Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
Am J Vet Res ; 71(10): 1178-88, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20919904

ABSTRACT

OBJECTIVE: To compare iatrogenic transmission of Anaplasma marginale during sham vaccination between needle and needle-free injection techniques. ANIMALS: 26 Holstein steers confirmed negative for anaplasmosis by use of a competitive ELISA (cELISA) and an A marginale-specific reverse transcription (RT)-PCR assay. PROCEDURES: An isolate of A marginale was propagated to a circulating parasitemia of 2.0% in a splenectomized steer. Sham vaccination was performed in the left cervical muscles of the splenectomized parasitemic steer with a hypodermic needle fitted to a multiple-dose syringe. The same needle and syringe were used to sham vaccinate a naïve steer. This 2-step procedure was repeated until 10 naïve steers (group ND) were injected. Similarly, sham vaccination of the left cervical muscles of the splenectomized parasitemic steer and another group of 10 naïve steers (group NF) was performed by use of a needle-free injection system. Five control steers were not injected. Disease status was evaluated twice weekly for 61 days by use of light microscopy, a cELISA, and an A marginale-specific RT-PCR assay. RESULTS: Iatrogenic transmission was detected in 6 of 10 steers in group ND. Disease status did not change in the NF or control steers. Sensitivity of light microscopy, cELISA, and RT-PCR assay was 100% on days 41, 41, and 20 after sham vaccination, respectively; however, only cELISA and RT-PCR assay sustained a sensitivity of 100% thereafter. CONCLUSIONS AND CLINICAL RELEVANCE: Needle-free injection was superior to needle injection for the control of iatrogenic transmission of A marginale.


Subject(s)
Anaplasma marginale , Anaplasmosis/transmission , Cattle Diseases/transmission , Iatrogenic Disease/veterinary , Needles/veterinary , Vaccination/veterinary , Animals , Cattle , Cattle Diseases/microbiology , Injections, Jet/veterinary , Male , Needles/adverse effects , Vaccination/instrumentation
2.
Vet Microbiol ; 145(1-2): 69-75, 2010 Sep 28.
Article in English | MEDLINE | ID: mdl-20346598

ABSTRACT

Chemosterilization is reported in cattle fed chlortetracycline hydrochloride (CTC) at dosages ranging from 1.1mg/kg for 120 days to 11 mg/kg for 30-60 days. The relationship between plasma CTC drug concentration and carrier clearance has not been described. Chronic carrier status was established in 21 steers with a Virginia isolate of Anaplasma marginale and confirmed by cELISA and an A. marginale-specific RT-PCR. Four negative, splenectomized steers served as active disease transmission sentinels. Steers were randomized to receive 4.4 mg/kg/day (LD); 11 mg/kg/day (MD); or 22 mg/kg/day (HD) of oral chlortetracycline; or placebo (CONTROL) for 80 days. The LD, MD and HD treatment groups consisted of 5 infected steers and 1 splenectomized steer; CONTROL group had six infected steers and 1 splenectomized steer. The daily treatments and ration were divided equally and fed twice daily. Blood samples were collected semi-weekly for determining plasma drug concentration by ultrahigh performance liquid chromatography-mass spectrometry/mass spectrometry method and assessment of disease status by both cELISA and RT-PCR. Mean (CV%) chlortetracycline plasma drug concentrations in the LD, MD, and HD groups were 85.3 (28%), 214.5 (32%) and 518.9 (40%)ng/mL during days 4 through 53 of treatment. A negative RT-PCR assay result was confirmed in all CTC-treated groups within 49 days of treatment; however, cELISA required an additional 49 to 88 days before similar results. Subinoculation of splenectomized steers confirmed chemosterilization. These results are important for influencing future chemosterilization strategies and impacting free trade policy among countries and regions of contrasting endemicity.


Subject(s)
Anaplasma marginale/drug effects , Anaplasmosis/drug therapy , Cattle Diseases/drug therapy , Chlortetracycline/therapeutic use , Anaplasmosis/diagnosis , Animals , Carrier State/drug therapy , Carrier State/microbiology , Carrier State/veterinary , Cattle , Cattle Diseases/diagnosis , Cattle Diseases/microbiology , Chlortetracycline/administration & dosage , Chromatography, High Pressure Liquid/veterinary , Dose-Response Relationship, Drug , Drug Administration Schedule/veterinary , Enzyme-Linked Immunosorbent Assay/veterinary , Gas Chromatography-Mass Spectrometry/veterinary , Male , Reverse Transcriptase Polymerase Chain Reaction/veterinary
3.
Vet Clin Pathol ; 37(3): 353-6, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18761532

ABSTRACT

Pleural effusion was examined from a 5-year-old, female Brittany Spaniel with a 7-day history of dyspnea, anorexia, and diarrhea. The fluid was yellow, cloudy, and slightly gelatinous, and had a total protein concentration of 2.8 g/dL, a total nucleated cell concentration of 1.1 x 10(3)/microL, and a triglyceride concentration of 177 mg/dL. A cytocentrifuged preparation contained a mixed inflammatory cell population with a predominance of small lymphocytes and abundant mucinous material in the background. The dog died 3 days later and a mass was found within the lumen and wall of the right auricle of the heart at necropsy. Histopathologic sections of the mass contained a population of anaplastic spindle cells diffusely suspended in a pale basophilic matrix, consistent with myxosarcoma. The cells were positive for vimentin and negative for cytokeratin, desmin, and von Willebrand factor VIII-related antigen. A myxoid matrix was confirmed by positive staining with Alcian blue. Myxosarcoma is a rare cardiac tumor in dogs that should be considered, along with mucus-producing carcinomas and bile, as a cause of muculent effusion.


Subject(s)
Dog Diseases/pathology , Heart Neoplasms/veterinary , Myxosarcoma/veterinary , Pleural Effusion/veterinary , Animals , Dog Diseases/diagnosis , Dogs , Female , Heart Neoplasms/diagnosis , Heart Neoplasms/pathology , Myxosarcoma/diagnosis , Myxosarcoma/pathology , Pleural Effusion/diagnosis , Pleural Effusion/pathology
SELECTION OF CITATIONS
SEARCH DETAIL
...