| Literature DB >> 29906638 |
Teivi Laurimäe1, Liina Kinkar1, Thomas Romig2, Rihab A Omer3, Adriano Casulli4, Gérald Umhang5, Robin B Gasser6, Abdul Jabbar6, Mitra Sharbatkhori7, Hossein Mirhendi8, Francisco Ponce-Gordo9, Lorena E Lazzarini10, Silvia V Soriano10, Antonio Varcasia11, Mohammad Rostami Nejad12, Vanessa Andresiuk13, Pablo Maravilla14, Luis Miguel González15, Monika Dybicz16, Jakub Gawor17, Mindaugas Šarkūnas18, Viliam Šnábel19, Tetiana Kuzmina20, Urmas Saarma21.
Abstract
Cystic echinococcosis (CE) is a zoonotic disease caused by the larval stage of the species complex Echinococcus granulosus sensu lato. Within this complex, genotypes G6 and G7 have been frequently associated with human CE worldwide. Previous studies exploring the genetic variability and phylogeography of genotypes G6 and G7 have been based on relatively short mtDNA sequences, and the resolution of these studies has often been low. Moreover, using short sequences, the distinction between G6 and G7 has in some cases remained challenging. The aim here was to sequence complete mitochondrial genomes (mitogenomes) to obtain deeper insight into the genetic diversity, phylogeny and population structure of genotypes G6 and G7. We sequenced complete mitogenomes of 94 samples collected from 15 different countries worldwide. The results demonstrated that (i) genotypes G6 and G7 can be clearly distinguished when mitogenome sequences are used; (ii) G7 is represented by two major haplogroups, G7a and G7b, the latter being specific to islands of Corsica and Sardinia; (iii) intensive animal trade, but also geographical isolation, have likely had the largest impact on shaping the genetic structure and distribution of genotypes G6 and G7. In addition, we found phylogenetically highly divergent haplotype from Mongolia (Gmon), which had a higher affinity to G6.Entities:
Keywords: Cystic echinococcosis; Genotype G6; Genotype G7; Hydatid disease; Mitochondrial genome; Zoonosis
Mesh:
Year: 2018 PMID: 29906638 DOI: 10.1016/j.meegid.2018.06.016
Source DB: PubMed Journal: Infect Genet Evol ISSN: 1567-1348 Impact factor: 3.342