Perubahan Profil Proteomik Plasmodium falciparum Galur Papua 2300 Akibat Paparan Antimalaria Artemisinin In Vitro
DOI:
https://doi.org/10.21776/ub.jkb.2016.029.01.10Keywords:
artemisinin, Plasmodium falciparum galur Papua 2300, proteomic, resistensiAbstract
Perkembangan resistensi Plasmodium falciparum dan penurunan kepekaan parasit terhadap obat antimalaria artemisinin menjadi salah satu permasalahan kesehatan di dunia. Sampai saat ini belum ada obat baru pengganti artemisinin. Penelitian ini bertujuan untuk membuktikan bahwa paparan obat antimalaria artemisinin berulang in vitro dapat menyebabkan perubahan profil protein melalui pendekatan proteomik P. falciparum galur Papua 2300. Waktu penelitian dilaksanakan mulai bulan Pebruari sampai dengan Nopember 2014. Tempat penelitian di Laboratorium Biomedik Fakultas Kedokteran Universitas Brawijaya, Fakultas Kedokteran Hewan Universitas Airlangga. Airlangga Influenza Research Center, Laboratorium bersama Kimia  Universitas Negeri Surabaya (UNESA) dan jurusan Kimia Politeknik Malang. Desain penelitian yang digunakan adalah Experimental Design dengan Post test only control group design. Kultur P. falciparum galur Papua 2300 dipapar antimalaria artemisinin berulang dengan menggunakan Inhibitory Concentration 50 (IC50). Pengamatan dilakukan terhadap profil protein dengan SDS Page 2 dimensi, FT- IR dan LCMS. Hasil penelitian menunjukkan ada variasi berat protein, spektrum infra merah (bilangan gelombang)  dan nilai massa molekul ion (m/z)  antara kelompok kontrol (K) dan kelompok perlakuan (PO1, PO2, Po3, PO4). Dapat disimpulkan bahwa paparan obat antimalaria artemisinin berulang secara  in vitro dapat mempengaruhi pola ekspresi protein Plasmodium falciparum galur Papua 2300.
Â
Downloads
References
World Health Organization. World Malaria Report 2009. Geneva, Switzerland: WHO Press; 2009.
Afonso A, Hunt P, Cheesman S, et al. Malaria Parasites Can Develop Stable Resistance to Artemisinin but Lack Mutations in Candidate Genes atp6 (Encoding the Sarcoplasmic and Endoplasmic Reticulum Ca2+ ATPase) tctp, mdr1, and cg10. Antimicrobial Agents and Chemotherapy. 2006; 50(2): 480-489.
Noedl H, Se Y, Schaecher K, et al. Evidence of Artemisinin Resistant Malaria in Western Cambodia. The New England Journal of Medicine. 2008; 359(24): 2619-2620.
Wongsrichanalai C and Meshnick SR. Declining Artesunat-Mefloquine Efficacy against Falciparum Malaria on Cambodia-Thailand Border. Emerging Infectious Diseases. 2008; 14(5): 716-719.
Maslachah L. Efek Paparan Artemisini Berulang terhadap Perkembangan Plasmodium falciparum Resisten In Vitro. [Disertasi]. Universitas Airlangga, Surabaya. 2013.
LaCrue AN, Scheel M, Kennedy K, Kumar N, and Kyle DE. Effect of Artesunat on Parasite Recrudescence and Dormancy in the Rodent Malaria Model Plasmodium Vinckei. PLoS One. 2011; 6(10): e26689.
Torrentino-Madamet MT, Almeras L, Desplans J, et al. Global Response of Plasmodium Falciparum to Hyperoxia: A Combined Transcriptomic and Proteomic Approach. Malaria Journal. 2011; 10(4): 1-15.
Silverstein RM, Webster FX, Kiemle DJ, and Bryce DL. Spectrometric Identification of Organic Compounds. 8th edition. Danvers; John Wiley & Sons Inc; 1998; 87.
Mok S, Imwong M, Mackinnon MJ, et al. Artemisinin Resistance in Plasmodium Falciparum is Associated with an Altered Temporal Pattern of Transcription. BMC Genomics. 2011; 12: 391-405.
Lodish H, Berk A, Zipursky LS, Matsudaira P, Baltimore D, and Darnell J. Molecular Cell Biology. 4th edition. New York: WH Freeman and Co; 2002; pp. 246-928.
Witkowski B, Lelievre J, Barragan MJ, et al. Increased Tolerance to Artemisinin in Plasmodium falciparum is Mediated by a Quiescence Mechanism. Antimicrobial Agents and Chemotherapy. 2010; 54(5): 1872-1877.
Veiga MI, Ferreira PE, Schmidt BA, et al. Antimalarial Exposure Delays Plasmodium Falciparum Intraerytrocytic Cycle and Drives Drug Transporter Genes Expression. Plos One. 2010; 5(8): e12408.
Deplaine G, Lavazec C, Bischoff E, et al. Artesunat Tolerance in Transgenic Plasmodium Falciparum Parasites Overexpressing a Tryptophan Rich Protein. Antimicrobial Agents and Chemotherapy. 2011; 55(6): 2576-2584.
Chavchich M, Gerena L, Peters J, Chen N, Cheng Q, and Kyle DE. Role of Pfmdr1 Amplification and Expression in Induction of Resistance to Artemisinin Derivatives in Plasmodium Falciparum. Antimicrobial Agents and Chemotherapy. 2010; 54(6): 2455–2464.
Chen N, Chavchich M, Peters JM, Kyle DE, Gatton ML, and Cheng Q. Deamplification of Pfmdr1-Containing Amplicon on Chromosome 5 in Plasmodium Falciparum is Associated with Reduced Resistance to Artelinic Acid in Vitro. Antimicrobial Agents and Chemotherapy. 2010; 54(8): 3395–3401.
Tao D, King JG, Tweedell RE, Josts PJ, Boddey JA, and Dinglasan RR. The Acute Transcriptomic and Proteomic Response of HC-04 Hepatoma Cell Tohepatocyte Growth Factor and its Implications for Plasmodium Falciparum Sporozoite Invasion. Molecular & Cellular Proteomics. 2014; 13(5): 1153-1164.
Siqueira-Batista R, Gomes AP, Mendonca EG, et al. Plasmodium falciparum Malaria: Proteomic Studies. The Revista Brasileira de Terapia Intensiva. 2012; 24(4): 394-400.
Madamet MT, Almeras L, Travaille C, et al. Proteomic Analysis Revealed Alterations of the Plasmodium Falciparum Metabolism Following Salicylhydroxamic Acid Exposure. Tropical Medicine. 2011; 2: 109-119.
Oehring SC, Woodcroft BJ, Moes S, et al. Organellar Proteomics Reveals Hundreds of Novel Nuclear Proteins in the Malaria Parasite Plasmodium Falciparum. Genome Biology. 2012; 13(11): R108-R129.
Downloads
Published
Issue
Section
License
Authors who publish with this journal agree to the following terms:- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).