DNA samples from dogs presenting with symptoms suggestive of canine ehrlich
iosis, but with no morulae detected on blood smears, frequently failed to g
ive a positive reaction with a North American Ehrlichia canis-specific PCR
assay targeting the 165 rRNA gene. We suspected the presence of a pathogen
genetically different from North American E. canis, and we performed experi
ments to test this hypothesis. DNA from one canine blood sample was subject
ed to PCR with primers designed to amplify Ehrlichia (Cowdria) ruminantium
ruminantium 165 and, map l genes. Amplicon sequencing yielded 16S and map1
sequences which were more closely related to other E. ruminantium sequences
than to those of any other Ehrlichia species. Fifty canine DNA samples wer
e subjected to a PCR assay, previously found to be Cowdria-specific, which
targets the pCS20 gene. Thirty-seven (74%) gave a positive signal, and 16 (
32%) also gave visible amplicons after gel electrophoresis, suggesting that
this E. ruminantium organism is common in the Pretoria-Johannesburg area.
The organism has not been isolated in culture, so we cannot definitively st
ate that it was responsible for the canine ehrlichiosis symptoms, although
the occurrence of several similar cases suggests this to be so. Most import
antly, we also do not yet know whether the organism is infective for, or ca
uses heartwater in, ruminants.