DOI QR코드

DOI QR Code

Surveillance on the Vivax Malaria in Endemic Areas in the Republic of Korea Based on Molecular and Serological Analyses

  • Lee, Seong-Kyun (Department of Medical Environmental Biology and Tropical Medicine, School of Medicine, Kangwon National University) ;
  • Hu, Fengyue (Department of Pathogenic Biology, School of Medicine, Yangzhou University) ;
  • Firdaus, Egy Rahman (Department of Medical Environmental Biology and Tropical Medicine, School of Medicine, Kangwon National University) ;
  • Park, Ji-Hoon (Department of Medical Environmental Biology and Tropical Medicine, School of Medicine, Kangwon National University) ;
  • Han, Jin-Hee (Department of Medical Environmental Biology and Tropical Medicine, School of Medicine, Kangwon National University) ;
  • Lee, Sang-Eun (Division of Vectors and Parasitic Diseases, Bureau of Infectious Disease Diagnosis Control, Korea Disease Control and Prevention Agency) ;
  • Shin, Hyun-Il (Division of Vectors and Parasitic Diseases, Bureau of Infectious Disease Diagnosis Control, Korea Disease Control and Prevention Agency) ;
  • Cho, Shin Hyeong (Division of Vectors and Parasitic Diseases, Bureau of Infectious Disease Diagnosis Control, Korea Disease Control and Prevention Agency) ;
  • Park, Won Sun (Department of Physiology, School of Medicine, Kangwon National University) ;
  • Lu, Feng (Department of Pathogenic Biology, School of Medicine, Yangzhou University) ;
  • Han, Eun-Taek (Department of Medical Environmental Biology and Tropical Medicine, School of Medicine, Kangwon National University)
  • Received : 2020.06.18
  • Accepted : 2020.11.02
  • Published : 2020.12.31

Abstract

Plasmodium vivax reemerged in 1993. It has been sustained for more than 25 years and become one of the important indigenous parasitic diseases in northern and western parts of the Republic of Korea near the demilitarized zone. In particular, relapse is a significant concern for the control of malaria, as short- and long-term incubation periods vary among those infected in Korea. In this study, the prevalence of asymptomatic carriers was examined among residents of high endemic areas of vivax malaria during nonseasonal transmission of mosquitoes. Blood samples from 3 endemic regions in northwestern Korea were evaluated by microscopic examination, rapid diagnostic testing, and nested PCR to identify asymptomatic patients carrying malaria parasites in the community. However, no positive malaria case among residents of endemic areas was detected. Additionally, serological analysis was carried out to measure antibodies against 3 antigenic recombinant proteins of P. vivax, merozoite surface protein 1-19, circumsporozoite surface protein-VK210, and liver-stage antigen (PvLSA-N), by the protein array method. Interestingly, seropositivity of sera between previous exposure and samples without exposure to malaria was significantly higher using the PvLSA-N antigen than the other antigens, suggesting that PvLSA-N can be used as a serological marker to analyze the degree of exposure for malaria transmission in endemic areas. This indicates a very low asymptomatic carrier prevalence during the nonmalaria season in the endemic areas of Korea.

Keywords

References

  1. Mendis K, Sina BJ, Marchesini P, Carter R: The neglected burden of Plasmodium vivax malaria. Am J Trop Med Hyg 2001; 64 (suppl): 97-106. https://doi.org/10.4269/ajtmh.2001.64.97
  2. Chai JY. Re-emerging Plasmodium vivax malaria in the Republic of Korea. Korean J Parasitol 1999; 37: 129-143. https://doi.org/10.3347/kjp.1999.37.3.129
  3. Sturrock HJ, Hsiang MS, Cohen JM, Smith DL, Greenhouse B, Bousema T, Gosling RD. Targeting asymptomatic malaria infections: active surveillance in control and elimination. PLoS Med 2013; 10: e1001467. https://doi.org/10.1371/journal.pmed.1001467
  4. White NJ. Determinants of relapse periodicity in Plasmodium vivax malaria. Malar J 2011; 10: 297. https://doi.org/10.1186/1475-2875-10-297
  5. Warhurst DC, Williams JE. ACP Broadsheet no 148. July 1996. Laboratory diagnosis of malaria. J Clin Pathol 1996; 49: 533-538. https://doi.org/10.1136/jcp.49.7.533
  6. Kain KC, Harrington MA, Tennyson S, Keystone JS. Imported malaria: prospective analysis of problems in diagnosis and management. Clin Infect Dis 1998; 27: 142-149. https://doi.org/10.1086/514616
  7. Komaki-Yasuda K, Vincent JP, Nakatsu M, Kato Y, Ohmagari N, Kano S. A novel PCR-based system for the detection of four species of human malaria parasites and Plasmodium knowlesi. PLoS One 2018; 13: e0191886. https://doi.org/10.1371/journal.pone.0191886
  8. Nyunt MH, Soe TN, Shein T, Zaw NN, Han SS, Muh F, Lee SK, Han JH, Park JH, Ha KS, Park WS, Hong SH, Kyaw MP, Han ET. Estimation on local transmission of malaria by serological approach under low transmission setting in Myanmar. Malar J 2018; 17: 6. https://doi.org/10.1186/s12936-017-2170-8
  9. Nyunt MH, Kyaw MP, Thant KZ, Shein T, Han SS, Zaw NN, Han JH, Lee SK, Muh F, Kim JY, Cho SH, Lee SE, Yang EJ, Chang CL, Han ET. Effective high-throughput blood pooling strategy before DNA extraction for detection of malaria in low-transmission settings. Korean J Parasitol 2016; 54: 253-259. https://doi.org/10.3347/kjp.2016.54.3.253
  10. Ndao M, Bandyayera E, Kokoskin E, Gyorkos TW, MacLean JD, Ward BJ. Comparison of blood smear, antigen detection, and nested-PCR methods for screening refugees from regions where malaria is endemic after a malaria outbreak in Quebec, Canada. J Clin Microbiol 2004; 42: 2694-2700. https://doi.org/10.1128/JCM.42.6.2694-2700.2004
  11. Tsuboi T, Takeo S, Iriko H, Jin L, Tsuchimochi M, Matsuda S, Han ET, Otsuki H, Kaneko O, Sattabongkot J, Udomsangpetch R, Sawasaki T, Torii M, Endo Y. Wheat germ cell-free systembased production of malaria proteins for discovery of novel vaccine candidates. Infect Immun 2008; 76: 1702-1708. https://doi.org/10.1128/IAI.01539-07
  12. Chen JH, Jung JW, Wang Y, Ha KS, Lu F, Lim CS, Takeo S, Tsuboi T, Han ET. Immunoproteomics profiling of blood stage Plasmodium vivax infection by high-throughput screening assays. J Proteome Res 2010; 9: 6479-6489. https://doi.org/10.1021/pr100705g
  13. Hassanpour G, Mohebali M, Zeraati H, Raeisi A, Keshavarz H. Asymptomatic malaria and its challenges in the malaria elimination program in Iran: a systematic review. J Arthropod Borne Dis 2017; 11: 172-181.
  14. Zhao Y, Zeng J, Liu Q, He Y, Zhang J, Yang Z, Fan Q, Wang Q, Cui L, Cao Y. Risk factors for asymptomatic malaria infections from seasonal cross-sectional surveys along the China-Myanmar border. Malar J 2018; 17: 247. https://doi.org/10.1186/s12936-018-2398-y
  15. Wang B, Han SS, Cho C, Han JH, Cheng Y, Lee SK, Galappaththy GN, Thimasarn K, Soe MT, Oo HW, Kyaw MP, Han ET. Comparison of microscopy, nested-PCR, and Real-Time-PCR assays using high-throughput screening of pooled samples for diagnosis of malaria in asymptomatic carriers from areas of endemicity in Myanmar. J Clin Microbiol 2014; 52: 1838-1845. https://doi.org/10.1128/JCM.03615-13
  16. Yin J, Li M, Yan H, Zhou S. Considerations on PCR-based methods for malaria diagnosis in China malaria diagnosis reference laboratory network. Biosci Trends 2018; 12: 510-514. https://doi.org/10.5582/bst.2018.01198
  17. Cassiano GC, Furini AA, Capobianco MP, Storti-Melo LM, Almeida ME, Barbosa DR, Póvoa MM, Nogueira PA, Machado RL. Immunogenetic markers associated with a naturally acquired humoral immune response against an N-terminal antigen of Plasmodium vivax merozoite surface protein 1 (PvMSP-1). Malar J 2016; 15: 306. https://doi.org/10.1186/s12936-016-1350-2
  18. Baum E, Sattabongkot J, Sirichaisinthop J, Kiattibutr K, Jain A, Taghavian O, Lee MC, Huw Davies D, Cui L, Felgner PL, Yan G. Common asymptomatic and submicroscopic malaria infections in Western Thailand revealed in longitudinal molecular and serological studies: a challenge to malaria elimination. Malar J 2016; 15: 333. https://doi.org/10.1186/s12936-016-1393-4
  19. Chen E, Salinas ND, Huang Y, Ntumngia F, Plasencia MD, Gross ML, Adams JH, Tolia NH. Broadly neutralizing epitopes in the Plasmodium vivax vaccine candidate Duffy Binding Protein. Proc Natl Acad Sci USA 2016; 113: 6277-6282. https://doi.org/10.1073/pnas.1600488113
  20. Drakeley CJ, Corran PH, Coleman PG, Tongren JE, McDonald SL, Carneiro I, Malima R, Lusingu J, Manjurano A, Nkya WM, Lemnge MM, Cox J, Reyburn H, Riley EM. Estimating mediumand long-term trends in malaria transmission by using serological markers of malaria exposure. Proc Natl Acad Sci USA 2005; 102: 5108-5113. https://doi.org/10.1073/pnas.0408725102
  21. Branch OH, Udhayakumar V, Hightower AW, Oloo AJ, Hawley WA, Nahlen BL, Bloland PB, Kaslow DC, Lal AA. A longitudinal investigation of IgG and IgM antibody responses to the merozoite surface protein-1 19-kiloDalton domain of Plasmodium falciparum in pregnant women and infants: associations with febrile illness, parasitemia, and anemia. Am J Trop Med Hyg 1998; 58: 211-219. https://doi.org/10.4269/ajtmh.1998.58.211
  22. Teo A, Feng G, Brown GV, Beeson JG, Rogerson SJ. Functional antibodies and protection against blood-stage malaria. Trends Parasitol 2016; 32: 887-898. https://doi.org/10.1016/j.pt.2016.07.003
  23. Arnot DE, Barnwell JW, Tam JP, Nussenzweig V, Nussenzweig RS, Enea V. Circumsporozoite protein of Plasmodium vivax: gene cloning and characterization of the immunodominant epitope. Science 1985; 230: 815-818. https://doi.org/10.1126/science.2414847

Cited by

  1. Recent Spatial and Temporal Trends of Malaria in Korea vol.59, pp.6, 2020, https://doi.org/10.3347/kjp.2021.59.6.585