Peer-reviewed veterinary case report
Key immune proteins linked to Babesia canis infection in dogs
By Galán, Asier et al.·Published in PloS one·2018·Clinic for Internal Diseases·View original on PubMed →
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Original publication title: MCP-1, KC-like and IL-8 as critical mediators of pathogenesis caused by Babesia canis.
- Species:
- dog
Plain-English summary
A group of dogs infected with the tick-borne parasite Babesia canis showed symptoms of babesiosis, which can include fever, weakness, and anemia. They were treated with a medication called Imizol, and researchers monitored their cytokine levels, which are substances that help regulate immune responses. The study found that higher levels of certain cytokines, like MCP-1 and KC-like, were linked to more severe complications in the dogs. While one dog unfortunately died during the study, the findings could help veterinarians predict which cases might worsen and guide future treatments for this disease.
People also search for: dog Babesia canis symptoms · Imizol treatment for dog babesiosis · what to do if my dog has tick-borne disease
Abstract
Canine babesiosis caused by the intraerythrocytic protozoan parasite Babesia canis is a tick-borne disease characterized by a host response that involves both cellular and humoral immunity. This study focuses on the secretion of cytokines Granulocyte-Macrophage Colony-Stimulating Factor (GM-CSF), Keratinocyte Chemotactic-like (KC-like), Interleukins (IL)-2, IL-7, IL-8, IL-10, IL-15, IL-18 and Monocyte Chemotactic Protein-1 (MCP-1) in babesiosis caused by Babesia canis upon treatment with Imizol®. We assessed time dependent changes in cytokine levels and tested whether these changes correlate with pathogenesis of the disease. Sixteen healthy dogs and 31 dogs infected with Babesia canis, of which 18 showed complications, were treated with Imizol®. One dog died during the study (3.2%). Longitudinal study was perfomed by monitoring dogs at the first day of presentation (day 1) and 6 days later (day 7). Our results show that higher MCP-1 levels on day 1 are positively associated with the occurrence of complications, (complicated vs. uncomplicated; p = 0.00016). A similar pattern was observed for KC-like on day 1 (p = 0.0326) and day 7 (p = 0.044). Moreover, babesiosis caused by B. canis produced a steady increase in IL-8 levels with a moderate to strong negative correlation with erythrocyte counts and hematocrit in uncomplicated diseased dogs only (Spearman's rank correlation coefficient rs = -0.582 and rs = -0.598 respectively). Like for MCP-1, KC-like levels also differed in complicated and uncomplicated diseased dogs on day 1 (p = 0.03236) and day 7 (p = 0.044). Furthermore, KC-like levels were strongly correlated with IL-8 levels (rs = 0.663-0.7) and non-segmented neutrophil counts (rs = 0.572-0.732) in both diseased groups. Analysis of ROC suggests the use of serum levels of MCP-1 and IL-7 as predictors of the occurrence of complications with an AUC of 0.906 and 0.896 respectively and linear combinations of MCP-1, KC-Like, IL-7 and GM-CSF with values up to AUC = 0.983. Cytokine cluster analysis presented in this study can contribute to a better understanding of the pathogenesis of babesiosis and serve as a prognostic tool for the early detection of cases with highest likelihood of developing complications. Overall, our studies show that infection by B. canis elicits a cytokine pattern that is distinct from that observed with B. rossi, and that some of the inflammatory mediators can be useful to predict complications. Our results also suggest targets for the development of novel therapeutic strategies in babesiosis caused by B. canis.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/29304171/