Jean E. Sander

Investigation of Bacterial Resistance to Hatchery Disinfectants

Three commercial chicken hatcheries were sampled for environmental bacteria. Isolated bacteria were tested for resistance to commercial preparations of quaternary ammonia, phenolic, and glutaraldehyde liquid disinfectants. Bacterial isolates were exposed to several disinfectant dilutions bracketing the dilutions recommended by the manufacturer for 5-, 10-, and 15-min exposure periods before subculturing to broth medium. Approximately 8% of the isolates from two of three hatcheries were resistant to disinfectant concentrations at and above the manufacturers recommended dilution and time of exposure. Resistant bacteria included Serratia marcescens, Bacillus cereus, Bacillus thuringiensis, Bacillus badius, Enterococcus faecalis, Enterococcus faecium, Pseudomonas stutzeri, and Enterobacter agglomerans.

Investigation of resistance of bacteria from commercial poultry sources to commercial disinfectants.

SUMMARY. Concern by consumers about food safety has resulted in increased pressure on poultry companies to develop effective sanitation programs. Salmonella isolates in hatcheries are often the same species isolated from processing plants. Resistance develops in bacteria after prolonged exposure to disinfectants. The methods available in published literature to detect the efficacy of disinfectants are labor intensive and do not consider how bacteria behave when adhered to a solid surface. We used a recently developed technique, which utilizes the actual surfaces on which the disinfectant is to be applied, to evaluate the degree of resistance to four commercially available disinfectants of 17 bacterial isolates from poultry hatcheries. We found that bacterial isolates within the same genus and species have different sensitivities to the same disinfectant. In addition, disinfectants with similar but not identical chemical formulations have different efficacies against the same bacteria.

Dynamics of Salmonella contamination in a commercial quail operation.

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.

Isolation and Characterization of a 6/85-like Mycoplasma gallisepticum from Commercial Laying Hens

Abstract Eighty-three-week-old table egg layers with swollen sinuses were presented with a history of increased mortality. Serology revealed positive titers to Mycoplasma gallisepticum (MG). The birds were part of a flock in which some birds had been vaccinated with 6/85 live MG vaccine at 18 wk of age. Tracheal cultures were obtained from both vaccinated and unvaccinated birds within the flock. The cultures were indistinguishable from 6/85 vaccine by both random amplified polymorphic DNA analysis and DNA sequence analysis. Challenge studies were performed to compare the field isolates with 6/85 vaccine and the R strain of MG. The field isolates produced a greater antibody response by serum plate agglutination than did the 6/85 vaccine. The isolates effectively colonized the trachea without increasing the tracheal mucosal thickness; however, they did not extensively colonize the air sacs or cause airsacculitis in the experimental birds.

Formaldehyde vaporization in the hatcher and the effect on tracheal epithelium of the chick

Chicken embryos were exposed to formaldehyde vapors in the hatcher during the final 3 days of incubation. Measured formaldehyde levels approached 130 ppm. Tracheas collected at hatch and 5 days post-hatch were evaluated for functional and morphologic changes. Tracheal cilia motility was reduced in formaldehyde-exposed chicks. Scanning electron microscopy revealed blunted cilia and blebs occurring in the cilia surfaces. At 5 days of age, excessive tracheal mucus was present. Sloughing of the tracheal epithelium was visible by light microscopy.

Disseminated Mycosis in Layer Cockerels and Pullets

SUMMARY. Eight-wk-old layer cockerels and pullets were presented to the diagnostic lab with a history of increased mortality, ruffled feathers, lameness, and recent vaccination. At necropsy, the birds had large multifocal granulomas in multiple tissues. Only light bacterial growth was seen on culture. On histopathology, a mixed population of fungi was seen within the granulomas including zygomycetes and Aspergillus, with the zygomycetes being the predominant organism. Because of the coinfection with Aspergillus and Penicillium, obtaining the zygomycetes in pure culture was unsuccessful. The source of the zygomycete fungi remains unknown; however, zygomycetes are known to be ubiquitous. Serology was performed to evaluate the flocks immune status. There was no evidence of immunosuppression caused by chicken anemia virus or bursal disease infections. No flock treatment was initiated.

The Effect of Inoculating Enterococcus faecalis into the Yolk Sac on Chick Quality and Maternal Antibody Absorption

Four hundred thirty-two 1-day-old specific-pathogen-free chicks were randomly divided into 36 groups of 12. All chicks were given 0.2 ml of Newcastle disease antiserum (hemagglutination-inhibition [HI] titer 1:5120) by injection into the yolk sac at hatch. Half of the groups received 0.2 ml of Enterococcus faecalis (4.0 x 10(8) colony-forming units/ml) by injection into the yolk sac at hatch (treatment). The remaining 18 groups received no bacteria (control). Two treatment groups and two control groups were weighed, bled, killed, and yolk sac weighed daily for the first 9 days of life. Feed was weighed at placement and at the end of the trial. Blood was tested for packed cell volume (PCV), total plasma protein, and Newcastle disease HI titer. No significant difference was observed between treatment and control groups for chick body weight, PCV, and feed consumption. Total plasma protein and retained yolk weight were significantly higher for treatment groups over control (P < 0.01 and P < 0.0001, respectively). Also, the geometric mean serum HI titer (log2) for Newcastle disease antibody was significantly higher in the control chicks vs. the treatment chicks (P < 0.01).

EVALUATION OF ELISA TITERS TO INFECTIOUS LARYNGOTRACHEITIS

Infectious laryngotracheitis (ILT), a highly infectious upper respiratory disease of chickens, can cause serious economic loss in areas where the poultry industry is concentrated. To determine the antibody levels associated with vaccine administration, field challenge, and protection, six groups of 20 specific-pathogen-free leghorn chickens were housed in biosecured isolation units. Individual groups served as either negative controls, vaccinated (one full dose per bird of chicken embryo origin [CEO] administered by the eyedrop method) and challenged (intratracheal administration with USDA strain ILT virus at 10(4.1) 50% embryo infective dose [EID50]), or unvaccinated and challenged with USDA strain ILT virus at various dose levels (10(2.1), 10(5.1), or 10(4.1) EID50). Chickens in each group were bled weekly, and their sera were tested for antibody using a commercially available enzyme-linked immunosorbent assay test kit. The antibody response using CEO vaccine resulted in a 400-600 geometric mean titer that appeared to be protective against severe field challenge. Negative controls had no titers, whereas vaccinated and/or challenged chickens had detectable titers within 2 wk of exposure, and these titers remained high for the next 4-7 wk. Mortality in nonvaccinated controls began at 3 days post-challenge and continued for up to 10 days.

Copper Sulfate Toxicosis in Commercial Laying Hens

A flock of 51-week-old leghorn hens experienced a 16% drop in egg production in a single week. The layer ration contained 1477 ppm copper from the addition of copper sulfate. Severe oral ulcers were present in the pharynx. Oral ulcers, reduced feed intake, and a drop in egg production occurred when a ration containing 1437 ppm copper was evaluated experimentally.

Evaluation of Three Water-Suspensible Formulations of Fenbendazole Against Ascaridia galli Infection in Broiler Chickens

Three formulations of water-suspensible fenbendazole, at target doses of 30.3 or 60.6 ppm in the drinking water, were administered to broilers infected with Ascaridia galli. The medication was administered in the water through automatic medicators for 6 hours on 3 consecutive days. Three days after treatment, chickens were killed and their worms were counted. Efficacy of fenbendazole was 99.2-100% and 69.0-89.6% at administration doses of 60.6 ppm and 30.3 ppm, respectively. Worm burden and percentage of broilers infected were lower in treated broilers than in controls (P < or = 0.05). Formulation A was dispensed most consistently and in the highest concentration through automatic medicators into the drinking water.