Experimental diet-induced atherosclerosis in Quaker parrots (Myiopsitta monachus).

Spontaneous atherosclerosis is common in psittaciformes, and clinical signs associated with flow-limiting stenosis are encountered in pet birds. Nevertheless, a psittacine model of atherosclerosis has not been developed for research investigations. Sixteen captive-bred Quaker parrots (Myiopsitta monachus) were used in this study. While 4 control birds were fed a maintenance diet, 12 other birds were fed an atherogenic diet composed of 1% cholesterol controlling for a calorie-to-protein ratio for periods ranging from 2 to 8 months. The birds were euthanized at the end of their respective food trial period. Histopathology, transmission electron microscopy, and cholesterol measurement were performed on the ascending aorta and brachiocephalic and pulmonary arteries. Plasma lipoproteins, cholesterol, and triglycerides were also measured on a monthly basis. Significant atherosclerotic lesions were induced within 2 months and advanced atherosclerotic lesions within 4 to 6 months. The advanced lesions were histologically similar to naturally occurring lesions identified in the same parrot species with a lipid core and a fibrous cap. Ultrastructurally, there were extracellular lipid, foam cell, and endothelial changes. Arterial cholesterol content increased linearly over time. Plasma cholesterol and low-density lipoprotein (LDL) significantly increased over time by an average of 5- and 15-fold, respectively, with a shift from high-density lipoprotein to LDL as the main plasma lipoprotein. Quaker parrots also exhibited high plasma cholesteryl ester transfer protein activity that increased, although not significantly, over time. This experiment demonstrates that in Quaker parrots fed 1% cholesterol, advanced atherosclerosis can be induced relatively quickly, and lesions resemble those found in other avian models and humans.

A modified biopsy technique to improve histopathological evaluation of avian skin.

Skin biopsies are a viable diagnostic tool in avian dermatology, however, the thinness of avian skin makes it difficult to prevent rolling and contraction of skin biopsy specimens during collection and fixation. The difficulty orienting such rolled samples during processing ultimately interferes with the establishment of a histopathological diagnosis. We describe a modified skin biopsy procedure for obtaining avian skin biopsy specimens. In this technique nontranslucent self-adhesive tape (Scotch tape) was attached to skin biopsy sites before obtaining skin biopsies using a standard skin biopsy punch instrument. A total of 23 skin biopsy specimens were obtained: 15 from nonfeathered skin of 12 normal Hispaniolan parrots, 3 from feathered skin of 2 normal birds and 5 from feathered skin of 3 psittacines presented for pathologic feather-picking. All 23 skin specimens consistently adhered to the tape during the biopsy procedure. The specimens were fixed in 10% neutral phosphate-buffered formalin. During processing, no curling or rolling of specimens occurred, and all specimens could be easily orientated for correct trimming and subsequent histopathological evaluation. The tape technique did not produce any appreciable artefacts. Remnants of the tape were microscopically evident above the stratum corneum assuring that none of the stratum corneum was lost during processing. Obtaining avian skin biopsy specimens using this modified tape technique is easy and ensures flat fixation of the skin biopsy specimens, which later allows trimming at right angles, and through the longitudinal diameter of feather follicles for accurate histopathologic evaluation.

Psittacine therapeutics.

Psittacine therapeutics incorporates a number of clinical parameters. These parameters include fluid therapy, nutritional support, blood transfusions, and administration of medications. This article highlights the basic therapeutic techniques utilized in a veterinary practice that treats psittacine species. Considerations on the practical application of these techniques, as it relates to patient presentation and owner compliance, are discussed within each section of the article.

Production of a rabbit anti-cockatiel immunoglobulin G and characterization of its cross-reactivities with immunoglobulin G of other psittacine species.

The purpose of this work was to produce rabbit anti-cockatiel immunoglobulin G (IgG) and compare its cross-reactivity with sera from eight other psittacine birds: Quaker parakeet, budgerigar, green-wing macaw, blue-fronted Amazon parrot, eclectus parrot, African grey parrot, Patagonian conure, Moluccan cockatoo. Cockatiel IgG did not bind to protein A or G; therefore, these proteins could not be used in column chromatography to isolate the IgG. A combination of serum IgG precipitation by ammonium sulfate and yolk IgG extraction from egg was loaded in sodium dodecyl sulfate-polyacrylamide gel upon which the IgG was resolved by electrophoresis. The resolved IgG in sodium dodecyl sulfate-polyacrylamide gel was stained with Coomassie blue, cut, crushed in phosphate-buffered saline, and injected into rabbits. The rabbit anti-cockatiel IgG produced in this way reacted with a single protein in gel immunodiffusion assay with all nine psittacine bird sera but not with those of chicken and ostrich. Immunoelectrophoresis confirmed the cross-reactivity of different psittacine sera with the anti-cockatiel IgG serum but not with ostrich and chicken sera. This antiserum detected antibody responses in sera from cockatiels vaccinated against chlamydial major outer membrane protein in an immunoblot assay.

Health examinations and clinical diagnostic procedures of ratites.

It is important to remember when performing health examinations and clinical diagnostic procedures on ratites that all protocols mentioned in this article should be followed; this includes reviewing history, environmental evaluation, proper handling, complete hands-on physical examination, diagnostic testing, and postmortem examination. The individual ratite examination is becoming rare, but veterinarians and producers must remember that individual birds make up the flock. Flock health is maintained by diagnosing disease and health problems early in the most susceptible animals. The most successful producers will use veterinarians as a major element to their management program to raise the most desirable birds for the future of the industry.

Intracellular Campylobacter-like organisms associated with rectal prolapse and proliferative enteroproctitis in emus (Dromaius novaehollandiae).

Rectal prolapse was the presenting clinical finding in a group of juvenile emus (Dromaius novaehollandiae). Gross findings included severely thickened and rugose distal rectal mucosae. Histologically, there were thickened villi, enterocyte hyperplasia, dilated glands filled with mucus and heterophils, and a dense infiltrate of heterophils, macrophages, lymphocytes, and plasma cells in the lamina propria. Examination of Warthin-Starry silver-stained sections revealed numerous apically located comma-shaped intracytoplasmic bacteria approximately 1 x 3 microns in size. Campylobacter-like organisms morphologically compatible with ileal symbiont intracellularis now known as Lawsonia intracellularis were seen via electron microscopy. Bacteria were further characterized by indirect immunofluorescence using monoclonal antibody specific for the 25-27-kd outer membrane protein of L. intracellularis.

Comparison of procedures to detect Chlamydia psittaci antibodies in cockatiels (Nymphicus hollandicus).

Diagnostic serologic procedures for psittacine chlamydiosis were evaluated using experimentally inoculated cockatiels (Nymphicus hollandicus). Chlamydia psittaci was recovered from subjects on day 16 postinoculation. Seroconversion was confirmed by the direct complement fixation (DCF) test. The blocking enzyme-linked immunosorbent assay was demonstrated to be the most sensitive of three serodiagnostic procedures evaluated from inoculation until day 24 postinfection, with 92% sensitivity and 73% specificity. The DCF test was progressively more sensitive over the duration of the experiment, attaining 100% sensitivity and specificity on the day 24 postinfection. This study confirms the ability of the DCF procedure to adequately detect C. psittaci antibodies. Limitations relating to reproducibility of serologic results under clinical conditions found in this study indicate that a further refinement of tests is required to consistently detect and quantify antibodies.

Husbandry practices as related to infectious and parasitic diseases of farmed ratites.

Over the past decade, there has been a world-wide increase in the number of farm-raised ratites. The focus of ostrich production remains in South Africa, but other countries are initiating production of this bird in addition to the emu and rhea. Ostriches, emus and rheas are being produced commercially outside their native habitat, resulting in new and unique disease presentations. The authors describe bacterial, viral and parasitic diseases which are emerging in production settings. Biosecurity, together with adequate management and nutrition, will reduce the likelihood of flock exposure and limit mortality in the event of infection. The problem currently facing the industry is that most ratite facilities do not incorporate separate quarantine areas. Newly-introduced birds may contaminate soil and facilities with pathogens such as Mycobacterium spp. and Salmonella spp. Ratites have excellent production potential if producers can profitably multiply and rear healthy stock. The authors discuss the currently-known diseases which may affect the viability of an intensive production facility.

Tourniquet-induced hypertension in an ostrich.

Surgery was performed on a 3-year-old 110-kg male ostrich (Struthio camelus) to remove a sequestrum from the dorsal aspect of the left tarsometatarsal bone. A pneumatic tourniquet was positioned proximal to the surgical site and inflated to 600 mm of Hg. Systolic blood pressure increased 35% over 105 minutes while the tourniquet was inflated. Systolic blood pressure decreased 31.5% within 30 seconds after removal of the tourniquet pressure. Recovery from anesthesia and surgery was routine. The tourniquet-induced hypertension in this ostrich was similar to that reported for human beings and horses.

Elementary body agglutination for rapidly demonstrating chlamydial agglutinins in avian serum with emphasis on testing cockatiels.

The development and use of a stained chlamydial elementary body agglutination (EBA) antigen for detecting antibody activity in avian sera is described. Examples of serologic results on serum samples from various types of birds indicate the usefulness of EBA, latex agglutination (LA), and direct complement fixation (DCF) in diagnosing avian chlamydiosis. Results of tests on 10 cockatiels examined in clinics indicate that a combination of serology, culture, and/or antigen-detection enzyme-linked immunosorbent assay may be helpful when testing this type of bird. Agreement between EBA, LA, and DCF was 81.8% when testing 407 serum samples from cockatiels of unknown health status. The relationship between positive (> or = 10 titer) antibody activity and known health status of 77 cockatiels revealed that agreement between the two criteria was only 59.7%. Of 13 Chlamydia-inoculated cockatiels, seven birds seroconverted from negative to positive by EBA; five seroconverted by DCF. Only the five birds that seroconverted by both EBA and DCF were culture-positive for chlamydiae. None of 15 sham-inoculated control cockatiels developed detectable antibody activity, and none of 10 cultured were positive. In tests with column-separated IgM and IgG, EBA detected only IgM activity, LA detected IgM and IgG activity, and DCF detected only IgG activity.

Chlamydiosis in commercial rheas (Rhea americana).

Mild to marked splenomegaly was observed in three of four rheas that died acutely in three unrelated commercial ratite facilities in Southeastern Louisiana. Mortalities occurred within a 5-week period in birds ranging from 2 months to 3 years of age. Multifocal hepatic and splenic necrosis with mononuclear cell infiltrates, typical of chlamydiosis in other avian species, was present on histopathologic sections. The diagnoses were confirmed by demonstration of inclusion bodies in splenic impression smears and fluorescent-antibody testing performed on Vero cell cultures.

Tuberculosis in commercial emus (Dromaius novaehollandiae).

Extensive granuloma formation typical of tuberculosis was observed in a mature female emu. The diagnosis was confirmed by demonstration of acid-fast bacilli in lesions and culture of a Mycobacterium with growth characteristics resembling M. avium from liver tissue. Individual emus on the affected farm and an epidemiologically related unit gave a positive skin reaction to intradermal M. avium tuberculin. The implication of tuberculosis in commercial emus is noted in relation to the growth of the industry in North America and to management and commercial practices that encourage dissemination of infection within the species and to other exotic and domestic animals.

Verminous encephalitis apparently caused by the filarioid nematode Chandlerella quiscali in emus (Dromaius novaehollandiae).

Verminous encephalitis attributed to Chandlerella quiscali was diagnosed in a flock of emus (Dromaius novaehollandiae). Clinically affected birds showed torticollis and progressive ataxia. Filarioid parasites with morphological characteristics resembling C. quiscali were identified in one case. Histologic lesions in the brain and spinal cord consisted of mild to moderate perivascular cuffing and scattered areas of variable mild necrosis. Parasites observed within the parenchyma of the brain and spinal cord often were not associated with either necrosis or an inflammatory reaction. Ivermectin administered subcutaneously at 4-week intervals at a dose rate of 200 micrograms/kg body weight appeared to prevent clinical signs in flocks in the presumed endemic area.

Eastern equine encephalitis in a flock of emus (Dromaius novaehollandiae).

Eastern equine encephalitis (EEE) was diagnosed in a flock of emus in southeastern Louisiana. The outbreak involved juvenile and adult breeders ranging in age from 20 to 36 months, with an attack rate of 76% and a case fatality rate of 87%. The diagnosis was confirmed by isolation and characterization of the viral agent, and by detection of EEE antibody in two recovered emus. High mortality was preceded by marked depression, hemorrhagic diarrhea, and emesis of blood-stained ingesta. On postmortem examination, hemorrhagic enteritis and multiple petechia of viscera were observed. Microscopic changes included severe necrosis of hepatocytes, intestinal mucosa, and necrotizing vasculitis of the spleen and lamina propria of the intestine. No nervous system lesions were observed. This outbreak occurred concurrently with EEE in horses and was attributed to unseasonably heavy rainfall with an abundance of arthropod vectors and proximity to free-living reservoir host species.