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Distribution of immunoglobulin-bearing cells in the gut-associated lymphoid tissues of the turkey: effect of antibiotics.

Distribution of immunoglobulin (Ig)-bearing cells in the gut-associated lymphoid tissues of antibiotic treated and untreated control turkeys (Meleagris gallopavo) was compared. Antibiotic treatment was similar to a regimen used in commercial turkey production, which included preincubation dipping of fertile eggs in gentamicin solution, injection of turkeys with gentamicin at hatching, and inclusion of chlortetracycline in the diet. Tissues were examined from turkeys at 3, 7, 14, and 21 days of age with a direct immunofluorescence procedure. Cell distribution in control turkeys was as follows: In the bursa of Fabricius, IgA-carrying cells predominated at 3 days of age, but at later intervals, the 3 classes of Ig-bearing cells were in equal numbers. In the cecal tonsils, IgM- and IgA-bearing cells were in larger numbers at 3 days of age, whereas, the IgG-bearing cells were sparsely distributed. By 7 days of age, IgM cells became more numerous in the cecal tonsils and remained numerous until 21 days of age. At 3 days of age, IgA cells predominated in the small intestines and IgM cells predominated in the large intestine. At 7 and 14 days of age, IgM cells were more numerous in the small and large intestines, but by 21 days of age, IgA cell population equaled that of IgM. The IgG cells were generally sparse in the intestines. Antibiotic treatment often resulted in lower numbers of Ig-positive cells, especially those bearing IgM and IgA. Normal development of the bursa of Fabricius was also retarded in this group.

Animals↗

Response of young chickens and turkeys to virulent and avirulent Pasteurella multocida administered by various routes.

Groups of 20 young chickens and turkeys obtained from commercial flocks and placed in pens with pine shavings over concrete floors or from the hatchery and grown on wire, were exposed to avirulent Pasteurella multocida serotype 3,4 cross or virulent P. multocida serotype 3 by drinking water, ocular, subcutaneous, intracutaneous, or palatine cleft routes. A secondary exposure to virulent P. multocida serotype 1 by the palatine cleft route was given 14 days later, except that birds exposed by palatine cleft on the initial exposure were reexposed by drinking water. There was a group of each species for each floor type and each exposure route except palatine cleft, which was performed on litter only. Chickens were more resistant to initial exposure to virulent P. multocida by all routes than turkeys. Chickens showed much less resistance to subsequent exposure to P. multocida serotype 1 than turkeys after exposure to the avirulent organism by the drinking-water route. Avirulent P. multocida administered to chickens or turkeys by subcutaneous or intracutaneous routes and turkeys by drinking water route produced a high degree of resistance to subsequent exposure to P. multocida serotype 1. In a second experiment it was found that wire floors caused many more breast blisters than pine shavings on Pasteurella-exposed or unexposed chickens.

Animals↗

Effect of Mycoplasma iowae infection on the immune system of the young turkey.

Studies were conducted in turkey poults of the effect of Mycoplasma iowae on the humoral antibody response to sheep red blood cells (SRBC) and on the weight and histological appearance of the bursa of Fabricius. Day-old turkeys were infected with M. iowae via the air sac and control turkeys received sterile broth. In the first experiment infected and control birds were inoculated intravenously with SRBC at 12 and 33 days of age, and hemagglutination (HA) tests were carried out on serum collected at intervals. Infected birds showed a slightly delayed response compared with control birds, but there was no delay in secondary response. Moreover, those birds with clinical disease gave significantly higher peak HA titres than did clinically healthy birds. In the second experiment the body weight and bursa to body weight ratio of M. iowae infected turkeys were compared with those of the control birds at 7 and 21 days of age. There was no significant difference in body weight, but at 7 days the mean bursa to body weight ratio of infected birds was significantly less (P less than 0.01) than that of the control birds and microscopic changes were seen in some bursae. These preliminary observations suggest that M. iowae infection of young turkeys may cause temporary damage to the bursa of Fabricius, accompanied by a transient immunosuppression.

Animals↗

Lysates of turkey-grown Pasteurella multocida: protection against homologous and heterologous serotype challenge exposures.

Pastereulla multocida organisms were separated from the blood of experimentally infected turkeys by differential centrifugation. An average of 92% of the residual host-cell contamination was removed from the pasteurellas by density gradient centrifugation in sucrose. Sucrose suspensions of the turkey-grown pasteurellas partially lysed after freezing and thawing. Treatment of freeze-thawed suspensions with DNAse, hyaluronidase, lysozyme, EDTA, and Triton X-100 did not influence their ability to induce protection against homologous and heterologous serotype challenge exposures. Lysozyme, EDTA, and Triton X-100 completely lysed the pasteurellas and rendered the cross-protection factor(s) filterable. Addition of adjuvant to completely lysed P multocida did not appear to enhance protection in turkeys against heterologous serotype challenge exposure. Adjuvant added to the pellet or supernatant fraction of centrifuged complete lysate enhanced protection in turkeys. Vaccines prepared from different serotypes of turkey-grown P multocida protected chickens and mice against homologous and heterologous serotype challenge exposures.

Animals↗

Lysates of turkey-grown Pasteurella multocida: effects of solubilizing agents on the immunologic properties of membrane vesicles.

Membrane vesicles from lysed suspensions of turkey-grown Pasteurella multocida were treated with various solubilizing agents to release protein that may contain cross-protection factor. Potassium thiocyanate, NaOH-glycine, lithium diiodosalicylate, guanidine hydrochloride, n-butanol, dimethyl sulfoxide, Triton X-100, and sodium lauryl sarcosinate were each tested as solubilizing agents. Vaccines made from combining solubilized membrane vesicles with complete lysate supernatant fluid produced various degrees of protection against challenge exposure with a heterologous serotype of P multocida in turkeys. Only vaccines prepared from membranes that were solubilized with potassium thiocyanate and sodium lauryl sarcosinate protected as well as complete lysate from turkey-grown P multocida. The amount of protein in each vaccine did not relate to protection. Distinct chemical differences were observed between lysates prepared from turkey-grown P multocida and lysates prepared from 41 C broth-grown P multocida. The external morphology of P multocida, after treatment with lysozyme and EDTA, was similar whether grown in broth or in turkeys.

Animals↗

Characterization of isolates of Newcastle disease virus from migratory birds and turkeys.

The susceptibility of wild birds to infection with Newcastle disease virus (NDV) has resulted in speculation about the role of these free-flying birds in the origin and transmission of the virus infection. Since several NDV isolates from free-flying waterfowl and turkey flocks in the Midwest were avirulent for chickens and had thermostable hemagglutinins, isolates were collected from both waterfowl and turkeys over a seven-year period, 1974-1980, for comparison. Strains from both waterfowl and turkeys were avirulent, based on mean death times in chicken embryos, and could be differentiated from licensed vaccine strains with similar mean death times by in vitro markers. Waterfowl strains were generally thermostable, were slow to elute from chicken red blood cells, and produced plaques in chicken embryo fibroblasts. Some of the turkey isolates were similar to the waterfowl strains in thermostability, elution, and production of plaques in chick embryo fibroblasts. However, in the latter years of the study, there was a tendency toward isolation from turkey flocks of vaccine-like strains that did not produce plaques without additives and whose hemagglutinin was thermolabile. The appearance of these strains reflects either a selection for this virus type by the host or replacement of field strains by vaccine strains as the result of an increased usage of vaccines by producers.

Animals↗

The food intakes and growth of choice-fed turkeys offered balancer mixtures of different compositions.

1. Choice-fed growing turkeys were offered whole wheat and each of six balancer mixtures. The compositions of the balancers were identical except for the content of ground cereals. 2. In a second experiment, choice-fed growing turkeys were offered whole wheat and each of four balancers which varied only in their calculated metabolisable energy (ME) content and the type of protein concentrate. 3. The turkeys which were fed on balancers of high white fish meal content ate more whole wheat and correspondingly less balancer than the turkeys offered balancers of high meat and bone meal content. 4. The ME content of the balancer did not affect the food intakes of the turkeys in the total feeding period. A high proportion of barley in the balancer hastened the increase in whole wheat intake after the introduction of the choice-feeding regime.

Animals↗

Amino acid sequence of alpha- and beta-polypeptide chains of turkey (Meleagris gallopavo) hemoglobin.

Two hemoglobin components are recognized in erythrocytes of the adult turkey (Meleagris gallopavo). We determined the amino acid sequences of turkey alpha A-, alpha D- and beta-globin from intact globin chains and chemical cleavage fragments. The sequences are highly similar to the hemoglobin of the Phasianidae, chicken, Japanese quail and pheasant. Turkey and pheasant beta-globin are identical. The amino acid sequence of turkey alpha A-globin differs by only one residue from chicken alpha A-globin. Phylogeny trees from alpha A-, alpha D- and beta-globin were constructed by the neighbor-joining method. Although the trees generated from alpha A- and beta-globin were similar, that from turkey alpha D-globin differed.

Amino Acid Sequence↗

A lipid-conjugated immunostimulating complex subunit vaccine against Salmonella infection in turkeys.

Immunostaining complexes (ISCOMs) are multimeric particles and have been used successfully for presentation of membrane proteins. In this study, outer-membrane proteins (OMPs) from Salmonella heidelberg were incorporated into lipid-conjugated ISCOM particles and evaluated for their use in a vaccine for turkeys against homologous and heterologous Salmonella challenge. Two types of lipid-conjugated ISCOMs were examined: ISCOM-phospholipid and ISCOM-sphingolipid preparations. The turkeys were challenged with one of the three Salmonella serotypes: S. heidelberg, S. reading, or S. enteritidis. The turkeys were monitored for clinical signs, shedding pattern post-challenge, and clearance of the challenge Salmonella from selected internal organs. Vaccines containing OMP with either lipid-conjugated ISCOM preparation produced significantly greater (P < 0.01) immune response than OMP alone. Cloacal swabs from turkeys given OMP along with ISCOM-phospholipid and challenged with a homologous serotype were completely negative for Salmonella. A certain degree of cross-protection against heterologous Salmonella was afforded by both OMP-ISCOM vaccines. The isolation rate of Salmonella from internal organs was significantly lower (P < 0.0001) in vaccinated turkeys than in unvaccinated controls.

Animals↗

Experimental infection of young turkeys with eastern equine encephalitis virus and highlands J virus.

Depression, somnolence, and increased mortality were observed in 2-week-old turkeys inoculated intramuscularly with either eastern equine encephalitis (EEE) virus or Highlands J (HJ) virus. Mortality rates in EEE virus- and HJ virus-inoculated turkeys were 7/30 (23%) and 9/30 (27%), respectively; no sham-inoculated controls died. Both EEE virus- and HJ virus-inoculated turkeys developed viremia that lasted 2 days; peak mean titers were 5.5 and 3.2 log10 plaque-forming units per ml of blood, respectively. Pathologic changes in both EEE virus- and HJ virus-inoculated turkeys consisted primarily of multifocal necrosis in the heart, kidney, and pancreas, and lymphoid necrosis and depletion in the thymus, spleen, and bursa of Fabricius. The findings indicate that EEE virus and HJ virus are pathogenic for young turkeys.

Alphavirus↗

Protection against hemorrhagic enteritis and Newcastle disease in turkeys by embryo vaccination with monovalent and bivalent vaccines.

The feasibility of embryo vaccination against Hemorrhagic enteritis (HE) and Newcastle disease (ND) in specific-pathogen-free turkey embryos was studied. Turkey eggs were injected with marble spleen disease virus (MSDV) at embryonation day (ED) 24, and tissues of poults hatching from virus-injected eggs were examined for MSDV. The virus was detected in spleen, intestine, liver, and bursa between 4 to 10 days postinoculation (PI). The peak titer of MSDV was present in the spleen at 6 days PI. Poults hatching from eggs injected with MSDV produced antibodies to the virus and resisted a challenge with virulent hemorrhagic enteritis virus (HEV) at 4 weeks of age. The B1 strain of NDV (NDV-B1) injected in turkey eggs at ED 24 killed the embryos. NDV-B1 modified by treatment with ethylmethane sulfonate (NDV-B1-EMS) was not lethal for turkey embryos. Poults hatching from eggs injected at ED 24 with NDV-B1-EMS developed antibodies to NDV and were protected from challenge exposure with virulent NDV at 4 weeks of age. Poults from eggs inoculated at 24 ED with a bivalent vaccine containing MSDV and NDV-B1-EMS developed antibodies to both viruses and were resistant to challenge with both virulent viruses. The study showed that SPF turkeys may be immunized by in ovo injection of live viral vaccines.

Animals↗

Salinomycin toxicosis in male breeder turkeys.

A sudden outbreak of mortality in one house of 600 48-week-old male breeder turkeys on a five-house turkey breeder farm was suspected to be feed-related. The turkeys gasped and became recumbent; 21.7% of affected turkeys died. No significant gross lesions were found at necropsy. Histological lesions, limited to skeletal muscle, consisted of degeneration and necrosis and were judged compatible with ionophore toxicosis. Feed samples from the affected house were analyzed by three techniques and shown to contain 13.4 to 18.4 g of salinomycin per ton of feed. An error at the feed mill was blamed for allowing contamination of the turkey feed with broiler starter feed containing salinomycin.

Animals↗

Experimental infection in turkeys and chickens with Ornithobacterium rhinotracheale.

Ornithobacterium rhinotracheale was found to cause growth retardation in both turkeys and chickens after experimental intra-air sac administration and to cause growth retardation together with airsacculitis and pneumonia after aerosol administration. Both turkey and chicken isolates of O. rhinotracheale were able to induce the same kind of respiratory inflammations and weight-gain losses in chickens as well as turkeys. Turkey rhinotracheitis virus was found to have a triggering effect on the O. rhinotracheale infection in turkeys, and Newcastle disease virus and to a lesser extent infectious bronchitis virus showed triggering effects on the O. rhinotracheale infection in chickens. Ornithobacterium rhinotracheale could be reisolated from affected organs of experimentally infected birds.

Aerosols↗

Investigation of the vascular supply of the pectoral muscles of the domestic turkey and comparison of experimentally produced infarcts with naturally occurring deep pectoral myopathy.

Naturally occurring deep pectoral myopathy in 9 chickens and 6 turkeys was reviewed. The arterial blood supply to the pectoral and supracoracoid muscles was studied in normal mature turkey hens by preparation of arterial casts following perfusion with methyl methacrylate. Also, a latex-perfused turkey was dissected and the blood vessels supplying these muscles were identified. Six mature turkeys (under general anesthesia) were subjected to unilateral surgical obstruction of selected cranial and caudal pectoral arteries and veins and then were euthanatized and necropsied at various postsurgical times. tin 2 of the turkeys, infarction of pectoral and supracoracoid muscles was produced. Gross and microscopic examinations of these infarcts revealed that they were very similar to the lesions of deep pectoral myopathy.

Animals↗

Ornithobacterium rhinotracheale infection in turkeys: experimental reproduction of the disease.

This report details the first experimental production of clinical disease, mortality, and pathology resembling that of field infections by using Ornithobacterium rhinotracheale alone. Twenty-two-week-old male turkeys were exposed to O. rhinotracheale or lung homogenate from O. rhinotracheale-infected turkeys. Within 24 hr after inoculation, turkeys given O. rhinotracheale or lung homogenate intratracheally were depressed and coughing and had decreased feed intake. By 48 hr, several birds were coughing blood and ultimately died. Grossly, the lungs were reddened, wet, and heavy, failed to collapse, and were covered by tenacious tan-to-white exudate. Microscopically, the parabronchi and air capillaries were filled with fibrin, heterophils, macrophages, and small numbers of gram-negative bacteria. The pleura was often covered by a thick layer of fibrin, heterophils, and macrophages. Turkeys that survived to day 7 postinoculation had severe, subacute pneumonia. Ornithobacterium rhinotracheale was recovered from the lungs of most birds with pneumonia and was also cultured from the air sacs, sinuses, tracheas, spleens, and livers. All turkeys inoculated with O. rhinotracheale developed antibodies to O. rhinotracheale detectable by the serum plate agglutination test.

Animals↗

Resistance to Salmonella enteritidis organ invasion in day-old turkeys and chickens by transformed T-cell line-produced lymphokines.

We previously reported an increased resistance to Salmonella enteritidis (SE) organ invasion in chicks and turkey poults injected prophylactically with SE-immune lymphokines (ILK). In the present study, concanavalin A (Con-A)-activated splenic T cells isolated from SE-hyperimmunized hens were transformed in vitro with reticuloendotheliosis virus strain T (REV-T) (chicken syncitial virus). These transformed T cells were then maintained as a long-term (> 1 yr) cell line for the harvest of immune lymphokines (VILK). The efficacy of VILK to protect turkey poults and chicks against SE organ invasion and the correlation between organ invasion and peripheral blood heterophilia were then evaluated. Three groups of day-old poults and chicks were injected intraperitoneally with either phosphate-buffered saline (PBS; group A), ILK (group B), or VILK (group C). Thirty minutes postinjection, poults and chicks were challenged per os with 5 x 10(5) colony-forming units (CFU) SE and 5 x 10(4) CFU SE, respectively. At 24 hr posttreatment, birds in groups A, B, and C were euthanatized and liver samples were cultured for the presence of SE. Both the VILK- and ILK-treated turkeys and chicks had significant reductions in organ invasion when compared with the PBS-injected controls (P < 0.005). For peripheral blood studies, turkeys and chicks were treated as above, and at 4 hr post-PBS, ILK, or VILK injection; total and differential peripheral blood counts were performed on birds from each group. A significant (P < 0.05) peripheral blood heterophilia at 4 hr postinjection was observed in the ILK- and VILK-treated birds, with no such increase found in the PBS-injected group. Correlation analysis revealed a direct relationship between the peripheral blood heterophilia in turkeys and chicks seen at 4 hr postinjection and the reduction in SE organ invasion seen in the VILK and ILK treatment groups (r = 0.991, r = 0.91, respectively). T cells isolated and transformed from nonimmune chickens did not produce factors that protected chicks from SE organ invasion and did not cause the peripheral blood heterophilia observed with ILK and VILK. These results show that the virally transformed SE-immune T-cell line produces lymphokines that result in the same level of peripheral blood heterophilia as ILK and was equally protective against SE organ invasion as ILK.

Animals↗

Observations on the involvement of wildlife in an epornitic of chlamydiosis in domestic turkeys.

In an investigation of potential wildlife reservoirs of Chlamydia psittaci at the site of an acute, highly fatal epornitic of chlamydiosis in domestic turkeys in Texas, various species of wild birds and rodents were captured and tested for chlamydial serum antibodies and chlamydiae in their tissues. Thirteen (65%) of 20 blackbirds (Agelaius sp), 4 (44%) of 9 killdeer (Oxyechus vociferus), 3 (27%) of 11 sparrows (Passer sp) and 1 of 4 mourning doves (Zenaidura macroura) were seropositive, but chlamydiae were not isolated from their tissues. Two of 3 rats (2 cotton rats, Sigmodon hispidus, and 1 roof cat, Rattus rattus) were seropositive, but 7 gophers (Citellus sp), 1 ground squirrel (Tamias sp), an opossum (Didelphis virginiana), and a domestic cat (Felis domesticus) were seronegative; however, chlamydiae were recovered from the livers and spleens of the opossum and domestic cat, both of which had been observed scavenging carcasses of turkeys dead of chlamydiosis. Cultures of these isolants were inoculated experimentally into turkeys and produced lesions of chlamydiosis that were indistinguishable from those caused by the strain originally recovered from diseases turkeys on the premises. Nine of 50 domestic goats quartered near the diseased turkeys were tested, and all were seropositive.

Animals↗

Comparative pathogenesis of haemorrhagic enteritis virus (HEV) infection in turkeys and chickens.

The pathogenesis of haemorrhagic enteritis virus (HEV) infection in chickens 3-4 days post-infection was compared with that in turkeys. As expected, infected turkeys showed HEV-specific lesions that included enlargement and mottling of the spleen, as well as haemorrhagic enteritis. In infected chickens, only splenomegaly was observed. The number of HEV-infected cells in the spleen was significantly (P < 0.05) higher in the turkey than in the chicken. In both species, the immunohistochemical labelling of B-cell surface determinants was diminished and the splenic B-cell areas were undetectable after HEV infection. Infection with HEV resulted in an increase in nitric oxide production by macrophages in chickens but not in turkeys.

Animals↗