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At least 19 recordsLinked to original sources

On the muscular fuel of the air sac in an air breathing fish.

The hyohyoideus muscle which is responsible for inflating and contracting the air sac in an air breathing fish, Amphipnous cuchia, belongs to white fibre type as it lacks muscle myoglobin. The muscle shows appreciable amount of glycogen and extracellular phospholipid globules. Staining of I bands in the muscle fibres with Alcian blue (1.0 less than or equal to pH less than or equal to 3.0) indicates presence of acid mucosubstances. The muscle does not show change in phospholipid content at the histochemical level but lowering of glycogen content (25 to 30%) when put to 51/2h of continuted physiological exercise. At the same time, increase in blood sugar level (20 to 30%) possibly indicates utilization of glycogen as the source of energy by the muscle. However, a clear cut priority of glycogen or phospholipid break down for energy source by the muscle could not be established.

Animals

Spectrographic analysis of laryngeal air sac resonance in rhesus monkey.

Laryngeal air sacs are circular out-pocketings, located in the hyoid bone with their ostium in the midline of the anterior part of the larynx. From previous cadaver studies of the rhesus monkey it was deduced that the function of the air sac is to act as a resonating chamber. The present study was designed to test this hypothesis. Recordings were made of three rhesus monkeys before and after surgical removal of the air sac. Spectrographic analysis of the monkeys' vocalizations indicated that differences in formant frequency characteristics between pre-and post-surgical recordings were negligible. This finding suggests that the laryngeal air sac does not play an important role in the resonant properties of the monkeys' vocal tracts.

Animals

Histology of air sac lesions induced in chickens by contact exposure to Mycoplasma synoviae.

Chickens were housed when 1 day old with chickens experimentally infected with Mycoplasma synoviae. Air sacs from 16 of the 2-week-old and eight of the 3-week-old contact-exposed chickens were given gross lesion scores and embedded in glycol methacrylate for slide preparation. Histologic lesions in air sacs with gross scores of 0-2 were mild edema resulting in a two to eightfold increase in air sac thickness, capillary proliferation, and exudate consisting largely of heterophils and necrotic debris. Histologic lesions in air sacs with gross scores of 3 and 4 were marked hyperplasia of epithelial cells and diffuse infiltration of the air sac connective tissue by mononuclear cells. Nine of 10 air sacs with gross scores of 0 had no histologic evidence of inflammation. The most severe histologic lesions were in those air sacs with gross scores of 4. The glycol methacrylate procedure resulted in 2-mum sections with excellent cellular detail.

Air Sacs

Surgical drainage of a submandibular air sac in an orangutan.

Continuous enlargement of a submandibular air sac was observed in a 7-year-old female orangutan. The animal was treated with tetracycline orally prior to administering phencyclidine and establishing surgical drainage. The incision into the air sac remained patent for 5 days and the cutaneous wound healed 2 weeks later.

Animals

Serological responses of broiler-type chickens, with and without Newcastle disease and infectious Bronchitis vaccine, to experimental infection with Mycoplasma synoviae by foot pad, air sac and aerosol.

Serum plate (SP) and tube agglutination (TA) reactions and geometric mean Mycoplasma synoviae (Ms.) hemagglutination-inhibition (HI) titers were determined on chickens infected at 21 days of age with Ms. by foot pad, air sac and aerosol. One-half had been given Newcastle disease (ND) and infectious bronchitis (IB) vaccine in the water at 20 days of age, and the other half had not been vaccinated with ND and IB vaccine. Blood was taken at 3, 4, 6 and 8 weeks after Ms. infection. Geometric mean HI titers were determined on serums of chickens that had a foot pad injection of Ms. 8 weeks after Ms. infection and were bled at 1, 3 and 5 weeks after foot pad booster. Three weeks after aerosol exposure with Ms., the geometric mean HI titer was significantly higher in the ND- and IB-vaccinated birds than in the nonvaccinated birds. In the Ms. air sac-infected group of nonvaccinated birds the geometric mean HI titer had increased significantly 3 weeks after food pad challenge with Ms. In the Ms. air sac-infected group of vaccinated birds, the geometric mean HI titer had significantly increased 3 and 5 weeks after foot pad challenge with Ms.

Administration, Oral

Local immunity against Newcastle disease virus in the newly hatched chicken's respiratory tract.

Inoculation of 200 mean egg infectious doses (EID(50)) of lentogenic Newcastle disease virus strain B1 (NDV-B1) into the air sac of 4-day-old specific-pathogen-free chicks provided significant protection against challenge of the air sac with 100 chicken mean lethal doses (LD(50)) of velogenic NDV-H but no protection against reinfection when the challenge was by the eye. Conversely, inoculation of the eye with 200 EID(50) of NDV-B1 provided significant protection against challenge of the eye but not of the air sac with 100 chicken LD(50) of NDV-H. Birds that received both antiserum and intraocular immunization were subsequently protected against both eye and air-sac challenge. On the other hand, birds that received antiserum and air-sac immunization were protected only against air-sac challenge but not against ocular challenge. Low levels of passively administered antibody did not prevent infection of the eye or air sac but greatly reduced the mortality rate after inoculation of either the vaccine or the challenge viruses. Passively administered antibody also suppressed hemagglutination-inhibiting and virus-neutralizing antibody formation stimulated by air-sac infection but not antibody formation stimulated by ocular infection. These data are consistent with the hypothesis that local immunity is responsible for prevention of infection, since birds were immune to reinfection at one site and simultaneously susceptible at the other site of infection.

Air Sacs

Organ culture studies on the efficiency of infection of chicken tissues with avian infectious bronchitis virus.

Long-term organ cultures of a range of tissues collected from specific pathogen-free chickens were employed to determine their susceptibility, and their capacity for subsequent virus production, following inoculation with avian infectious bronchitis (AIB) virus. When inoculated with approximately 2-0 log10 median ciliostatic doses (CD50) of a classical highly egg-adapted vaccine strain (H120) of AIB virus, 9 of 23 tissues were shown to be susceptible, namely the nasal turbinates, trachea, air sac membranes,lungsasal turbinates, trachea, air sac membranes, lungs, proventriculus mucosa, thyroid, kidney, ovary and oviduct. When the remaining 14 tissues were inoculated with a high dose of virus (6.8 log10 CD50), the conjunctiva, caecel tonsil, testis and bursa of Fabricius were susceptible whereas the oesophagus and cloaca responded minimally. Inoculation of the same range of tissues with a high or low dose of a field strain (HVI9) of AIB virus produced similar results, except for a number of individual variations in response, due possibly to strain differences in pathogenicity. Determinations of the minimal infectious dose requirements of the susceptible tissues revealed that the efficiency of infection with the H120 strain was highest for the nasal turbinate and tracheal tissues, and thereafter, in order of decreasing efficiency, were the air sac membranes, lung, oviduct, proventriculus mucosa, conjunctiva, kidney, ovary, bursa of Fabricius, thyroid, testis, caecal tonsil, cloaca and oesophagus. The relevance of these results is discussed in connection with the early events in the pathogenesis and the clinical syndrome of AIB infection in chickens.

Animals

An epornitic of avian cholera in waterfowl and common crows in Phelps County, Nebraska, in the spring, 1975.

In the spring of 1975, many species of waterfowl and common crows (Corvus brachyrhynchos) were found dead in Phelps County, Nebraska. About 25,000 water fowl and at least 3,000 crows died in the epornitic. Few waterfowl were seen dying, but the crows experienced a chronic illness during which they became debilitated and were lethargic and dyspneic. Gross and microscopic lesions in the waterfowl were typical for acute avian cholera. The crows had dark, firm areas within the lungs, loosely adhered yellow fibrous material in the pericardial sac and air sacs and, occasionally, liver abscesses. Microscopically, focal purulent pneumonia was present and a fibrinopurulent exudate overlaid a granulomatous reaction on the heart and lung surfaces. Isolation of Pasteurella multocida serotype 1 confirmed the diagnosis of acute and chronic avian cholera in the waterfowl and crows, respectively.

Animals

Pathogenicity studies in poultry with an undefined serotype of Mycoplasma.

Pathogenicity trials in poultry are reported with an isolate of mycoplasma, designated 'W8', which is serologically unrelated to Mycoplasma gallisepticum, M synoviae or M meleagridis. W8 killed fowl and turkey embryos when injected into the yold sacs of embryonating eggs. Infection of one-day-old fowls, turkeys and pheasants by the air sac route caused marked growth depression and a high incidence of osteomyelitis of the vertebral column in all species. A large proportion of infected turkeys and a smaller proportion of infected pheasants also developed chondrodystrophic changes of the long bones similar to those of turkey syndrome '65. Infection did not cause mortality or macroscopic air sacculitis. No obvious pathological changes occurred in fowls following W8 infection by the air sac route at two weeks of age and only minimal changes when infection was given at one week. Infection did not appear to spread to in-contact controls. W8 was recovered most frequently and in greatest profusion from the air sacs, tracheas, kidneys and vertebral columns of fowls and turkeys following air sac infection at one day of age.

Animals

Airsacculitis induced in broilers with a combination of Mycoplasma gallinarum and respiratory viruses.

Mycoplasma gallinarum was isolated from tracheas and air-sac lesions from broilers in flocks having higher than normal condemnations due to airsacculitis. A representative M. gallinarum isolant, given by aerosol or by air-sac inoculation, produced air-sac lesions in young chickens when given in combination with a vaccine combining Newcastle disease and infectious bronchitis or with a field strain of infectious bronchitis virus.

Agglutination Tests

Medical and surgical approach to laryngeal air sacculitis in a baboon caused by Pasteurella multocida.

Air sacculitis was diagnosed in a chronically chaired baboon, Papio anubis. Pasteurella multocida was repeatedly isolated from the air sac for a period of 1 year. The condition was characterized by the continuous accumulation of either mucoserous or purulent fluid. Biopsies of the air sac taken during the course of the disease initially revealed goblet cell hyperplasia. Later a subepithalial mononuclear or polymorphonuclear infiltrate and necrosis was the predominate finding. Medical therapy was only intermittently successful and consisted of frequent drainage and antibiotics administered locally and intravenously. The condition was resolved after surgical resection of the air sac lining membrane.

Ampicillin