Determinants of Malaria Re-emergence in Coastal and Island Elimination Settings: A PRISMA-Based Systematic Review

  • Rahmah RA AZ Master of Environmental Health, Faculty of Public Health, Diponegoro University, 50275, Prof. Soedarto Street No. 13, Semarang, Indonesia
  • Mursid Raharjo Master of Environmental Health, Faculty of Public Health, Diponegoro University, 50275, Prof. Soedarto Street No. 13, Semarang, Indonesia
  • Sulistiyani Master of Environmental Health, Faculty of Public Health, Diponegoro University, 50275, Prof. Soedarto Street No. 13, Semarang, Indonesia
Keywords: Malaria Re-Emergence, Coastal Areas, Island Settings, Surveillance, Systematic Review

Abstract

Introduction: Malaria elimination remains vulnerable in receptive coastal and island settings where ecological change, vector adaptation, human mobility, imported infections, surveillance gaps, and governance constraints may interact. This systematic review aimed to synthesize determinants of malaria re-emergence, resurgence, reintroduction, and re-establishment of local transmission in coastal and island elimination settings, with relevance to Indonesia and other tropical archipelagic regions.

Method: A systematic review was conducted following PRISMA 2020 guidelines. Literature was searched in Scopus, ScienceDirect, and PubMed for studies published from 2019 to 2025. Eligible studies addressed malaria re-emergence, elimination sustainability, ecological receptivity, vector or parasite factors, imported transmission, surveillance capacity, or governance issues in coastal, island, archipelagic, low-transmission, or elimination-related contexts. From 1,054 identified records, 30 studies met the inclusion criteria and were synthesized thematically.

Result: Malaria re-emergence in coastal and island elimination settings was not attributable to a single determinant. Ecological and climatic factors, including land-use change, wetland formation, coastal modification, rainfall variability, and rising temperature, may increase suitable habitats for Anopheles vectors. Vector behavioral adaptation, outdoor biting, altered resting behavior, and insecticide resistance may reduce the effectiveness of indoor-based interventions. Human mobility through migration, fishing, mining, tourism, port activity, and inter-island travel may facilitate parasite importation into receptive areas. Plasmodium vivax relapse, low-density infection, and asymptomatic carriage may further complicate case detection and classification. Surveillance weaknesses, limited molecular diagnostic capacity, delayed investigation, fragmented reporting, unstable financing, and weak intersectoral coordination may reduce elimination resilience.

Conclusion: Sustaining malaria elimination in coastal and island settings requires integrated, adaptive surveillance linking epidemiological, entomological, climatic, mobility, and laboratory data. Strengthening port-based surveillance, vector monitoring, molecular diagnostics, community participation, intersectoral coordination, and sustainable financing is essential to prevent reintroduction and local transmission re-establishment.

References

World Health Organization. Global messaging briefing kit World malaria report 2023 [Internet]. Geneva; World Health Organization. Available from: https://www.who.int/teams/global-malariaprogramme/reports/world-malaria-report-2023.

Morlighem C, Chaiban C, Georganos S, Brousse O. Spatial Optimization Methods for Malaria Risk Mapping in Sub-Saharan African Cities Using Demographic and Health Surveys GeoHealth. 2023 ; 7(10):1–15. https://doi.org/10.1029/2023GH000787

Arisco NJ, Peterka C, Diniz C. Ecological change increases malaria risk in the Brazilian Amazon. Proc Natl Acad Sci U S A. 2024;121(44):1–10. https://doi.org/10.1073/pnas.2409583121

He Q, Li Z, Daleo P, Lefcheck JS, Thomsen MS, Adams JB, et al. Coastal wetland resilience through local , regional and global conservation. Nat Rev Biodivers. 2025;1(1):50-67. https://doi.org/10.1038/s44358-024-00004-x

Guerra CA, Kang SY, Citron DT, Hergott DEB, Perry M, Smith J, et al. Human mobility patterns and malaria importation on Bioko Island. Nat Commun. 2019;10(1):2332. https://doi.org/10.1038/s41467-019-10339-1

Uate NR, Antó N, Vidane S, Augusto G. Dynamics in Malaria Transmission in the Cross-Border Areas of Mozambique , South Africa and Eswatini ( Mosaswa ), from March 2017 to March 2019. Cent Afr J Public Health. 2025;11(2):53–61. https://doi.org/10.11648/j.cajph.20251102.12

Perera R, Wickremasinghe R, Newby G, Caldera A, Fernando D. Review Article Malaria Control , Elimination, and Prevention as Components of Health Security : Am J Trop Med Hyg. 2022;107(4):747–53. https://doi.org/10.4269/ajtmh.22-0038

Hasyim H, Marini H, Misnaniarti M, Flora R, Liberty IA. Evaluation of the malaria elimination programme in Muara Enim Regency : a qualitative study from Indonesia. Malar J. 2024; 23 (1) : 43. https://doi.org/10.1186/s12936-024-04857-7

Chan CW, Kaneko A. Malaria control and elimination in Vanuatu and Papua New Guinea : Multidisciplinary and collaborative research with island communities, 1985 – 2024. Parasitol Int. 2025;109:103111. https://doi.org/10.1016/j.parint.2025.103111

Khan N, Awasthi G, Das A. How can the complex epidemiology of malaria in India impact its elimination. Trends Parasitol. 2023;39(6):432–44. https://doi.org/10.1016/j.pt.2023.03.006

Ebhuoma O, Gebreslasie M, Villena OC, Arab A. Environmental and geographical factors influence malaria transmission in KwaZulu-Natal province, South Africa. Geospat Health. 2025;20(1):1370. https://doi.org/10.4081/gh.2025.1370

Polo B, Bennett KL, Barasa S, Brenas J, Agumba S, Mwangangi J, et al. Genomic surveillance reveals geographical heterogeneity and differences in known and novel insecticide resistance mechanisms in Anopheles arabiensis across Kenya. BMC Genomics. 2025; 26 : 599. https://doi.org/10.1186/s12864-025-11788-3

Oruni A, Tchouakui M, Tagne CSD, Hearn J, Kayondo J, Wondji CS. Temporal evolution of insecticide resistance and bionomics in Anopheles funestus, a key malaria vector in Uganda. Sci Rep. 2024;1–14. https://doi.org/10.1038/s41598-024-83689-6

Connelly S V, Brazeau NF, Msellem M, Ngasala BE, Aydemir O, Goel V, et al. Strong isolation by distance and evidence of population microstructure reflect ongoing Plasmodium falciparum transmission in Zanzibar. elife.2023;1–18. https://doi.org/10.7554/elife.90173

Yan H, Li M, Xia Z, Yin J. Competency of malaria laboratory diagnosis at national and provincial levels at the beginning of malaria post ? elimination phase , China. Malar J. 2024;1–6. https://doi.org/10.1186/s12936-024-04883-5

Kramyoo M, Boonpeng K, Janchoo C, Siriwattanakul K, Phankhod K, Vongthanom N, et al. Acta Tropica High-sensitivity detection of asymptomatic malaria in high-risk Thai populations using droplet digital PCR. 2025;270:107831. https://doi.org/10.1016/j.actatropica.2025.107831

Aregawi MW, Maiteki C, Rek JC, Agaba B, Katureebe C, Ranjbar M, et al. Malaria epidemics and its drivers in Uganda in 2022. Malar J.2025. https://doi.org/10.1186/s12936-025-05351-4

Okumu F, Odero JO, Monroe A, Charlwood JD, Knols BGJ. Safeguarding malaria control gains in Africa through ‘species sanitation’ and structural resilience. 2025;41(9):720–33. https://doi.org/10.1016/j.pt.2025.07.004

Zhou G, Taffese HS, Zhong D, Wang X, Lee M chieh, Degefa T, et al. Resurgence of Clinical Malaria in Ethiopia and Its Link to Anopheles stephensi Invasion: Pathogens. 2024;1–11. https://doi.org/10.3390/pathogens13090748

Sekine S, Chan CW, Kalkoa M, Yamar S, Iata H, Taleo G, Kc A. Tracing the origins of Plasmodium vivax resurgence after malaria elimination on Aneityum Island in Vanuatu; Commun Med. 2024;4:91 https://doi.org/10.1038/s43856-024-00524-9

Li Y, Huang Y, Chen R, Huang W, Xu H, Ye R, et al. An innovative three ? layer strategy in response to a quartan malaria outbreak among forest goers in Hainan Island , China : a retrospective study. Infect Dis Poverty. 2022; 11 : 97. https://doi.org/10.1186/s40249-022-01015-6

Hewavitharane M, Ranawaka G, Saparamadu MDJS, Premaratne R. Seasonal abundance and climatic determinants of Anopheles vectors in Sri Lanka : its implications in the malaria post ? elimination era. Malar J. 2025; 24 (1) : 256. https://doi.org/10.1186/s12936-025-05497-1

Kagaya W. Parasitology International Low-density Plasmodium falciparum infection ; “Even a parasite will turn.” Parasitol Int. 2025;107:103052. https://doi.org/10.1016/j.parint.2025.103052

Kojom LP, Sharma A. Indigenous Plasmodium vivax upsurge in the Eastern Mediterranean, Western Pacific, and South East Asia regions – beyond the constant culpability of climate change, COVID-19, and armed conflicts. Int J Parasitol. 2025;55(14):755–65. https://doi.org/10.1016/j.ijpara.2025.08.009

Mosnier E, Dusfour I, Lacour G, Saldanha R, Guidez A, Gomes MS, et al. Resurgence risk for malaria, and the characterization of a recent outbreak in an Amazonian border area between French Guiana and Brazil. BMC Infect Dis. 2020; 20 : 373. https://doi.org/10.1186/s12879-020-05086-4

Lenakoly TY, Tulak ZL. Mapping the malaria receptivity area in Biak Regency, Papua Province . Miracle J Public Health.2022;5(2):108–117. https://doi.org/10.36566/mjph.v5i2.293

Khan J, Zhang D, Gholizadeh S, Deng Y, Aziz A, Chen J, et al. Phylogeographic Patterns and Genetic Diversity of Anopheles stephensi : Implications for Global Malaria Transmission. Trop Med Infect Dis. 2025;10(4):109. https://doi.org/10.3390/tropicalmed10040109

Feng X, Feng J, Zhang L, Tu H, Xia Z. Vector control in China , from malaria endemic to elimination and challenges ahead. Infect Dis Poverty. 2022;11(1):54. https://doi.org/10.1186/s40249-022-00971-3

Li Y, Stewart K, Han KT, Han ZY, Aung PP, Thein ZW, et al. Understanding Spatiotemporal Human Mobility Patterns for Malaria Control Using a Multiagent Mobility Simulation Model. Clin Infect Dis. 2023;76(3):e867–e874. https://doi.org/10.1093/cid/ciac568

White NJ. Anti ? malarial drug effects on parasite dynamics in vivax malaria. Malar J. 2021; 20 (1) : 161. https://doi.org/10.1186/s12936-021-03700-7

Ashley EA, Phyo AP, Carrara VI, Tun KM, Nosten F, Smithuis F, et al. Plasmodium vivax Relapse Rates Following Plasmodium falciparum Malaria Reflect Previous Transmission Intensity. J Infect Dis. 2019;220(1):100–104. https://doi.org/10.1093/infdis/jiz052

Lesmana SD, Afandi D, Rosdiana D, Murtono H, Azzuhra MN, Panjaitan GR. Postmalaria elimination : Overview of recurrent malaria cases in Riau Province, Indonesia. Trop Parasitol. 2025;15(2):91–98. https://doi.org/10.4103/tp.tp_58_24.

Hasyim H, Dewi WC, Lestari RAF, Flora R, Novrikasari N, Liberty IA, et al. Risk factors of malaria transmission in mining workers in Muara Enim, South Sumatra, Indonesia. Sci Rep. 2023;13(1):14755. https://doi.org/10.1038/s41598-023-40418-9.

Kementerian Kesehatan Republik Indonesia. Peraturan Menteri Kesehatan Republik Indonesia Nomor 2Tahun 2022 tentang Penanggulangan Malaria;[Internet]. Jakarta: Kementerian Kesehatan Republik Indonesia; 2022. Available from: https://peraturan.go.id/id/permenkes-no-22-tahun-2022.

World Health Organization. Global technical strategy for malaria 2016–2030, 2021 update [Internet]. Geneva: World Health Organization; 2021. Available from: https://www.who.int/publications/i/item/9789240031357.

Published
2026-07-16
How to Cite
RA AZ, R., Raharjo, M., & Sulistiyani. (2026). Determinants of Malaria Re-emergence in Coastal and Island Elimination Settings: A PRISMA-Based Systematic Review. Media Publikasi Promosi Kesehatan Indonesia (MPPKI), 9(7), 1444-1456. https://doi.org/10.56338/mppki.v9i7.9252
Section
Article