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Genetic Diversity of Merozoite Surface Protein 2 (MSP2) Plasmodium falciparum Clinical Isolate in Wamena General Hospital

JURNAL BIOLOGI PAPUA · Vol. 12 No. 2 (2020) · pp. 123–132

DOI
10.31957/jbp.1319
ISSN
2503-0450, 2086-3314
Published
2020-09-30
Publisher
Jurusan Biologi FMIPA Universitas Cenderawasih
Language
eng

Abstract

The genetic diversity of typical clinical isolated Plasmodium falciparum in the malaria population varies greatly, especially at the location where malaria disease were recorded at high incidence rate. MSP2 is known as glycoprotein expressed on the surface of merozoites, which is an antigenic protein and has a potential to act as vaccine candidate for malaria. The MSP2 gene has two main allelic groups called FC27 and 3D7/IC. Block 3 from MSP2 gene is the most polymorphic to describe the diversity of parasite populations. The P. falciparum parasite population is often characterized by wide genetic diversity in areas of high transmission intensity. Therefore, the study on P. falciparum diversity is useful to describe the level of malaria transmission. The study of genetic diversity focused on clinical isolated species at Wamena General Hospital was aimed to determine the presence of the MSP2 gene, variety of MSP2 gene allele and the dominant frequency of the MSP2 gene allele. This research has been carried out from March 2018 to February 2019 using a cross sectional approach. The research sample was taken and prepared from Wamena Regional Hospital and followed by the analyzing of DNA isolation, PCR, electrophoresis of the research samples was done at the genetic science laboratory in Jakarta, Indonesia. The samples studied were patients who met the inclusion criteria, namely a single P. falciparum infection with an asexual parasite density >1000 parasites/µl or >3+ (1-10 P/Lp), and were agreed to become respondents by signing an informed consent. A total of 26 clinical isolates of P. falciparum were isolated with the MSP2 gene distribution on the FC27 allele with the highest as many as 25 samples (96.2%), 22 samples (84.6%) of the 3D7 / IC allele while the mixture of the two alleles was 22 samples (84.6%). From a total of 26 samples, there were samples with the male gender category counted for 77.3% and female 41%. The results of the identification of clinical isolated P. falciparum at Wamena Hospital with a total of 26 samples were found in productive age, between 15-34 years with a single allele (95.8%), while 23 cases and mix (both alleles 87.5%) about 21 cases, meanwhile in cases of before-productive age, in which ages were 12 and 14 years of age with a single allele 100% (FC27) 2 cases and 50% (3D7/IC) found to be 1 case, The mixture of the two alleles is 50% was only 1 case and there was no sample at non-productive age observed. Key words: Malaria; MSP-2; P. falciparum; Wamena

Collaboration network of the authors

40 authors · 124 co-authorship links · showing the 40 most connected

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Co-authorOrganisationJoint articles
Suharno SuharnoAffiliation unknown11
Hendra K. MauryAffiliation unknown5
Daniel LantangAffiliation unknown5
Supeni SufaatiAffiliation unknown4
Daniel Z. K. WambrauwAffiliation unknown4
Kalvin PaikiAffiliation unknown3
Tri GunaediAffiliation unknown3
Lisye I. ZebuaAffiliation unknown3
Yulindra M. NumberiAffiliation unknown3
Henderina J. KeiluhuAffiliation unknown3
Suwito SuwitoAffiliation unknown2
Mesak KamareaAffiliation unknown2
Maklon WarpurAffiliation unknown2
Imam MishbachAffiliation unknown2
Irma RahayuAffiliation unknown2
Farmawaty FarmawatyAffiliation unknown2
Wigati YektiningtyasAffiliation unknown2
Efray WanimboAffiliation unknown2
Marcelino N. YonasAffiliation unknown2
Leonard SiregarAffiliation unknown2
Ervina IndrayaniAffiliation unknown2
John D. KalorAffiliation unknown2
Korinus RejauwAffiliation unknown2
Rini S. KelanitAffiliation unknown1
Dewi SulistiowatiAffiliation unknown1
Eva S. SimaremareAffiliation unknown1
Agustina RubanAffiliation unknown1
Alum TurnipAffiliation unknown1
Agnes KabelenAffiliation unknown1
Alfred AntohAffiliation unknown1
Erni UnenorAffiliation unknown1
Verena AgustiniAffiliation unknown1
Nurtanti HAndonoAffiliation unknown1
Sulistianingsih SulistianingsihAffiliation unknown1

Affiliations come from OpenAlex; journal OAI-PMH metadata carries none. Authors without an OpenAlex ID are matched by name, which can merge or split people.

Metadata source: OAI-PMH (metadata jurnal) https://ejournal.uncen.ac.id/index.php/JBP/oai, first harvested 1 Nov 2026, last seen 1 Nov 2026.
Original metadata (oai_dc)
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	<dc:title xml:lang="en-US">Genetic Diversity of Merozoite Surface Protein 2 (MSP2) Plasmodium falciparum Clinical Isolate in Wamena General Hospital</dc:title>
	<dc:creator>Runtuboi, Dirk Y.P.</dc:creator>
	<dc:creator>Tanjung, Rosye H.R.</dc:creator>
	<dc:creator>Sarungu, Yulius</dc:creator>
	<dc:creator>Imbiri, Meidy J.</dc:creator>
	<dc:creator>Resmol, Irma A.</dc:creator>
	<dc:creator>Suyono, Ign. Joko</dc:creator>
	<dc:description xml:lang="en-US">The genetic diversity of typical clinical isolated Plasmodium falciparum in the malaria population varies greatly, especially at the location where malaria disease were recorded at high incidence rate. MSP2 is known as glycoprotein expressed on the surface of merozoites, which is an antigenic protein and has a potential to act as vaccine candidate for malaria. The MSP2 gene has two main allelic groups called FC27 and 3D7/IC. Block 3 from MSP2 gene is the most polymorphic to describe the diversity of parasite populations. The P. falciparum parasite population is often characterized by wide genetic diversity in areas of high transmission intensity. Therefore, the study on P. falciparum diversity is useful to describe the level of malaria transmission. The study of genetic diversity focused on clinical isolated species at Wamena General Hospital was aimed to determine the presence of the MSP2 gene, variety of MSP2 gene allele  and the dominant frequency of the MSP2 gene allele. This research has been carried out from March 2018 to February 2019 using a cross sectional approach. The research sample was taken and prepared from Wamena Regional Hospital and followed by the analyzing of DNA isolation, PCR, electrophoresis of the research samples was done at the genetic science laboratory in Jakarta, Indonesia. The samples studied were patients who met the inclusion criteria, namely a single P. falciparum infection with an asexual parasite density &amp;gt;1000 parasites/µl or &amp;gt;3+ (1-10 P/Lp), and were agreed to become respondents by signing an informed consent. A total of 26 clinical isolates of P. falciparum were isolated with the MSP2 gene distribution on the FC27 allele with the highest as many as 25 samples (96.2%), 22 samples (84.6%) of the 3D7 / IC allele while the mixture of the two alleles was 22 samples (84.6%). From a total of 26 samples, there were samples with the male gender category counted for 77.3% and female 41%. The results of the identification of clinical isolated P. falciparum at Wamena Hospital with a total of 26 samples were found in productive age, between 15-34 years with a single allele (95.8%), while 23 cases and mix (both alleles 87.5%) about 21 cases, meanwhile in cases of before-productive age, in which ages were 12 and 14 years of age with a single allele 100% (FC27) 2 cases and 50% (3D7/IC) found to be 1 case, The mixture of the two alleles is 50% was only 1 case and there was no sample at non-productive age observed. Key words: Malaria; MSP-2; P. falciparum; Wamena</dc:description>
	<dc:publisher xml:lang="en-US">Jurusan Biologi FMIPA Universitas Cenderawasih</dc:publisher>
	<dc:date>2020-09-30</dc:date>
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	<dc:identifier>https://ejournal.uncen.ac.id/index.php/JBP/article/view/1319</dc:identifier>
	<dc:identifier>10.31957/jbp.1319</dc:identifier>
	<dc:source xml:lang="en-US">JURNAL BIOLOGI PAPUA; Vol. 12 No. 2 (2020); 123-132</dc:source>
	<dc:source xml:lang="id-ID">Jurnal Biologi Papua; Vol 12 No 2 (2020); 123-132</dc:source>
	<dc:source>2503-0450</dc:source>
	<dc:source>2086-3314</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://ejournal.uncen.ac.id/index.php/JBP/article/view/1319/1069</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2020 JURNAL BIOLOGI PAPUA</dc:rights>
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