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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Tehran University of Medical Sciences
2009-09-01
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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.
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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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1721566653385277440 |