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[Development of the mitochondrial apparatus and blood supply of skeletal muscle fibers during ontogenesis of domestic fowl].

The diameter, length, and numerical density of capillaries, diameter of muscle fibers, size and numerical density of their profiles, and relative volume of mitochondria in them were determined in the chicken red oxidative gastrocnemius and white glycolytic pectoral muscle during development from day 10 of embryogenesis to six month of postnatal life. The bulk blood flow was measured in these muscles by hydrogen clearance during postembryonic development. During embryogenesis, the fibers of gastrocnemius muscle develop and grow at a higher rate, while during postembryonic development, those of the pectoral muscle develop faster. The density of mitochondrial profiles increases during embryogenesis and decreases after hatching, while their mean size increases, especially in the oxidative fibers, but it somewhat decreases in 6-month old chicks. Redistribution of mitochondria by the fiber section during development takes place in both muscles: they are localized predominantly in the center in 18-day embryos and in the periphery, especially in the gastrocnemius fibers, in 6-month old fowl. At hatching, the lengths of capillaries are similar in both muscles, but as chicks grow, the proportion of longer (more than 600 microm) capillaries in the pectoral muscle sharply increases, while their density and bulk blood flow decrease. Ratios were determined between structural parameters of the capillary bed and mitochondria, on the one hand, and oxygen consumption (ml/min per 1 mm fiber and 100 g muscle mass), on the other.

Animals↗

Nucleotide sequence analysis of the L1 loop variable region of hexon gene of fowl adenovirus 4 isolates from India.

Three fowl adenovirus 4 (FAV4) isolates from chicken and one from quail, all from Tamil Nadu, India were analyzed. The L1 loop variable region of hexon gene of these isolates was amplified by PCR and sequenced. The nucleotide sequences (442 bp) and deduced amino acid sequences of the four isolates were compared with those of other isolates of FAV4. The nucleotide sequences of the four isolates had a 98% homology with other Indian isolates and a 96% homology with Belgian and Russian isolates. The amino acid sequences of the four Indian isolates had a more than 98% homology with other Indian isolates and a more than 92% homology with Belgian and Russian isolates. Hence, the variable of L1 loop region of hexon gene was found to be highly homologous in all the FAV4 isolates tested both at nucleotide and amino acid level.

Adenoviridae Infections↗

Association of fowl adenovirus serotype 12 with hydropericardium syndrome of poultry in India.

Eight fowl adenovirus (FAdV) isolates obtained from different geographical regions of India were typed by a virus-neutralization test (VNT) using rabbit antisera against all the 12 serotypes of FAdV and by PCR for the hyper-variable region of hexon gene combined with restriction fragment length polymorphism (RFLP) analysis using AluI and MboI restriction enzymes. It was found that six isolates belonged to FAdV-4, one to FAdV-12 and one to both of them. This study revealed the involvement of FAdV-12 alone or in association with FAdV-4 in precipitating inclusion body hepatitis--hydropericardium syndrome (IBH-HPS) among poultry flocks in the country.

Adenoviridae Infections↗

Acaricidal efficacy of Myrrh (Commiphora molmol) on the fowl tick Argas persicus (Acari: Argasidae).

Five concentrations of purified extract of Myrrh from Commiphora molmol tree were prepared to study its effects on the fowl tick Argas persicus under laboratory conditions. The results revealed that Myrrh had dependant dose toxic effect on the adult female of A. persicus. Toxicity increased gradually daily post treatment. The LC50 was 1.28%, 0.88%, 0.84%, 0.50% and 0.42% at Ist, 2nd, 3rd, 6th and 12th days respectively. At 12th day, the recorded mortality rates were 63, 67, 76, 87 and 94% for concentrations, 0.625, 1.25, 2.5, 5 and 10%, respectively against 5% in control. Histopathological and Transmission election microscope (TEM) examinations showed the lysing of epithelial gut cells in treated groups. The lysed epithelial gut cells showed irregularly distributed nucleus, commonly at low concentrations and rarely in high concentrations of Myrrh. The lysed epithelial gut cells, without nucleus or with aggregated one beside the basal lamina, were common at high concentrations and rare in low concentrations of Myrrh. Consequently, Myrrh can rapidly penetrate the cuticle to body cavity, destroy the epithelial gut cells and finally cause the death of ticks.

Animals↗

[Recombinant viruses of poultry as vector vaccines against fowl plague].

To help in the control of fowl plague caused by highly pathogenic avian influenza A viruses of hemagglutinin (HA) subtypes H5 and H7 several vaccines have been developed. A prophylactic immunization of poultry with inactivated influenza viruses in non-endemic situations is questionable, however, due to the impairment of serological identification of field virus-infected animals which hinders elimination of the infectious agent from the population. This problem might be overcome by the use of genetically engineered marker vaccines which contain only the protective influenza virus hemagglutinin. Infected animals could then be unambiguously identified by their serum antibodies against other influenza virus proteins, e.g. neuraminidase or nucleoprotein. For such a use, purified HA or HA-expressing DNA vaccines are conceivable. Economically advantageous and easier to apply are modified live virus vaccines in use against other poultry diseases, which have been modified to express influenza virus HA. So far, recombinant HA-expressing fowlpox virus (FPV) as well as infectious laryngotracheitis and Newcastle disease viruses have been asssessed in animal experiments. An H5-expressing FPV recombinant is already in use in Central America and Southeast Asia but without accompanying marker diagnostics. Advantages and disadvantages of the different viral vectors are discussed.

Animals↗

Social status and availability of females determine patterns of sperm allocation in the fowl.

Where sperm competition occurs, the number and quality of sperm males inseminate relative to rival males influences fertilization success. The number of sperm males produce, however, is limited, and theoretically males should allocate sperm according to the probability of gaining future reproductive opportunities and the reproductive benefits associated with copulations. However, the reproductive opportunities and value of copulations males obtain can change over their lifetime, but whether individuals respond to such changes by adjusting the way they allocate sperm is unclear. Here we show that, in the fowl, Gallus gallus, dominant males, which have preferential access to females, modulate the number of sperm they ejaculate according to the availability of females. When presented with two females, dominant males allocated more sperm to higher quality females, whereas when females were on their own, only copulation order had an affect on their sperm numbers. In contrast, subordinate males, whose mating activity is restricted by dominant males, allocated high numbers of sperm to initial copulations, irrespective of female availability. We further show, by manipulating male social status, that sperm allocation is both phenotypically plastic, with males adjusting their patterns of sperm allocation according to their dominance rank, and intrinsic, with males being consistently different in the way they allocate sperm, once the effects of social status are taken into account. This study suggests that males have evolved sophisticated patterns of sperm allocation to respond to frequent fluctuations in the value and frequency of reproductive opportunities.

Animals↗

[Retinal projections into the diencephalon in the fowl (Gallus gallus domesticus)].

The localization of the primary visual centers in the hen diencephalon was determined by anterograde transport horseradish peroxidase (HRP) techniques. Twelve fowls (Gallus gallus domesticus) were used for HRP study and four were used for cytoarchitectural study (Nissl and Klüver-Barrera stained preparation). One-hundred microliter of 30% HRP solution in physiological saline was injected into the vitreous body of one eye of each hen under anesthesia of sodium pentobarbital (30 mg/kg body wt). After a postoperative period of 48 hours, the animals were deeply anesthetized and perfused with an injection of 1,000 ml of Ringer solution which was followed by 2,000 ml of 1% paraformaldehyde and 1.25% glutaraldehyde in a 0.1 M phosphate buffer (pH 7.4) which was then followed by 1,000 ml of 10% sucrose in the same buffer. The brain was cut into serial transverse sections of 60 microns on freezing microtome. Every section was treated with tetramethylbenzidine (TMB). Retinal projections were found in the hypothalamic area, lateral geniculate nucleus (GL), lateral part of dorsolateral thalamus (DLL), medial part of dorsolateral thalamus (DLM), ventrolateral thalamus (VLT), rostrolateral part of dorsolateral anterior thalamus (DLAlr), magnocellular part of dorsolateral anterior thalamus (DLAmc), lateral anterior thalamus (LA), ectomammillary nucleus (EM), external nucleus (NE), and nucleus superficial synencephalica (SS), contralaterally. No labeled terminals were found in the ipsilateral brain stem. In the hypothalamic region, terminals were found to be just lateral to the rostral part of the third ventriculus and the bottom of the lateral margins of the hypothalamus, which we termed medial (MRH) and lateral (LRH) retinorecipient hypothalamic nucleus. LRH had high density terminals compared with MRH and caudal MRH continued into rostral LRH so that there was no boundary between MRH and LRH in HRP preparation. MRH is contained large cells (25-35 microns in diameter) and occupied rostral 1/4 of retinorecipient of hypothalamus (RH), whereas LRH contained small type cells (about 15 microns in diameter) and occupied caudal 3/4 of RH. In the retinorecipient nuclei of the thalamus, high density terminals were found in GL, LA, DLAlr, NE, SS and EM. In DLAlr and EM, granulae of HRP product were bigger than in other terminal nuclei and also the density of those terminals was high. GL and LA have large nuclei which receive retinal afferents. Labeled terminals of those nuclei were distributed homogeneously throughout the whole nucleus except for the inner layer of GL. Cytoarchitectonically, GL was divided into two layers.

Animals↗

Serologic examination of birds from the area of Southern Moravia for the presence of antibodies against arboviruses of the groups alfa, flavo, Bunyamwera supergroup, and the virus Yaba 1-Lednice 110. I. Domestic fowls.

196 geese, 141 ducks, and 100 hens from 9 localities of the South Moravian region (District of Breclav) were examined by means of the haemagglutination-inhibition test (HIT) for the presence of antibodies against 12 arbovirus antigens of the groups Alfavirus (Western Equine Encephalitis (WEE), Eastern Equine Encephalitis (EEE), Semliki, Sindbis, Chikungunya, O'nyong-nyong), Flavovirus (Tick-borne Encephalitis (TBE), Dengue and West Nile Virus (WN), Bunyamwera Supergroup (Tahna and Beta Calovo), and the Yaba 1-Lednice 110 Virus. In tested fowls antibodies were mostly found against Yaba 1-Lednice 110 Virus, namely 3.6% in geese and 17.7% in ducks. Antibodies against Calovo Virus were found in only 1 of the tested ducks. All sera of hens were negative. Antibodies against arboviruses of the Alfa-and Flavovirus groups were not detected.

Animals↗

The effect of enterotoxin of Clostridium welchii (perfringens) type A on fowls.

Lethal doses of enterotoxin of Clostridium welchii (perfringens) type A injected intravenously into young fowls caused immediate lassitude, with partial recovery, followed by death seven to 35 h after inoculation. Lesions found were ascites, hydropericardium, oedema of the muscles, hepatic congestion, urate deposits on the peritoneum and the pericardium, and intestinal hyperaemia. Sublethal doses produced no clinical signs or lesion. The LD50 of this enterotoxin was 74-84 mug/kg of body weight.

Animals↗

Enzyme variants of Eimeria parasitizing the domestic fowl and possibilities of species diagnostics.

Electrophoretic variation of the enzymes lactate dehydrogenase (LDH) and glucosephosphate isomerase (GPI) of Eimeria parasitizing the domestic fowl in Czechoslovakia is summarized and the differentiation of species of poultry coccidia is discussed. A new method for evaluation of zymograms of coccidial enzymes is presented. This method enables the results of different experiments to be compared by calculating standardized rates of mobility of each enzyme band relative to the positions of reference variants coded LDH-8 or GPI-9.

Animals↗

Comparison of live avirulent M-9, Minnesota, and CU fowl cholera vaccines.

The M-9 and Minnesota (MN) avirulent Pasteurella multocida vaccines were evaluated and compared with the Clemson University (CU) vaccine, which had been shown to be highly effective in preventing fowl cholera in turkeys. Neither the M-9 nor the MN vaccine given in the drinking water was as effective as the CU vaccine in protecting turkeys against challenge with virulent P. multocida. When grown in brain-heart infusion (BHI) agar as recommended, the M-9 was not as efficacious as when it was grown in BHI broth. The M-9 was as effective as the CU vaccine only when grown in BHI broth and given at 10 times the standard dosage. Injection of the M-9 vaccine into the air spaces of the head at a site near the caudal rim of the ear after one vaccination in the drinking water was not as effective for hyperimmunizing potential breeders as was the CU vaccine injected at the same site. A microtiter agglutination test demonstrated a significant (P less than 0.05) correlation between the level of anti-P. multocida antibody found 1 week after vaccination and survival after challenge with virulent P. multocida.

Administration, Oral↗

Differentiation of species of Eimeria from the fowl using a computerized image-analysis system.

Oocysts of Eimeria species from the fowl have been identified using a computerized image-analysis system (Leitz T.A.S. Plus Image-Analyser). The system enabled semiautomatic measurement of oocyst dimensions with subsequent species of diagnosis based on graphic statistical evaluation of size and shape of measured parasites. E. mitis, E. acervulina, E. brunetti, E. maxima, E. tenella and complex of E. necatrix and E. praecox were distinguishable both in pure cultures and in mixtures. It was not possible to distinguish E. praecox from E. necatrix using this system.

Animals↗

Subclinical pneumonia associated with an experimental adenovirus infection in the domestic fowl and the effect of concurrent infectious laryngotracheitis virus.

A CELO-type adenovirus (AV) isolated from fowls with respiratory disease was inoculated experimentally into the tracheas of young birds. No symptoms referable to respiratory infection were evident. Post mortem examination between days 2 and 5 after inoculation revealed pneumonia involving up to 30 per cent of the surface of the lungs. Histologically, a focal to diffuse interstitial lymphocytic infiltration and bronchiolar degeneration were present. Concurrent infections with a mild strain of infectious laryngotracheitis virus (ILT) failed to enhance the pathogenicity of either the AV or ILT infections.

Adenoviridae Infections↗

Effect of gossypol on domestic fowl, Gallus domesticus.

Domestic fowls (Gallus domesticus) were administered gossypol (10 mg/kg body weight/day) by oral intubation for 15 weeks. Drug treatment did not have any effect on body growth rate. The drug treatment, however, caused a marked decrease in the weights of testis and epididymis. Predominant changes in the histoarchitecture of testis (desquamation of germinal epithelium and inhibition of spermatogenesis) were observed following gossypol treatment. Epididymal tubules in gossypol treated animals were devoid of spermatozoa. Gossypol treatment had no effect on hematological parameters (total erythrocyte count, total leucocyte count, hematocrit and hemoglobin) studied in the present investigations.

Animals↗

Massive occurrence of rickettsiae of the spotted fever group in fowl tampan, Argas persicus, in the Armenian S.S.R.

Fowl tampans (Argas persicus) collected in Oktemberyan in the Armenian S.S.R. in 1974 were found to be massively infected with rickettsiae of the spotted fever (SF) group. One isolated rickettsial strain, designated Armenia 9, is antigenically related to, and probably identical with, strain Armenia 11 and strain B of Rickettsia slovaca, isolated from Dermacentor marginatus ticks. Strain Armenia 9 grows readily in chick embryo yolk sacs and in chick embryo cell (CEC) and L-cell cultures. It causes generalized infection in both soft and hard ticks. A fatal disease was produced in Clethrionomys glareolus after subcutaneous inoculation. Similar inoculation of other small wild rodents (Mus musculus, Microtus arvalis, Apodemus flavicollis), hens and laboratory animals (guinea pigs, white mice and hamsters) resulted only in an antibody response.

Animals↗

Suspected reticuloendotheliosis in turkeys with cutaneous lesions reminiscent of fowl pox.

Twelve turkeys from a flock of 2,500 had cutaneous lesions somewhat resembling fowl pox. Lymphoid-like tumors were evident in livers and spleens. Closer examination of cutaneous lesions, and histopathological examinations indicated skin lesions were also infiltrative and not unlike reticuloendotheliosis. Electron micrographs revealed the presence of C-type virus particles.

Animals↗