A native soluble form of CTLA-4.

CTLA-4 is an immunoregulatory receptor expressed on the surface of activated T and B lymphocytes. The counterreceptors for CTLA-4 are the B7 family molecules. We describe alternatively spliced mRNAs expressed in hematolymphoid tissues of humans, mice, and rats that lack the transmembrane domain coded by exon 3 of the CTLA-4 gene. These alternate transcripts were detected by RT-PCR in B cells and resting T cells of both the CD4 and the CD8 phenotype. Activation of human blood mononuclear cells with PHA or anti-CD3 + anti-CD28 monoclonal antibodies appears to effect a decrease in the amount of the alternative transcript relative to the full-length transcript. Recombinant sCTLA-4 is a B7-binding protein and has immunomodulatory effects as measured by inhibition of the mixed leukocyte response. Human serum contains immunoreactive material consistent with a native soluble form of CTLA-4.

Probing essential oil biosynthesis and secretion by functional evaluation of expressed sequence tags from mint glandular trichomes.

Functional genomics approaches, which use combined computational and expression-based analyses of large amounts of sequence information, are emerging as powerful tools to accelerate the comprehensive understanding of cellular metabolism in specialized tissues and whole organisms. As part of an ongoing effort to identify genes of essential oil (monoterpene) biosynthesis, we have obtained sequence information from 1,316 randomly selected cDNA clones, or expressed sequence tags (ESTs), from a peppermint (Mentha x piperita) oil gland secretory cell cDNA library. After bioinformatic selection, candidate genes putatively involved in essential oil biosynthesis and secretion have been subcloned into suitable expression vectors for functional evaluation in Escherichia coli. On the basis of published and preliminary data on the functional properties of these clones, it is estimated that the ESTs involved in essential oil metabolism represent about 25% of the described sequences. An additional 7% of the recognized genes code for proteins involved in transport processes, and a subset of these is likely involved in the secretion of essential oil terpenes from the site of synthesis to the storage cavity of the oil glands. The integrated approaches reported here represent an essential step toward the development of a metabolic map of oil glands and provide a valuable resource for defining molecular targets for the genetic engineering of essential oil formation.

Tracheal resection and anastomosis for an intratracheal chondroma in a ball python.

A 9-year-old female ball python was evaluated for lethargy and respiratory compromise. Radiographic and endoscopic examination revealed a 1-cm intratracheal mass occluding the tracheal lumen. A partial tracheal resection and anastomosis was performed to remove the mass. On histologic examination, the mass was determined to be an intratracheal chondroma. Eosinophilic cytoplasmic inclusions observed within the tissue were calcium deposits. Electron microscopy was used to differentiate these from viral inclusion bodies often associated with neoplasms in reptiles. Endoscopic evaluation of the trachea 5 weeks after surgery revealed complete healing and minimal stenosis at the surgery site. Indications of tumor regrowth were not evident. Clinical signs of recurrence of respiratory compromise had not been observed 9 months after surgery.

Aspergillosis in an ostrich.

A 4-month-old sexually intact blue-neck ostrich was examined because of chronic respiratory tract disease and poor performance. The bird was coughing and dyspneic on physical examination. Thoracic radiographs were consistent with air sacculitis. Bronchoscopy was used to view and to biopsy plaques within the bronchus and lower airways. Aspergillus spp was identified in culture and in biopsy specimens examined microscopically. Aspergillosis was confirmed on postmortem examination. Bronchoscopy may aid in the early diagnosis and treatment of this disease.

Survival of pigeon red blood cells after transfusion into selected raptors.

Survival time of 51Cr-labeled pigeon RBC transfused into 5 raptors was determined. Mean +/- SD estimated RBC survival time was 0.51 +/- 0.19 days. This was considerably shorter than estimated survival time of autologous RBC in a Red-tailed Hawk (estimated survival, 35.1 days) and in a pigeon (estimated survival, 26.8 days). Estimated survival time after homologous transfusion of RBC from one pigeon to another was 7.1 days. Although single heterologous blood transfusions have been recommended as a safe and efficacious means of whole blood replacement in birds, results of this study suggest that heterologous RBC transfused from pigeons to selected raptor species are rapidly destroyed.

Evaluation of selected plants for their toxic effects in canaries.

Leaves or fruit from 14 plants considered to be toxic to pet birds were administered by gavage to 15 pairs of canaries (Serinus canaria). Each bird was given 0.12 to 0.70 g of plant material. One pair served as a control and was given distilled water. The plant materials were flash-frozen in liquid nitrogen, pulverized, and resuspended in deionized water for administration. Of the plants tested, 5 (oleander, lupine, foxglove, yew leaves, and dieffenbachia) were considered highly toxic and were associated with acute death of birds. The remaining plant samples caused no, or only transient, clinical illness.

Evaluation of selected plants for acute toxicosis in budgerigars.

Pairs of budgerigars were given samples, by gavage, of plants considered potentially toxic to pet birds. Samples were prepared by flash-freezing and powdering fresh plant material in liquid nitrogen and resuspending the material in deionized water for administration. Of the 19 plants tested, only 6 induced clinical signs of illness; these plants included yew, oleander, clematis, avocado, black locust, and Virginia creeper (Taxus media, Nerium oleander, Clematis sp, Persea americana, Robinia pseudoacacia, Parthenocissus quinquefolio).

[The content of beta-carotene, vitamin A and ascorbic acid in different tissues of bulls, short-scrotum bulls and oxen of different body weights]. / Untersuchungen über den Gehalt an beta-Carotin, Vitamin A und Ascorbinsäure in verschiedenen Geweben von Bullen, Muchsen und Ochsen unterschiedlicher Körpermasse.

Analyses of the liver of bulls of different age show, that the concentration of beta-carotene in the age of 6 to that of 25 weeks increased only from 0.43 +/- 0.16 to 1.66 +/- 0.27 and that of vitamin A from 11.49 +/- 5.87 to 13.90 +/- 5.21 micrograms/g fresh weight. The concentration of beta-carotene and of vitamin A in the testis of bulls and of short scrotum bulls up to an age of 15 weeks was similar; thereafter the concentration in the short scrotum bulls was higher. At an age of 72 weeks the concentration of vitamin A in the liver of bulls (219.17 +/- 51.86) was higher (p less than 0.01) than in that of the short scrotum bulls (144.11 +/- 27.79) and that of the oxen (135.51 +/- 41.26 micrograms/g fresh weight). Analyses of the concentration of ascorbic acid in 8 different tissues of bulls and short scrotum bulls at 6 various periods show, that the highest values mostly were found in December.

[Content of beta-carotene, vitamin E and ascorbic acid in blood plasma of female calves, cattle, bulls, castrates and ox throughout the course of the year]. / Untersuchungen über den Gehalt an beta-Carotin, Vitamin E und Ascorbinsäure im Blutplasma von weiblichen Kälbern, Kühen, Bullen, Muchsen und Ochsen im Jahresverlauf.

The concentration of beta-carotin, of vitamin E and of ascorbic acid in the plasma of female calves (beginning with an age of 4 weeks), of cows in the 2nd and 5th lactation, of bulls, of short scrotum bulls and of oxes in the course of the year was analysed. The concentration of beta-carotin in the plasma of calves after driving up to pasture increased slower than that of cows. After transition to stable feeding there was a significant decrease in the concentration after 4 weeks. During the period of suckling the concentration of vitamin E in the plasma of calves was low. After transition to pasture the concentration of vitamin E in the plasma of calves increased slower than in that of the cows. The concentration of ascorbic acid in the plasma during the winter was higher than during the summer. There was no influence of experimental cryptorchism or castration on the mentioned values.

Polyostotic hyperostosis associated with oviductal tumor in a cockatiel.

A 10-year-old female cockatiel in a thin and depressed condition and with a 1 X 2-cm soft abdominal swelling was hospitalized. Radiography revealed a well-circumscribed mass containing punctate areas of mineralization, displacing the gizzard cranially in the caudodorsal portion of the abdomen. There was bilateral, symmetric, generalized, increased medullary opacity of the radius, ulna, carpometacarpus, femur, tibiotarsus, and tarsometatarsus. These findings were compatible with polyostotic hyperostosis secondary to an estrogen-secreting tumor. Euthanasia and necropsy were requested. A small area of neoplastic cells in the oviduct was identified histologically, but most of the tissue mass consisted of necrotic cellular debris. There was no metastasis. Sagittal secretions of decalcified radiopaque bones revealed up to 60% filling of medullary cavities with bone spicules. Although clinical and radiographic findings were compatible with an estrogen-secreting tumor, osteopetrosis, metastatic neoplasia, hypertrophic osteopathy, and metabolic bone disease were included in the initial differential diagnosis. The absence of metastasis and the confinement of the tumor within the oviduct would have made surgical removal a possible approach to treatment.

Mast cell tumors in three ferrets.

Pruritic open skin lesions (5 mm diameter) on the thorax, neck, or head of 3 ferrets were diagnosed as mast cell tumors. Diagnosis of the tumors was based on histologic examination of biopsy specimens. Histologic diagnosis was necessary because the lesions had been treated as mycotic or bacterial ulcers and did not respond to conventional treatment. Excised mast cell tumors did not recur, and malignant behavior of the tumors was not observed.

Avocado (Persea americana) intoxication in caged birds.

Avocados of 2 varieties were mashed and administered via feeding cannula to 8 canaries and 8 budgerigars. Two control budgerigars were given water via feeding cannula. Six budgerigars and 1 canary died within 24 to 47 hours after the first administration of avocado. Deaths were associated with administration of both varieties of avocado. Higher dose was associated with greater mortality. The 2 budgerigars given water were normal throughout the observation period. Results indicated that avocados are highly toxic to budgerigars and less toxic to canaries. Postmortem findings observed in some birds included subcutaneous edema in the pectoral area and hydropericardium.

A survey of the aerobic bacteria in the feces of captive raptors.

Feces of 47 captive raptors belonging to the order Falconiformes or Strigiformes were cultured for bacteria. Gram-negative bacteria, which were cultured from the feces of 45 of the 47 raptors, were the most common isolates. A wide variety of species were identified, including a newly described genus (Moellerella wisconsensis), two newly described species (Escherichia fergusonii and Proteus penneri), and a member of a newly described enteric group (CDC Enteric group 41). Additional organisms identified that have not been reported in previous bacteriological surveys of raptors were Salmonella heidelberg, Salmonella braenderup, Morganella morganii, Yersinia ruckeri, Serratia spp., and Kluyvera sp. Escherichia coli, isolated from the feces of 42 of the 47 raptors, was the most frequently recovered. Streptococcus faecalis, the second most common isolate, was cultured from 30 birds. Several differences were observed between fecal bacteria isolated from raptors fed commercially prepared chicken and those isolated from raptors not fed chicken. The most obvious difference was that birds fed chicken had more varied gram-negative bacterial species and in greater numbers per fecal sample. The potential for the isolated bacteria from raptors as pathogens in humans and avian species is discussed.

A survey of aerobic bacteria and fungi in the feces of healthy psittacine birds.

Fecal samples from 61 clinically healthy psittacine birds of a wide variety of species were cultured for bacteria and fungi. The most common bacterial isolates were gram-positive bacilli, which were recovered from 60 of the 61 birds. These organisms included Lactobacillus, Bacillus, Corynebacterium, and Streptomyces. Gram-positive cocci, cultured from the feces of 21 of the birds, included Staphylococcus epidermidis, Streptococcus spp., Aerococcus spp., and Micrococcus spp. Only 6 of the 61 psittaciformes yielded gram-negative bacteria, with Escherichia coli being the most frequent isolate. Gram-negative bacilli were recovered from 4 of the 31 privately owned birds and 2 of the 30 petshop birds sampled. In addition to the bacteria, Candida albicans, Cryptococcus laurentii, and Aspergillus sp. were isolated from 13 fecal cultures. Candida albicans was isolated exclusively from 5 petshop birds. The number of birds yielding Corynebacterium and gram-negative bacteria increased with age, whereas the number of birds yielding lactobacilli and yeasts decreased with age. The organisms isolated and their significance as potential pathogens in psittacine birds are discussed.

Seroepizootiology of types 3 and 7 adenoviruses and bovine viral diarrhea virus infections of beef cattle from birth to first parturition.

Twenty-nine female Angus cattle were monitored from birth until 24 months of age for infection with types 3 and 7 adenoviruses (AV3, AV7) and bovine viral diarrhea (BVD) virus by virus isolation and neutralization tests. Twenty-seven animals remained in the study for 450 days, whereas 16 animals remained at the conclusion of the tests. Viruses were not isolated from test animals. Seroepizootiologic examination indicated that there were 28 infections with AV3, 33 infections with AV7, and 13 infections with BVD virus. Of these infections, 5 with AV3, 6 with AV7, and 2 with BVD virus were reinfections. All but 1 primary AV3 infection had occurred between 180 and 360 days after parturition. Infection with AV7 occurred earlier than that with AV3, as shown by 6 seropositive animals by 180 days. Most adenovirus infections were documented after animals had left confinement and were turned out to pasture. Most BVD virus infections occurred within the first 90 days after parturition. At completion of the study, only 1 animal had not shown evidence of AV3 infection, 2 animals had not been infected with AV7, and 7 cows had remained free of BVD virus infection.

Association of parainfluenza-3 virus with bovine macrophages and blood cells: an in vitro study.

Bovine blood cells and peritoneal and lung macrophages were exposed in vitro to parainfluenza-3 (PI-3) virus. Residual nonadsorbed PI-3 virus (expressed in percentage of input virus) in the supernate of the various cell fractions 1 hour after incubation at 37 C was as follows: lung macrophages, 11%; peritoneal macrophages, 59%; monocytes, 26%; RBC, 14%; lymphocytes, 28%; and polymorphonuclear cells (PMN), 63%. Lung macrophages, monocytes, lymphocytes, and PMN were monitored over a 72-hour period for hemadsorption of chicken RBC. Hemadsorption increased for lung macrophages and monocytes, whereas it decreased for lymphocytes and PMN. Infective virus could not be recovered from PMN, RBC, lymphocytes, or monocytes for more than 24 hours after PI-3 infection. Recovery of infective PI-3 virus from infected peritoneal and lung macrophages extended over 4 to 8 days, respectively.

Variation of virus replication in primary bovine kidney cell cultures derived from 68 three-day-old calves.

Primary kidney cell cultures were prepared from 68 three-day-old calves. Complete monolayers of these cultures were infected separately with viral diarrhea, infectious bovine rhinotracheitis, parainfluenza, and adenovirus 7 viruses. The yield of virus from all infected cultures was calculated by plaque titer assay after 2 to 4 days' incubation. The variation of virus yield was substantial between individual cultures.