni. No Campylobacter was isolated from any of the caecal contents or broiler carcasses analyzed.

Background: Broilers are a reservoir of Campylobacter (C.), an important causal agent of gastroenteritis mostly associated to handling and consumption of broiler meat. The majority of broiler fl ocks are colonized by thermophilic Campylobacter at the slaughter age, and carcasses might be contaminated throughout the processing line. Since surveillance is crucial to evaluate and improve approaches to reduce Campylobacter spread during broiler processing, a cross-sectional study was carried out to detect the level of Campylobacter contamination in a broiler at slaughter.Materials, Methods & Results: Cloacal swabs, caeca and whole carcasses were taken from a broiler fl ock slaughtered in Southern Brazil. Samples were individually inoculated in Bolton Broth (BB) and incubated at 41.5C in a microaerobic atmosphere for 44 h, when the enriched culture was inoculated onto modifi ed Charcoal Cefoperazone Deoxycholate Agar (mCCDA) and Campy-Cefex Agar (CCA) plates. All plates were incubated at 41.5C in the microaerobic atmosphere for 44 h. Aliquots of each enriched BB were collected and submitted to polymerase chain reaction (PCR), while the genetic relatedness of isolates was analyzed by pulsed-fi eld gel electrophoresis (PFGE). A total of 3 (9.4%) cloacal swabs were positive for C. jejuni. No Campylobacter was isolated from any of the caecal contents or broiler carcasses analyzed.

RESUMO

Com o objetivo de avaliar as condições higiênico-sanitárias das carcaças de frango in natura comercializadas em mercados públicos do Município de São Luís, MA, foram colhidas quarenta amostras de carcaças de frango e analisadas quanto à pesquisa de Salmonella spp., Staphylococcus coagulase positivos e contagem padrão de micro-organismos mesófilos pelos métodos convencionais. Do total de amostras analisadas, 18 (45%) apresentaram contaminação por Staphylococcus coagulase positivos, 5 (12,5%) estavam contaminadas por Salmonella spp., identificadas como Salmonella Albany. A contagem padrão de micro-organismos mesófilos variou de 103 a 107 UFC/g no alimento analisado. Os resultados obtidos indicam que as condições higiênico-sanitárias das carcaças de frango in natura analisadas são insatisfatórias e que este produto pode ser um importante veículo de toxi-infecção alimentar.

The objective of this study was to evaluate the hygienic-sanitary conditions of in natura broiler carcasses commercialized in the market from São Luiz City, MA. Forty samples were collected and analyzed to research of Salmonella spp., coagulase positive Staphylococcus and of mesophilic microorganisms count. Among the analyzed samples, eighteen (45%) were contaminated with coagulase positive Staphylococcus, five (12,5%) were contaminated with Salmonella sp, being identified Salmonella Albany and counting of 103 to 107 UFC/g of mesophilic microorganisms. The results showed the hygienic-sanitary conditions samples analyzed were unsatisfactory and the consumption of this products can lead to an intoxication.

Assuntos

RESUMO

ABSTRACT The objective of this study was to evaluate the hygienic-sanitary conditions of in natura broiler carcasses commercialized in the market from São Luiz City, MA. Forty samples were collected and analyzed to research of Salmonella spp., coagulase positive Staphylococcus and of mesophilic microorganisms count. Among the analyzed samples, eighteen (45%) were contaminated with coagulase positive Staphylococcus, five (12,5%) were contaminated with Salmonella sp, being identified Salmonella Albany and counting of 103 to 107 UFC/g of mesophilic microorganisms. The results showed the hygienic-sanitary conditions samples analyzed were unsatisfactory and the consumption of this products can lead to an intoxication.

RESUMO Com o objetivo de avaliar as condições higiênico-sanitárias das carcaças de frango in natura comercializadas em mercados públicos do Município de São Luís, MA, foram colhidas quarenta amostras de carcaças de frango e analisadas quanto à pesquisa de Salmonella spp., Staphylococcus coagulase positivos e contagem padrão de micro-organismos mesófilos pelos métodos convencionais. Do total de amostras analisadas, 18 (45%) apresentaram contaminação por Staphylococcus coagulase positivos, 5 (12,5%) estavam contaminadas por Salmonella spp., identificadas como Salmonella Albany. A contagem padrão de micro-organismos mesófilos variou de 103 a 107 UFC/g no alimento analisado. Os resultados obtidos indicam que as condições higiênico-sanitárias das carcaças de frango in natura analisadas são insatisfatórias e que este produto pode ser um importante veículo de toxi-infecção alimentar.

RESUMO

ABSTRACT Processing of poultry products requires a severe microbiological quality control, considering they are one of the main sources of foodborne infections. The objective of this research was to perform the isolation of enterobacteria in broiler carcasses from commercial establishments in the Metropolitan Region of Fortaleza in Ceará State, Brazil. Broiler carcasses were collected and selected as fresh (n = 14), refrigerated (n = 18) and frozen (n = 19). Carcasses were submitted to a rinsing method, followed by pre-enrichment and enrichment with Rappaport-Vassiliadis and Selenite-Cystine, streaked on plates with Brilliant Green, MacConkey and Salmonella-Shigella agars, and to a presumptive biochemical identification. It was verified that all broiler carcasses categories presented enterobacteria contamination, with the following frequency of isolation: Proteus sp., 66.7%; Enterobacter sp., 15.7%; Citrobacter sp., 2%; Escherichia coli, 47.1%; Klebsiella sp., 11.8%; Shigella sp., 5.9%, and Salmonella sp. 11.8%. It was observed that no combination of culture media was able to detect all enterobacteria contamination in the broiler carcasses. Thus, it may be necessary the use of several combinations of culture media to determine the real microbiological quality of broiler carcasses.

RESUMO A carne de frango requer um rígido controle de qualidade microbiológica em seu processamento, uma vez que é uma das principais fontes de infecção alimentar para o homem. Desta forma, a presente pesquisa teve como objetivo realizar o isolamento de enterobactérias em carcaças de frango de corte obtidas em estabelecimentos comerciais na região metropolitana de Fortaleza no Estado do Ceará, Brasil. As carcaças foram coletadas e agrupadas em três categorias: frescas (n = 14), refrigeradas (n = 18) e congeladas (n = 19). As amostras foram submetidas a um método de enxaguadura, seguido por pré-eriquecimento e enriquecimento seletivo com os meios Rappaport-Vassiliadis e Selenito-Cistina, plaqueamento nos meios sólidos Verde Brilhante, MacConkey e Salmonella-Shigella e, posteriormente, a provas bioquímicas de identificação. Foram realizadas diversas combinações entre os meios para o processamento das amostras. Todas as categorias de carcaças apresentaram contaminação por enterobactérias, com as seguintes freqüências de isolamentos Proteus sp., 66,7%; Enterobacter sp., 15,7%; Citrobacter sp., 2%; Escherichia coli, 47,1%; Klebsiella sp., 11,8%; Shigella sp., 5,9% e Salmonella sp., 11,8%. Nenhuma combinação dos meios de cultura empregados foi capaz de isolar todas as contaminações por enterobactérias nas carcaças. Desta forma, é necessário o uso de várias combinações de meios de cultura para determinação real da qualidade microbiológica de carcaças de frango.