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1358  Leptospira Diagnostic Tests                                                          Leukocyte Function Tests




            Leptospira Diagnostic Tests
  VetBooks.ir  Definition                                                        Drug Effects



                                                cine (≤1 : 400).
           Leptospirosis is a zoonotic disease caused by   usually much lower by 3-6 months postvac-  Antibiotic therapy may cause a blunt rise in
           pathogenic serovars of Leptospira interrogans, a   •  Positive  ELISA  or  IgM  LFA:  exposure  to   serologic titer and cause negative PCR and
           motile, spiral-shaped bacterium (spirochete).   Leptospira spp. or vaccination (<6 months   culture results.
           Multiple serovars cause clinical disease.  interference postvaccination for IgM LFA
                                                and > 1 year for ELISA).         Specimen Collection and Handling
           Physiology                         •  Positive PCR: supportive of infection  MAT: 2 mL of serum (red top tube). Stable
           •  Organisms  penetrate  abraded  skin  and/                          5 days at 2°C-8°C or longer if frozen. ELISA
            or mucous membranes,  replicate  in the   Next Diagnostic Steps to Consider   or IgM LFA: 1 mL of serum (red top tube).
            bloodstream, and rapidly disseminate to   if Levels Are High         Stable 7 days at 2°C-8°C. PCR/RT-PCR: 2 mL
            multiple organs, most importantly liver and   •  Treat if signs suggest active disease. Consider   EDTA whole blood (lavender top tube) and
            kidney (allows shedding in urine). Organisms   PCR/RT-PCR (urine, blood, cerebrospinal   2 mL urine in sterile container. Stable 10 days
            replicate in the renal tubular epithelium,   fluid,  aqueous humor, or tissue); direct   at 2°C-8°C or longer if frozen. For in-clinic
            causing chronic tubulointerstitial nephritis   fluorescent  antibody  testing  on  tissue   tests, follow manufacturer’s directions.
            and  a  persistent  carrier  state  if  untreated.   (kidney, liver) collected before antibiotic
            See p. 583.                         administration.                  Relative Cost:  $ (ELISA and IgM LFA);
           •  Serovars  included  in  vaccines:  canicola,   •  Darkfield  microscopy  or  culture  (blood,   $$ (MAT)
            icterohaemorrhagiae,  grippotyphosa,  and   urine) is technically difficult and not widely
            pomona.                             available.                       Pearls
                                                                                 •  The  diagnosis  can  be  missed  if  relevant
           Reference Interval                 Causes of Abnormally Low Levels      serovars are excluded from serologic testing,
           •  Microscopic  agglutination  test  (MAT):   Serologic  tests:  early  infection,  antibiotic   because  there is no  consistent  serologic
            reported as titer values; panel of serovars   treatment, infecting serovar not included in   cross-reactivity from one serovar to another.
            varies among laboratories.        test. Negative PCR/RT-PCR due to insufficient   Serovars currently recommended for testing:
           •  Rapid IgM immunochromatographic lateral   nucleic acid, chronic carrier state, antibiotic   canicola, pomona, grippotyphosa, bratislava,
            flow assay (IgM LFA), ELISA for antibody   treatment, or occurrence of new strains/serovars  icterohaemorrhagiae, hardjo, and autumnalis.
            and  PCR/RT-PCR:  positive  or  negative                             •  It may be useful to evaluate urine PCR and
            result                            Next Diagnostic Steps to Consider    serologic tests concurrently.  Vaccination
                                              if Levels Are Low                    interferes with IgM LFA test for shorter
           Causes of Abnormally High Levels   Repeat IgM LFA in 3-7 days or MAT titer or   period of time (most are negative by 12-16
           •  MAT: active disease suggested by a fourfold   ELISA in 1-2 weeks. PCR can detect infection   weeks postvaccination) than ELISA or MAT
            rise (paired serum samples 2-4 weeks apart).   earlier than MAT or ELISA.  (several months to ≥1 year).
            A single titer of ≥ 1 : 800 in a nonvaccinated
            dog, or dog vaccinated > 6 months prior, is   Important Interspecies Differences  AUTHOR: Patty J. Ewing, DVM, MS, DACVP
                                                                                 EDITOR: Lois Roth-Johnson, DVM, PhD, DACVP
            also suggestive of infection. Vaccine-induced   Cats are less susceptible than dogs to clinical
            titers may be as high as 1 : 3200, but are   disease, but may have positive titers.





            Leukocyte Function Tests



           Definition                         •  Monocytes are tested for ability to phago-  Specimen Collection and Handling
           Tests of the  in vitro ability of neutrophils,   cytose particles and for cellular markers.  The laboratory performing tests should be
           monocytes, and lymphocytes to perform specific   •  Lymphocyte  tests  include  proliferative   contacted for specific sample collection and
           functions unique to that cell type. These tests   response to specific mitogens (i.e., lym-  shipment handling; many function tests must
           are not routinely available. For several tests,   phocyte blastogenesis), expression of B- and   be performed on freshly isolated cells.
           the specific leukocyte must be freshly isolated   T-cell receptors and other markers, and
           from blood and tested within hours.  quantitation of serum antibodies.  Relative Cost:  $$-$$$

           Physiology                         Causes of Abnormally Low Levels    Pearls
           •  Neutrophil function tests include measuring   Though both congenital and acquired causes   Animals with suspected congenital immuno-
            response to chemotactic stimuli, oxidative   of leukocyte dysfunction exist, these tests are   deficiency states (e.g., pups or kittens with
            burst and release of oxidative metabolites,   most often performed in young dogs or cats   recurrent infections) are best evaluated in a
            phagocytosis and killing of bacteria, and   with suspected congenital immunodeficiency   referral setting.
            expression  of adhesion  and activation  cell   (e.g., canine leukocyte adhesion defect, severe
            markers (e.g., CD18). See p. 1260.  combined immunodeficiency), or in a research   AUTHOR: Stephen D. Gaunt, DVM, PhD, DACVP
                                                                                 EDITOR: Lois Roth-Johnson, DVM, PhD, DACVP
                                              setting.



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