AI Article Synopsis

  • Ehrlichia canis is a significant health concern in dogs, often causing high morbidity and mortality, and can be difficult to diagnose due to asymptomatic cases and cross-reactivity in serological tests.
  • A study examined 59 euthanized dogs with ticks but no clinical symptoms, finding that while 52.55% tested negative for E. canis in blood samples, 61.30% were positive in tissue biopsies.
  • Results indicated that E. canis DNA was present in various organs despite blood tests being negative, highlighting the limitations of blood PCR and the need for more comprehensive testing in tissues.

Article Abstract

Background: Nowadays, Ehrlichia canis receives increasing attention because of its great morbidity and mortality in animals. Dogs in the subclinical and chronic phases can be asymptomatic, and serological tests show cross-reactivity and fail to differentiate between current and past infections. Moreover, there could be low parasitaemia, and E. canis might be found only in target organs, hence causing results to be negative by polymerase chain reaction (PCR) on blood samples.

Methods: We evaluated by PCR the prevalence of E. canis in blood, liver, spleen, lymph node and bone marrow samples of 59 recently euthanised dogs that had ticks but were clinically healthy.

Results: In total, 52.55% of the blood PCRs for E. canis were negative, yet 61.30% yielded positive results from tissue biopsies and were as follows: 63.15% from bone marrow; 52.63% from liver; 47.36% from spleen; and 15.78% from lymph node. In addition, 33% had infection in three tissues (spleen, liver and bone marrow).

Conclusions: Our results show the prevalence of E. canis from tissues of dogs that were negative by blood PCR. Ehrlichia canis DNA in tissue was 30% lower in dogs that tested negative in PCR of blood samples compared to those that were positive. However, it must be taken into account that some dogs with negative results were positive for E. canis in other tissues.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7561240PMC
http://dx.doi.org/10.1186/s13071-020-04363-0DOI Listing

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