Canine ehrlichiosis is an important tick-borne rickettsial disease mainly caused by Ehrlichia canis. This study aimed to detect and characterise E. canis in dogs in Abeokuta, Nigeria by microscopy and nested PCR. Blood samples were collected from 205 dogs, thin smears were made, field-stained, and DNA was extracted from the blood samples. A partial region of the 16S rRNA gene was amplified by polymerase chain reaction (PCR) and sequenced unidirectionally. Ehrlichial morulae were detected in three dogs (1.5%). The PCR test revealed that 47 dogs (22.9%) were positive for E. canis. The lengths of the sequences obtained range from 374 bp to 376 bp with an average G-C content of 37% and 98-99% homology with the reference sequences in GenBank. The aligned autochthonous sequences were less polymorphic. The phylogenetic analysis separated sequences reported previously in Nigeria from the autochthonous sequences. The present work shows that the strain of E. canis detected in the study area is genetically different from those reported in the northern part of Nigeria and more closely related to sequences from Brazil and India.

Adequate knowledge of the genetic diversity among Babesia species infecting dogs is necessary for a better understanding of the epidemiology and control of canine babesiosis. Hence, this study determined the genetic diversity among the Babesia rossi detected in dogs presented for routine examination in Veterinary Hospitals in Abeokuta, Nigeria. Blood were randomly collected from 209 dogs. Field-stained thin smears were made and DNA extracted from the blood. Partial region of the 18S small subunit ribosomal RNA (rRNA) gene was amplified, sequenced and analysed. Babesia species was detected in 16 (7.7%) of the dogs by microscopy. Electrophoresed PCR products from 39 (18.66%) dogs revealed band size of 450 bp and 2 (0.95%) dogs had band size of 430 bp. The sequences obtained from 450 bp amplicon displayed homology of 99.74% (387/388) with partial sequences of 18S rRNA gene of Babesia rossi in the GeneBank. Of the two sequences that had 430 bp amplicon, one was identified as T. annulata and second as T. ovis. A significantly (p<0.05) higher prevalence of B. rossi was detected by PCR compared to microscopy. The mean PCV of Babesia infected dogs was significantly (p<0.05) lower than non-infected dogs. Phylogenetic analysis revealed minimal diversity among B. rossi with the exception of one sequence that was greatly divergent from the others. This study suggests that more than one genotype of B. rossi may be in circulation among the dog population in the study area and this may have potential implication on clinical outcome of canine babesiosis.

African animal trypanosomosis (AAT) is one of the major constraints to the development of effective livestock production systems. Dogs are human companion and are believed to be sentinels for infection with the human species. This study was to detect subclinical and clinical infection of trypanosomes among hunting dogs in Abeokuta and its environs using molecular technique. A total of 87 dogs comprising of 49 males and 38 females were ramdomly screened for trypanosomes by polymerase chain reaction technique. Among 87 dogs screened, 17.2% were positive for Trypanosoma congolense and Trypanosoma brucei. Prevalence of trypanosomosis in males was 14.3% while the females accounted for 21.1%.Hematological examination revealed a significant increase (p < 0.05) in mean white blood cells (20.9 ± 2.11) and monocyte counts (5.9 ± 0.62) of the infected dogs compared to uninfected dogs. Packed Cell Volume (36.0 ± 3.73) and haemoglobin concentration (13.9 ± 2.10) decreased insignificantly, while, red blood cells (7.1 ± 0.87), lymphocyte (60.9 ± 9.63), neutrophil (33.3 ± 9.16) and eosinophil (1.4 ± 0.42) counts increased insignificantly (p > 0.05) in infected dogs compared to uninfected dogs. In conclusion, trypanosomosis is prevalent in hunting dogs, in Abeokuta.

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