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Prevalence of selected infectious disease agents in cats from Arizona
Jason M Eberhardt1, Karter Neal, Tom Shackelford
1Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, 300 West Drake Road, Fort Collins, CO 80523, USA. Jason.Eberhardt@colostate.edu
Abstract:
The objective of this study was to use polymerase chain reaction (PCR) assays to determine the prevalence of Ehrlichia species, Anaplasma phagocytophilum, Mycoplasma haemofelis, 'Candidatus Mycoplasma haemominutum' and Bartonella species from feral and relinquished cats in Phoenix and Nogales, Arizona. DNA from one or more of the organisms was amplified from 31 of 112 blood samples (27.7%). DNA consistent with Bartonella clarridgeiae 15 (13.4%), Bartonella henselae 14 (12.5%), 'Candidatus M haemominutum' 9 (8.0%), and M haemofelis 5 (4.5%) were detected. DNA of Ehrlichia species, Neorickettsia risticii, or A phagocytophilum was not amplified. Failure to amplify DNA of A phagocytophilum may relate to the absence of appropriate tick vectors. Failure to amplify Ehrlichia species DNA suggests that cats were not exposed, exposed but not infected, or infected but the DNA was not detected by the PCR assay used in this study. The Bartonella species and hemoplasma results suggest flea control should be maintained.
Insights
Prevalence of Bartonella species and hemoplasma in Arizona cats was investigated using PCR assays. Results indicate a need for ongoing flea control in feline populations to manage these common infections.
Area of Science:
- Veterinary Microbiology
- Infectious Diseases
- Feline Health
Background:
- Feral and relinquished cats can harbor various tick- and flea-borne pathogens.
- Understanding the prevalence of these agents is crucial for public health and animal welfare.
Purpose of the Study:
- To determine the prevalence of Ehrlichia species, Anaplasma phagocytophilum, hemotropic Mycoplasma, and Bartonella species in cats from Arizona.
- To assess the utility of PCR assays for detecting these pathogens in feline blood samples.
Main Methods:
- Polymerase chain reaction (PCR) assays were employed to detect DNA of target pathogens.
- Blood samples were collected from feral and relinquished cats in Phoenix and Nogales, Arizona.
- Specific primers were used to amplify DNA sequences of Ehrlichia, Anaplasma, Mycoplasma, and Bartonella species.
Main Results:
- DNA from one or more target organisms was detected in 27.7% of the 112 analyzed blood samples.
- Bartonella clarridgeiae (13.4%) and Bartonella henselae (12.5%) were the most frequently detected Bartonella species.
- 'Candidatus Mycoplasma haemominutum' (8.0%) and Mycoplasma haemofelis (4.5%) were also detected.
- DNA of Ehrlichia species, Neorickettsia risticii, and Anaplasma phagocytophilum was not amplified.
Conclusions:
- Bartonella species and hemotropic Mycoplasma are prevalent in the studied cat population in Arizona.
- The absence of Ehrlichia and Anaplasma DNA may be due to lack of exposure, infection, or limitations of the PCR assay.
- Findings underscore the importance of consistent flea control measures for cats to prevent transmission of Bartonella and hemoplasma.
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