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FIV also induces a lentiviral encephalopathy and has been used in this capacity as a model for HIV neurologic disease 36 - Information on the tissue tropism, viral kinetics, and pathogenesis of LLV is much more Airis VM PC Camera in scope. Lymphoma in one lion and retinitis in several LLV-infected lions have been described, and T-cell-subset profile alterations have been substantiated in several captive lions 6192242 and in free-ranging individuals This study describes the neurologic manifestations of lion lentivirus infection in three captive lions, which were found to be analogous to FIV and HIV neuropathies, and characterizes the viral distribution and selected immunological phenotypes associated with LLV infection. These findings illustrate an association between chronic LLV infection and clinical neurologic disease in lions, despite a low viral load, analogous to the lentiviral encephalopathy in cats and humans, and also provides insights into the viral load and distribution that contribute to the relatively low level of pathogenicity of this virus for its natural host.
The approximate ages of lions EL, DJ, and TT at the initiation of these studies were 19, 17, and 15 years, respectively. Three seronegative lions, one female and two males, ages 18, 21, and 23 months, served as uninfected control blood donors.
All animals were housed Airis VM PC Camera the Columbus Zoo in two separate exhibits. No utensils or equipment were shared between the exhibits. Both infected female lions were euthanized because of progressive physical deterioration, while the male died due to a severe progressive anemia.
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Physical examination and observation. General health evaluation consisted of serum biochemical profile analysis, complete blood count with differential analysis, platelet count, urinalysis, hemostasis screening one-stage prothrombin time, activated partial thromboplastin time, fibrinogen, fibrin degradation productsand thoracic radiographs performed at the Ohio State University Veterinary Teaching Hospital Columbus, OH. Observational changes in the behaviors and activities of lions TT and EL were assessed on a monthly basis by Columbus Zoo animal handlers.
Selected elapsed-time videos were reviewed by a veterinary neurologist M. The frequencies of behavior changes were scored on a discrete scale from 0 to 3, as follows: Electrodiagnostic examination. Quantitative neurophysiologic changes were analyzed by using auditory evoked Airis VM PC Camera AEP and quantitative electroencephalography QEEG tests performed while the animals were under isoflurane gas anesthesia by use of the Biologic Brain Atlas system Biologic System Co.
Venous blood gas, pulse oximetry, and end-tidal partial CO2 pressure were monitored to stabilize the blood pH and ensure constant levels of arterial oxygen and carbon dioxide tension to remove confounding variables of the QEEG. The QEEG data were analyzed by comparison of the spectral analysis results for the infected and the control animals within each group and between groups Airis VM PC Camera Spectral differences between hemispheres for each individual recording were evaluated during each recording session. Electrode placement, signal filtering, and averaging and data analysis for AEP were performed as described previously 39 by using a Airis VM PC Camera electrodiagnostic system Neuropak 4; Nihon-Kodon, Irvine, CA.
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Magnetic resonance imaging MRI of the brain was performed with one affected female lion lion EL by using a 0. The lion was positioned in sternal recumbency while she was under general isoflurane anesthesia.
The contrast medium was intravenously administered gadopentetate-dimeglumine 0. Lymphocyte phenotyping. The immune profiles of all infected lions were monitored by lymphocyte subtype analysis and determination of total granulocyte counts at four time points during one 9-month period after clinical signs were recognized. Lymphocyte subpopulations were enumerated by immunostaining and flow cytometry with an Epics Elite flow cytometer Beckman Coulter, Inc. The titers of antibodies to LLV in serum were determined by immunoblotting, as described previously Feline leukemia virus titers were determined by enzyme-linked immunosorbent assay Ohio State University Veterinary Teaching Hospital Clinical Laboratory. Assays for the detection of serum and cerebrospinal antibodies to canine distemper virus, feline infectious peritonitis virus, Toxoplasma gondii, Neospora caninum, and cryptococcosis were performed by the Laboratory Corporation of America Dublin, OH.
Postmortem evaluation. The animals were subjected to a postmortem examination immediately following euthanasia, and gross lesions were noted at that time. At necropsy, samples were Airis VM PC Camera from the following tissues: One million peripheral blood mononuclear cells PBMCs from lions TT and EL were collected at three time points and cocultivated with an equal number of the following cell types by standard techniques: Supernatants were collected biweekly and were assayed for reverse transcriptase RT activity between days 14 and 35 of culture by using a microtiter RT assay 18 The outer and the inner primers amplified fragments of bp and bp, respectively.
These primers were used to generate PCR products from lion EL, which were similarly cloned and sequenced.
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