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At least 613 records · Page 34Linked to original sources
PubMed1992

Effects of corticosteroids on short-circuit current across the cecum of the domestic fowl, Gallus domesticus.

Both avian corticosteroid hormones, aldosterone and corticosterone, increased short-circuit current across the wall of the ceca of the domestic fowl (Gallus domesticus) in vitro. About 80% of this short-circuit current was inhibited by the Na-channel blocking drug amiloride. Corticosterone was about ten times less potent than aldosterone in increasing short-circuit current and it exerted a similar maximal effect. Cortisol (an endogenous corticosteroid hormone in mammals but not birds) was about ten times less potent than corticosterone and this difference appeared to reflect the presence of the 17 alpha-OH group in cortisol. Carbenoxolene, which inhibits 11 beta-hydroxysteroid dehydrogenase, increased the effect of corticosterone. This effect is consistent with inhibition of the metabolism of corticosterone to 11-dehydrocorticosterone. The latter was found to be about 100 times less potent than corticosterone. The effects of both aldosterone and corticosterone (also dexamethasone) were abolished by the mineralocorticoid receptor antagonist spironolactone. The results suggest that corticosterone has an effect similar to aldosterone but in vivo its action may be depressed by the activity of 11 beta-hydroxysteroid dehydrogenase. The sensitivity of the cecal preparations to corticosterone indicates that this hormone could contribute to the regulation of transcecal Na transport (absorption) in vivo.

Adrenal Cortex Hormones↗
PubMed1989

The capacity of normal and talpid3 mutant fowl myogenic cells to migrate in quail limb buds.

Talpid3 is a recessive lethal mutant of the fowl. It has been shown previously that, in vitro, talpid3 limb mesenchyme cells are more adhesive and less mobile than normal cells. It is therefore of interest to investigate the effect of the gene on cell movement in vivo, in the limb bud itself, in cells in which it is known to occur in normal embryos. Myogenic cells, which normally migrate into the limb bud from the somites, continue to move distalwards when grafted into the limb bud at a later stage. Blocks of normal or talpid3 limb mesenchyme containing myogenic cells were transplanted into quail limb buds in ovo. Since quail cells are histologically distinguishable from chick cells the progress of myogenic cell movement 5 days after transplantation could be observed. In 10 out of 14 cases normal myogenic cells migrated extensively in a proximo-distal direction within the limb bud of the quail host. In contrast, only 2 out of 11 talpid3 transplants showed a moderate degree of distalwards movement.

Animals↗
PubMed1993

Water loss from eggs of domestic fowl and calcium status of hatchlings.

Water balance in eggs of domestic fowl was manipulated by drilling holes (each 3 mm in diameter) through the calcareous layer into the air cell on day 10 of incubation. Water loss between days 0 and 18 averaged 6 g for eggs in the control group (no hole) but increased to 8, 12, and 15 g for eggs with 1, 2, or 3 holes, respectively. Hatching success was 79-87% for eggs with 0-2 holes through the eggshell but only 43% for eggs with three holes. Live mass of hatchlings declined as the number of holes drilled in the eggshell increased, but dry mass of carcasses was unaffected by the treatments. The quantity of Ca2+, Mg2+, and phosphorus in residual yolks and yolk-free carcasses of hatchlings was not influenced by the amount of water lost from eggs. Plasma Ca2+ and Mg2+ were elevated in hatchlings from eggs with high rates of water loss. The inability to regulate plasma Ca2+ may be a negative consequence of excessive water loss and could contribute to increased mortality of embryos.

Animals↗
PubMed1982

The distribution of polypeptide YY (PYY) - and pancreatic polypeptide (PP) - immunoreactive cells in the domestic fowl.

The distribution of the polypeptide which has an N-terminal tyrosine and a C-terminal tyrosine (PYY) - and pancreatic polypeptide (PP) - immunoreactive cells were investigated in the gut of the domestic fowl. PPY-immunoreactive cells were observed in the duodenum and jejunum. PP-immunoreactive cells were seen in the duodenum, jejunum, ileum and colon. Both PYY- and PP-immunoreactive cells were extended from the basal lamina to the gut lumen i.e. of open type. PYY-immunoreactive cells occurred mainly in the basal and middle portion of the villi. On the other hand, PP-immunoreactive cells were located mostly in the crepts. The occurrence of PYY-immunoreactive cells in the upper part of the small intestine is rather similar to that of amphibians and reptiles, than to that of mammals, where PYY-immunoreactive cells are located in the distal part of the small intestine and in the large intestine.

Animals↗
PubMed1982

Ultrastructural localization of phosphatases in the testes of the domestic fowl: acid phosphatase and thiamine pyrophosphatase.

ACPase and TPPase activity has been examined in the germinal epithelium of the testes in the domestic fowl. ACPase activity in spermatogonia and spermatocytes was confined to the Golgi complex. In spermatids ACPase activity was seen in the endoplasmic reticulum and nuclear envelope in the phase I and especially in the phase II (the elongating phase). This activity gradually decreased during the next phase III (the elongating phase). This activity gradually decreased during the next phase III, and had disappeared in the final phase IV. The membrane body showed ACPase reaction in the small peripheral vacuoles and cisternal structures surrounding large central vacuoles. ACPase was also present in vesicles surrounding the developing tail. Late spermatids showed an abundance of autophagic vacuoles which had a complex array of ACPase positive delimiting membranes. In Sertoli cells ACPase activity was predominant in the lysosomes. TPPase activity was seen in the cisternae of the Golgi complex in spermatogonia and spermatocytes. In spermatids activity was present in the endoplasmic reticulum during the phase II, but it is lost in later stages. The smaller vacuoles and cisternal structures in the membrane body also showed reaction products. According to the present results it is thought likely that the smaller vacuoles and cisternal structures of the membrane body are of endoplasmic reticulum origin. The autophagic vacuoles in spermatids and the lysosomes of Sertoli cells are considered responsible for the degradation of residual bodies cast off by spermatids.

Acid Phosphatase↗
PubMed1982

Time course of adaptation to low and high NaCl diets in the domestic fowl. Effects on electrical behaviour of isolated epithelia from the lower intestine.

Short circuit currents (Isc), resting electrical potential differences (p.d.) and resistances were measured in vitro for stripped rectal ("colonic") and coprodeal epithelia from fowls transferred to low from high NaCl diet for 1, 2, 4 or 8 days (NaCl depletion), and from birds adapted to low NaCl diet and sacrificed 8, 16 and 24 h after NaCl-loading (resalination). NaCl-depletion enhanced Isc and p.d. fully by 4 days in rectum but took 8 days in coprodeum (half times 1.2 days and 4 days respectively); rectal amino acid-sensitive Isc was abolished and amiloride-sensitive Isc was established by 4 days (half-time 1 day). Resistance changes were transient and relatively small in rectum, but coprodeal resistance decreased. Resalination reversed these changes very rapidly in both tissues (within 25-50 h; half times 10-20 h). It is concluded that responses to NaCl-depletion are mediated by aldosterone (and possibly by some other unknown agonist); responses to resalination may be due in part to suppressed aldosterone secretion and possibly to the evocation of some other controller (perhaps prolactin or corticosterone) antagonising aldosterone.

Adaptation, Physiological↗
PubMed1992

Ca2+-ATPase in mucous and oxyntico-peptic cells of the fowl proventriculus.

Calcium adenosine triphosphatase (Ca(2+)-ATPase) was localized by means of histo-and ultracytochemistry in the secretory cells of the proventriculus of the domestic fowl. The mucous cells exhibited plasmalemmal-associated enzyme activity on the external aspect of the basolateral cell membrane. Intracellularly, the luminal aspect of Golgi-membranes and of secretory vesicle membranes reacted positively for Ca(2+)-ATPase activity, as did the apical cytosol and the matrix of lysosomes. Oxyntico-peptic cells were characterized by apical and apico-lateral plasmalemmal activity and by an organelle-associated distributional pattern similar to that in the mucous cells. In addition, Ca(2+)-ATPase was associated either with the matrix of mitochondria or with tubuli of the rough-surfaced endoplasmic reticulum. The results are discussed with respect to messenger and effector functions of calcium in the process of proventricular mucus secretion. In addition, Ca(2+)-ATPase distributional patterns in the oxyntico-peptic cell are related to the unique structure and function of these cells.

Animals↗
PubMed1988

Relationship of transmural electrical parameters to the luminal Na concentration in the colon of the fowl (Gallus domesticus).

Electrical parameters: PD, resistance, Isc and amiloride-sensitive-Isc across the fowl colon (in vitro) change in response to the Na content of the diet. On a low-Na diet these changes appear to reflect increases in ion transport, especially amiloride-inhibitable Na transport. In vitro the magnitudes of the changes are related to the Na concentration in the luminal (mucosal) fluid and in birds on a low-Na diet peak at a concentration of about 12.5 mM. Such Na concentrations are similar to those in the colonic fluid of Na-deprived birds. Typical Michaelis-Menten kinetics do not appear to apply, possibly reflecting a local adaptation of the ion transport process in response to its external Na concentration.

Animals↗
PubMed1995

Eimeria spp. of the domestic fowl: analysis of genetic variability between species and strains using DNA polymorphisms amplified by arbitrary primers and denaturing gradient-gel electrophoresis.

The genetic relatedness of 5 Eimeria spp. of the domestic fowl, including 11 strains of E. acervulina, 2 strains of E. tenella and 1 precocious line of E. acervulina, was assayed by means of random amplified polymorphic DNA (RAPD) and denaturing gradient-gel electrophoresis (DGGE). Seven different oligonucleotides were used to generate similarity coefficients for the species and strains of Eimeria infecting chickens. Between 1 and 13 DNA segments, depending on the species/strain-primer combination, were amplified with the various primers. Amplification products ranged in size from 0.16 to 3.8 kb. E. acervulina strains demonstrated two to four major common bands unique to the species. These strains also exhibited major and minor differences in their DNA patterns. Band-match analyses from both polyacrylamide and denaturing gradient gels were used to calculate similarity coefficients for the Eimeria spp. and strains tested. Species differences, readily detected upon examination of DNA banding patterns, gave similarity coefficients of 4%-38% and 3%-18% when analyzed by polyacrylamide- and denaturing gradient-gel electrophoresis, respectively. A similar analysis of E. acervulina strains, yielded similarity coefficients of 55%-95% and 51%-85%, respectively. The differences observed between both species and strains were greater when the RAPD-assay products were analyzed via DGGE, indicating that a combination of these two techniques may provide a more stringent analysis of the genetic relatedness of these coccidia.

Animals↗
PubMed1980

Bionomics and health importance of fowl tick Argas (Persicargas) persicus (Oken, 1818) (Ixodoidea: ARgasidae).

The fowl tick Argas (Persicargas) persicus occurs in warm areas of Slovakia, where its distribution is limited by the 650-700 mm annual average isohyet and the +8 degrees C annual average isotherm. In Slovakia, larvae hatch from spring to autumn, and nymphal and adult moultings occur chiefly in July and August. Larvae feed for four days, nymphs and adults for less than one hour. The tick develops and reproduces during the warm season in the wild but throughout the year under favourable laboratory conditions in which the life cycle requires 17 months.

Animals↗
PubMed1993

Species and strain differentiation of Eimeria spp. of the domestic fowl using DNA polymorphisms amplified by arbitrary primers.

Eimeria spp. from the domestic fowl were examined for genetic relatedness by the random amplified polymorphic DNA (RAPD) assay. Nine different oligonucleotide decamers with arbitrary DNA sequences were tested as primers to amplify DNA from six Eimeria species infecting chickens. Two strains each of E. acervulina and E. tenella were used. Depending on the species/strain-primer combination, between 1 and 12 DNA segments ranging in size from 0.16 to 4.95 kb were amplified. The two strains of E. acervulina showed minor and major differences in their amplified DNA patterns, giving a similarity coefficient of 61%. The two strains of E. tenella seemed to be more closely related, yielding a similarity coefficient of 98%. The differences observed between species were greater than those found between strains with every primer used, indicating that the RADP assay could be a useful tool for the study of relationships among these coccidia. The results obtained in this study also indicate the presence of unique, species-specific, amplified DNA segments that could be exploited to identify Eimeria species of the chicken.

Animals↗
PubMed1982

Immunoreactive neuropeptide systems in avian embryos (domestic mallard, domestic fowl, Japanese quail).

In embryos of the domestic mallard, domestic fowl, and Japanese quail vasotocin-, mesotocin-, luliberin (LHRH)-, met-enkephalin-, corticotropin-, and somatostatin-immunoreactive perikarya and fiber formations were visualized at different incubation stages by means of the PAP technique (Sternberger 1979). The most striking results were: (1) Vasotocin-, mesotocin-, and luliberin-immunoreactive systems display, up to the late embryonic period, morphological features most probably related to a neurohormonal function. (2) Met-enkephalin immunoreactivity appears very late during embryonic life; it is restricted to fiber networks and not found in perikarya. (3) Corticotropin immunoreactivity is observed in the tuberal region temporarily at the end of the second and the beginning of the last third of the incubation period. (4) Somatostatin-immunoreactive material is present (i) at the end of the first third of incubation, in association with the olfactory system; (ii) during the same period, adjacent to thin-layered portions of the roof of the brain; (iii) shortly thereafter, in cells of both pancreatic primordia and thyroid gland; and (iv) onward from the middle of the incubation period, in a mesencephalic cell group. The striking difference, in the early embryo, between the mature somatostatin plays a role in the development of the brain, as well as the pancreas, and the thyroid gland.

Adrenocorticotropic Hormone↗
PubMed1993

The identification of genes for the major core proteins of fowl adenovirus serotype 10.

The sequence analysis of 1218 base pairs containing the probable fowl adenovirus (FAV) equivalents to the major core genes of human adenovirus (HAV) located on the late transcription unit number 2 (L2) has been completed. Two open reading frames (ORF) 3 prime to the gene for the penton base have been identified (41.3 to 43.4 map units). The putative poly A recognition sequence signalling the end of the L2 transcription unit has also been located. The two ORFs identified encode polypeptides that are highly basic in nature, especially rich in arginine. Both ORF appear to encode the FAV equivalents to the HAV major core polypeptides. The genomic map locations of these two ORFs have been determined and compared to the map locations of HAV-2 pV, pVII, and mu genes. A possible third core protein gene of FAV-10 that reads in the reverse direction was also tentatively identified.

Amino Acid Sequence↗
PubMed1983

Functional defects of fowl plague virus temperature-sensitive mutant having mutation in the neuraminidase.

A fowl plague virus (FPV) temperature-sensitive mutant ts 5 having mutation lesions in the gene coding for the neuraminidase has been obtained. The mutant induced synthesis of cRNA, vRNA and proteins in cells under non-permissive conditions, but formation of virions including non-infectious ones was defective. The neuraminidase and haemagglutinin synthesized under non-permissive conditions possessed functional activity and could migrate from the rough endoplasmic reticulum into plasma membranes; however, cleavage of the haemagglutinin was reduced. In ts 5-infected cells under non-permissive conditions the synthesis of segments 5 and 8 of cRNA and vRNA was predominant both early and late in the reproduction cycle, and the synthesis of P1, P2, P3, HA and M proteins was reduced after approximately 3 hours. The data obtained suggest that involvement of the neuraminidase in the formation of infectious virions may have no direct association with the enzymatic activity of this protein, and that the mutation in the neuraminidase may affect regulation of replication and transcription processes.

Cell Membrane↗
PubMed1982

Synthesis of RNA segments 1-3 during generation of incomplete influenza A (fowl plague) virus.

Incomplete influenza A virus (fowl plague Dobson strain) was prepared by undiluted passage in primary chick embryo fibroblast cells. Analysis of released virus RNA revealed a deficiency in RNA segments 1-3, characteristic of incomplete virus formation. The virus yield from a high multiplicity infection with standard virus always showed this deficiency, even when analysed as early as 6 hours post-infection, whereas infection at low multiplicity gave rise to virus indistinguishable in RNA composition from the parent virus. The relative amounts of intracellular, non-polyadenylated, complementary RNA (template RNA) were found to reflect accurately the eventual RNA composition of released virus, and were altered in phase with PFU:HAU ratio, throughout a von Magnus cycle.

Animals↗
PubMed1982

The fibers of fowl adenoviruses.

Purified virions from 14 strains of fowl adenoviruses (FAV) representing 11 serotypes were examined by electron microscopy. Pentons of all strains turned out to have two projections at their penton bases. It is shown that the double fibers also protrude from the intact virion. The length of both fibers was measured on free pentons and is given for each serotype. Double fibers seem to be a common feature of FAV. The serologically unrelated Egg Drop Syndrome (EDS) avian adenovirus strain 127 was confirmed to have single fibers only.

Adenoviridae↗
PubMed1981

Intrinsic interference between swine influenza and fowl plague virus.

Multiplication of swine influenza (SW) virus is inhibited by fowl plaque virus (FPV) at the level of RNA synthesis when host cells are infected with both viruses at a high multiplicity of infection. Under these conditions reassortment between the two viruses cannot be detected. The inhibitory effect of FPV is highly reduced and recombinants between the two viruses could be obtained when the cells were superinfected with FPV 1--2 hours after infection with SW virus, or after simultaneous infection with a low multiplicity of infection. The phenomenon is compatible with the intrinsic interference.

Animals↗
PubMed1975

Electron microscopical study of initial and final stages of fowl plague virus-replication in chick embryo cells.

Cellular uptake of fowl plague virus occurs 10-30 minutes after inoculation of chick embryo cells. The penetration of the virions is by pinocytosis (viropexis); fusion with the cellular membrane has not been observed. After pinocytosis the virions become gradually disintegrated. Budding of newly formed virions from the cellular membrane starts 3 hours post inoculation (p.i.) and reaches its maximum 8 hours p.i. At the same time budding takes place into electron microscopically empty and autophagic vacuoles. Eight hours p.i. about 3 per cent of the infected cells show budding of virions from the surface and into cytoplasmic vacuoles. Labelling of the cellular membrane with ruthenium red demonstrated that these cytoplasmic vacuoles are not simple cross-sections of invaginations of the cellular membrane. Cluster-like structures were found at 6 hours p.i. in the nuclei of infected cells; however, the suggestion that the clusters develop from nucleoli could not be confirmed.

Animals↗