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Bioinformation. 2009; 3(7): 314–320.
Published online 2009 February 28.
PMCID: PMC2655052
Use of sequence motifs as barcodes and secondary structures of Internal Transcribed spacer 2 (ITS2, rDNA) for identification of the Indian liver fluke, Fasciola (Trematoda: Fasciolidae)
PK Prasad,1 V Tandon,1* DK Biswal,2 LM Goswami,1 and A Chatterjee3
1Department of Zoology, North Eastern Hill University, Shillong, Meghalaya, 793022, India
2Bioinformatics Centre, North Eastern Hill University, Shillong, Meghalaya, 793022, India
3Department of Biotechnology and Bioinformatics, North Eastern Hill University, Shillong, Meghalaya, 793033, India
*PK Prasad: pramod812/at/gmail.comTel.: (+91) 0364 2722312; Fax: (+91) 0364 2722301
Received October 10, 2008; Revised January 16, 2009; Accepted February 7, 2009.
Abstract
Most phylogenetic studies using current methods have focused on primary DNA sequence information. However, RNA secondary structures are particularly useful in systematics because they include characteristics that give “morphological” information which is not found in the primary sequence. Also DNA sequence motifs from the internal transcribed spacer (ITS) of the nuclear rRNA repeat are useful for identification of trematodes. The species of liver flukes of the genus Fasciola (Platyhelminthes: Digenea: Fasciolidae) are obligate parasitic trematodes residing in the large biliary ducts of herbivorous mammals. While Fasciola hepatica has a cosmopolitan distribution, the other major species, i.e., F. gigantica is reportedly prevalent in the tropical and subtropical regions of Africa and Asia. To determine the Fasciola sp. of Assam (India) origin based on rDNA molecular data, ribosomal ITS2 region was sequenced (EF027103) and analysed. NCBI databases were used for sequence homology analysis and the phylogenetic trees were constructed based upon the ITS2 using MEGA and a Bayesian analysis of the combined data. The latter approach allowed us to include both primary sequence and RNA molecular morphometrics and revealed a close relationship with isolates of F. gigantica from China, Indonesia and Japan, the isolate from China with significant bootstrap values being the closest. ITS2 sequence motifs allowed an accurate in silico distinction of liver flukes. The data indicate that ITS2 motifs (≤ 50 bp in size) can be considered promising tool for trematode species identification. Using the novel approach of molecular morphometrics that is based on ITS2 secondary structure homologies, phylogenetic relationships of the various isolates of fasciolid species have been discussed.
Keywords: Fasciola hepatica, Fasciola gigantica, secondary structure, internal transcribed spacer, bar coding, motifs
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