2008
DOI: 10.1017/s0031182008004198
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First report of Echinococcus granulosus G8 in Eurasia and a reappraisal of the phylogenetic relationships of ‘genotypes’ G5-G10

Abstract: In this study, we investigated the presence of the larval stage of the tapeworm Echinococcus granulosus in wild ungulates in Estonia, genetically characterized E. granulosus isolates using mitochondrial gene sequences and used the sequence data, together with those available in a public database, to infer the phylogenic relationships of E. granulosus 'genotypes' G5-G10. While 0.8% of the 2038 moose (Alces alces) examined were found to be infected with E. granulosus, the parasite was not detected in other wild … Show more

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Cited by 98 publications
(106 citation statements)
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“…Later, economic and social changes caused a decrease in the numbers of family farms, (Moks et al, 2008). Of these, 11 belonged to genotype G8 and 5 to genotype G10.…”
Section: U N C O R R E C T E D P R O O Fmentioning
confidence: 99%
“…Later, economic and social changes caused a decrease in the numbers of family farms, (Moks et al, 2008). Of these, 11 belonged to genotype G8 and 5 to genotype G10.…”
Section: U N C O R R E C T E D P R O O Fmentioning
confidence: 99%
“…Consequently, a taxonomic reappraisal relying mainly on mitochondrial data has proposed that E. granulosus species splits to four valid species including: 1) E. granulosus sensu stricto (G1-G3 complex), 2) E. equines (G4), 3) E. ortleppi (G5), and 4) E. canadensis (G6-G10). 17,21,22 Moreover, E. felidis (lion strain) is closely related to E. granulosus sensu stricto and is placed within the E. granulosus complex. 23 Recently, based on more complex data containing nuclear sequences and the epidemiological aspects, it was recommended that genotypes G6-G10 should be broken into two distinct species including E. canadensis (G8 and G10 genotypes) and E. intermedius (G6/ G7 genotypes).…”
Section: Introductionmentioning
confidence: 99%
“…These informal groupings were retained for many years but with the advent of molecular characterization they were shown to be genetically distinct (Thompson and McManus, 2001). PCR-based techniques using a variety of genetic loci, and sequencing of nuclear and mitochondrial DNA, coupled with molecular epidemiological studies in endemic areas, confirmed the genetic and morphological distinctness of the host-adapted strains and revealed phylogenetic relationships which support a robust, meaningful taxonomy based on a previously documented nomenclature (Table 2; Bowles et al, 1994;Cruz-Reyes et al, 2007;Harandi et al, 2002;Huttner et al, 2009;Jenkins et al, 2005Lavikainen et al, 2003Moks et al, 2008;Nakao et al, 2013;Pednekar et al, 2009;Romig et al, 2006Romig et al, , 2015Saarma et al, 2009;Thompson et al, 1995Thompson et al, , 2006Thompson, 2001Thompson, , 2008Thompson and McManus, 2002;Tigre et al, 2016). Interestingly, the nomenclature used for these 'species' conforms to that proposed by observational parasitologists in the 1920se60s, before molecular tools were available to confirm and support their morphological descriptions and epidemiological observations Thompson and McManus, 2002;Thompson, 2008).…”
Section: U N C O R R E C T E D P R O O Fmentioning
confidence: 63%