2015
DOI: 10.1186/s13028-016-0189-4
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Fatal Babesia canis canis infection in a splenectomized Estonian dog

Abstract: A previously splenectomized dog from Estonia was presented with a sudden lack of appetite and discoloration of the urine. Despite supportive therapy, its condition deteriorated dramatically during 1 day. Severe thrombocytopenia and high numbers of protozoan hemoparasites were evident in blood smears, and the hematocrit dropped from 46 to 33 %. The dog was euthanized before specific antibabesial treatment was initiated. Blood samples from the dog and from two other dogs in the same household tested positive for… Show more

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Cited by 14 publications
(12 citation statements)
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“…In 2015, a previously splenectomized dog was admitted to a small animal clinic of the Estonian University of Life Sciences in Tartu, Estonia, showing signs of lethargy, a change in urine color, and lack of appetite, was diagnosed with babesiosis by blood smear microscopy [ 277 ]. The clinical status of the dog worsened within 8 h, with the onset of unresponsive seizures; therefore, with the owner’s consent, the dog was euthanized.…”
Section: Northern and Northeastern Europementioning
confidence: 99%
“…In 2015, a previously splenectomized dog was admitted to a small animal clinic of the Estonian University of Life Sciences in Tartu, Estonia, showing signs of lethargy, a change in urine color, and lack of appetite, was diagnosed with babesiosis by blood smear microscopy [ 277 ]. The clinical status of the dog worsened within 8 h, with the onset of unresponsive seizures; therefore, with the owner’s consent, the dog was euthanized.…”
Section: Northern and Northeastern Europementioning
confidence: 99%
“…DNA isolation from blood was performed according to the method of Tiškina et al 9 Primary and nested PCR were performed in a final volume of 25 μl reaction mixtures containing 1 × Taq Buffer with (NH4) 2 SO 4 , 2.5 mM MgCl 2 , 200 μM dNTP mixture, 0.2 μM of each primer and 0.8 U Taq DNA polymerase (recombinant) (Thermo Fisher Scientific) and 2 μl DNA template (2 μl of products from the primary PCR were used as a template for the nested PCRs). The negative control was a PCR mix with DNA substituted by water.…”
Section: Methodsmentioning
confidence: 99%
“… Spectrophotometry was used to measure the concentration and purity of the DNA (ND-1000 UV–VIS Spectrophotometer; NanoDrop Technologies) 9 bp = base pairs …”
Section: Methodsmentioning
confidence: 99%
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