Page 946 - Clinical Small Animal Internal Medicine
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884  Section 9  Infectious Disease

            to rat neurons in culture and may play a role in neuro­    Diagnosis
  VetBooks.ir  logic disease pathogenesis. The neurologic disease is   Complete blood count (CBC) abnormalities may include
            more prevalent  with certain isolates of the virus, which
            may point to certain envelope protein sequences being
            more toxic and/or relate to the ability of virus to replicate   anemia, lymphopenia, and neutropenia. Thrombocy­
                                                              topenia may sometimes occur. Hyperglobulinemia is the
            in the feline nervous system.                     most common biochemical abnormality. Proteinuria
                                                              may be seen in cats with glomerulonephritis.
                                                                Antibodies to FIV infection persist for life and thus
              Epidemiology                                    patient‐side ELISA antibody testing is recommended as
                                                              a screen for FIV infection. However, false‐positive and ‐
            Feline immunodeficiency virus infection is common   negative results may occur. If a kitten under 6 months of
            around the world. The incidence of FIV varies (from 4%   age is antibody positive, it should be retested after 60
            to 47%) geographically, correlating with the percentage   days, as maternal antibody could be the cause of the pos­
            of free‐roaming and feral cats in the population.  itive assay. If an animal is negative after a recent possible
                                                              exposure, it should be retested after 60 days, allowing
                                                              sufficient time for an active immune response to develop.
              Signalment                                      Tests used to detect antibody cannot distinguish between
                                                              infection and vaccination. Positive tests in healthy cats
            Although it is possible for any cat to be infected with FIV,   should be confirmed using ELISA from another manu­
            free‐roaming, nonpure‐bred, sexually intact, mature,   facturer, western blotting, or PCR. In cases where the
            male cats are more likely to contract an FIV infection.   vaccination history is not known, real‐time quantitative
            This is largely due to cat bites being the primary mode of   PCR should be considered, as this assay can detect a low‐
            virus transmission.                               grade viremia, indicative of an active infection. However,
                                                              sensitivity and specificity of PCR are variable. PCR may
                                                              be negative due to low levels of viremia or mutations,
              History and Clinical Signs                      and false‐positive results have been reported in vacci­
                                                              nated cats.
            Acute clinical signs of the infection are generally mild
            and often consist of the nonspecific signs of lethargy,
            anorexia, pyrexia, diarrhea, and  lymphadenopathy.     Management
            Generally, these clinical signs coincide with the viremia.
            Once the viremia subsides, the virus appears to go into   The best therapy for FIV is prevention. Keeping cats
            a clinical latent phase, with virus not detected in the   indoors and only allowing exposure to known FIV‐nega­
            blood and the apparent absence of most clinical signs.   tive cats is the best way to prevent the infection. The vac­
            This clinical latent phase is of variable length but often   cine for FIV is controversial, as efficacy is variable.
            lasts for years, as the virus slowly suppresses the   Additionally, using standard FIV screening assays, a vac­
            immune system. The last phase of the infection is   cinated  cat  currently  cannot  be  distinguished  from  an
            feline acquired immune deficiency syndrome (FAIDS).   infected cat. Since shelters may not perform a confirma­
            Clinical signs of FAIDS are the result of opportunistic   tory assay on an animal that is found FIV positive by a
            infections, various neoplasias, and/or neurologic dis­  screening assay, it is advised to microchip the cat at the
            ease. Thus, clinical signs are variable depending upon   time of vaccination with a chip whose data are linked to
            how the immune suppression is manifested. Stomatitis   vaccination status to assist shelter personnel in the inter­
            is very common and can occur during any phase of the   pretation of a positive result.
            infection. Persistent diarrhea is also fairly common, as   The use of the routine feline vaccines in FIV‐positive
            is respiratory disease. Neoplasia is common in FAIDS,   cats is controversial due to the suppressed immune system
            with B cell lymphoma being the most frequent.     of the FIV‐infected cat. Since it is best to keep infected cats
            Neurologic signs such as behavioral changes, disrupted   indoors to reduce the risk of FIV exposure to other cats,
            sleep, impaired learning,  paresis,  and seizures have   the exposure of the infected cat to other common patho­
            been reported. A wasting condition has also been   gens is also reduced, thereby decreasing the need for vac­
            described late in the FAIDS phase of the disease.   cination. Additionally, the duration of immunity to most of
            Increased circulating immune complexes can result in   the vaccinatable feline pathogens likely lasts for years. If
            immune complex disease manifested as uveitis and   the cat has been vaccinated earlier in life, protective immu­
            glomerulonephritis.                               nity likely still remains. If, however, vaccines are to be used,
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