2017
DOI: 10.1016/j.cimid.2016.11.008
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Molecular evidence of tick-borne hemoprotozoan-parasites (Theileria ovis and Babesia ovis) and bacteria in ticks and blood from small ruminants in Northern Algeria

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Cited by 70 publications
(54 citation statements)
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“…Small ruminants are also affected by babesiosis caused by Babesia ovis, B. motasi, B. crassa, B. foliata, B. taylori, and Babesia sp. (China) [52]. Babesia ovis is considered highly pathogenic with mortality rates of 30-50% in susceptible sheep.…”
Section: Tick-borne Pathogens In Small Ruminantsmentioning
confidence: 99%
See 1 more Smart Citation
“…Small ruminants are also affected by babesiosis caused by Babesia ovis, B. motasi, B. crassa, B. foliata, B. taylori, and Babesia sp. (China) [52]. Babesia ovis is considered highly pathogenic with mortality rates of 30-50% in susceptible sheep.…”
Section: Tick-borne Pathogens In Small Ruminantsmentioning
confidence: 99%
“…uilenbergi,T. recondita and T. separata [52]. In susceptible sheep, the disease can be highly pathogenic, especially when it is caused by T. lestoquardi, causing a lymphoproliferative disease with mortality and high morbidity.…”
Section: Tick-borne Pathogens In Small Ruminantsmentioning
confidence: 99%
“…A limited number of human cases of coxiellosis have been reported in Algeria and most cases occurred in the northern part of the country (Angelakis et al 2014 ; Benslimani et al 2005 ). More recently, evidence of Q fever infection based on polymerase chain-reaction (PCR) amplification and sequencing of C. burnetii target genes has been reported in ticks from bats (Leulmi et al 2016 ), Rhipicephalus bursa ticks, dog and cat spleens (Bessas et al 2016 ) and blood from sheep and goats (Aouadi et al 2017 ). The true incidence of the disease in humans remains unknown in Algeria because of a lack of published data and the non-specific clinical signs of Q fever which lead to underreporting of the disease (Van der Hoek et al 2012 ).…”
Section: Introductionmentioning
confidence: 99%
“…and Theileria spp. were also screened by qPCR targeting fragments of the 18S and 28s genes respectively [17]. Bartonella elizabethae, Rickettsia montanensis, C. burnetii, A. phagocytophilum and Borrelia crocidurae DNAs were used as positive qPCR controls for the primers and probe targeting respectively Bartonella spp., Rickettsia spp., C. burnetii, Anaplasmataceae spp.…”
Section: Methodsmentioning
confidence: 99%