hbv s gene premature stop codon in strains from middle eastern patients
نویسندگان
چکیده
conclusions: premature stop codon in the s gene was observed in all countries with evaluable hbv genome sequences. co-existence of detectable hepatitis b surface antigen (hbsag) and s gene premature stop codon was inconsistent with other studies. investigations on yield truncated hbsag are suggested to determine if they can affect elisa hbsag results. background: we have previously reported on a premature stop codon in hepatitis b virus (hbv) s gene among iranian patients. this mutation may cause undetectable hbv by conventional elisa methods. objectives: in this study, we aimed to determine the presence of premature stop codon in hbv s gene from middle eastern countries with predominant hbv genotype d, subtype ayw2. materials and methods: submitted hbv sequences to ncbi genome database from middle eastern countries (iran, iraq, turkey, pakistan, afghanistan, united arab emirates (uae) and yemen) were retrieved. the s genes of submitted hbv sequences were analyzed by the bioedit software to evaluate the genotype and premature stop codon in the s gene. results: premature stop codon in the s gene was observed for all countries with appropriate sequences for analysis. the frequency of mutant strains to total evaluated sequences was 17/711, 1/2, 4/110 and 1/30 for iran, iraq, turkey and yemen, respectively. in other countries (pakistan, afghanistan and uae), there were no submitted sequences or the submitted sequences were inappropriate for analysis. moreover, this mutation in the s gene of hbv was derived from 2 blood donors.
منابع مشابه
A global investigation of gene deletion strains that affect premature stop codon bypass in yeast, Saccharomyces cerevisiae.
Protein biosynthesis is an orderly process that requires a balance between rate and accuracy. To produce a functional product, the fidelity of this process has to be maintained from start to finish. In order to systematically identify genes that affect stop codon bypass, three expression plasmids, pUKC817, pUKC818 and pUKC819, were integrated into the yeast non-essential loss-of-function gene a...
متن کاملA hereditary bleeding disorder resulting from a premature stop codon in thrombomodulin (p.Cys537Stop).
In this study, we describe a novel thrombomodulin (TM) mutation (c.1611C>A) that codes for a change from cysteine 537 to a premature stop codon (p.Cys537Stop). Three members of a family with a history of posttraumatic bleeding were identified to be heterozygous for this TM mutation. All coagulation screening tests, coagulation factor assays, and platelet function test results were within normal...
متن کاملPresence of HBV S-gene mutants in immunocompromised patients.
Hepatitis B virus (HBV) is responsible for a serious, potentially fatal disease that affects approximately two billion people worldwide. Although an extended HBV immunization program has run since 1991, representing the most effective preventive measure possible, leading to a dramatic reduction of HBV hepatitis incidence, 4.5 million new HBV infections still occur every year. In 1988 the emerge...
متن کاملMolecular Characterization of HBV Strains Circulating among the Treatment-Naive HIV/HBV Co-Infected Patients of Eastern India
Previously we reported that the exposure to hepatitis B virus (HBV) infection serves as a major threat among the treatment naive HIV infected population of eastern India. Hence, molecular characterization of these strains is of utmost importance in order to identify clinically significant HBV mutations. A total of 85 treatment naive HIV/HBV co-infected participants were included of whom the com...
متن کاملFamilial apolipoprotein E deficiency and type Ill hyperlipoproteinemia due to a premature stop codon in the apolipoprotein E gene
A kindred with apolipoprotein E deficiency and a truncated lower molecular weight apoE mutant, designated a p 0 E 3 ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ , has been identified. Gel electrophoresis demonstrated complete absence of the normal apoE isoproteins and the presence of a small quantity of a lower molecular weight apoE. Plasma apoE levels in the proband were approximately 4% of normal. This marked deficie...
متن کاملFamilial apolipoprotein E deficiency and type III hyperlipoproteinemia due to a premature stop codon in the apolipoprotein E gene.
A kindred with apolipoprotein E deficiency and a truncated lower molecular weight apoE mutant, designated apoE-3Washington, has been identified. Gel electrophoresis demonstrated complete absence of the normal apoE isoproteins and the presence of a small quantity of a lower molecular weight apoE. Plasma apoE levels in the proband were approximately 4% of normal. This marked deficiency of apoE re...
متن کاملمنابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
archives of clinical infectious diseasesجلد ۸، شماره ۱، صفحات ۳-۷
کلمات کلیدی
میزبانی شده توسط پلتفرم ابری doprax.com
copyright © 2015-2023