Hostname: page-component-cd9895bd7-8ctnn Total loading time: 0 Render date: 2024-12-28T06:12:11.292Z Has data issue: false hasContentIssue false

High genetic diversity of Echinococcus canadensis G10 in northeastern Asia: is it the region of origin? – CORRIGENDUM

Published online by Cambridge University Press:  22 May 2024

Marion Wassermann*
Affiliation:
Department of Parasitology, University of Hohenheim, Stuttgart, Germany Center for Biodiversity and Integrative Taxonomy, University of Hohenheim, Stuttgart, Germany
Francis Addy
Affiliation:
Faculty of Biosciences, Department of Biotechnology and Molecular Biology, University for Development Studies, Tamale, Ghana
Ludmila Kokolova
Affiliation:
Yakut Scientific Research Institute of Agriculture, Siberian Branch of the Russian Academy of Science, Yakutsk, Russia
Innokentiy Okhlopkov
Affiliation:
Institute for Biological Problems of Cryolithozone, Siberian Branch of the Russian Academy of Science, Yakutsk, Russia
Sarah Leibrock
Affiliation:
Department of Parasitology, University of Hohenheim, Stuttgart, Germany
Jenny Oberle
Affiliation:
Department of Parasitology, University of Hohenheim, Stuttgart, Germany
Antti Oksanen
Affiliation:
Finnish Food Authority, Animal Health Diagnostic Unit (FINPAR), Oulu, Finland
Thomas Romig
Affiliation:
Department of Parasitology, University of Hohenheim, Stuttgart, Germany Center for Biodiversity and Integrative Taxonomy, University of Hohenheim, Stuttgart, Germany
*
Corresponding author: Marion Wassermann, E-mail: [email protected]

Abstract

Type
Corrigendum
Creative Commons
Creative Common License - CCCreative Common License - BYCreative Common License - NC
This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial licence (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. The written permission of Cambridge University Press must be obtained for commercial re-use.
Copyright
Copyright © The Author(s), 2024. Published by Cambridge University Press

The authors apologise for errors that appeared in the published article. The values for nucleotide diversity given in Table 3 (page 7) were erroneously taken from the results of the software Arlequin v 3.5.2.2 and not from DnaSP 6.12 as stated. This resulted in incorrect information in the results section in Table 3, first section of the paragraph ‘Population diversity and neutrality indices’ (page 7), and in the last column of ‘Discussion’ (page 8). The corrected table and text can be found below. Corrections made are highlighted in bold.

Table 3. Diversity and neutrality indices of Echinococcus canadensis G10 based on complete cox1 gene (1608 bp)

n, number of isolates (sequences); n H, number of haplotypes; H d, haplotype diversity; N d, nucleotide diversity; s.d., standard deviation.

a including sequences from Sakha and additional from eastern Russia.

b including sequences from eastern Russia, Mongolia, and Tibet.

* Significant at p < 0.05.

Results

Population diversity and neutrality indices

Analyses of the haplotype (H d) and nucleotide diversity (N d) indices show low values in Europe, compared to the diversity found in Northeast Asia, which are 8.3 (H d) and 11.75 (N d) times higher, respectively (Table 3). The value of European diversity H d was 0.0987 and that of nucleotide diversity N d was 0.00016. The indices from Sakha determined in the present study are almost 1 order of magnitude higher compared to Europe (H d: 0.7526; N d: 0.00138) and increase further with the inclusion of the other sequences from eastern Russia, Mongolia and China (H d: 0.8204; N d: 0.00188). The Alaskan samples also show high haplotype diversity values (H d: 0.8000); the nucleotide diversity (N d: 0.00062) is lower than that in northeast Asia, but still higher compared to Europe.

Discussion

As for E. canadensis, the genetic haplotype diversity has only been investigated from the G6/7 genotypic cluster. Although some geographical structuring can be seen with the ‘G6’ variants originating mostly from camel-raising regions and G6/7 contains a large number of haplotypes, most of these cluster closely together suggesting close relationship and recent ancestry (Addy et al., 2017; Laurimäe et al., 2018b). In contrast, many haplotypes of G10 analyzed in this study are widely separated from each other as reflected by the far higher value of nucleotide diversity (N d = 0.00188) as compared to G6/7 (N d = <0.00173) (Addy et al., 2017).

The remarkably high genetic diversity of G10 in Northeast Asia, the occurrence of all E. canadensis genotypes in this region and the phylogenetically basal position of genotypes 8 and 10 may be circumstantial evidence that this parasite might have evolved in this region.

References

Wassermann, M, Addy, F, Kokolova, L, Okhlopkov, I, Leibrock, S, Oberle, J, Oksanen, A, Romig, T (2023). High genetic diversity of Echinococcus canadensis G10 in northeastern Asia: is it the region of origin? Parasitology 19. https://doi.org/10.1017/S0031182023001191Google ScholarPubMed
Figure 0

Table 3. Diversity and neutrality indices of Echinococcus canadensis G10 based on complete cox1 gene (1608 bp)