Serological and molecular analysis of feline vector-borne anaplasmosis and ehrlichiosis using species-specific peptides and PCR

Abstract

Background

With the exception of Bartonella spp. or Cytauxzoon felis, feline vector-borne pathogens (FVBP) have been less frequently studied in North America and are generally under-appreciated as a clinical entity in cats, as compared to dogs or people. This study investigated selected FVBP seroreactivity and PCR prevalence in cats using archived samples.

Methods

Feline blood samples submitted to the Vector Borne Diseases Diagnostic Laboratory (VBDDL) at North Carolina State University College of Veterinary Medicine (NCSU-CVM) between 2008 and 2013 were tested using serological assays and PCR. An experimental SNAP® Multi-Analyte Assay (SNAP® M-A) (IDEXX Laboratories, Inc. Westbrook, Maine, USA) was used to screen all sera for antibodies to Anaplasma and Ehrlichia genus peptides and A.phagocytophilum, A.platys, B.burgdorferi, E.canis, E.chaffeensis, and E.ewingii species-specific peptides. PCR assays were used to amplify Anaplasma or Ehrlichia DNA from extracted ethylenediaminetetraacetic acid (EDTA)-anti-coagulated blood samples. Amplicons were sequenced to identify species.

Results

Overall, 7.8 % (56/715) of cats were FVBP seroreactive and 3.2 % (13/406) contained Anaplasma or Ehrlichia DNA. Serologically, B.burgdorferi (5.5 %) was the most prevalent FVBP followed by A.phagocytophilum (1.8 %). Ehrlichia spp. antibodies were found in 0.14 % (12/715) of cats with species-specific seroreactivity to E.canis (n = 5), E.ewingii (n = 2) and E.chaffeensis (n = 1). Of seropositive cats, 16 % (9/56) were exposed to more than one FVBP, all of which were exposed to B.burgdorferi and either A.phagocytophilum (n = 7) or E.ewingii (n = 2). Based upon PCR and DNA sequencing, 4, 3, 3, 2, and 1 cat were infected with A.phagocytophilum, A.platys, E. ewingii, E. chaffeensis and E.canis, respectively.

Conclusions

Cats are exposed to and can be infected with vector-borne pathogens that commonly infect dogs and humans. To our knowledge, this study provides the first evidence for E.chaffeensis and E.ewingii infection in naturally-exposed cats in North America. Results from this study support the need for regional, serological and molecular FVBP prevalence studies, the need to further optimize serodiagnostic and PCR testing for cats, and the need for prospective studies to better characterize clinicopathological disease manifestations in cats infected with FVBP.

Background

In North America, fleas, mosquitoes and ticks are considered the most important vectors for transmission of a spectrum of infectious agents that can induce disease in mammalian species, including dogs and humans; however, with the exceptions of Dirofilaria immitis (mosquito-borne feline heartworm disease) [1], Cytauxzoon felis (tick-borne feline cytauxzoonosis) [2] and Bartonella henselae (flea or tick-borne feline bartonellosis) [1], other known canine and human tick-borne pathogens have not been detected in, or have been minimally studied, in cats in the US and throughout much of the world when compared to dogs or humans. Anaplasma, Borrelia and Ehrlichia species infect cows, sheep, dogs, horses and human beings; however, the role of these pathogens as a cause of disease in cats remains incompletely defined [3]. As compared to dogs and humans, the smaller number of FVBP studies may be due to the lack of standardized serological tests, either ELISA or IFA, as are used routinely in canine veterinary practices. Also, veterinarians’ perception of the risk of FVBD may be a factor because there have been fewer research studies defining the regional serological or PCR prevalence of anaplasmosis, ehrlichiosis, and Lyme disease in cats. This factor is undergoing rapid change as researchers around the world have begun to investigate FVBP prevalence among various cat populations (feral, healthy, sick, etc.). Serological, and to a lesser extent molecular-based, FVBP studies have been reported from the US [4–6], Brazil [7–9], France [10], Portugal [11], Italy [12] Spain [13, 14], Sweden [15], Kenya [16], and the Far East [17, 18]. In parts of Spain and Italy, stray and domestic cat A.phagocytophilum seroprevalence rates ranged from 2–8 % [7, 19, 20]. In the US, A.phagocytophilum seroprevalences range from 4.3 % [6] in southeastern US to as high as 38 % in northeastern US endemic regions [5]. E.canis seroprevalence rates have ranged from 6–18 % in Europe [7, 13, 14, 19, 20]. In the Western hemisphere fewer Ehrlichia spp. seroprevalence studies have been performed; however, E.canis seroprevalence was 5.5 % amongst 200 domestic cats in Brazil [8]. B.burgdorferi seroprevalence rates as high as 47 % were found in cats from areas endemic for Lyme in the US [5]. Currently, veterinary diagnostic serological assays rely upon A.phagocytophilum, B.burgdorferi and E.canis antigens and assays that were originally validated for testing dogs and in most instances have not been optimized for testing cats.

Molecular-based evidence, such as PCR, indicates that cats can potentially be infected with A.phagocytophilum [4, 12, 15], A.platys [21, 22] and E.canis [9, 11, 23–25]. In Sweden, Bjoersdorff et al. was first to report PCR amplification of A.phagocytophilum from a cat [15]. The DNA sequence in a 14-month-old shorthaired cat with lethargy and fever was 100 % identical to dog and horse A.phagocytophilum strains from the same region. Subsequently, Lappin et al. confirmed infection with A.phagocytophilum in 5 young clinically-ill cats from the northeastern US by PCR amplification and DNA sequencing [4]. To date, A.platys infections, with PCR amplification of the pathogen, have been reported in only two thrombocytopenic cats [21, 22]. Other clinical manifestations included anorexia and platelet inclusion bodies in a cat from Brazil [21] and chronic hyperglobulinemia in a cat from North Carolina that was also PCR positive for Mycoplasma hemominutum, Bartonella henselae and Bartonella koehlerae [22]. Using PCR, Ehrlichia species DNA has been amplified from cats located in Italy [12], France [10, 23] and the Americas [8, 9, 23–25]. DNA evidence of possible E.canis (98 % identity) and E.chaffeensis (97 % identity) infections was reported by Braga Mdo et al. in cats from Brazil [8]. Positive E.canis PCR results were also reported for 11 thrombocytopenic and lymphopenic Brazilian cats [9, 25]. Based upon PCR amplification and DNA sequencing of the Ehrlichia 16S rDNA gene, our research group described E.canis infection (100 % identical to E.canis DNA obtained from dog isolates) in cats from France [23] and in 3 young, sick cats from the southeastern United States or eastern Canada [24].

IDEXX Laboratories, Inc. (Westbrook, Maine, USA) developed a qualitative enzyme-linked immunosorbent assay (ELISA) test, SNAP® M-A, using Anaplasma genus EENZ1 and Ehrlichia genus p30/p30-1 peptides to broadly detect Anaplasma spp. and Ehrlichia spp. antibodies in conjunction with A.phagocytophilum p44 Aph, A.platys p44 Apl, E.canis p16, E.chaffeensis VLPT, E.ewingii p28, and B.burgdorferi C6 species-specific peptides as a research tool to characterize regional trends in seroprevalence to specific vector-borne pathogens in dogs [26, 27]. Although developed as a canine assay, the assay does not use a host species-specific conjugate, and can therefore be used on a research basis to screen mammalian species other than dogs. An earlier ELISA based assay, the SNAP® 3Dx®, was used in a serosurvey of cats naturally exposed to B.burgdorferi [28] and the SNAP®4Dx® has been utilized to test horses for borreliosis [29] and ehrlichiosis [30, 31]. Recently, Qurollo et al. reported seroprevalence data using SNAP® M-A in over 6500 archived canine serum samples from the US, Canada and the Caribbean. Overall and regional seroprevalence and co-seroprevalence (exposure to more than one pathogen) was determined, as well as seroprevalence trends between 2008 and 2010 [26]. Although currently SNAP® M-A is not available commercially, the use of a broad range of genus and species-specific immunodominant peptides in diagnostic tests would allow veterinarians to determine Anaplasma or Ehrlichia species exposures in dogs and cats in their region. This information could benefit both clinical decision making, as well as human and veterinary zoonotic disease education [32–34].

The purpose of this study was to evaluate a wide range of FVBPs in cats suspected of exposure to a vector-borne pathogen. Specifically, we determined the seroprevalence of Anaplasma spp., B.burgdorferi and Ehrlichia spp. and the presence of Anaplasma or Ehrlichia sp. DNA, as determined by PCR amplification and DNA sequencing.

Methods

All samples were de-identified, so no ethical approval necessary.

Clinical accessions and sample availability

Feline clinical accessions (n = 858) submitted to the NCSU-CVM-VBDDL between January 1, 2008, and December 31, 2013, for FVBP testing originated from veterinary hospitals located in the United States (n = 827), Canada (n = 28) and the Caribbean (n = 3). Sample submission information included date of collection, date received, and the cat owner or veterinary practice address while individual identifications were not revealed. Of these 858 cats, 715 sera were available for testing using the SNAP® M-A kit for Anaplasma, Borrelia, and Ehrlichia antibodies and EDTA-anti-coagulated whole blood was available from 406 cats for PCR testing. Prior to the study, Anaplasma and Ehrlichia diagnostic PCR results were known for 163 of these 406 cats. Stored, frozen (−80 °C) blood was retrievable for additional PCR testing for 331/406 diagnostic accessions. When adequate serum volumes were available, a subset of 59 SNAP® M-A seropositive and 4 PCR positive samples were tested by SNAP®4Dx®Plus assay (IDEXX Laboratories, Inc. Westbrook, Maine, USA) and by indirect fluorescent antibody (IFA) assays using whole cell antigens. Medical record data was obtainable for 7 PCR positive cats, 4 of which were referrals to the NC State Veterinary Hospital and 3 were from other veterinary hospitals or universities. Medical records were reviewed for the signalment, history and physical examination findings, complete blood count (CBC), serum biochemistry profile abnormalities and for additional diagnostic testing that were performed, including abdominal ultrasound, radiographs, or coagulation profiles.

Serological assays

Cat serum specimens (n = 715) were retrospectively tested by SNAP® M-A for A.phagocytophilum, A.platys, B.burgdorferi, E.canis, E.chaffeensis, and E.ewingii antibodies. This kit uses a reversible chromatographic flow of sample and automatic, sequential flow of wash solution and enzyme substrate. Archived cat serum stored at − 80 °C was thawed to room temperature prior to mixing 4 drops of serum with 4–5 drops of SNAP® M-A conjugate. The mixture was allowed to move across a flow matrix where peptide-specific antibody could bind to peptide-horse radish peroxidase conjugate before color reactant release. Color development, indicating a positive reaction, was read after 15 min per manufacturer’s instructions (IDEXX Laboratories, Inc, Westbrook, Maine, USA).

PCR testing

DNA from 200 μL of feline EDTA-anti-coagulated whole blood was extracted with a QIAsymphony™ robotic extractor using MagAttract® DNA Mini M48 kit (Qiagen, USA cat: 953336). DNA quality was assayed by quantitative PCR (qPCR) amplification of the glyceraldehyde 3-phosphate dehydrogenase gene on feline genomic DNA. A conventional PCR assay targeting a conserved region of the Anaplasma and Ehrlichia 16S rRNA gene [35] and two qPCR assays targeting the Anaplasma genus Tr-1 and Ehrlichia genus sodB [36] genes were performed on stored, frozen blood samples (n = 331). Species were identified by amplicon sequencing (Genewiz, Research Triangle Park, NC, USA) and additional, species-specific qPCRs were used in an attempt to confirm positive samples. The Anaplasma genus Tr-1 assay and species-specific assays (A.phagocytophilum p44, A.platys p44, E.chaffeensis nadA, and E.ewingii sodB) used in this study have not been previously reported; primer sequence and amplicon size for each of these qPCRs are listed in Table 1. The reactions were performed in a CFX96™ Real-Time Detection System combined with C1000™ Thermal Cycler (Bio-Rad, USA) under the following conditions: 25 μl final volume reaction containing 12.5 μl of SYBR®Green Supermix, 0.2 μM of the Tr-1 primers and 0.3 μM of each species-specific primer (Sigma-Aldrich, St Louis, MO, USA), 7 μl of filter-sterilized, molecular-grade water and 5 μl of DNA template. Thermocycler conditions consisted of a single cycle at 98 °C for 2 min, followed by 40 cycles of denaturation at 98 °C for 15 s, annealing at 57 °C (Tr-1) or 67 °C (all species-specific assays) for 15 s, and extension at 72 °C for 15 s. Melting temperature measurements were made between 65–88 °C at 0.5 s intervals.

Table 1 Primer targets, sequences and amplicon base pair size for previously unreported quantitative PCR assays used in this study. F: Forward primer; R: reverse primer

Comparison of serological assays

Fifty-nine stored, frozen sera from SNAP® M-A seropositive and/or PCR positive cats were retested using the SNAP®4Dx®Plus assay (IDEXX Laboratories, Inc. Westbrook, Maine, USA) according to manufacturer’s directions. SNAP® M-A and PCR positive cats were also tested by IFA using A.phagocytophilum (ProtaTek International Inc. St. Paul, MN, USA), E.canis (strain NC Jake), E.chaffeensis (strain E.chaffeensis Ark) and B.burgdorferi (MBL Bion, Des Plaines, IL, USA) antigen slides as appropriate for the seroreactivity detected by SNAP® M-A. For IFA testing, serum samples were diluted two fold from 1:16 to 1:512 in phosphate buffered saline (PBS) solution containing 1 % normal goat serum, 0.05 % Tween-20 and 0.5 % powdered nonfat dry milk (BioRad, Hercules, CA, USA). Antibody responses were detected by IFA with fluorescein conjugated goat anti-cat IgG (Thermo Fisher Scientifics, Waltham, MA, USA) [37]. Seropositive samples were defined as having endpoint titers ≥ 1:64 based upon laboratory criteria used by the VBDDL.

Results

Seroreactivity

Of the 715 cat serum samples tested with SNAP® M-A, the overall FVBP seroprevalence (Table 2) was 7.8 % (56/715) with B.burgdorferi the most seroprevalent at 5.5 % (39/715). By SNAP® M-A testing, seroreactivity to an Anaplasma or Ehrlichia spp. peptide was detected in 2.9 % (21/715) of cat serum accessions tested. Based upon the 3 Anaplasma spp. analytes, 1.8 % of cats (13/715) were exposed to an Anaplasma spp., of which 12 were A.phagocytophilum seroreactive and one cat was seroreactive with only the genus analyte. No cat was SNAP® M-A A.platys seroreactive. Using SNAP® M-A, Ehrlichia genus seroreactivity was found in 1.7 % (12/715) of cats. Based upon reactivity to a species-specific peptide, 5 of the 12 cats were seroreactive to E.canis (0.7 %), 2 cats to E.ewingii (0.3 %),1 cat to E.chaffeensis (0.2 %) and 4 cats were seroreactive with only the genus analyte. Seroreactivity to more than one FVBP was found in 16.1 % (9/56) of seroreactive cats. For each of these 9 cats, B.burgdorferi seroreactivity was detected in conjunction with either A.phagocytophilum (n = 7) or E.ewingii (n = 2) seroreactivity.

Table 2 Regional Seroprevalence by SNAP® M-A shown as percentages of 715 feline serum samples

PCR amplification of Anaplasma and Ehrlichia

Based upon conventional Anaplasma and Ehrlichia 16S rDNA PCR diagnostic results, performed at the time of sample submission to the VBDDL (n = 163), 7 cats were infected with either A.phagocytophilum (n = 4), A.platys (n = 2), or E.canis (n = 1). When archived frozen EDTA-whole blood (n = 331) was accessed for testing by 16S rDNA PCR, 7 cats were infected with either an Anaplasma or Ehrlichia spp., including E.ewingii (n = 3), E.chaffeensis (n = 2), A.phagocytophilum (n = 1) and A.platys (n = 1). Based upon diagnostic and archival PCR testing, the total number of cats infected with an Anaplasma or Ehrlichia sp. was 3.2 % (13/406), with one A.phagocytophilum PCR positive cat represented in both the diagnostic and archival PCR results (Table 3). Additional retrospective Anaplasma and Ehrlichia genus- and species-specific PCRs confirmed several 16S rDNA PCR positive samples, and included cats infected with A.phagocytophilum, E.chaffeensis, and E.ewingii (Table 3).

Table 3 State of origin, VBDDL diagnostic and archived sample Anaplasma and Ehrlichia PCR results, SNAP® M-A, SNAP® 4Dx®Plus and IFA (antigen) serology results for individual cats infected with FVBD

Clinical data

Clinical data for 7 PCR positive cats is summarized in Table 4. The FVBP PCR positives for which records were available included 3 A.platys infected cats, one of which was a cat diagnosed with multiple myeloma, as previously described in a case report [22], 2 A.phagocytophilum infections, 1 E.chaffeensis infection (limited to CBC and biochemistry panel), and 1 E.ewingii infection. Four of the 6 cats were reported as being indoor/outdoor, 2 were indoor only, one unknown, and one cat had a tick removed immediately prior to becoming ill. Presenting complaints included anorexia, lethargy or epistaxis. Three cats were febrile at the time of physical examination and one cat was icteric, however this cat was co-infected with Cytauxazoon felis and A.platys. Feline Leukemia and Feline Immunodeficiency Virus (FeLV/FIV) results were negative for 6 of 6 cats tested. The most common hematological abnormalities included anemia (n = 5), thrombocytopenia (n = 5) and neutrophilia (n = 3). Other blood abnormalities reported by the attending veterinarian included hyperglobulinemia, lymphocytosis or thrombocytosis. One E.ewingii positive cat was found to be hyperthyroid.

Table 4 Abbreviated clinical data available for 7 Anaplasma or Ehrlichia PCR positive cats

Comparison among serological assays

Fifty-nine SNAP® M-A positive serum samples had sufficient volume for SNAP®4Dx®Plus and/or IFA comparative testing. Of the 13 cats that were seroreactive to SNAP® M-A Anaplasma sp. analytes (EENZl and P44 Aph), only 3 (23 %) were seroreactive by SNAP®4Dx®Plus (EENZ1 analyte), whereas 11 (85 %) were IFA positive for A.phagocytophilum antibodies. When compared to the SNAP® M-A Ehrlichia sp. analytes (p30/p30-1, p16, VLPT, p28), there was variable agreement with the SNAP®4Dx®Plus and E.chaffeensis or E.canis IFA using whole cell antigen preparations (Table 5). By E.chaffeensis IFA, only one E.chaffeensis and one Ehrlichia genus reactive cat were seropositive at titers of 1:256 and 1:64, respectively. Only the E.chaffeensis IFA seroreactor was E.canis IFA seroreactive at a titer of 1:256. None of the five SNAP® M-A E.canis p16 reactors were positive by SNAP®4Dx®Plus (p16 not present in this assay) or by IFA testing using E.chaffeensis or E.canis whole cell antigens. Of the 39 SNAP® M-A B.burgdorferi C6 peptide positives, 23 (59 %) and 27 (69 %) were positive by SNAP®4Dx®Plus or a whole cell B.burgdorferi antigen preparation, respectively.

Table 5 Comparison of SNAP® M-A results for 59 sera with SNAP®4Dx®Plus and Anaplasma phagocytophilum, Ehrlichia chaffeensis, Ehrlichia canis, or Borrelia burgdorferi Immunofluorescence results

Serum samples, available for 4 PCR positive cats, (2 E.chaffeensis and 2 E.ewingii) were not seroreactive by any of the three serological assays with the exception of an antibody response of 1:128 against E.canis by IFA for a cat that was PCR positive for E.chaffeensis (Table 3). A serum sample available from a fifth cat PCR positive for A.phagocytophilum was reactive to the C6 B.burgdorferi analyte in both SNAP® M-A and SNAP®4Dx®Plus but was not reactive to any A.phagocytophilum antigens.

Discussion

To the authors’ knowledge, this is one of the largest feline tick-borne pathogen prevalence studies reported for cats suspected of vector-borne infections from North America. Using species-specific peptides or PCR testing, this study identified two tick-borne pathogen species (E.chaffeensis and E.ewingii) that to our knowledge have not been previously reported to infect cats in North America. In addition, antibodies to B.burgdorferi (5.5 %) and A.phagocytophilum (1.8 %) were found frequently in serum submitted from sick cats in Lyme disease endemic regions of the northeastern and mid-Atlantic United States. These two pathogens share a common vector, Ixodes scapularis. Similarly, B.burgdorferi and A.phagocytophilum co-exposures were the most frequently detected. While exposure to, or infection with, a spectrum of FVBP were identified among these cats, the overall serological and PCR prevalence of tick-borne infections were relatively low compared to dogs tested during a similar time frame [26, 38]. For example, using SNAP® M-A to test over 6500 dog serum samples submitted to the NCSU-CVM-VBDDL from the United States, Canada and the Caribbean, primarily between 2008 and 2010, the overall canine seroprevalence was 8.3 % for B.burgdorferi and 3.4 % for A.phagocytophilum, both nearly double the prevalences in cats [26]. Reasonable explanations for the lower FVBP seroprevalences include shorter tick-attachment times due to fastidious grooming, thus reducing the opportunity for pathogen transmission. Also, although demographic and environmental data was not available for these diagnostic accessions, the cats included in this study were likely client-owned and therefore were more likely to be maintained primarily indoors and thus exposed to fewer ticks than their canine counterparts.

Historical or more recent documentation of exposure to, or infections with, A.platys, E.canis, E.chaffeensis and E.ewingii in cats provides a justification for future studies that investigate specific disease presentations associated with each of these infections. Similar to dogs, cats can be sequentially or concurrently exposed to more than one FVBP; therefore, co-infections can influence clinical, hematological and pathological findings [26]. In this study, complete or partial medical data obtained for 7 PCR positive cats (Table 4) underscores potential clinical and hematological disease similarities among cats and dogs in association with vector-borne infectious diseases. For example, four of seven cats were anemic and thrombocytopenic and epistaxis was reported in one of the markedly thrombocytopenic E.ewingii infected cats. Also, two A.platys infected cats were thrombocytopenic; however, co-infections were detected in both cats, so it is impossible to know the degree to which the A.platys infection contributed to thrombocytopenia in either cat.

In conjunction with published and ongoing studies of cat populations throughout the world, expanded FVBP test offerings by diagnostic laboratories are warranted. The sensitivity of a serological test is contingent upon the type, configuration and specificity of peptides chosen in the design of the assay. In addition, it should be determined if cats’ immunological reactivity to currently used diagnostic peptides is the same or different than dogs. Although assays being used in canine VBD diagnostic panels, whether ELISA or IFA based, will be a first step in facilitating the detection of FVBP in cats, improvements are in order. As an example, five cats were seroreactive using the E.canis p16 peptide, whereas none of these 5 cats were seroreactive by SNAP®4Dx®Plus (p16 not present in this assay) or by IFA testing using E.chaffeensis or E.canis whole cell antigens. Whether this discrepancy represents a lack of specificity of the p16 analyte, a lack of sensitivity of the commercial ELISA and IFA, or enhanced analytical sensitivity of this analyte for testing cat sera remains to be determined. Also, only one of the E.chaffeensis or E.ewingii infected cats (PCR+ with DNA sequence confirmation) was seroreactive, using any of the three assays assessed in this study. If as a general rule applicable to tick exposed cats, this finding could contribute to falsely low Ehrlichia seroprevalences, both diagnostically and during cat serosurvey studies. Isolation of FVBP from cats in conjunction with the detailed characterization of immunologic response to specific antigens may lead to assays that are more specific and hopefully more sensitive in the clinical diagnosis of acute or chronic vector-borne diseases in cats. The combination of serology and PCR testing has been recommended for the evaluation of canine VBDs [39]. Based upon the results of this study, using panels combining serology, with IFA being demonstrated as slightly more sensitive than ELISA in this study for A.phagocytophilum, Ehrlichia spp., and B.burgdorferi, along with genus and species-specific PCR in cats seems warranted, as this approach would facilitate more accurate diagnoses and targeted therapy for sick cats.

There were several inherent limitations to this study. The cat serum and blood specimens submitted by veterinarians to the VBDDL were from cats presumably suspected of an infection with a FVBP. However, based upon the historical research priorities of our laboratory, it is likely that many of these specimens were submitted from cats in which cytauxzoonosis (C. felis transmitted by ticks) or bartonellosis (Bartonella henselae and other Bartonella sp. most often transmitted by fleas) were suspected. Thus, seroprevalence rates in these cats are presumably higher than in the healthy, client-owned cat population. Although cats were regionalized based on local veterinary hospitals or owner zip codes, individual travel histories were not available; therefore, where exposures or infections occurred remains uncertain. Also, as medical histories were not provided in conjunction with sample submission information, it was not possible to determine risk factors such as outdoor exposure potential (living primarily indoors, indoors and outdoors, or outdoors only), vector exposure and other environmental factors that would influence the prevalence results. Despite obtaining clinical data for 7 PCR positive cats; incomplete medical record entries, variability in the clinical data obtained for each cat and the documentation of co-infections in two cats, does not allow specific clinical or hematological abnormalities to be attributed to infection with a specific FVBP.

Conclusions

Cats are exposed to and can be infected with vector-borne pathogens that commonly infect dogs and humans. Anaplasma phagocytophilum, A.platys, E.canis, E.chaffeensis and E.ewingii infections were confirmed by PCR amplification and DNA sequencing. To our knowledge, this study provides the first evidence for E.chaffeensis and E.ewingii infection in naturally-exposed cats in North America. Results from this study support the need for regional, serological and molecular FVBP prevalence studies, the need to further optimize serodiagnostic and PCR testing for cats, and the need for prospective studies to better characterize clinicopathological disease manifestations in cats infected with FVBP.