A study on the semen obtained from breeding goats suffering from mild to severe chronic besnoitiosis revealed marked changes in semen volume, colour, density, concentration, mass and individual motility and percentage live. There were also many neutrophils and spermatozoa with primary and secondary defects, including missing tails and deformed heads and tails. The observed changes were considered to be severe enough to account for the infertility observed in the flock. Sections of testes obtained for histopathology were characterised by massive blockage of the pampiniform plexus, degeneration of the germinal epithelium, tubular necrosis with an inflammatory infiltrate and, in some cases, accumulation of haemosiderin-like material in the tunica vaginalis

Anaplasma marginale and Babesia bigemina are important tick-borne pathogens of cattle. A cross-sectional survey was undertaken to determine the seroprevalence of A. marginale and B. bigemina infections and identify associated risk factors on traditional smallholder farms in Machakos County, Kenya. A total of 421 cattle from 127 farms from four divisions in the county were sampled and visited between September and November 2007. The farms were selected by a proportional allocation approach based on the number of farms in the four divisions previously selected by stratified random sampling method. Information on animal and individual farm management variables was obtained using standardized questionnaires. Prevalence of serum antibodies due to A. marginale and B. bigemina pathogens was determined using the enzyme-linked immunosorbent assay (ELISA) technique. The relationship between the seropositivity and associated risk factors was assessed by multivariable analyses using standard logistic regression models. The overall estimation (and their 95% confidence intervals) of A. marginale and B. bigemina seropositivity at the animal level was 53.4% (48.5%, 58.2%) and 40.6% (35.8%, 45.4%), respectively. Two variables, "animal age" and "administrative division," were significantly associated with the A. marginale seroresponse. Three variables, "animal age" "grazing system" and "administrative division" were significantly associated with the B. bigemina seroresponse. These findings suggest possible indicators of existence of endemic instability for the two infections. The study identifies characterization of environmental suitability for the vectors and how they interact with grazing systems to cause the infections as an area for further studies, for improved understanding of the infections and in designing disease control programs.

The principle objective of this study was to estimate the infection seroprevalence and identify risk factors associated with Theileria parva infection in cattle on smallholder farms in Machakos County, Kenya. A total of 127 farms were selected by a proportional allocation approach based on the number of farms in four divisions in the county previously selected by stratified random sampling method. Subsequently, a total sample of 421 individual animals was randomly selected from the farms. Information on animal and relevant individual farm management practices was gathered using a standardized questionnaire. Prevalence of serum antibodies was determined using the enzyme-linked immunosorbent assay (ELISA). Multivariable logistic models incorporating random effects at the farm level evaluated the association between the presence of T. parva antibodies and the identified risk variables. The overall estimation of T. parva antibodies in the county was 40.9% (95% confidence interval of 36.1, 45.7%). Seroprevalence to T. parva was significantly associated with animal age, vector tick infestation in the animal, tick control frequency, and administrative division. Further analyses suggested a confounding relationship between administrative division and both breed and grazing system and the T. parva seropositivity. Random effects model yielded intra-farm correlation coefficient (ICC) of 0.18. The inclusion of farm random effect provided a substantially better fit than the standard logistic regression (P = 0.032). The results demonstrate substantial variability in the T. parva infection prevalence within all categories of the cattle population of Machakos County of Kenya, where East Coast fever is endemic.

A preliminary survey on the prevalence of besnoitiosis in domestic ruminants in Kenya based on field and farmvisits, clinical and <em>post mortem</em> examinations and histopathological examination of tissues and biopsies, showed that goats are the most affected, followed by cattle, while sheep were unaffected. Caprine besnoitiosis occurred in a continuous belt in of the 8 provinces in Kenya stretching from the Coast, Eastern, North Eastern, Nairobi and the Rift Valley Provinces. Mandera, in the North Eastern Province, had the highest prevalence rate of 36 %, followed by Kwale (35 %), Isiolo (35 %), Marsabit (33 %), Wajir (28 %), Nairobi (26 %), Meru (24 %), Garissa (21 %), Taita Taveta (18 %), Embu (17 %), Kitui (9 %), Machakos (7 %), Laikipia (3 %), Kajiado (2 %) and Turkana and Elgeyo-Marakwet (1 % each). In all flocks where the prevalence rates were over 6 %, kids were observed to be affected. There were no significant differences (P &lt; 0.05) between the prevalence rates in bucks and does (18 % and 18.4 %, respectively), but kids were less (4 %) affected. Bovine besnoitiosis was found only in the Tana River District, with an infection rate of 11 %

Peste des petits ruminants virus that causes a highly infectious and often fatal disease of sheep and goats is confirmed by various diagnostic techniques among them being isolation of the virus from cell culture systems, viral ribonucleic acid (RNA) detection by molecular assays, and viral antigen detection by immunocapture enzyme-linked immunosorbent assay (IC ELISA), immunohistochemistry (IHC), and AGAR gel test. Whereas most of the confirmatory diagnostic procedures require pathological samples to be stored frozen to preserve integrity of the peste des petits ruminants (PPR) virus RNA, samples for IHC tests are preserved in 10% formalin. In this study, nine formalin-fixed pathological samples from three goats suspected of PPR were processed for extraction of PPR viral RNA and analyzed for detection with real-time reverse transcription-polymerase chain reaction (qRT-PCR) assay. The results showed that five out of the nine tested samples returned positive for presences PPR viral genome. This study has established that field pathological samples of PPR-suspected cases, collected and stored in 10% formalin for up 2 years, could be used for PPR virus RNA extraction for disease virus confirmation.