Disseminated candidiasis secondary to fungal and bacterial peritonitis in a young dog

Objective – To describe a severe case of bacterial sepsis and disseminated candidiasis in a previously healthy dog.
Case Summary – Fungal sepsis was identified in a 2-year-old dog following intestinal dehiscence 4 days after abdominal surgery. Septic peritonitis was identified at admission and evidence of dehiscence at the previous enterotomy site was found during an exploratory laparotomy. Both gram-positive cocci and Candida albicans were cultured from the abdominal cavity. Candida sp. was also subsequently cultured from a central venous catheter. Euthanasia was performed due to failure to respond to therapy. Fungal organisms, morphologically consistent with Candida spp., were found in the lungs and kidney on postmortem histopathologic examination indicating disseminated candidiasis.
New or Unique Information Provided – Candida peritonitis is a well-recognized entity in humans and contributes to morbidity and mortality in critically ill patients. Abdominal surgery, intestinal perforation, presence of central venous catheters, and administration of broad-spectrum antibiotics are all considered to be suspected risk factors. This report describes the first known case of systemic candidiasis occurring secondary to Candida peritonitis and bacterial sepsis in a critically ill dog.     

Parasitemia in an immunocompetent horse experimentally challenged with Sarcocystis neurona sporocysts

Equine protozoal myeloencephalitis (EPM) is a serious neurological disease of horses in Americans. Most cases are attributed to infection of the central nervous system with Sarcocystis neurona. Parasitemia has not been demonstrated in immunocompetent horses, but has been documented in one immunocompromised foal. The objective of this study was to isolate viable S. neurona from the blood of immunocompetent horses. Horses used in this study received orally administered S. neurona sporocysts (strain SN 37-R) daily for 112 days at the following doses: 100/day for 28 days, followed by 500/day for 28 days, followed by 1000/day for 56 days. On day 98 of the study, six yearling colts were selected for attempted culture of S. neurona from blood, two testing positive, two testing suspect and two testing negative for antibodies against S. neurona on day 84 of the study. Two 10 ml tubes with EDTA were filled from each horse by jugular venipuncture and the plasma fraction rich in mononuclear cells was pipetted onto confluent equine dermal cell cultures. The cultures were monitored weekly for parasite growth for 12 weeks. Merozoites grown from cultures were harvested and tested using S. neurona-specific PCR with RFLP to confirm species identity. PCR products were sequenced and compared to known strains of S. neurona. After 38 days of in vitro incubation, one cell culture from a horse testing positive for antibodies against S. neurona was positive for parasite growth while the five remaining cultures remained negative for parasite growth for all 12 weeks. The Sarcocystis isolate recovered from cell culture was confirmed to be S. neurona by PCR with RFLP. Gene sequence analysis revealed that the isolate was identical to the challenge strain SN-37R and differed from two known strains UCD1 and MIH1. To our knowledge this is the first report of parasitemia with S. neurona in an immunocompetent horse.     

Simulation of flow patterns and ion-exchange in soil percolation experiments

An increased understanding of ion-exchange processes in raw-humus was obtained by simulations using quantitative mathematical models. The work is based on a series of percolation experiments with a water flow of about 1 mm min^?1 through raw-humus samples of 4 cm thickness. For the input solutions consisting of 10^?3 N H₂SO₄, HNO₃, HCl and NaCl the results indicate that cation-exchange reactions are the most important processes for the chemical composition of the run-off. Since a large part of the water flows quickly through the soil, both the water residence time and the ion-exchange kinetics must be taken into account. As a basis for the chemical model, a hydrologic sub-model reproducing the residence time distribution of the flow in the soil is used. Considering the ions H⁺, M⁺ (monovalent metal ions) and M²⁺ (divalent metal ions), four different chemical models were tried but only one of them gave satisfactory agreement with the experimental results. This model has 5 independent parameters and consists of first and second order chemical processes.     

A simple procedure for the extraction of trypanosome DNA and host protein from dried blood meal residues of haematophagous diptera.

A two step elution method is described for the extraction of host serum proteins and trypanosome DNA from a single dried insect gut smear preparation. The first low temperature elution yields material suitable for use in ELISA to determine the host species on which the fly last fed while the results of the second, high temperature, elution can be used in a PCR assay to detect the presence of trypansosomal DNA. The method can be used to extract material from both fly squashes and blood spots dried onto filter paper and could simplify the collection and processing of samples for epidemiological studies on trypanosomoses and other vector borne pathogens.