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. 2020 Jul;13(7):1294-1302.
doi: 10.14202/vetworld.2020.1294-1302. Epub 2020 Jul 9.

Clinicopathological and molecular profiles of Babesia vogeli infection and Ehrlichia canis coinfection

Thanakorn Rawangchue  1 , Sivapong Sungpradit  1   2
Affiliations

Clinicopathological and molecular profiles of Babesia vogeli infection and Ehrlichia canis coinfection

Thanakorn Rawangchue et al. Vet World. 2020 Jul.

Abstract

Background and aim: Canine babesiosis, a tick-borne parasitic disease, is caused by the hemoprotozoa, Babesia vogeli, and Babesia gibsoni. Infection with these parasites, which is endemic globally, leads to life-threatening immunosuppression in dogs. The merozoites invade the red blood cells (RBCs) of infected dogs. Ehrlichia canis, an intracellular bacterium that infects monocytes, is transmitted by the same tick species (Rhipicephalus sanguineus) during blood consumption and coinfection with B. vogeli and E. canis has been reported. Although the hematology and biochemistry of canine babesiosis have been studied, more studies are needed to develop a better understanding of the hematobiochemical and molecular profiles associated with cases of single infection and coinfection of canine babesiosis in Thailand. This study aimed to investigate the hematological, biochemical, and molecular profiles of B. vogeli infection and E. canis coinfection.

Materials and methods: The study included 33 B. vogeli-positive blood samples and 11 E. canis-coinfected blood samples. To exclude coinfection with Hepatozoon canis and Anaplasma platys, only dogs with B. vogeli infection and B. vogeli-E. canis coinfection were included in the study. A multiplex polymerase chain reaction (PCR) assay was conducted to detect B. vogeli, E. canis, and H. canis, and a conventional PCR assay was conducted for the detection of A. platys. Besides, the PCR assay and sequencing, comprehensive data analysis was conducted, including a microscopic blood parasite examination and hematological and biochemical data analysis.

Results: The comparison of the hematobiochemical data between the B. vogeli-positive and E. canis coinfection groups identified that there were statistically significant differences in the RBC parameters, including RBC count, hemoglobin concentration, hematocrit, and RBC distribution width (p=0.001). Neither B. vogeli infection nor coinfection with E. canis was associated with the sex, breed, recorded clinical signs, geographic origin of the dog and also B. vogeli 18S rRNA gene sequencing results.

Conclusion: Coinfection with E. canis increased the severity of babesiosis. The pathogenic mechanisms underlying this infection, such as destruction of RBCs, require further investigation. This study may enhance diagnosis, treatment, and prevention of canine babesiosis.

Keywords: 18S rRNA gene; Babesia vogeli; Ehrlichia canis; coinfection; hematobiochemical data; red blood cell.

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Figures

Figure-1
Figure-1
Geographic distribution of the babesiosis cases in this study.
Figure-2
Figure-2
Phylogenetic tree analysis of Babesia vogeli 18S rRNA and Ehrlichia canis 16S rRNA gene sequences of dog samples from Nakhon Pathom, Thailand (asterisk), and other provinces and countries. Bootstrap values are provided at the beginning of each branch.
See this image and copyright information in PMC

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