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1.
Avian Dis ; 45(4): 1044-9, 2001.
Article in English | MEDLINE | ID: mdl-11785876

ABSTRACT

Control of carcass contamination requires knowledge of the source and dynamics of spread of Salmonella in commercial poultry production. We examined Salmonella contamination at a U.S. commercial quail operation. Pulsed-field gel electrophoresis (PFGE) was used to type isolates in order to trace Salmonella throughout this production environment. During a 6-mo survey, Salmonella serotypes hadar, typhimurium, typhimurium variant Copenhagen, and paratyphi were encountered within this poultry operation. Ninety-four percent of the Salmonella isolated from breeder and production houses and from carcass rinses belonged to Salmonella serotypes typhimurium variant Copenhagen and hadar. There were six distinct S. typhimurium variant Copenhagen genetic types, as identified by PFGE, present within this particular poultry operation. Seventy-nine percent of S. typhimurium variant Copenhagen identified from the environment of the breeder and production houses produced the same PFGE pattern. Thirty-eight percent of S. typhimurium Copenhagen isolated from carcass rinses and the breeder house shared the same PFGE DNA pattern. This study demonstrates the transmission of salmonellae throughout this production environment, from the breeders to their progeny and to the birds ultimately processed for human consumption.


Subject(s)
Coturnix , Poultry Diseases/microbiology , Salmonella Infections, Animal/transmission , Salmonella/isolation & purification , Animal Husbandry , Animals , Disease Transmission, Infectious/veterinary , Electrophoresis, Gel, Pulsed-Field/veterinary , Food Contamination , Food Microbiology , Meat/microbiology , Poultry Diseases/diagnosis , Poultry Diseases/transmission , Salmonella/classification , Salmonella Infections, Animal/diagnosis , Salmonella Infections, Animal/microbiology , Serotyping/veterinary
2.
Avian Dis ; 45(4): 953-61, 2001.
Article in English | MEDLINE | ID: mdl-11785899

ABSTRACT

Antibiotics are used in food animal production to treat diseases and also to improve performance. Antibiotics are not used on all farms, and antibiotic resistance is occasionally found on farms that do not use antibiotics. Rendered animal protein products are often included in poultry feeds and could potentially serve as a source of antibiotic-resistant bacteria. One hundred sixty-five rendered animal protein products from cattle, poultry, and fish were aseptically collected from poultry feed mills. Fifty-five percent of the poultry meal samples had detectable levels of gram-negative bacteria ranging from 40 to 10,440 colony-forming units/g of sample. Poultry meal and meat and bone meal had the greatest number of samples with bacteria resistant to five or more antibiotics. A high percentage of feed samples (85%) contained bacteria resistant to amoxicillin, ampicillin, clavulanic acid, or cephalothin, whereas few samples contained bacteria resistant to ciprofloxacin, kanamycin, or trimethoprim/sulfamethoxazole. Acinetobacter calcoaceticus, Citrobacter freundii, and Enterobacter cloacae were the most commonly isolated antibiotic-resistant bacteria. Isolation for Salmonella was also performed, with 14% of the meat and bone meal samples containing Salmonella sp. Only one of the meat and bone meal isolates, Salmonella livingstone, was resistant to five or more antibiotics. Many of the antibiotic-resistant bacteria contained integrons, genetic elements that mediate multiple drug resistance.


Subject(s)
Animal Feed/microbiology , Anti-Bacterial Agents/pharmacology , Gram-Negative Bacteria/drug effects , Proteins/administration & dosage , Animal Feed/analysis , Animals , Cattle , Chickens , Colony Count, Microbial , Drug Resistance, Multiple, Bacterial , Fish Products/microbiology , Fishes , Gram-Negative Bacteria/growth & development , Meat Products/microbiology , Microbial Sensitivity Tests
3.
Avian Dis ; 42(3): 431-51, 1998.
Article in English | MEDLINE | ID: mdl-9777144

ABSTRACT

Escherichia coli is a common inhabitant of the gastrointestinal tract of most animals. Like most pathogenic E. coli, avian isolates cannot be distinguished biochemically from the normal commensals inhabiting the gastrointestinal tract of birds. Using a molecular approach, we were able to identify genetic differences among avian E. coli isolates by restriction fragment length polymorphism (RFLP) and random amplification of polymorphic DNA (RAPD) by the polymerase chain reaction (PCR). Several different RFLPs were observed among avian E. coli isolates using DNA probes for 16S ribosomal RNA genes (rrn) and insertion sequence elements (IS2). We were also able to observe differences in DNA banding patterns generated by RAPD analysis. Similarities and differences among avian E. coli were discernible using RFLPs and RAPD analysis, whereas conventional bacteriological methods failed to differentiate these isolates. Based on RAPD patterns, avian E. coli appear to be genetically diverse. Of 16 different RAPD types (RT) encountered, 84% of E. coli fell into seven major RTs. One RT was present in clinical isolates but absent from the commensals isolated in this study. Many of these different E. coli RTs were not geographically restricted to northern Georgia but were also observed in other southern states in the United States. Resistance to various antibiotics was randomly associated with different E. coli RTs. Sarafloxacin resistance was present among different E. coli RTs, suggesting that antibiotic usage is not selecting for a clonal population in avian E. coli. RAPD provides a rapid and powerful tool to study the epidemiology of avian E. coli.


Subject(s)
Escherichia coli/genetics , Animals , Chickens/microbiology , DNA Fingerprinting , DNA Primers/genetics , DNA, Bacterial/genetics , Oligonucleotides/genetics , Polymorphism, Restriction Fragment Length , Random Amplified Polymorphic DNA Technique , Turkeys/microbiology
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