Genotypic and Phenotypic Analysis of Fasciola Isolates

Background: To identify the fasciolid species by morphometric and molecular methods in Zanjan, north­west of Iran. Methods: Adult Fasciola worms (n=584) were obtained from cattle and sheep in Zanjan slaughterhouse in 2007. Living flukes were washed, then worms' images were taken by 3CCD camera...

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Main Authors: MB Ghavami, P Rahimi, A Haniloo, SN Mosavinasab
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2009-09-01
Series:Iranian Journal of Parasitology
Subjects:
Online Access:https://ijpa.tums.ac.ir/index.php/ijpa/article/view/109
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spelling doaj-d607094a3ce64a2e82710fe4b922f3ca2021-04-02T13:04:56ZengTehran University of Medical SciencesIranian Journal of Parasitology1735-70202008-238X2009-09-0143Genotypic and Phenotypic Analysis of Fasciola Isolates MB Ghavami0P Rahimi1A Haniloo2SN Mosavinasab3 Background: To identify the fasciolid species by morphometric and molecular methods in Zanjan, north­west of Iran. Methods: Adult Fasciola worms (n=584) were obtained from cattle and sheep in Zanjan slaughterhouse in 2007. Living flukes were washed, then worms' images were taken by 3CCD camera and finally apical zone of each worm was obtained. Morphometric values such as body length, body width, body area, body pe­rimeter and the distance between ventral sucker and posterior end of body were obtained using Auto­CAD image analysis software. Total gDNA was extracted from individual flukes by modified phenol-chloroform method. PCR amplification of ITS2 fragment was performed the isolated DNA samples and the amplicons were consequently subjected to RFLP assay and nucleotide sequencing to distinguish be­tween fasciolid species. Results: Mean of morphometric values in flukes from sheep was greater than those of cattle. Accordingly, the identified species included 31% F. hepatica-like, 7% F. gigantica-like and 62% intermediate forms. How­ever, ITS2 fragment of 535 amplified specimens, showed no variation at the species-specific nucleo­tide sites 230, 340 and 341. The amplified fragment composed of partial 5.8S sequence (62bp), the com­plete ITS2 sequence (361bp) and partial 28S sequence (34bp). The nucleotide contents of ITS2 region were 69 A, 116 T, 81 C and 95 G and the average G+C content was approximately 49%. Comparing of ITS2 sequences with the BLAST GenBank database, also confirmed that all specimens were F. hepatica. Conclusion: A simple and rapid PCR-RFLP assay can be used for distinguishing between these species. https://ijpa.tums.ac.ir/index.php/ijpa/article/view/109FasciolaMorphometric valuesITS2PCR-RFLPRestriction enzymesIran
collection DOAJ
language English
format Article
sources DOAJ
author MB Ghavami
P Rahimi
A Haniloo
SN Mosavinasab
spellingShingle MB Ghavami
P Rahimi
A Haniloo
SN Mosavinasab
Genotypic and Phenotypic Analysis of Fasciola Isolates
Iranian Journal of Parasitology
Fasciola
Morphometric values
ITS2
PCR-RFLP
Restriction enzymes
Iran
author_facet MB Ghavami
P Rahimi
A Haniloo
SN Mosavinasab
author_sort MB Ghavami
title Genotypic and Phenotypic Analysis of Fasciola Isolates
title_short Genotypic and Phenotypic Analysis of Fasciola Isolates
title_full Genotypic and Phenotypic Analysis of Fasciola Isolates
title_fullStr Genotypic and Phenotypic Analysis of Fasciola Isolates
title_full_unstemmed Genotypic and Phenotypic Analysis of Fasciola Isolates
title_sort genotypic and phenotypic analysis of fasciola isolates
publisher Tehran University of Medical Sciences
series Iranian Journal of Parasitology
issn 1735-7020
2008-238X
publishDate 2009-09-01
description Background: To identify the fasciolid species by morphometric and molecular methods in Zanjan, north­west of Iran. Methods: Adult Fasciola worms (n=584) were obtained from cattle and sheep in Zanjan slaughterhouse in 2007. Living flukes were washed, then worms' images were taken by 3CCD camera and finally apical zone of each worm was obtained. Morphometric values such as body length, body width, body area, body pe­rimeter and the distance between ventral sucker and posterior end of body were obtained using Auto­CAD image analysis software. Total gDNA was extracted from individual flukes by modified phenol-chloroform method. PCR amplification of ITS2 fragment was performed the isolated DNA samples and the amplicons were consequently subjected to RFLP assay and nucleotide sequencing to distinguish be­tween fasciolid species. Results: Mean of morphometric values in flukes from sheep was greater than those of cattle. Accordingly, the identified species included 31% F. hepatica-like, 7% F. gigantica-like and 62% intermediate forms. How­ever, ITS2 fragment of 535 amplified specimens, showed no variation at the species-specific nucleo­tide sites 230, 340 and 341. The amplified fragment composed of partial 5.8S sequence (62bp), the com­plete ITS2 sequence (361bp) and partial 28S sequence (34bp). The nucleotide contents of ITS2 region were 69 A, 116 T, 81 C and 95 G and the average G+C content was approximately 49%. Comparing of ITS2 sequences with the BLAST GenBank database, also confirmed that all specimens were F. hepatica. Conclusion: A simple and rapid PCR-RFLP assay can be used for distinguishing between these species.
topic Fasciola
Morphometric values
ITS2
PCR-RFLP
Restriction enzymes
Iran
url https://ijpa.tums.ac.ir/index.php/ijpa/article/view/109
work_keys_str_mv AT mbghavami genotypicandphenotypicanalysisoffasciolaisolates
AT prahimi genotypicandphenotypicanalysisoffasciolaisolates
AT ahaniloo genotypicandphenotypicanalysisoffasciolaisolates
AT snmosavinasab genotypicandphenotypicanalysisoffasciolaisolates
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