2009
DOI: 10.1016/j.parint.2008.09.001
|View full text |Cite
|
Sign up to set email alerts
|

Mitochondrial DNA divergence in populations of the tapeworm Diphyllobothrium nihonkaiense and its phylogenetic relationship with Diphyllobothrium klebanovskii

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

1
35
0

Year Published

2009
2009
2023
2023

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 41 publications
(36 citation statements)
references
References 24 publications
1
35
0
Order By: Relevance
“…Diphyllobothrium klebanovskii Kuratov et Posokhov, 1988, was isolated from the lower Amur River basin in the Russian Far East (72). Synonymy with D. nihonkaiense has been confirmed by molecular data (12).…”
Section: Europementioning
confidence: 61%
See 3 more Smart Citations
“…Diphyllobothrium klebanovskii Kuratov et Posokhov, 1988, was isolated from the lower Amur River basin in the Russian Far East (72). Synonymy with D. nihonkaiense has been confirmed by molecular data (12).…”
Section: Europementioning
confidence: 61%
“…In most analyses, D. pacificum and/or D. stemmacephalum (type species of the genus) represent the most basal taxa of the genus (12,22,81,150). Diphyllobothrium nihonkaiense is the basal taxon to the clade formed by D. latum, D. dendriticum, and D. ditremum, which also contains members of the genera Ligula and Digramma, the adults of which are parasites of fish-eating birds (44).…”
Section: Taxonomy and Phylogenetic Relationshipsmentioning
confidence: 99%
See 2 more Smart Citations
“…A custom primer pair was designed to amplify a 349-bp region of the Diphyllobothrium cytochrome c oxidase subunit 1 (cox1) gene based on publicly available sequences (forward primer, 5=-TGCACTCTCTACACAGCGTTT-3=; reverse primer, 5=-ATGCCCCCACACAACACTAC-3=). This specific region was selected because it contained residues that discriminate between D. nihonkaiense and Diphyllobothrium klebanovskii (12). The PCR was performed using the AccuPrime Pfx DNA polymerase kit (Invitrogen, Carlsbad, CA) with the following cycling conditions: 95°C for 2 min followed by 35 cycles at 95°C for 15 s, 55°C for 30 s, and 68°C for 90 s, and a final extension at 68°C for 2 min.…”
mentioning
confidence: 99%