Author/Authors :
RAYANI, Mohammad Dept. of Medical Microbiology and Parasitology - Faculty of Medicine and Health Sciences - University Putra Malaysia, Serdang, Malaysia , HATAM, Gholamreza Basic Sciences in Infectious Diseases Research Center - School of Advanced Medical Sciences and Technologies - Shiraz University of Medical Sciences, Shiraz, Iran , UNYAH, Ngah Zasmy Dept. of Medical Microbiology and Parasitology - Faculty of Medicine and Health Sciences - University Putra Malaysia, Serdang, Malaysia , ASHRAFMANSORI, Abdolmajid Basic Sciences in Infectious Diseases Research Center - School of Advanced Medical Sciences and Technologies - Shiraz University of Medical Sciences, Shiraz, Iran , ABDULLAH, Wan Omar Dept. of Medical Microbiology and Parasitology - Faculty of Medicine and Health Sciences - University Putra Malaysia, Serdang, Malaysia , HAMAT, Rukman Awang Dept. of Medical Microbiology and Parasitology - Faculty of Medicine and Health Sciences - University Putra Malaysia, Serdang, Malaysia
Abstract :
Background: This study is the first phylogenetic genotype analysis of Giardia lamblia in
Iran. The main objective was to determine genotyping and identify the sub-assemblages of
Giardia lamblia isolates involved in the transmission of giardiasis in Fars Province, south of
Iran, in 2012.
Methods: Forty G. lamblia isolates were collected from the patient’s fecal samples with
gastrointestinal discomfort referred to the health centers and hospitals in Shiraz, Fars
Province, south of Iran. Purification of G. lamblia cysts from fecal samples and DNA
extraction were performed using monolayer of sucrose density gradient and Phenol-
Chloroform-Isoamylalcohol (PCI) respectively. Semi-nested PCR and sequence analysis
were then performed using the primers (GDHeF, GDHiF, and GDHiR) which amplified a
432-bp fragment of Giardia glutamate dehydrogenase (gdh) gene. Phylogenetic analysis was
carried out using a neighbor-joining tree composed of the nucleotide sequences of G.
lamblia isolates obtained in this study and the known sequences isolates published in
GenBank.
Results: G. lamblia sub-assemblage AII was the most prevalent genotype with 80% of the
cases and 20% of the cases belong to sub-assemblage BIII and BIV based on the DNA
sequence of the gdh. G. lamblia isolates at Fars Province were widely distributed within
assemblage A cluster (sub-assemblage AII) and the remaining isolates were dispersed
throughout the assemblage B cluster (sub-assemblage BIII and BIV).
Conclusion: PCR Sequencing and phylogenetic analysis was a proper molecular method
for genotyping and discriminating of the of G. lamblia sub-assemblages in fecal samples,
using the glutamate dehydrogenase gene that suggests a human contamination origin of
giardiasis.
Keywords :
Giardia lamblia , Genetic variation , Glutamate dehydrogenase (gdh) , Iran