2008
DOI: 10.1007/s00436-008-1280-1
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Cytochrome oxidase subunit 1 and mitochondrial 16S rDNA sequences of Trichuris skrjabini (Tricocephalida: Trichuridae)

Abstract: The partial mitochondrial cytochrome c-oxidase subunit 1 gene (cox 1) and partial mitochondrial 16S ribosomal DNA of Trichuris skrjabini (Baskakov 1924) isolated from Capra hircus have been amplified and sequenced. The analyses of multiple sequence alignments of mitochondrial 16S rDNA and cox 1 of T. skrjabini revealed high homology with those of Trichinella species. For the first time, the mitochondrial DNA gene sequences of one species of trichurid nematode have been cited.

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Cited by 13 publications
(6 citation statements)
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“…However, COI gene amplified all the samples thus demonstrating that COI is a better gene for this purpose. The effectiveness of COI gene in species classification has also been reported before in wildlife [9], nematodes [32], reedbuck [10], birds [33], rodents [15], and lepidoptera [34]. The COI genes have been the most frequent methods used for species identification in animal biological studies due to its high degree of phylogenetic species differentiation as compared to other mtDNA genes [33].…”
Section: Discussionmentioning
confidence: 64%
“…However, COI gene amplified all the samples thus demonstrating that COI is a better gene for this purpose. The effectiveness of COI gene in species classification has also been reported before in wildlife [9], nematodes [32], reedbuck [10], birds [33], rodents [15], and lepidoptera [34]. The COI genes have been the most frequent methods used for species identification in animal biological studies due to its high degree of phylogenetic species differentiation as compared to other mtDNA genes [33].…”
Section: Discussionmentioning
confidence: 64%
“…found in ruminants (both domesticated and non-domesticated). Four Trichuris spp.-T. discolor, T. ovis, T. globulosa and T. skrjabini-have been identified as inhabiting the caecum and colon of ruminants [35][36][37][38][39][40][41][42][43][44][45]. One of the major discoveries was the identification of T. globulosa and T. ovis as the same species by isoenzymes [35], using second, internally transcribed spacer ribosomal DNA (ITS2 rDNA) [38] and ITS1-5.8S-1TS2 [37].…”
Section: Molecular Identification Of Trichuris Spp In Domestic and Non-domestic Ruminantsmentioning
confidence: 99%
“…PCR was performed using the following conditions: an initial denaturation at 96 °C for 3 min and then 30 cycles of 1 min at 94 °C, 1 min at 58 °C and 1 min at 72 °C, followed by 10 min at 72 °C. Finally, a 419 bp fragment of the cox1 gene was amplified using the forward primer L6625 (5'-TTYTGRTTYTTYGGNCAYCC-3') and reverse primer H7005 (5'-ACTACGTAGTAGGTATCATG-3'), which were together with PCR conditions modified by Callejón et al (2009). Each PCR mixture included: 12.5 μl of commercial Combi PPP Master Mix (Top-Bio, Praha, Czech Republic), 9.5 μl of PCR water, 1 μl of each primer mix (0.01 mM each) and 1 μl of template DNA.…”
Section: Pcr Amplification and Sequencingmentioning
confidence: 99%