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1.
Avian Dis ; 64(3): 324-329, 2020 09 01.
Article in English | MEDLINE | ID: mdl-33205179

ABSTRACT

Ornithobacterium rhinotracheale (ORT) is an important bacterial pathogen of great economic significance to poultry production. This bacterium causes severe disease in chickens and turkeys worldwide. The objective of this study was to characterize ORT isolates from two different geographic locations in the United States by multilocus sequence typing (MLST). A total of 60 isolates were included in this study; 36 from California and 24 from Minnesota. All 60 isolates were confirmed to be ORT by PCR that targeted the 16S rRNA gene. The results of MLST revealed eight different sequence types (ST) of ORT. Out of these, four were novel and were assigned numbers ST-32, ST-33, ST-34, and ST-35. ST-1 was the predominant sequence type among all isolates followed by ST-9 and ST-8. Only one isolate was identified as ST-2. No significant variation was seen in STs in ORT isolated from different years. In turkeys, 76.3% (29/38) of isolates belonged to ST-1 and 7.9% (3/38) to ST-8. Of the chicken isolates, 72.2% (13/18) belonged to ST-1 and 16.6% (3/18) to ST-9. Isolates from both states showed low genetic variability. Of the 32 isolates from California, 24 (75%) were identified as ST-1 and 4 (12.5%) were identified as ST-9. The most prevalent sequence type was ST-1 (17/24) followed by ST-8 (3/24) in Minnesota. Three isolates from turkeys in Minnesota belonged to the same ST (ST-8) as the already known ORT strain RefO, which isolated from a rook in Germany in 2000. Whether this sequence type had evolved from wild birds could not be ascertained in this study.


Subject(s)
Chickens , Flavobacteriaceae Infections/veterinary , Genetic Variation , Ornithobacterium/genetics , Poultry Diseases/epidemiology , Turkeys , Animals , California/epidemiology , Flavobacteriaceae Infections/epidemiology , Flavobacteriaceae Infections/microbiology , Minnesota/epidemiology , Multilocus Sequence Typing/veterinary , Polymerase Chain Reaction/veterinary , Poultry Diseases/microbiology , Prevalence , RNA, Bacterial/analysis , RNA, Ribosomal, 16S/analysis , United States
2.
J Avian Med Surg ; 29(4): 326-35, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26771322

ABSTRACT

An asymptomatic 14-year old, male black swan ( Cygnus atratus ) housed at a zoological institution was presented for routine preshipment examination. Hematologic findings indicated that the bird had a severe lymphocytic leukocytosis, consistent with chronic lymphocytic leukemia. Radiographs showed the presence of multiple soft tissue masses within the caudal coelomic cavity; ultrasound showed one mass to be an enlarged spleen, a cystic mass near the gonads, and a mass suspected to be associated with the ventriculus. Results of further antemortem diagnostics, including bone marrow aspiration, fine-needle aspirate cytology of the coelomic masses, and immunohistochemical staining confirmed T-cell leukemia with infiltration of the bone marrow and the spleen. The bird showed partial response to treatment with chlorambucil, lomustine, prednisone, l-asparaginase, and whole-body radiation, with neither evidence of adverse effects nor clinical signs of disease. Although the leukemia showed response, there was no evidence of remission at any point. The swan died 433 days after initial evaluation and initiation of therapy. Necropsy, histopathologic findings, and immunohistochemistry results confirmed extensive infiltration of multiple organs, including the liver, spleen, heart, lungs, and kidneys with neoplastic T-cell lymphocytes.


Subject(s)
Anseriformes , Antineoplastic Agents/therapeutic use , Bird Diseases/diagnosis , Leukemia, T-Cell/veterinary , Animals , Animals, Zoo , Bird Diseases/drug therapy , Leukemia, T-Cell/drug therapy , Male
3.
J Vet Diagn Invest ; 25(6): 775-81, 2013 Nov.
Article in English | MEDLINE | ID: mdl-24081928

ABSTRACT

A total of 5 psittacine birds in an enclosed zoological exhibit, including 2 princess parrots and 3 cockatoos of 2 different species, developed severe central nervous system clinical signs over a 2-3-month period and died or were euthanized. Histologically, all birds had a lymphoplasmacytic and histiocytic encephalitis with intralesional protozoa consistent with a Sarcocystis species in addition to intramuscular tissue sarcocysts. By immunohistochemical staining, merozoites in brain and tissue cysts in muscle did not react with polyclonal antisera against Sarcocystis falcatula, Sarcocystis neurona, Toxoplasma gondii, and Neospora caninum, or with a monoclonal antibody to S. neurona. Transmission electron microscopy on sarcocyst tissue cyst walls from 2 birds was morphologically consistent with Sarcocystis calchasi. Polymerase chain reaction (PCR) amplification and sequencing of partial 18S ribosomal RNA from muscle tissue cysts and brain schizonts from 3 birds was consistent with a clade containing S. calchasi and Sarcocystis columbae but could not distinguish these closely related Sarcocystis species. However, PCR amplification and sequencing of the internal transcribed spacer 1 RNA segment in the brain from 2 birds and muscle from 2 birds specifically identified the isolates as S. calchasi. The current report documents that multiple psittacine species are susceptible intermediate hosts of S. calchasi, and that infection can cause encephalitis resulting in significant morbidity and mortality in psittacine aviaries.


Subject(s)
Bird Diseases/parasitology , Central Nervous System Diseases/veterinary , Parrots , Phylogeny , Sarcocystis/isolation & purification , Sarcocystosis/veterinary , Animals , Animals, Zoo , Base Sequence , Bird Diseases/pathology , Central Nervous System Diseases/parasitology , Central Nervous System Diseases/pathology , DNA, Protozoan/chemistry , DNA, Protozoan/genetics , Disease Outbreaks/veterinary , Fatal Outcome , Immunohistochemistry/veterinary , Microscopy, Electron, Transmission , Molecular Sequence Data , Polymerase Chain Reaction/veterinary , RNA, Ribosomal, 18S/chemistry , RNA, Ribosomal, 18S/genetics , Sarcocystis/genetics , Sarcocystis/ultrastructure , Sarcocystosis/parasitology , Sarcocystosis/pathology , Sequence Alignment , Sequence Analysis, DNA
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