The prevalence of helminth infection, species spectrum and worm burdens in Kenyan pigs was examined. A total of 115 gastrointestinal tracts (GIT) from 61 growers and 54 adult pigs were examined between February 2005 and January 2006. Seventy eight (67.8%) had one or more helminth parasites, of which thirty six (31.3%) were mixed infection. Ten types of helminth parasites encountered in descending order of prevalence were, Oesophagostomum dentatum (39.1%), Trichuris suis (32.2%), Ascaris suum (28.7%), Oesophagostomum quadrispinulatum (14.8%), Trichostrongylus colubriformis (10.4%), Trichostrongylus axei (4.3%), Strongyloides ransomi (4.3%), Hyostrongylus rubidus (1.7%), Ascarops strongylina (1.7%) and Physocephalus sexalutus (0.9%). Oesophagostomum dentatum was the most prevalent species (51.9%) in the adult pigs, while Trichuris suis was the most prevalent species (44.3%) in growers. The highest worm counts were recorded in the out door production system. Oesophagostomum quadrispinulatum, Trichostrongylus colubriformis, Trichostrongylus axei, Hyostrongylus rubidus, Ascarops strongylina and Physocephalus sexalutus were recorded in Kenya for the first time. The high prevalence and wide spectrum observed in the present study suggests that helminth infection may be a constraint to economic pig production in the country and there is need to institute control measures.
Background Gastrointestinal parasites are neglected infections, yet they cause significant burden to animal and human health globally. To date, most studies of gastrointestinal parasites focus on host-parasite systems that involve either a single parasite or a host species. However, when hosts share habitat and resources, they may also cross-transmit generalist gastrointestinal parasites. Here we explore multi-host-parasite interactions in a single ecosystem to understand the infection patterns, especially those linked to livestock-wildlife interfaces and zoonotic risk. Methods We used both coprological methods (flotation and sedimentation; N = 1,138 fecal samples) and molecular identification techniques (rDNA and mtDNA; N = 18 larvae) to identify gastrointestinal parasites in nine sympatric host species (cattle, sheep, goats, wildebeest, Grant’s gazelles, Thomson’s gazelles, impala, vervet monkeys and baboons) in the Amboseli ecosystem, Kenya. Results We found that the host community harbored a diverse community of gastrointestinal helminths, including 22 species and/or morphotypes that were heterogeneously distributed across the hosts. Six zoonotic gastrointestinal helminths were identified: Trichuris spp., Trichostrongylus colubriformis , Enterobius spp. Oesophagostomum bifurcum , Strongyloides stercoralis and Strongyloides fuelleborni . The dominant parasite was Trichuris spp, whose ova occurred in two morphological types. Baboons were co-infected with Strongyloides fuelleborni and S . stercoralis . Conclusions We found that the interface zone shared by wild ungulates, livestock and non-human primates is rich in diversity of gastrointestinal helminths, of which some are extensively shared across the host species. Closely related host species were most likely to be infected by the same parasite species. Several parasites showed genetic sub-structuring according to either geography or host species. Of significance and contrary to expectation, we found that livestock had a higher parasite richness than wild bovids, which is a health risk for both conservation and livestock production. The zoonotic parasites are of public health risk, especially to pastoralist communities living in areas contiguous to wildlife areas. These results expand information on the epidemiology of these parasites and highlights potential zoonotic risk in East African savanna habitats.
Rhipicephalus decoloratus causes serious economic losses in cattle industry every year in East Africa. Biological control using entomopathogenic fungi is seen as a promising alternative to chemical acaricides being used for their control. The pathogenicity of Metarhizium anisopliae and of Beauveria bassiana isolates was tested in the laboratory against amitraz-resistant and amitraz-susceptible strains of R. decoloratus. Unfed larvae were sprayed with conidial suspensions of 1×10(9) conidia ml(-1). Fungal isolates were pathogenic to R. decoloratus larvae, causing mortality of between 10.0 and 100% and between 12.1 and 100% of amitraz-susceptible and amitraz-resistant strains, respectively. The LT50 values of selected fungal isolates varied between 2.6-4.2days in amitraz-susceptible strain and between 2.8-3.9days in amitraz-resistant strain. The LC50 values varied between 0.4±0.1 and 200.0±60×10(3) conidia ml(-1) and between 0.1±0.1 and 200.0±31.0×10(3) conidia ml(-1) in amitraz-susceptible and amitraz-resistant strains, respectively. Metarhizium anisopliae isolate ICIPE 7 outperformed the other isolates and was selected for compatibility study with amitraz and field trial. ICIPE 7 was compatible with amitraz. In the field, four treatments including control, ICIPE 7 alone, amitraz alone and ICIPE 7/amitraz were applied on cattle. All the treatments significantly reduced the number of ticks on all the sampling dates: day 7 (F3,8=3.917; P=0.0284), day 14 (F3,8=9.090; P=0.0275), day 21 (F3,8=37.971; P=0.0001) and day 28 (F3,8=8.170; P=0.0016) compared to the control. Results of the present study indicate that ICIPE 7 can be used for the management of amitraz-resistant strain of R. decoloratus.
A study was carried out on a ranch in the semi-arid area of Kajiado District in Kenya during the period July 2000 to June 2001 to determine the seasonal patterns of development and survival of gastrointestinal nematodes of sheep on pastures. A series of plots were contaminated with sheep faeces every month and pasture samples were collected weekly for the recovery and identification of larvae. The availability of infective larvae on naturally contaminated pastures was also monitored on the paddocks grazed by sheep and around the night pen and the watering point every month from July 2000 to June 2001. The results from the examination of the pasture samples indicated that rainfall distribution was the major factor governing the development and survival of the pre-parasitic stages. No parasitic larvae were detected from the plots contaminated during the dry months from July to October 2000, but development and translocation of infective larvae on pastures occurred on plots contaminated during the rainy seasons and soon after when relatively high moisture was present in the herbage (November 2000 to June 2001). During this period, peak larval counts occurred between the first and the second week post contamination, then declined to undetectable levels between week 4 and 16 post contamination. The lack of development of infective larvae during the dry season and the relatively rapid decline of their population during the wet season presents an opportunity for the use of pasture spelling as a means of helminth control in the study area. The availability of infective larvae on naturally contaminated pastures, around the night pen and around the watering point also followed the rainfall distribution pattern. Infective larvae were consistently recovered around the watering point throughout the study period. This indicated that the point is an important source of infection for sheep, especially during the dry season when other pastures are non-infective.
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