Publication:
Plasmodium vivax rhomboid-like protease 1 gene diversity in Thailand

dc.contributor.authorTouchchapol Mataradchakulen_US
dc.contributor.authorChairat Uthaipibullen_US
dc.contributor.authorFrancois Nostenen_US
dc.contributor.authorJoel Vega-Rodriguezen_US
dc.contributor.authorMarcelo Jacobs-Lorenaen_US
dc.contributor.authorUsa Lek-Uthaien_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.contributor.otherNuffield Department of Clinical Medicineen_US
dc.contributor.otherJohns Hopkins Bloomberg School of Public Healthen_US
dc.date.accessioned2018-12-21T07:52:53Z
dc.date.accessioned2019-03-14T08:03:44Z
dc.date.available2018-12-21T07:52:53Z
dc.date.available2019-03-14T08:03:44Z
dc.date.issued2017-10-01en_US
dc.description.abstract© 2017 Mahidol University Background Plasmodium vivax infection remains a major public health problem, especially along the Thailand border regions. We examined the genetic diversity of this parasite by analyzing single-nucleotide polymorphisms (SNPs) of the P. vivax rhomboid-like protease 1 gene (Pvrom1) in parasites collected from western (Tak province, Thai-Myanmar border) and eastern (Chanthaburi province, Thai-Cambodia border) regions. Methods Data were collected by a cross-sectional survey, consisting of 47 and 45 P. vivax-infected filter paper-spotted blood samples from the western and eastern regions of Thailand, respectively during September 2013 to May 2014. Extracted DNA was examined for presence of P. vivax using Plasmodium species-specific nested PCR. Pvrom1 gene was PCR amplified, sequenced and the SNP diversity was analyzed using F-STAT, DnaSP, MEGA and LIAN programs. Results Comparison of sequences of the 92 Pvrom1 831-base open reading frames with that of a reference sequence (GenBank acc. no. XM001615211) revealed 17 samples with a total of 8 polymorphic sites, consisting of singleton (exon 3, nt 645) and parsimony informative (exon 1, nt 22 and 39; exon 3, nt 336, 537 and 656; and exon 4, nt 719 and 748) sites, which resulted in six different deduced Pvrom1 variants. Non-synonymous to synonymous substitutions ratio estimated by the DnaSP program was 1.65 indicating positive selection, but the Z-tests of selection showed no significant deviations from neutrality for Pvrom1 samples from western region of Thailand. In addition McDonald Kreitman test (MK) showed not significant, and Fst values are not different between the two regions and the regions combined. Interestingly, only Pvrom1 exon 2 was the most conserved sequences among the four exons. Conclusions The relatively high degree of Pvrom1 polymorphism suggests that the protein is important for parasite survival in face of changes in both insect vector and human populations. These polymorphisms could serve as a sensitive marker for studying plasmodial genetic diversity. The significance of Pvrom1 conserved exon 2 sequence remains to be investigated.en_US
dc.identifier.citationExperimental Parasitology. Vol.181, (2017), 1-6en_US
dc.identifier.doi10.1016/j.exppara.2017.06.007en_US
dc.identifier.issn10902449en_US
dc.identifier.issn00144894en_US
dc.identifier.other2-s2.0-85024371982en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/42705
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85024371982&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.titlePlasmodium vivax rhomboid-like protease 1 gene diversity in Thailanden_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85024371982&origin=inwarden_US

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