Merozoite surface protein-3α is a reliable marker for population genetic analysis of <it>Plasmodium vivax</it>

<p>Abstract</p> <p>Background</p> <p>The knowledge on population structure of the parasite isolates has contributed greatly to understanding the dynamics of the disease transmission for designing and evaluating malaria vaccines as well as for drug applications. <it&g...

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Main Authors: Zakeri Sedigheh, Barjesteh Hesam, Djadid Navid D
Format: Article
Language:English
Published: BMC 2006-07-01
Series:Malaria Journal
Online Access:http://www.malariajournal.com/content/5/1/53
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spelling doaj-a04c70e1fb1a4cc4becec956280e503d2020-11-25T00:05:20ZengBMCMalaria Journal1475-28752006-07-01515310.1186/1475-2875-5-53Merozoite surface protein-3α is a reliable marker for population genetic analysis of <it>Plasmodium vivax</it>Zakeri SedighehBarjesteh HesamDjadid Navid D<p>Abstract</p> <p>Background</p> <p>The knowledge on population structure of the parasite isolates has contributed greatly to understanding the dynamics of the disease transmission for designing and evaluating malaria vaccines as well as for drug applications. <it>msp-1 </it>and <it>msp-3α </it>genes have been used as a genetic marker in population studies of <it>Plasmodium vivax </it>isolates. In this study, <it>msp-3α </it>was compared and assessed with <it>msp-1 </it>marker in order to find whether <it>msp-3α </it>is a reliable genetic marker for <it>P. vivax </it>population studies.</p> <p>Methods</p> <p>This comparative study was designed and carried out as the first assessment of diversity in <it>Pvmsp-3α </it>gene by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) in the 50 northern and 94 southern <it>P. vivax </it>isolates from Iran, which had been analysed before for <it>msp-1 </it>gene.</p> <p>Results</p> <p>Three allele size as, Type A (1.8 kb), Type B (1.5 kb) and Type C (1.2 kb) have been detected among both northern and southern isolates based on PCR results. Type C (70%) and Type A (68.7%) were the predominant fragments among northern and southern parasites, respectively. 99 distinct <it>Pvmsp</it>-3α fragments defined by the size were detected in the 94 southern samples by PCR analysis. However, no mixed genotype infections have been detected among northern isolates. Based on restriction pattern from digestion with <it>Hha I </it>and <it>Alu I </it>12 and 49 distinct allelic variants have been detected among 50 northern and 94 southern isolates. However, based <it>on msp-1 </it>gene, 30 distinct variants identified in all 146-sequenced Iranian <it>P. vivax </it>isolate.</p> <p>Conclusion</p> <p>The results suggested that PCR-RFLP on <it>msp-3α </it>gene is an adequate, applicable and easily used technique for molecular epidemiology studies of <it>P. vivax </it>isolates without the need for further sequencing analysis.</p> http://www.malariajournal.com/content/5/1/53
collection DOAJ
language English
format Article
sources DOAJ
author Zakeri Sedigheh
Barjesteh Hesam
Djadid Navid D
spellingShingle Zakeri Sedigheh
Barjesteh Hesam
Djadid Navid D
Merozoite surface protein-3α is a reliable marker for population genetic analysis of <it>Plasmodium vivax</it>
Malaria Journal
author_facet Zakeri Sedigheh
Barjesteh Hesam
Djadid Navid D
author_sort Zakeri Sedigheh
title Merozoite surface protein-3α is a reliable marker for population genetic analysis of <it>Plasmodium vivax</it>
title_short Merozoite surface protein-3α is a reliable marker for population genetic analysis of <it>Plasmodium vivax</it>
title_full Merozoite surface protein-3α is a reliable marker for population genetic analysis of <it>Plasmodium vivax</it>
title_fullStr Merozoite surface protein-3α is a reliable marker for population genetic analysis of <it>Plasmodium vivax</it>
title_full_unstemmed Merozoite surface protein-3α is a reliable marker for population genetic analysis of <it>Plasmodium vivax</it>
title_sort merozoite surface protein-3α is a reliable marker for population genetic analysis of <it>plasmodium vivax</it>
publisher BMC
series Malaria Journal
issn 1475-2875
publishDate 2006-07-01
description <p>Abstract</p> <p>Background</p> <p>The knowledge on population structure of the parasite isolates has contributed greatly to understanding the dynamics of the disease transmission for designing and evaluating malaria vaccines as well as for drug applications. <it>msp-1 </it>and <it>msp-3α </it>genes have been used as a genetic marker in population studies of <it>Plasmodium vivax </it>isolates. In this study, <it>msp-3α </it>was compared and assessed with <it>msp-1 </it>marker in order to find whether <it>msp-3α </it>is a reliable genetic marker for <it>P. vivax </it>population studies.</p> <p>Methods</p> <p>This comparative study was designed and carried out as the first assessment of diversity in <it>Pvmsp-3α </it>gene by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) in the 50 northern and 94 southern <it>P. vivax </it>isolates from Iran, which had been analysed before for <it>msp-1 </it>gene.</p> <p>Results</p> <p>Three allele size as, Type A (1.8 kb), Type B (1.5 kb) and Type C (1.2 kb) have been detected among both northern and southern isolates based on PCR results. Type C (70%) and Type A (68.7%) were the predominant fragments among northern and southern parasites, respectively. 99 distinct <it>Pvmsp</it>-3α fragments defined by the size were detected in the 94 southern samples by PCR analysis. However, no mixed genotype infections have been detected among northern isolates. Based on restriction pattern from digestion with <it>Hha I </it>and <it>Alu I </it>12 and 49 distinct allelic variants have been detected among 50 northern and 94 southern isolates. However, based <it>on msp-1 </it>gene, 30 distinct variants identified in all 146-sequenced Iranian <it>P. vivax </it>isolate.</p> <p>Conclusion</p> <p>The results suggested that PCR-RFLP on <it>msp-3α </it>gene is an adequate, applicable and easily used technique for molecular epidemiology studies of <it>P. vivax </it>isolates without the need for further sequencing analysis.</p>
url http://www.malariajournal.com/content/5/1/53
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