Fabricius Of Birds Research Articles

A teleost structural analogue to the avian bursa of Fabricius.

The bursa of Fabricius is a primary and secondary lymphoid organ considered exclusively present in birds, and studies of this structure have been vital to our current understanding of the adaptive immune system of vertebrates. In this study, we reveal substantial lymphoepithelial tissue in a previously undescribed bursa in Atlantic salmon (Salmo salar), situated caudal to the urogenital papilla of the cloaca and thus analogous to the anatomical placement of the bursa of Fabricius. We investigated three groups of Atlantic salmon at different maturational stages and characterized the structure by applying dissection, radiology, scanning electron microscopy and histological techniques, including immunohistochemistry and in situ hybridization. We found that the epithelial anlage of the salmon cloacal bursa developed into substantial lymphoepithelial tissue and subsequently regressed following sexual maturation. Such a dynamic development is also a key characteristic of the avian bursa. The presence of intraepithelial lymphocytes was concomitant with expression of the leukocyte‐attracting chemokine CCL19, indicative of lymphoid organ functions. We did not observe recombination or gene conversion in salmon bursal lymphocytes at any developmental stage, indicating the absence of primary lymphoid organ functions in contrast to the bursa of Fabricius. However, the possibility of the bursa to trap both enteric and environmental antigens, combined with the presence of several antigen‐presenting cells residing within the lymphoepithelium, suggest the structure has secondary lymphoid organ functions. We present the discovery of a lymphoid organ in Atlantic salmon with striking topographical similarities to that of the bursa of Fabricius in birds. In addition, the age‐dependent dynamics of its lymphoepithelium suggest functions related to the maturation processes of lymphocytes.

©ПАТОМОРФОЛОГІЧНІ ЗМІНИ У ЛІМФОЇДНІЙ ТКАНИНІ БУРСИ ФАБРІЦІУСА КУРЕЙ, ВИКЛИКАНІ РІЗНИМИ ВАКЦИННИМИ ТА ПОЛЬОВИМИ ШТАМАМИ ВІРУСУ ХВОРОБИ ГАМБОРО ВИЯВЛЕНИМИ В УКРАЇНІ

The infectious bursal disease virus was detected in the Gumboro рrovince of the United States in 1962 and since then has become widespread throughout the world. Gumboro disease is characterized by severe immunosuppression in affected birds, and often mortality. Since 1986, very virulent strains of IBDV appeared in central Europe, and caused up to 70% mortality of chickens. Vaccination became the main method of protection against the disease. It is important to differentiate the post-infectious and post-vaccination effects of the virus on the bursa of the Fabricius of birds to control the vaccination process. Therefore, the aim of the study was to detect the effects of various vaccine and very virulent IBDV strains on the bursa of Fabricius of chickens. For this purpose, histological examination of bursas of vaccinated and infected birds was carried out. Samples were taken from different poultry farms in Ukraine. In results of the study we observed positive correlation between degree of depletion of the cloacal bursa and the residual virulence of the vaccine strains. Also, we detected very severe (up to 100%) depletion of bursa follicles caused by very virulent strains. The results of the work can be further used for the analysis of the post-vaccination reaction in chickens during preventive measures in places of industrial bird production.

The relationship between parasites and spleen and bursa mass in the Icelandic Rock Ptarmigan Lagopus muta

The spleen and bursa of Fabricius in birds are organs that play an important role in fighting parasite infections. The size of these organs can be used by ecologists as a measure of immune investment, with larger size implying greater investment. The bursa only occurs in juvenile birds during the development of the B cell repertoire, whereas the spleen, which is the main site of lymphocyte differentiation and proliferation, is present in both juveniles and adults. We investigated spleen and bursa mass in relation to parasite measures for 541 Rock Ptarmigan Lagopus muta collected in northeast Iceland during October from 2007 to 2012. Of these 541birds, 540 carried at least one parasite species. Juveniles had heavier spleens than adults, and adult females had heavier spleens than adult males, but there were no sex differences in juveniles. Spleen mass increased from 2007 to 2009, then decreased up to 2011, before slightly increasing again in 2012. Spleen and bursa mass in juveniles increased with improved body condition, but decreased in adults, and this effect differed significantly among years. Spleen mass in juveniles was positively associated with parasite species richness and abundance, in particular endoparasite abundance, with coccidian parasites being the main predictors. Bursa mass was negatively associated with elevated ectoparasite abundance, with two chewing lice being the main predictors. These two immune defense organs appeared to relate to different stimuli. Mean annual spleen mass of juveniles changed in synchrony with Ptarmigan body condition and population density over the years of this study. The only parasite measure that showed any relation to density was coccidian prevalence in juvenile birds, with an approximately 2-year time-lag, suggesting that factors other than parasites are probably more important in triggering changes in spleen mass.

Dispersal, vaccination and regression of immune defence organs

The thymus in vertebrates and the bursa of Fabricius in birds regress before reproduction, while the immunological information of these organs is maintained as cell memory. Regression at a certain age presupposes that individuals have achieved exposure to a large fraction of parasites in the environment. Here we present a new scenario for regression of immune defence organs, based on optimality reasoning. This scenario links early involution of immune defence organs with (1) effects of exposure to parasites on adaptive immune responses to these parasites, (2) exposure to local parasite communities during natal dispersal and migration as a means of “vaccination” against local parasites, and (3) the function of visits to future breeding sites by juveniles as a means of exposure to local parasites. This scenario provides explanations for why natal dispersal is longer than breeding dispersal, for sex differences in dispersal, and for why the bursa of Fabricius regresses relatively early in life among bird species with delayed start of reproduction.

PANCREAS OF ASELLI IN SOME SPECIES OF THE SHREWS (SOREX ARANEUS&NEOMYS FODIENS) AS AN ANALOGUE OF THE BURSA OF FABRICIUS IN BIRDS

No organ equivalent to the bursa of Fabricius in birds, which is responsible for the production of B cells, has been found in mammals thus far. It has been suggested that Peyer's patches and the appendix along with the bone marrow play this role. In this study, the gland of Aselli of shrews was examined, whose function has not yet been clarified. The results of the study of the gland of Aselli in common and water shrews suggest this gland to be the key lymphoid organ analogous to the bursa of Fabricius. However, unlike the bursa of Fabricius, the gland of Aselli seems to fulfil two functions. It not only produces B cells, but also is the site of their terminal differentiation into plasma cells.

Infectious Bursal Disease Viral RNA Amplification Using RT/PCR from Bursa Tissue Following Phenol: Chloroform Inactivation of the Virus

The preservation of viable infectious agents for future studies could create complicated logistic problems, and at times it is not feasible. Methods for preserving the genetic integrity of inactivated agents would not only facilitate these studies but would also make it possible to transport inactivated preparations around the world. In this report, the effect of inactivation on the genetic material of infectious bursal disease virus (IBDV) was studied. Tissues from the bursa of Fabricius of birds experimentally infected 3 days earlier with the classic STC strain of IBDV were collected and immediately placed in a solution of phenol:chloroform:isoamyl alcohol (25:24:1) for 24, 48, 72, or 96 hr. Infected bursal tissue not treated with the phenol:chloroform solution and uninfected phenol: chloroform bursal tissue were used as controls. In a separate experiment, bursal tissues collected 5 days following infection of specific-pathogen-free birds with the classic STC or variant 1084-E strain were placed in the phenol:chloroform solution for 2 wk. All bursal samples were tested for viable IBDV following phenol:chloroform treatment. The tissues were washed in phosphate-buffered saline to remove phenol and then homogenized. Viability of the viruses in homogenized bursal tissue was examined by inoculation of embryonated chicken eggs. Viable IBDV was not observed in any phenol:chloroform-treated bursal tissue but was observed in the infected but non-phenol:chloroform-treated control bursa. The reverse transcriptase/polymerase chain reaction (RT/PCR) was used to test the integrity of the viral RNA. Viral RNA from the nontreated control and all infected bursal samples treated with phenol:chloroform solution at all the time points examined were transcribed into DNA, and a 394-bp fragment of the VP2 gene was amplified using specific primers in the PCR. The RT/PCR assay was negative using the phenol:chloroform-treated uninfected bursal tissue. This study clearly demonstrated that phenol:chloroform treatment of infected bursal tissue inactivated the classic and variant IBDV strains tested and preserved the viral RNA for use in the RT/PCR assay.

Morphology and pathology of immunologically competent cells in ruminants.

The distribution of lymphocyte populations in peripheral blood and lymphoid tissue in ruminants was examined using a panel of monoclonal antibodies, flow cytometry, and immunohisto-chemistry. In ruminants, the continuous Peyer's patch was proposed as a primary lymphatic organ, with a function similar to that of the bursa of Fabricius in birds. Our findings suggested that the arthritis caused by caprine arthritis-encephalitis virus is due to a hyperresponsive cellular immunity of the cytotoxic and suppressor T cells in the synovial fluid, and N cells in the peripheral blood lymphocytes are a major component of the immune system in this arthritis. The CD8+ T cells may play an effector role in suppressing bovine leukemia virus growth in recombinant vaccinia virus-vaccinated animals. Lymphomas of enzootic bovine leukosis were demonstrated as tumors of mature B cells with common characteristics.

The evolution and involution of Peyer's patches in fetal and postnatal sheep.

The Peyer's patches (PP) of sheep have a number of important anatomical features and functional characteristics which are similar to tissues that have been classified as primary lymphoid organs. The prenatal maturation of PP occurs in the absence of any antigenic stimulus as immunogenic molecules are not normally encountered by the sheep fetus. Primordial PP were first detected in the small intestine of fetal sheep at about 60-days gestation; lymphoid follicles were present by 75-days gestation and vigorous lymphopoiesis was occurring in these follicles by 100 days. From 120-days gestation until birth, at about 150 days, the PP follicles were histologically mature and they had the greatest density of proliferating lymphoid cells found anywhere in the body. The total number of PP and their constituent follicles had developed before birth when there were 25-40 discrete PP in the jejunum and proximal ileum and one single continuous PP in the terminal ileum. There was no evidence of any change in the rate of growth of the PP follicles at birth which could be related to the advent of the first antigens in the gut. The total weight of PP tissue was greater than any other single lymphoid tissue by about 6 weeks after birth weighing around 120 g or about 1.2% of the body weight; about 50-60 g of the PP tissue was calculated to be lymphoid tissue. At this time the ileocecal PP (IPP) extended 2.5 m along the terminal ileum and accounted for about 90% of the total mass of PP. From about 12 weeks after birth the IPP began to involute and only a few PP follicles remained in this region of the intestine by 18 months of age. Follicles in PP in other parts of the small intestine remained and continued to produce lymphocytes throughout the life of the animal. PP contain a number of anatomically and functionally distinct lymphoid compartments that could play different roles in the body's immune defense. Explicit in most theories on the function of PP is the notion that antigenic stimulation is the cause of the lymphopoiesis in the follicles; our results do not support this view. Instead they suggest that the follicles in the PP of sheep may play a role similar to that played by the bursa of Fabricius in birds.