Genotyping and Phylogenetic Analysis of Circumsporozoite Protein () Gene of Clinical Isolates in South-Eastern Iran.

Soudabeh Etemadi, Mehdi Nateghpour, Afsaneh Motevalli Haghi, Hamid Eslami, Mehdi Mohebali, Neda Setayesh, Leila Farivar, Aref Teimouri
Author Information
  1. Soudabeh Etemadi: Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
  2. Mehdi Nateghpour: Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
  3. Afsaneh Motevalli Haghi: Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
  4. Hamid Eslami: Department of Medical Biotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
  5. Mehdi Mohebali: Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
  6. Neda Setayesh: Department of Pharmaceutical Biotechnology, School of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
  7. Leila Farivar: Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
  8. Aref Teimouri: Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

Abstract

BACKGROUND: Circumsporozoite protein (CSP) is one of the most important surface sporozoite antigens in malaria, recently considered as a candidate for vaccination. Considering the importance of CSP, this study was conducted to investigate the polymorphism and genetic diversity of Circumsporozoite Protein () in the southeastern region of Iran during 2015-2016.
METHODS: To investigate polymorphism and genetic diversity, 20 blood samples were collected from patients with , then DNA was extracted and amplified using partial sequence of CSP gene. Polymerase chain reaction (PCR) products were sequenced and compared to sequences from genomic databases using BLAST. Genetic evaluation and phylogenic analysis were performed using MEGA7 and DnaSP5 software's on 38 sequences include 20 sequences of our study and 18 sequences of Gene Bank.
RESULTS: Eleven isolates were VK210 genotype and 9 isolates contained VK247. The result of variable segregation nucleotide site indicated that the differentiation of sequences in CSP were 25.67% in our 20 samples which are less than the 38 samples with a value of 26.67%. Comparing the ratio of dN/dS regions in the CSP gene indicates that the CSP varies more synonymously and amino acid has lower variation. Out of 38 samples, 35 unique haplotypes were identified based on 1042 nucleotide sequences in CSP, showing a variation percentage of 99.4%.
CONCLUSION: The Tajima D analyses showed that CSP gene in had a positive number in the total analyzed sequences, which means that the mutations are in order to select positive evolution.

Keywords

References

  1. J Mol Evol. 1980 Dec;16(2):111-20 [PMID: 7463489]
  2. Mol Biochem Parasitol. 1994 Nov;68(1):45-52 [PMID: 7891747]
  3. Mol Biol Evol. 1987 Jul;4(4):406-25 [PMID: 3447015]
  4. Bioinformation. 2011;6(8):320-3 [PMID: 21769195]
  5. Bull World Health Organ. 1975;52(1):21-32 [PMID: 764993]
  6. Mol Biochem Parasitol. 1993 Jan;57(1):177-80 [PMID: 8426613]
  7. Malar J. 2005 Apr 27;4:20 [PMID: 15854233]
  8. Trends Parasitol. 2008 Aug;24(8):333-6 [PMID: 18603475]
  9. Asian Pac J Trop Med. 2011 Dec;4(12):931-6 [PMID: 22118026]
  10. Trans R Soc Trop Med Hyg. 2000 Jul-Aug;94(4):377-81 [PMID: 11127238]
  11. Int J Parasitol. 2010 Sep;40(11):1229-35 [PMID: 20621627]
  12. Gene. 2013 Apr 15;518(2):381-7 [PMID: 23333606]
  13. Cell. 1992 Sep 18;70(6):1021-33 [PMID: 1326407]
  14. Trop Med Int Health. 2006 May;11(5):729-37 [PMID: 16640626]
  15. Malar J. 2016 Feb 24;15:117 [PMID: 26911803]
  16. Am J Trop Med Hyg. 2011 Feb;84(2 Suppl):51-7 [PMID: 21292878]
  17. Mem Inst Oswaldo Cruz. 2011 Aug;106 Suppl 1:12-26 [PMID: 21881753]
  18. Infect Genet Evol. 2010 Mar;10(2):298-303 [PMID: 20097310]
  19. Proc Natl Acad Sci U S A. 2005 Oct 25;102(43):15523-8 [PMID: 16227436]
  20. Cell. 2007 Nov 2;131(3):492-504 [PMID: 17981117]
  21. Exp Parasitol. 2001 Jul;98(3):152-61 [PMID: 11527438]
  22. J Exp Med. 2011 Feb 14;208(2):341-56 [PMID: 21262960]
  23. J Infect Dis. 2009 Nov 1;200(9):1465-9 [PMID: 19803728]
  24. J Mol Evol. 2004 Oct;59(4):528-35 [PMID: 15638464]
  25. Evolution. 1985 Jul;39(4):783-791 [PMID: 28561359]
  26. Int J Prev Med. 2013 Jan;4(1):88-94 [PMID: 23413116]
  27. Mol Biol Evol. 2016 Jul;33(7):1870-4 [PMID: 27004904]

Word Cloud

Created with Highcharts 10.0.0CSPsequencesCircumsporozoitesamplesIran20usinggene38proteinstudyinvestigatepolymorphismgeneticdiversityProteinanalysisGeneisolatesnucleotide67%variationpositiveGenotypingPhylogeneticBACKGROUND:oneimportantsurfacesporozoiteantigensmalariarecentlyconsideredcandidatevaccinationConsideringimportanceconductedsoutheasternregion2015-2016METHODS:bloodcollectedpatientsDNAextractedamplifiedpartialsequencePolymerasechainreactionPCRproductssequencedcomparedgenomicdatabasesBLASTGeneticevaluationphylogenicperformedMEGA7DnaSP5software'sinclude18BankRESULTS:ElevenVK210genotype9containedVK247resultvariablesegregationsiteindicateddifferentiation25lessvalue26ComparingratiodN/dSregionsindicatesvariessynonymouslyaminoacidlower35uniquehaplotypesidentifiedbased1042showingpercentage994%CONCLUSION:TajimaDanalysesshowednumbertotalanalyzedmeansmutationsorderselectevolutionAnalysisClinicalIsolatesSouth-EasternPlasmodiumvivax

Similar Articles

Cited By