2018
DOI: 10.1016/j.meegid.2018.02.005
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Molecular survey on the occurrence of arthropod-borne pathogens in wild brown hares ( Lepus europaeus ) from Central Italy

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Cited by 30 publications
(16 citation statements)
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“…A lower seroprevalence of L. infantum (0.9% compared with 12.4% in our study) was reported in L. europaeus in Italy (Ebani et al 2016). Molecular studies have revealed 56.3% L. infantum infection in Spain (Ruiz-Fons et al 2013), and more recent studies have revealed 1.9% L. infantum infection in central Italy (Rocchigiani et al 2018). In northern Greece, the L. infantum DNA prevalence reported for 2007-2011 was 23.49% (Tsokana et al 2015), which is consistent with our findings in the same region (20%) ( Table 1).…”
Section: Resultscontrasting
confidence: 57%
“…A lower seroprevalence of L. infantum (0.9% compared with 12.4% in our study) was reported in L. europaeus in Italy (Ebani et al 2016). Molecular studies have revealed 56.3% L. infantum infection in Spain (Ruiz-Fons et al 2013), and more recent studies have revealed 1.9% L. infantum infection in central Italy (Rocchigiani et al 2018). In northern Greece, the L. infantum DNA prevalence reported for 2007-2011 was 23.49% (Tsokana et al 2015), which is consistent with our findings in the same region (20%) ( Table 1).…”
Section: Resultscontrasting
confidence: 57%
“…On the basis of previous epidemiological studies in mammals and data relative to human infections, F. tularensis seems to not be largely present in Italy (Pascucci et al, 2015; Ebani et al, 2016, 2017; Graziani et al, 2016; Rocchigiani et al, 2018), thus the negative results of the tested waterfowl could reflect the true epidemiological status. F. tularensis has been proven to be able to infect different avian species, thus birds could be cause of infection for humans.…”
Section: Discussionmentioning
confidence: 96%
“…DNA was extracted from 200 µL of buffy coat by blood/cultured cells genomic DNA extraction mini kit (Trevose, PA, USA) and all samples were submitted to PCR assay. For detection of Leishmania DNA, the ITS1 gene was selected as PCR target, as previously described [13]. PCR amplifications were performed in 50 μL of reaction mixture, containing 200 μM of deoxynucleoside triphosphates, 0.5 μM of each primer, 1.25 U of Taq polymerase (Lucigen Corporation, Middleton, Wisconsin, USA), and 2 μL of genomic DNA.…”
Section: Methodsmentioning
confidence: 99%
“…On the other hand, rodents such as black rats [10] and hares [11,12,13] have previously been described as being infected. Moreover, bovine [14] and horses were proven to be affected by cutaneous leishmaniosis in both Central [15,16] and Southern Europe [17,18,19].…”
Section: Introductionmentioning
confidence: 99%