2014
DOI: 10.1016/j.ijpara.2014.06.009
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Genetic diversity of the Chinese liver fluke Clonorchis sinensis from Russia and Vietnam

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Cited by 27 publications
(14 citation statements)
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“…nov. differs from M. bilis, M. xanthosomus , and M. orientalis in most metrics, as well as the length/width body ratio and ventral/oral sucker ratio (Table ). Besides the determination of the phylogenetic status for the Metorchis representative in the Russian southern Far East, we analyzed the levels of nucleotide and haplotype diversities for the cox1 gene, which indicate long‐term isolation of a relatively small population (Avise, ), as was previously revealed for Clonorchis sinensis from the same geographic territory (Chelomina et al., ). Almost all M. ussuriensis sp.…”
Section: Discussionmentioning
confidence: 99%
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“…nov. differs from M. bilis, M. xanthosomus , and M. orientalis in most metrics, as well as the length/width body ratio and ventral/oral sucker ratio (Table ). Besides the determination of the phylogenetic status for the Metorchis representative in the Russian southern Far East, we analyzed the levels of nucleotide and haplotype diversities for the cox1 gene, which indicate long‐term isolation of a relatively small population (Avise, ), as was previously revealed for Clonorchis sinensis from the same geographic territory (Chelomina et al., ). Almost all M. ussuriensis sp.…”
Section: Discussionmentioning
confidence: 99%
“…and ( Paragonimus westermani ). The partial cox1 gene sequences were amplified using the forward 5cF22 (5′‐TAG‐ACT‐ATC‐TGT‐CTT‐CAA‐AAC‐A‐3′ (Chelomina, Tatonova, Hung, & Ngo, )) and reverse CO1‐Rv (5′‐AAC‐AAA‐TCA‐TGA‐TGC‐AAA‐AGG‐TA‐3′ (Katokhin et al., )) primers. The partial sequences of 28S were amplified using the following primers: forward dig12 (5′‐AAG‐CAT‐ATC‐ACT‐AAG‐CGG‐3′) and reverse 1500R (5′‐GCT‐ATC‐CTG‐AGG‐GAA‐ACT‐TCG‐3′) (Tkach, Littlewood, Olson, Kinsella, & Swiderski, ).…”
Section: Methodsmentioning
confidence: 99%
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“…Currently, most published molecular evidence seems to suggest that C. sinensis represents a single species and that genetic variation within the species is relatively low (Park and Yong, 2001;Lee and Huh, 2004;Petney et al, 2013). However, to date, most studies have used a relatively small number of genetic loci for specific identification (e.g., internal transcribed spacers of nuclear ribosomal DNA) and/or population genetic studies (e.g., act, tub, ef-1a, cox1, cox3, nad4 and nad5) (Park and Yong, 2001;Lee and Huh, 2004;Liu et al, 2007;Park, 2007;Katokhin et al, 2008;Lai et al, 2008;Shekhovtsov et al, 2009;Liu et al, 2012;Shin et al, 2013;Sun et al, 2013;Tatonova et al, 2013;Xiao et al, 2013;Chelomina et al, 2014), and it is not yet known whether "cryptic" (= morphologically similar, but genetically distinct) species exist within C. sinensis. Nonetheless, karyotypic differences in C. sinensis observed among China, Korea (2n = 56) and the Russian Far East (2n = 14) (Park and Yong, 2001;Zadesenets et al, 2012) do suggest that this might be the case.…”
Section: Introductionmentioning
confidence: 99%
“…There are ITS1 rDNA data for C. sinensis from different areas (Tatonova et al, 2012;Sun et al, 2013). Vietnam is the southernmost area for this parasite and previously, C. sinensis from Vietnam has been investigated using mitochondrial cox1 gene (Chelomina et al, 2014), while there are no data on the ITS1 marker in this area. Also, O. viverrini from Vietnam has not been analysed using the ITS1 rDNA marker.…”
Section: Introductionmentioning
confidence: 99%