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Fascioliasis is a freshwater snail‐borne zoonotic helminth disease caused by two species of trematodes: Fasciola hepatica of almost worldwide distribution and the more pathogenic F. gigantica restricted to parts of Asia and most of Africa. Of high pathological impact in ruminants, it underlies large livestock husbandry losses. Fascioliasis is moreover of high public health importance and accordingly included within the main neglected tropical diseases by WHO. Additionally, this is an emerging disease due to influences of climate and global changes. In Africa, F. gigantica is distributed throughout almost the whole continent except in the north‐western Maghreb countries of Morocco, Algeria and Tunisia where only F. hepatica is present. The present study concerns the DNA multimarker characterization of the first finding of F. gigantica in sheep in Algeria by the complete sequences of rDNA ITS‐1 and ITS‐2 and mtDNA cox1 and nad1 genes. Sequence comparisons and network analyses show sequence identities and similarities suggesting a south–north trans‐Saharan geographical origin, with introduction from Ghana, through the Sahel countries of Burkina Faso and Mali into Algeria. This way perfectly fits with nomadic pastoralism according to interconnecting intranational and transborder herd transhumance routes traditionally followed in this western part of Africa from very long ago. The risk for further spread throughout the three north‐western Maghreb countries is multidisciplinarily analysed, mainly considering the present extensive motorization of the intranational transhumance system in Algeria, the lymnaeid snail vector species present throughout the north‐western Maghreb, the increasing demand for animal products in the growing cities of northern Algeria and the continued human infection reports. Control measures should assure making anti‐fasciolid drugs available and affordable for herders from the beginning and along their transhumant routes and include diffusion and rules within the regional regulatory framework about the need for herd treatments.

Aim:The aim of the present study was to determine the prevalence and intensity of rabbit coccidiosis (Oryctolagus cuniculus) in North Algeria.Materials and Methods:During the study, 40 rabbit farms were investigated. The farms are located in the provinces of Tizi Ouzou, Médéa, and Djelfa which distributed, respectively, into three regions: East Tell Atlas Mountains, Central Tell Atlas Mountains, and High Plateaus. The number of oocyst per gram of feces (OPG) was determined by McMaster technique, and the Eimeria species were identified using morphological criteria.Results:In the farms investigated, the prevalence of coccidian infection was estimated to 90% (80.7-99.3%) in rabbits after weaning. The classification of the farms according to their parasite load allowed us to show that 37.5% of the prospective farms have an oocyst excretion between 104 and 5×104 oocysts per gram and 22.5% excrete >5×104 oocysts per gram. Excretion levels by region show that the region of East Tel Atlas Mountains ranks first with 79% of farms with a parasitic load >104 coccidians compared to the regions of Central Tel Atlas Mountains and High Plateaus. In total, eight species of Eimeria were identified from oocyst-positive samples. Mixed infections with four Eimeria species were common. E. magna is the dominant species in comparison with E. media and E. irresidua with respective frequencies of 42.5% and 17.6% and 14.9% (p<0.001). Our results showed that the farms using anticoccidial drugs for their rabbits were low (25%) and the percentage of farms with poor hygienic conditions was 65%. There was a significant association between increased oocysts excretion and control measures of coccidian infection.Conclusion:The study revealed an overall prevalence of 90% in the three Algerian regions. A strong association was observed between Eimeria infection and hygienic status and preventional chemotherapy.

To determine the presence and distribution of bovine theileriosis in the North Central region of Algeria, 358 DNA samples and 359 blood smears were analyzed from nine provinces. Theileria DNA extracted from cattle blood was amplified by fluorescence resonance energy transfer polymerase chain reaction (FRET-PCR). Blood smears were examined for Theileria piroplasms by microscopical examination (ME) of Giemsa-stained slides. While microscopical identification revealed only 42 animals being infected with Theileria piroplasms, PCR-positive amplification using Theileria genus-specific primers was obtained from 132 Theileria spp. (P < 0.0001). Among the 132 positives, 108 animals (81.8 %) were found positive of Theileria annulata, while 24 (18.2 %) were found positive for Theileria sp. (P < 0.0001). However, melting curve analysis of these latter samples revealed the presence of two different peaks, 51.5 ± 0.5 °C corresponding to Theileria sp1 and 52.5 ± 0.5 °C for Theileria sp2. Cloning and sequencing of Theileria sp1 and Theileria sp2 using the Cox primers indicated that these species are very closely related to Theileria buffeli. There is a highly significant difference in the distribution of theileriosis between different provinces (P < 0.0001). This disparity between provinces is probably due to differences in tick contact, influenced by the subhumid bioclimatic gradient and differences in agricultural land use.