Enteric bacteria are considered important potential pathogens in avian clinical medicine, causing either primary or opportunistic infections. The aim of this study was to evaluate the frequency of enterobacteria in the intestinal microbiota of psittacine birds and to determine the antimicrobial susceptibility of the Escherichia coli isolates cultured. Fecal samples were collected from 300 parrots captured from the illegal wildlife trade in Goiás, Brazil and were processed using conventional bacteriological procedures. A total of 508 isolates were obtained from 300 fecal samples: 172 E. coli (33.9% of isolates; 57.3% of individuals); 153 Enterobacter spp. (30.1% of isolates; 51.0% of individuals); 89 Klebsiella spp. (17.7% of isolates; 29.7% of individuals); 59 Citrobacter spp. (11.6% of isolates; 19.7% of individuals), 21 Proteus vulgaris (4.2% of isolates; 7.0% of individuals), 5 Providencia alcalifaciens (0.98% of isolates; 1.67% of individuals), 5 Serratia sp. (0.98% of isolates; 1.67% of individuals), 3 Hafnia aivei (0.59% of isolates; 1.00% of individuals), and 1 Salmonella sp. (0.20% of isolates; 0.33% of individuals). Escherichia coli isolates were subsequently tested for susceptibility to the following antibiotics: amoxicillin (70.93% of the isolates were resistant), ampicillin (75.58%), ciprofloxacin (23.25%), chloramphenicol (33.14%), doxycycline (64.53%), enrofloxacin (41.28%), tetracycline (69.19%), and sulfonamide (71.51%). Multi-resistance to three and four groups of antibiotics occurred in 40 samples (23.25%) and 4 samples (2.32%), respectively. These results demonstrate that illegally traded birds are carriers of potentially pathogenic bacteria, including E. coli strains with antimicrobial resistance.
Conventional bacteriology techniques and quantitative polymerasechain reaction (qPCR) were applied to the eggshell, albumen, and yolk of washed and unwashed commercial white and brown eggs, to detect Salmonella spp. Pooled samples of eggshells, albumen, and yolk of white and brown eggs were collected at the poultry house and at the egg-storage room. Salmonella spp. was detected by conventional bacteriology in 5.4% (21/387) of analyzed samples and in 16% (68/387) by qPCR. In the 114 unwashed white eggs samples of eggshell, albumen and yolk, the bacterium was identified in 2.6% of the eggs (3/114) by conventional bacteriology and in 13.2% (15/114) by qPCR. In the 90 samples of washed eggs, 6.7% (6/90) were contaminated as detected by conventional bacteriology and 10.0% (9/90) by qPCR. In the 81 samples of unwashed brown eggs, Salmonella spp. was detected in 6.1% of the eggs (5/81) by conventional bacteriology and 27.2% (22/81) by qPCR. In the 102 samples of brown washed eggs, 6.9% (7/102) where positive by conventional bacteriology and 35.3% (16/102) by qPCR. All samples detected as positive by conventional bacteriology were also positive by qPCR. Salmonella Agona represented 18.2% (4/22) of identified serovars, Salmonella enterica subs. enterica O: 4.5 18.2%
Este trabalho foi desenvolvido com objetivo de pesquisar Salmonella em amostras de fígado, coração, saco da gema e mecônio de pintos de corte de um dia; inglúvios e cecos obtidos em abatedouros e em suabes de arrasto; larvas ou adultos de Alphitobius diaperinus. Complementarmente, determinou-se o perfil de suscetibilidade aos antimicrobianos: amoxicilina (10 mcg), ampicilina (10 mcg), ciprofloxacina (5 mcg), enrofloxacina (5 mcg), florfenicol (30 mcg), neomicina (30 mcg), sulfonamida (300 mcg), tetraciclina (30 mcg) e trimetoprim-sulfametoxazol (25 mcg) dos serovares tipificados isolados. As amostras foram submetidas às análises microbiológicas pelos métodos bacteriológicos convencionais. Salmonella sp. foi isolada em 6,2% (4/64) do fígado, 4,7% (3/64) do coração, 3,1% (2/64) dos sacos da gema e 4,7% (3/64) do mecônio, num total de 4,7% (12/256) (pinto de um dia); em 10,2% (13/128) das amostras ambientais, sendo 9,4% (9/96) de suabes de arrasto 12,5%, (4/32) de larvas e adultos Alphitobius diaperinus e em 4,4% (28/640) das amostras em abatedouros, sendo 6,5% (21/320) dos inglúvios e 2,2% (7/320) dos conteúdos cecais de abatedouro. Salmonella enterica ser. Enteritidis foi identificada em suabes de arrasto e em amostras de Alphitobius diaperinus, enquanto Salmonella enterica ser. Typhimurium foi encontrada nos inglúvios e cecos. Salmonella enterica ser. Enteritidis apresentaram 75% (6/8) de resistência às sulfonamidas e Salmonella enterica ser. Typhimurium 100% (3/3). A amoxicilina foi outro antimicrobiano com elevada frequência de resistência. Adicionalmente, 20,7% (11/53) dos serovares apresentaram resistência simultânea a pelo menos dois princípios ativos. Conclui-se que Salmonella encontra-se amplamente distribuída no fluxo de produção de frangos de corte, e a via vertical continua sendo uma fonte de introdução de Salmonella sp. à cadeia de produção; cama e insetos podem perpetuar e veicular Salmonella de interesse zoonótico no ambiente avícola; a existência de cepas resistentes aos antimicrobianos, bem como a resistência múltipla, constituem ameaça à saúde pública.
RESUMO -Avaliaram-se os efeitos de Salmonella Enteritidis sobre a colonização e o desenvolvimento do trato intestinal, a conversão alimentar e o ganho de peso em perus. Um total de 135 perus de corte de 1 dia foi distribuído em três tratamentos:controle; perus oriundos de ovos inoculados com Salmonella Enteritidis via casca e perus desafiados com água de bebida com Effects of experimentally inoculated Salmonella Enteritidis on the gastrointestinal health of turkeysABSTRACT -The effects of Salmonella Enteritidis on the colonization and development of the intestinal tract, feed conversion and weight gain were evaluated. A total of 135 day old turkeys were assigned to three treatments: control; turkeys from eggs inoculated with Salmonella Enteritidis via shell and turkeys challenged with drinking water with Salmonella Enteritidis. At 10, 20 and 28 days, the performance variables were evaluated and samples were collected to perform bacterial assessment, biometrics and histomorphometry. On days one, 15 and 28, samples of meconium/excreta were collected from all birds. The intestinal colonization increased during the initial phase when Salmonella was inoculated via eggshell. The intestine showed greater weight on the first, tenth and 28th days when Salmonella was present, with no differences regarding the intestine length. Salmonella Enteritidis was able to colonize the intestinal tract, establish infection, reduce bird performance and modify the cellular structures of the intestine. Contamination of the eggshell before hatching generated birds susceptible to infection at birth and the frequency of isolation of Salmonella Enteritidis persisted until 28 days of age.Salmonella inoculation by drinking water generated infected birds, but with less recovery of the pathogen with age increase.Inoculated birds showed inferior performance, confirming the potential damage to poultry production.
This present study was developed with the objective of detect Salmonella sp. by conventional bacteriology and qPCR techniques in samples of flooring material from transport crates (meconium); raising environment (swab of cages and drinking fountains); cloacal swab; food and insects from growing, rearing and production phases in a commercial group of laying hens. A total of 864 samples were collected, among whom 248 originated from growing, 392 from rearing and 224 from production phase. Among the 864 samples, 2,8% where positives in bacteriologic technique and 15.3% in qPCR. Contamination was higher in growing and rearing phases and declined in production phase. Twenty four isolations of Salmonella where typified as Salmonella Agona (41.7%), Salmonella Livingstone (33.3%), Salmonella Cerro (16.7%), Salmonella Senftenberg (4.2%) and Salmonella Schwarzengrund (4.2%). During growing phase Salmonella Livingstone was identified. These findings suggest vertical contamination in the group. During rearing and production phases, isolated materials belong to serovars Agona, Cerro, Senftenberg and Schwarzengrund, pointing to horizontal contamination. It is possible to conclude that both vertical and horizontal contaminations are important during the cycle of commercial egg production and contamination in rearing phase is higher than in growing and production phases.
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