William R. Maslin

F Strain Mycoplasma gallisepticum Vaccination of Post-Production-Peak Commercial Leghorns and Its Effect on Egg and Eggshell Quality

Forty-five-week-old commercial leghorns negative for antibodies to Mycoplasma gallisepticum (MG) and M. synoviae were vaccinated with high-passage F strain MG (FMG). Hens were confined in modified Horsfall-Bauer isolation units through 60 weeks of age. Egg production (% hen day) and parameters of egg and eggshell quality were monitored, including egg weight, eggshell strength, Haugh unit score, pimpling, and blood/meat spot incidence. Egg production was significantly lower (P less than 0.05) for FMG vaccinates than controls (down 5.76% and 5.80% in Trials 1 and 2, respectively). However, vaccinates and controls did not differ significantly in eggshell strength, shell thickness, pimpling, or blood/meat spot incidence. Haugh unit scores were significantly (P less than 0.05) greater for FMG vaccinates. At necropsy, all reproductive tracts appeared grossly normal. These studies suggest that high-passage FMG vaccination of post-production-peak hens does not adversely affect oviduct function.

Ocular Responses to Ammonia in Broiler Chickens

Abstract In two trials, 60 male commercial broilers were placed in each of eight environmentally controlled chambers receiving 0, 25, 50, or 75 ppm aerial ammonia from 1 to 28 days. Birds exposed to 25 ppm (lower concentration) ammonia gas developed ocular abnormalities but at a slower rate when compared with birds exposed to 50 and 75 ppm (higher concentrations). Birds exposed to higher concentrations also developed more severe lesions. With little atmospheric ammonia present after 28 days of the grow-out stage, the corneas indicated signs of healing. Lymphocytes and heterophils were seen in the iris at 49 days in ammonia-exposed birds even when ammonia exposure was terminated at 28 days. The lower ammonia concentrations resulted in abnormalities that were slight when compared with those seen at the higher ammonia concentrations. As measured by the incidence of inflammatory infiltrates in the trachea, lung, and air sacs, respiratory tract tissues did not appear to be affected by any tested level of aerial ammonia. The findings in this investigation represent the first report indicating that ammonia-induced uveitis in chickens clears rapidly after exposure to ammonia ceases.

Attempts to Reproduce a Runting/Stunting-type Syndrome Using Infectious Agents Isolated from Affected Mississippi Broilers

Various organisms, including 12 aerobic and 2 anaerobic bacteria, an infectious bronchitis virus (IBV), a reovirus, and 2 bacteriophages, were isolated from intestinal tracts of commercial broiler chicks undergoing a runting/stunting-type condition. In a series of trials, these agents were given alone and in combination to 1-day-old chicks in an attempt to reproduce the field condition. Because the agents were isolated and evaluated over time, an augmented designs variation of the analysis of variance proved particularly useful in analyzing the data collected and minimizing bird usage. Chicks inoculated with tryptose phosphate broth served as negative controls, and those inoculated with the original intestinal tract material were positive controls. Relative to the negative control chicks, body weights of the positive control chicks and of chicks inoculated with several of the agent combinations were depressed at 7, 14, and 21 days postinoculation. Common to combinations that most consistently caused weight depression were reovirus + IBV + others of the agents isolated. However, because none of the agent combinations reproduced the lethargy or dry feces seen in the positive controls, none was considered to be the ultimate cause of this particular runting/stunting-type condition. Further characterization of the disease syndrome was based on the positive control chicks. These chicks consistently had lowered body weights and transient lethargy and dry fecal pellets. Microscopic lesions consisted of lymphocytic renal and pancreatic interstitial infiltrates, dilated or cystic duodenal and jejunal crypts of Lieberkühn, increased crypt depth, and increased cellularity in the intestinal lamina propria. Electron microscopy revealed regular arrays of 26-nm viral particles, usually in association with membrane debris, in intestinal epithelial cells and crypt lumens and in intestinal and renal mesenchymal cells. These viral particles were theorized to be essential to reproduction of the complete malady seen.

Canine Pythiosis - Isolation and Identification of Pythium Insidiosum

Pythium insidiosum was isolated from the subcutaneous tissue of a 1-year-old tan crossbreed dog and from the intestinal tract of an 18-month-old Samoyed male. Gomoris methenamine silver stain was superior to hematoxylin and eosin in demonstrating the organism in tissue sections. The agent was identified as P. insidiosum by zoospore formation in an aqueous yeast extract solution containing grass blades. Exoantigens produced in culture were shown to be identical to known P. insidiosum antigens by microimmunodiffusion.

The Effects of 6/85 Live Mycoplasma gallisepticum Vaccine in Commercial Layer Hens over a 43-Week Laying Cycle on Egg Production, Selected Egg Quality Parameters, and Egg Size Distribution When Challenged Before Beginning of Lay

SUMMARY. In each of two trials, 80 commercial leghorn-type pullets were separated into two treatments with four replicates of 10 chickens in each treatment. Forty pullets were designated as controls and received no inoculation, whereas the remaining 40 pullets received the 6/85 vaccine strain of Mycoplasma gallisepticum (MG) at 10 wk of age. Hen-day egg production, egg weight, eggshell strength, Haugh unit score, pimpling incidence, and blood/meat spot incidence were monitored and recorded weekly in each trial through an entire laying cycle of 43 wk. Further, eggs from all treatments were collected daily, Monday–Thursday, and individually weighed. No significant difference was observed between the treatments for 43-wk means for hen-day egg production, for any of the monitored egg or eggshell quality parameters, or for the number of extra large, large, medium, small, pee wee, or undergrade egg sizes. A significant (P ≤ 0.05) difference was observed for the number of jumbo-sized eggs between the two treatments. Results of this study suggest that vaccination of commercial layer chickens at 10 wk of age with 6/85 strain MG does not detrimentally impact egg production, egg size distribution, or ovary/oviduct function as evidenced by selected egg parameters monitored in this study.

VARIOUS BLOOD PARAMETERS IN COMMERCIAL HENS ACUTELY AND CHRONICALLY INFECTED WITH MYCOPLASMA GALLISEPTICUM AND MYCOPLASMA SYNOVIAE

Two trials were conducted to study the effects of acute (Trial 1) and chronic (Trial 2) mycoplasma infections on differential leukocyte counts in chickens. The trials initially included either 20 (Trial 1) or 40 (Trial 2) 6-wk-old commercial leghorn chickens negative for antibodies to Mycoplasma gallisepticum (MG) and Mycoplasma synoviae (MS). Chickens were inoculated with F strain MG (FMG), MS (WVU 1853), or both. One group of chickens remained uninoculated and served as a negative control for both trials. Chickens were housed in fiberglass isolation units from 6 to 10 wk (Trial 1) or 6 to 70 wk of age (Trial 2). Differential leukocyte counts were examined from 6 to 10 wk (Trial 1) or 66 to 70 wk of age (Trial 2) in all chickens. Also, in Trial 2, packed cell volumes (PCVs) and plasma protein values were examined from 66 to 70 wk of age. In the acute study (Trial 1), differential leukocyte counts revealed statistically significant differences (P < 0.05) in heterophil, lymphocyte, monocyte, eosinophil, and basophil values among treatments. In general, the differential counts of FMG- and MS-infected birds were characterized by heterophilia, lymphopenia, monocytosis, eosinopenia, and basopenia. Histopathologic examination of the spleen, liver, kidney, and bone marrow revealed a high degree of lymphoid foci within the spleen and bone marrow of all infected chickens. In the chronic study (Trial 2), no statistically significant differences (P < 0.05) were observed in differential leukocyte counts, PCV, and plasma protein values among treatments. Histopathologic examination of spleen, liver, kidney, and bone marrow did not reveal any difference among treatments.

The Effects of F Strain Mycoplasma gallisepticum, Mycoplasma synoviae, and the Dual Infection in Commercial Layer Hens Over a 44-Week Laying Cycle When Challenged Before Beginning of Lay. II. Egg Size Distribution

In each of two trials, 160 commercial pullets were separated into four treatments with four replicates of 10 chickens in each treatment. Forty pullets were designated as controls and received no inoculation; 40 pullets received F strain Mycoplasma gallisepticum (FMG); an additional 40 pullets received Mycoplasma synoviae (MS); and the final 40 pullets were inoculated with both FMG and MS (dual). All inoculations occurred at 10 wk of age. Eggs from all treatments were collected daily, Monday-Thursday, and individually weighed. No significant difference was observed among the treatments for percentages of jumbo, extra-large, medium, small, peewee, or undergrade eggs. As a percentage of eggs laid for the 4 days of each week over the 44-wk laying cycle of each trial, the FMG hens laid significantly fewer large size eggs (43.2%) as compared with either controls (51.17%) or dual-infected hens (49.95%). No significant difference was found in percentage of large eggs laid by FMG hens when compared with MS hens.

The Effects of F Strain Mycoplasma gallisepticum, Mycoplasma synoviae, and the Dual Infection in Commercial Layer Hens Over a 44-Week Laying Cycle When Challenged Before Beginning of Lay. I. Egg Production and Selected Egg Quality Parameters

In each of two trials, 160 commercial pullets were separated into four treatments with four replicates of 10 chickens in each treatment. Forty pullets were designated as controls and received no inoculation; 40 other pullets received F strain Mycoplasma gallisepticum (FMG); an additional 40 pullets received Mycoplasma synoviae (MS); and the final 40 pullets were inoculated with both FMG and MS (dual). Hen-day egg production, egg weight, eggshell strength, Haugh unit score, pimpling incidence, and blood/meat spot incidence were monitored and recorded in each trial through an entire laying cycle. No significant difference was observed among the treatments for hen-day egg production, egg weight, eggshell strength, or Haugh unit scores. Significant differences were observed for pimpling incidence among controls (1.63%), Mycoplasma gallisepticum (MG)-infected (2.09%), and dual-infected hens (2.41%). A significant difference in blood/meat spot incidence was observed between MG-infected hens (0.27%) and dual-infected hens (0.45%). Histopathologic examination of the ovary and all segments of the oviduct revealed no significant differences among the treatments. These results suggest that the majority of the hen reproductive tract functions similarly in FMG-vaccinated, MS-infected, or dual-infected hens as compared with Mycoplasma-clean hens.

A Comparison of the Gland of Harder Response and Head-Associated Lymphoid Tissue (HALT) Morphology in Chickens and Turkeys

The immunofunctional response of the gland of Harder (GH) was compared in chickens and turkeys using an in vivo assay previously developed for use in chickens. The GH were surgically removed (GHx) from leghorn chicks at 1 day of age and from poults at 2 days of age. Intact birds of each species served as controls. During the fourth week of age, both GH-intact and GHx chicks were exposed to killed Brucella abortus antigen by the ocular or intraperitoneal route. One week later, serum and tears were collected and assayed for antibodies to B. abortus. In addition, all birds were killed at the end of the trial period, and the heads were fixed and processed for histologic examination. Various components of the head-associated lymphoid tissue (HALT) including the GH, nasal glands, lacrimal glands, lacrimal ducts, eyelid conjunctiva, and nasal cavity mucosa/submucosa, were evaluated microscopically using a scoring system to estimate quantity and degree of development of immune tissue in those sites. Results of all analyses indicate that functional response and morphology of the HALT are comparable in turkeys and chickens.

Osteopetrosis, Anemia, Thrombocytopenia, and Marrow Necrosis in Beef Calves Naturally Infected with Bovine Virus Diarrhea Virus

Bovine virus diarrhea virus (BVDV) infection in cattle has a complex set of clinical manifestations, depending on the strain of infecting virus, the immunological status of the host, and the presence or absence of coinfecting stains. Transient BVDV can be caused by either cytopathic or noncytopathic viral infection of immunocompete nt cattle. Calves infected in utero with noncytopathic BVDV (NC-BVDV) before the age of immunocompete nce may become persistently infected immunotolerant carriers of the virus. These persistently infected cattle may serve as viral shedders, infecting herdmates. Mucosal disease, the most severe clinical manifestation of BVDV, occurs when cattle are persistently infected with an NC-BVDV and then are coinfected with a cytopathic strain of BVDV. 1,3