Biomedical subjects
Publications and source records attributed to D W Trampel.
Histologic features of chicken air-sac membranes harvested with rings were compared with those of membranes collected on cards. Ring stabilization of the tissues throughout fixation, dehydration, and embedment was found to reduce markedly the artifacts and the loss of normal tissue architecture observed within the wall of card-collected air sacs.
An avidin-biotin-immunoperoxidase diagnostic test was developed to facilitate rapid identification of Mycoplasma gallisepticum in respiratory tissues of turkeys. This procedure used polyclonal primary antibodies produced in rabbits. Turkeys were inoculated into the infraorbital sinus and trachea with the R strain of M. gallisepticum, Mycoplasma synoviae, Mycoplasma meleagridis, or Frey's media. The outer walls of the infraorbital sinuses, lungs, and tracheas were collected and fixed in either 10% neutral formalin or pentanedial methyl glycol at 1, 2, 3, and 4 wk postinoculation. Tissues were subdivided and remained in each fixative for 6 or 24 hr. The avidin-biotin-immunoperoxidase diagnostic test was sufficiently sensitive to detect M. gallisepticum antigen at 1, 2, 3, and 4 wk postinoculation. Staining of M. gallisepticum was significantly more intense on infraorbital sinus epithelium than on respiratory epithelium from the trachea or lung. Statistical analysis indicated that the 6-hr fixation time offered better antigen preservation than 24 hr in a fixative. There was no difference in intensity of M. gallisepticum antigen staining in tissues fixed in methyl pentanedial glycol when compared with tissues fixed in 10% neutral buffered formalin. Significant differences in staining intensity were observed between weeks. Specificity of the avidin-biotin-immunoperoxidase test was not complete. None of the tissues from the M. meleagridis and control groups showed staining. No staining was observed in the ciliated brush border of infraorbital sinus epithelial cells from turkeys infected with M. synoviae. However, weak to moderate staining was observed in several tracheas of turkeys inoculated with M. synoviae. Improved specificity of an avidin-biotin-immunoperoxidase diagnostic test to detect M. gallisepticum in respiratory tissues of turkeys probably will require the use of multiple monoclonal antibodies directed against several different epitopes specific to the cell membrane of M. gallisepticum.
Formalin-fixed kidney tissues from adult egg-laying chickens in two houses of an egg-production complex in the upper Midwest were submitted to Iowa State University for histopathologic examination. An increased incidence of visceral gout, average daily mortality 1%-2% higher than expected, and egg production within normal limits were observed in both houses. Numerous developing stages of Cryptosporidium were observed on the apical surface of epithelial cells lining renal collecting tubules and ureters. Scanning and transmission electron microscopy were used to visualize colonization of cryptosporidia, disruption of microvilli, and exfoliation of parasitized epithelial cells. Lymphoplasmacytic infiltration in the wall of ureters and hyperplasia of parasitized epithelial cells resulted in partial obstruction of ureters, which may have induced visceral gout in affected hens. This is the first report of urinary tract cryptosporidiosis occurring in adult hens in a modern commercial egg-production facility.
A retrospective study was conducted to evaluate the temporal relationship between flock seroconversion to hemorrhagic enteritis virus (HEV) and the appearance of adenoviral inclusions in the spleen and renal tubular epithelium. The study was conducted on samples of turkey poults submitted to the Fresno Branch of the California Veterinary Diagnostic Laboratory System during May to December 1988. The study included 78 submissions (four to eight poults per submission) of ages ranging from 6 to 15 weeks. Sera were tested for antibodies to HEV using the agar gel immunodiffusion test. Spleen and kidney samples were examined by light microscopy for the presence of inclusions in the mononuclear phagocytes of the spleen or in the renal tubular epithelium of the kidney. Logistic regression statistical analysis was used to evaluate the association between the age of the bird and the likelihood of the presence of inclusions in the spleen and kidney, as well as the likelihood of seroconversion to HEV. A significant association (P less than 0.05) was found between the presence of splenic inclusion bodies and the age of the bird. The probability of splenic inclusions was higher in younger birds (6 weeks of age), and decreased as the birds became older, approaching zero at 11 weeks of age. The kidney inclusions were significantly associated with age. The probability of detecting the inclusions increased with age, reached a maximum at 10 weeks, and then declined, approaching zero by 14 weeks. However, the probability of seroconversion to HEV increased significantly with age up to 10 weeks and then remained positive throughout the remainder of the study period.
Commercial turkeys from four Iowa flocks, two Illinois flocks, and three California flocks were submitted to state diagnostic laboratories because of a variety of health problems. The turkeys ranged in age from 5 to 12 weeks, included both hens and toms, and were owned by five different companies. Some flocks had previously been immunized with live hemorrhagic enteritis vaccine, and other flocks were unvaccinated. In all accessions, basophilic intranuclear inclusion bodies were observed in renal tubular epithelium by light microscopy. Transmission electron microscopy showed that the inclusions consisted of densely packed virus particles. The virions were identified as adenoviruses based upon the icosahedral morphology and average particle diameters of 72 nm. Avidin-biotin immunoperoxidase staining of formalin-fixed, paraffin-embedded kidneys was used to identify this adenovirus as hemorrhagic enteritis virus.
Experiments were conducted to establish a stunting syndrome (SS) model to facilitate research on nutritional aspects of enteric disorders of poults. One-day-old turkeys were dosed per os with tryptose phosphate broth (TPB) (controls) or inoculum (inoculated). The inoculum was prepared by homogenizing intestines from 11-day-old commercial poults diagnosed to have SS in TPB (1:0.5 [wt:wt]). Subsequently, intestines from 8-day-old inoculated poults from the previous experiment were used. Inoculation reduced growth (P less than 0.001) and feed consumption (P less than 0.001) at 8 and 14 days of age. In Expts. 1, 2, and 3, gain of inoculated poults was 60.9%, 58.8%, and 52.6% that of controls up to 8 days of age and 77.9%, 76.6%, and 80.9% that of controls from 8 to 15 days of age, respectively. Feed conversion was impaired (P less than 0.001) up to 8 days of age. The activity of maltase and sucrase in the jejunum and of pancreatic enzymes was determined every 2 days up to 13 days of age. Inoculation decreased (P less than 0.001) maltase and sucrase starting at 3 days of age (i.e., maltase activity was 17.45 and 1.70 mumols maltose hydrolyzed/hr.mg protein in control and inoculated poults, respectively). Inoculation had no effect on pancreatic lipase, amylase, or trypsin.
One-day-old turkeys were inoculated per os with material shown previously to induce stunting syndrome (SS). Weight gain and feed efficiency of inoculated poults from 1 to 13 days of age were impaired (P less than 0.01) compared with uninoculated poults. Examination of the jejunal mucosa by scanning and transmission electron microscopy showed the presence of long-segmented filamentous organisms (LSFOs) in poults that had been inoculated with SS. These organisms were not seen in jejuna of uninoculated poults. Further research is needed to characterize LSFOs and to determine their involvement, if any, in the adverse effects associated with SS.
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A viral enteric disease of young turkeys characterized by stunting of affected birds, diarrhea, and increased mortality is described. Eosinophilic intranuclear inclusion bodies were found in the absorptive epithelial cells of the ileum. Electron microscopy of formalin-fixed tissue revealed that the intestinal inclusions contained numerous loosely packed 15-to 20-nm hexagonal particles. The size, shape, and intranuclear location have been used to tentatively identify these particles as parvoviruses.
Cecal spirochetosis in chickens has been associated with enteric disease and reduced egg production in the United States and Europe. This report describes spirochete overgrowth of cecal mucosa in chickens from a flock of 100,000 commercial layers experiencing diarrhea and a 5% drop in egg production. Spirochetes were demonstrated in the ceca by darkfield and light microscopy. Apical surfaces of cecal enterocytes were covered by a dense layer of spirochetes aligned parallel to each other and perpendicular to the mucosal surface. Weakly beta-hemolytic, indole-negative spirochetes were isolated from the ceca on BJ media under anaerobic conditions at 42 C. Chicken cecal spirochetosis may represent an economically significant enteric disease of laying hens which has heretofore been infrequently recognized.
In September 1989, 17-day-old turkey poults were submitted to Iowa State University because of leg weakness and dehydration. These birds were commercial large white toms from a flock of 23,214. Lesions observed at necropsy included chondrodystrophy of the hock joints, clear fluid in hock joint spaces, valgus deformities and shortening of the tarsometatarsal bones, and curled toes. Mycoplasma iowae was isolated and identified from swabs of the air sac, cloaca, hock joint, and large intestine. Approximately 1.4% of the flock was culled between 2 and 8 weeks of age because of leg problems. M. iowae infection did not severely affect overall flock performance. Eighty-seven percent of the flock was marketed at 18 weeks of age with an average per turkey weight of 29.5 pounds.
Eye infections were initially observed in single-comb white leghorn breeder chicks at 5 days of age, and morbidity increased from 0.05% to 1.5% after debeaking at 7 days of age. All chicks necropsied at 15 days of age had cheesy yellow exudate within the conjunctival sac of one eye and small (1 mm diameter) white nodular lesions in lungs and on thoracic air-sac membranes. Histopathologic examination of the eyes revealed septate fungal hyphae and inflammatory cells in the anterior chamber, cornea, and conjunctival sac. Similar fungal hyphae were present within lung granulomas. Aspergillus fumigatus was isolated from the eyes. Eye infections were the only health problem reported for several consecutive flocks on this farm. Elimination of moldy feed from the diet and environment and proper management of sawdust litter have prevented fungal ophthalmitis in subsequent flocks.
This study included a complete factorial arrangement of three dietary levels of bacitracin methylene disalicylate (BMD) (0, 50, and 200 g/ton) and two health conditions (none and stunting syndrome [SS]). One-day-old turkeys were dosed per os with tryptose phosphate broth or a supernatant derived from gastrointestinal tracts of poults with SS. Body weight, feed intake, feed efficiency, water intake, and hydration efficiency were determined at 5, 9, 13, 21, and 27 days of age. BMD at 200 g/ton in the feed significantly improved body weight (P < 0.005) of poults with SS at all ages, and it improved feed efficiency (P < 0.05) from 1 to 9 days of age. BMD at 50 and 200 g/ton improved hydration efficiency (P < 0.05) of poults with SS during the first 9 days of life.
Intranuclear inclusions were observed with light microscopy in tissues from necropsy cases from three different species of birds. Because of the nature of these inclusions, the species affected, or their distribution, the inclusions were considered of unknown pathogenic significance. The inclusions were examined ultrastructurally. Parvovirus-like particles were observed in the intranuclear inclusions of pigeon hepatocytes and duodenal stromal cells from a quail. Finely granular eosinophilic intranuclear inclusion bodies from two unrelated pigeon cases were found to be composed of loosely organized filaments. One liver sample from a 16-week-old laying chicken had prominent eosinophilic hepatocellular intranuclear inclusions composed of electron-dense coarsely granular amorphous material.
Aluminium hydroxide-adjuvanted Escherichia coli bacterins were evaluated for efficacy in protecting turkeys against homologous challenge. In each of six trials involving four different E. coli serotypes, poults in one group received a single subcutaneous injection at 1 day of age, poults in a second group were vaccinated twice at 1 and 14 days of age, and those in a third nonvaccinated group served as controls. Vaccinated and control turkeys were challenged at 4 wk of age and survivors were necropsied 1 wk later. Mortality and gross lesion scores of both vaccinated groups were compared with those of the nonvaccinated group. Poults vaccinated twice had significantly lower mortality and less severe gross lesions than poults receiving no vaccine prior to challenge. Immunization with one or two injections of aluminum hydroxide-adjuvanted E. coli bacterin did not impair weight gain of poults.
Septicemia is an unwholesome condition diagnosed during postmortem inspection in poultry slaughter establishments on the basis of macroscopic lesions. Early identification of septicemia has important public health implications. In this study, Pasteurella multocida, Escherichia coli, and Staphylococcus aureus septicemia were induced in broilers in order to determine if lesions of acute septicemia can be grossly detected in the visceral organs of broiler carcasses prior to the development of changes in the skeletal muscle. Increased spleen and liver weights were observed during the acute phase of septicemia. Airsacculitis, pericarditis, and perihepatitis were observed during the acute phase of P. multocida- and E. coli-induced septicemia; and arthritis was the earliest indicator of S. aureus-induced septicemia. These macroscopic lesions were sufficient to identify unwholesome septicemic broiler carcasses prior to the development of changes in the skeletal muscle of the carcass.