2012
DOI: 10.1016/j.ttbdis.2011.11.003
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Prevalence of Rickettsia spp., Anaplasma phagocytophilum, and Coxiella burnetii in adult Ixodes ricinus ticks from 29 study areas in central and southern Sweden

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Cited by 37 publications
(37 citation statements)
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“…6,11 However, contrary to our present finding, C. burnetii was not detected in ticks studied in Hungary, 46 in Germany, 40 or in Sweden. 47 This variation is most probably attributed to differences in animal management factors, for example, that domestic animals are housed within farms throughout their lifespan and are not allowed to graze on pastures in some European countries and the systematic use of acaricides, such as deltamethrin, that reduce tick populations and alter the ability of ticks to carry C. burnetii. This is different from Ethiopia where animals graze in communal pastures throughout the year that serve as an infectious source for blood-feeding ticks, and there is no regular use of acaricides as has been shown before.…”
Section: Discussionmentioning
confidence: 99%
“…6,11 However, contrary to our present finding, C. burnetii was not detected in ticks studied in Hungary, 46 in Germany, 40 or in Sweden. 47 This variation is most probably attributed to differences in animal management factors, for example, that domestic animals are housed within farms throughout their lifespan and are not allowed to graze on pastures in some European countries and the systematic use of acaricides, such as deltamethrin, that reduce tick populations and alter the ability of ticks to carry C. burnetii. This is different from Ethiopia where animals graze in communal pastures throughout the year that serve as an infectious source for blood-feeding ticks, and there is no regular use of acaricides as has been shown before.…”
Section: Discussionmentioning
confidence: 99%
“…All cDNA samples from the ticks were individually assayed using a real-time PCR targeting the citrate synthase ( gltA ) gene of Rickettsia spp., as previously described [2, 14, 27]. Two to five μl cDNA was used as a template in each reaction, together with 0.25 μl LC Uracil-DNA glycosylase (UNG) (Roche Diagnostics, Mannheim, Germany) to minimize the risk of contamination.…”
Section: Methodsmentioning
confidence: 99%
“…For samples that were negative in gel electrophoresis (1% agarose) 5 μl of the PCR product from the first round were used for nesting the ompB PCR product yielding a 267 bp ompB fragment [25]. When species identification was unclear, additional PCR assays representing the 17 kDa gene and ompA gene were used as previously described, except for some minor changes [26-28]. The thermal cycle amplifying a fragment of the 17 kDa gene, was moderated to initial heating at 94ºC for 3 min followed by 40 repeated cycles (94°C 30s, 55°C 1 min, 72°C 1 min).…”
Section: Methodsmentioning
confidence: 99%
“…The PCR assay targeting the ompA gene, was moderated with an initial denaturation step at 95ºC for 3 min, amplification cycle of 45 repeats with denaturation (95ºC 20s), annealing (46ºC 60s) and elongation (63ºC 60s) followed by final elongation at 72ºC for 7 min (Table 1). For analysis of the samples collected during 2010, a semi-nested PCR assay targeting the gltA gene was used as well [26,29]. In all conventional PCR assays, Taq PCR Core Kit with Q-solution was used according to the manufacturer’s instructions (Qiagen GmbH, Hilden, Germany).…”
Section: Methodsmentioning
confidence: 99%