Page 1500 - Small Animal Internal Medicine, 6th Edition
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1472   PART XIV   Infectious Diseases


                           Anaplasma phagocytophilum
                             PCR and serology results
  VetBooks.ir     4
                Number of positive cats  2
                  3




                  1

                  0
                     0  1  2  3  4  5   6  7  8  9  1013
                                 Week of study

                                Ap PCR       Ap AB

            FIG 95.3
            Serologic and polymerase chain reaction assay test results   FIG 95.4
            over time in cats infected with Anaplasma phagocytophilum   Bilateral anterior uveitis in a dog consistent with E. canis–
            by exposure to wild-caught Ixodes scapularis ticks. The four   associated inflammation. (Courtesy Dr. Cynthia Powell,
            cats were exposed to wild-caught Ixodes scapularis ticks on   Colorado State University.)
            Day 0 of the study. AB, Antibodies detected by the SNAP
            4DX; Ap, A. phagocytophilum; PCR, polymerase chain
            reaction.
                                                                 infection in cats, acaricidal products approved for use on cats
                                                                 should be used. As for dogs, cats used for blood donors that
            seronegative when first assessed serologically, but all proven   reside in endemic areas should be screened for A. phagocy-
            cases to date have ultimately seroconverted.  Anaplasma   tophilum infections by serology and PCR assay; the ACVIM
            phagocytophilum DNA can be amplified from blood before   optimally recommends using only cats that are negative in
            development  of  detectable  serum  antibodies,  so  a  single   both tests (Wardrop et al., 2016). However, if PCR assay
            negative antibody result in an acutely infected cat does not   cannot be performed, the minimal standard recommended
            exclude infection. Therefore cats with suspected anaplasmo-  was to use only seronegative cats as donors.
            sis may need convalescent serum samples to prove infection.
            Alternately, antibody testing could be combined with PCR
            testing of whole blood in acute cases (Lappin et al., 2015). In   CANINE THROMBOCYTOTROPIC
            a recent study of cats (n = 4) exposed to wild-caught Ixodes   ANAPLASMOSIS
            scapularis ticks from Rhode Island, all cats developed anti-
            bodies that were detectable in a commercially available kit   Etiology and Epidemiology
            labeled for use with canine serum (SNAP 4DX, IDEXX) and   Anaplasma platys forms morulae in circulating platelets, and
            became PCR-positive (Lappin et al., 2015). However, none   this syndrome has been referred to as canine infectious cyclic
            of the cats developed measurable clinical signs of disease or   thrombocytopenia. Infected dogs have been detected primar-
            complete blood cell abnormalities (Fig. 95.3).       ily in the south and southeastern United States, Australia,
                                                                 Africa, Caribbean Islands, the Middle East, South America,
            Treatment                                            and parts of Europe. Inclusions morphologically similar to
            Supportive care should be administered as needed. Several   A. platys have been detected in one cat in Brazil, and other
            antibiotics have been administered to naturally infected cats,   cats have been positive for A. platys DNA in blood (Hegarty
            but most cats became clinically normal within 24 to 48 hours   et al.,  2015;  Lima  et al.,  2010;  Qurollo  et al.,  2014;  Zobba
            after initiation of tetracycline or doxycycline administration   et al., 2015). However, whether this agent is associated with
            and recurrence was not reported (Adaszek et al., 2013; Bjo-  significant disease in cats is unknown.  Anaplasma platys
            ersdorff et al., 1999; Lappin et al., 2004; Savidge et al., 2016).   DNA has been amplified from ticks, particularly Rhipicepha-
            Although clinically normal, two cats were still PCR-positive   lus spp. (Foongladda et al., 2011; Geurden et al., 2018), and
            17 days and 90 days after treatment (of 21-30 days’ duration),   trans-stadial transmission has been documented in this tick
            respectively, which suggests that treatment with tetracyclines   (Aktas and Ozubek, 2018). High co-infection rates with E.
            for 21 to 30 days may be inadequate for eliminating the   canis also support the hypothesis  that  Rhipicephalus spp.
            organism from the body (Lappin et al., 2004).        ticks are the vectors of A. platys (Yabsley et al., 2008).
                                                                   After intravenous inoculation, the incubation period is 8
            Zoonotic Aspects and Prevention                      to 15 days. Although cyclic thrombocytopenia and parasit-
            See the section on canine granulocytic anaplasmosis for a dis-  emia can occur at 10- to 14-day intervals, organism numbers
            cussion of zoonotic aspects. To prevent A. phagocytophilum   and severity of thrombocytopenia may lessen over time.
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