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F1000Research2024; 10; 645; doi: 10.12688/f1000research.53946.4

Preliminary Evidence of Human Plasmodium in Domestic Animals from a Malaria-Endemic Region in Indonesia.

Abstract: In Indonesia, malaria incidence is at a high rate despite maximum preventive efforts. Therefore, this study aims to determine the possibility of a reservoir among domestic animals in malaria-endemic areas. Animal blood was collected using EDTA tubes, then smeared and stained with Giemsa for microscopic identification. About 10 μl of blood was dropped on to a filter paper to capture DNA. Nested PCR was used for parasite molecular detection, while species were identified using the sequenced DNA. A total of 208 and 62 animal blood samples were collected from Gaura village, West Sumba and Fakfak village, West Papua, Indonesia respectively. In total, 32 samples from Gaura contained or , while the percentage in buffalo, horse, goat, and dogs were 20.7%, 14.3%, 5.8%, 16.7%, respectively. was not found in any of the samples, and no other species were detected in 18 pig blood samples. The human DNA in domestic animals within malaria-endemic regions suggests a potential link to the persistence and high prevalence of malaria in these areas. While the findings suggest a potential role of domestic animals in malaria transmission, they remain preliminary and do not definitively establish domestic animals as reservoirs. Further research is necessary to confirm these findings and to better understand the contribution of domestic animals to the transmission dynamics of malaria.
Publication Date: 2024-12-10 PubMed ID: 39931544PubMed Central: PMC11809677DOI: 10.12688/f1000research.53946.4Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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Overview

  • This study investigates whether domestic animals in malaria-endemic regions of Indonesia might act as reservoirs for human malaria parasites.
  • The research detected human Plasmodium DNA in several domestic animals, indicating a possible connection to persistent malaria transmission.

Background and Objective

  • Indonesia experiences a high incidence of malaria despite extensive preventive measures.
  • Understanding all potential reservoirs of malaria parasites is crucial to controlling and eliminating the disease.
  • The main goal of this study was to explore whether domestic animals in malaria-endemic areas harbor human malaria parasites and therefore contribute to ongoing transmission.

Methods

  • Sample Collection: Blood samples were collected from domestic animals using EDTA tubes from two villages — Gaura in West Sumba and Fakfak in West Papua.
  • Microscopic Examination: Blood smears were stained with Giemsa and microscopically examined for parasite identification.
  • DNA Collection: Approximately 10 μl of blood was placed on filter paper for DNA extraction.
  • Molecular Detection: Nested PCR was performed to detect Plasmodium DNA.
  • Species Identification: PCR products were sequenced to determine the specific Plasmodium species present.

Results

  • A total of 270 domestic animal blood samples were analyzed (208 from Gaura village, 62 from Fakfak village).
  • From Gaura, 32 samples tested positive for human Plasmodium DNA, specifically Plasmodium falciparum or Plasmodium vivax.
  • The prevalence rates of Plasmodium DNA in different animals from Gaura were:
    • Buffalo: 20.7%
    • Horse: 14.3%
    • Goat: 5.8%
    • Dogs: 16.7%
  • No Plasmodium falciparum DNA was detected in these samples.
  • 18 pig blood samples did not reveal any presence of Plasmodium species.

Implications

  • The detection of human Plasmodium DNA in domestic animals suggests these animals might act as silent reservoirs for malaria parasites.
  • This could be a factor contributing to the persistence and high malaria prevalence in these endemic regions.
  • Identifying animal reservoirs is significant since most malaria control programs focus exclusively on human transmission cycles.

Limitations and Future Research

  • The findings are preliminary and do not conclusively establish domestic animals as reservoirs capable of transmitting malaria back to humans.
  • Additional studies are necessary to:
    • Determine if domestic animals can sustain viable infections and transmit parasites to mosquito vectors.
    • Evaluate the epidemiological significance of these animal infections in malaria transmission dynamics.
    • Investigate the potential implications for malaria control and elimination strategies targeting both human and animal reservoirs.

Conclusion

  • This study provides initial molecular evidence of human malaria parasites in domestic animals in malaria-endemic areas of Indonesia.
  • While intriguing, these results highlight the need for deeper investigation into the role domestic animals may play in malaria persistence and transmission.

Cite This Article

APA
Munirah M, Wahyuni S, Wahid I, Hamid F. (2024). Preliminary Evidence of Human Plasmodium in Domestic Animals from a Malaria-Endemic Region in Indonesia. F1000Res, 10, 645. https://doi.org/10.12688/f1000research.53946.4

Publication

ISSN: 2046-1402
NlmUniqueID: 101594320
Country: England
Language: English
Volume: 10
Pages: 645
PII: 645

Researcher Affiliations

Munirah, Munirah
  • Doctoral Study Program, Faculty of Medicine, Hasanuddin University, Makassar, South Sulawesi, 90245, Indonesia.
Wahyuni, Sitti
  • Department of Parasitology, Faculty of Medicine, Hasanuddin University, Makassar, South Sulawesi, 90245, Indonesia.
Wahid, Isra
  • Department of Parasitology, Faculty of Medicine, Hasanuddin University, Makassar, South Sulawesi, 90245, Indonesia.
Hamid, Firdaus
  • Department of Microbiology, Faculty of Medicine, Hasanuddin University, Makassar. Jln. Perintis Kemerdekaan 10 Tamalanrea, Makassar, South Sulawesi, 90245, Indonesia.

MeSH Terms

  • Animals
  • Indonesia / epidemiology
  • Humans
  • Malaria / epidemiology
  • Malaria / veterinary
  • Malaria / parasitology
  • Plasmodium / genetics
  • Plasmodium / isolation & purification
  • Animals, Domestic / parasitology
  • Endemic Diseases
  • DNA, Protozoan / genetics

Conflict of Interest Statement

No competing interests were disclosed.

References

This article includes 56 references
  1. Barber MF, Fitzgerald JR. Mechanisms of host adaptation by bacterial pathogens.. 2024;48(4): fuae019.
    doi: 10.1093/femsre/fuae019pmc: PMC11308195pubmed: 39003250google scholar: lookup
  2. Bäumler A, Fang FC. Host specificity of bacterial pathogens.. 2013;3(12): a010041.
    doi: 10.1101/cshperspect.a010041pmc: PMC3839602pubmed: 24296346google scholar: lookup
  3. nBruce D, Harvey D, Hamerton A, et al. :nn sp.nnnn1913;87:45–47.
  4. Bruce D, Harvey D, Hammerton A. Trypanosomes and other parasites of animals in Nyasaland.. 1915;16:203–208.
  5. Cox FE. History of the discovery of the malaria parasites and their vectors.. 2010;3(5):1–9.
    doi: 10.1186/1756-3305-3-5pmc: PMC2825508pubmed: 20205846google scholar: lookup
  6. Davidson G, Chua T, Cook A. Defining the ecological and evolutionary drivers ofn transmission within a multi-scale framework.. 2019;18:66.
    doi: 10.1186/s12936-019-2693-2pmc: PMC6408765pubmed: 30849978google scholar: lookup
  7. Dixit J, Zachariah A, Sajesh P. Reinvestigating the status of malaria parasite (n) in Indian non-human primates.. 2018;12: e0006801.
  8. Donnelly B, Berrang-Ford L, Ross NA. A systematic, realist review of zooprophylaxis for malaria control.. 2015;14:313.
    doi: 10.1186/s12936-015-0822-0pmc: PMC4533963pubmed: 26264913google scholar: lookup
  9. Duval L, Fourment M, Nerrienet E. African apes as reservoirs ofn and the origin and diversification of the Laverania subgenus.. 2010;107(23):10561–10566.
    doi: 10.1073/pnas.1005435107pmc: PMC2890828pubmed: 20498054google scholar: lookup
  10. Duval L, Nerrienet E, Rousset D. Chimpanzee malaria parasites related ton in Africa.. 2009;4:e5520.
  11. Ellwanger JH, Chies JAB. Zoonotic spillover: Understanding basic aspects for better prevention.. 2021;44(1): e20200355.
  12. Erkenswick GA, Watsa M, Pacheco MA. Chronicn infections in wild Peruvian tamarins.. 2017;12:e0184504.
  13. Franco AO, Gomes MGM, Rowland M. Controlling malaria using livestock-based interventions: a one health approach.. 2014;9: e101699.
  14. Garnham P, Edeson J. Two new malaria parasites of the Malayan mousedeer.. 1962;41:1–8.
    pubmed: 13897015
  15. Garnham P, Kuttler K. Malaria parasite of the white-tailed deer (Odocoileus virginianus) and its relation with known species ofn in other ungulates.. 1980;206:395–402.
    doi: 10.1098/rspb.1980.0003pubmed: 6102388google scholar: lookup
  16. Green M, Sambrook J. Nested Polymerase Chain Reaction (PCR). 2019;2.
    doi: 10.1101/pdb.prot095182pubmed: 30710024google scholar: lookup
  17. Guy R, Liu P, Pennefather P. The use of fluorescence enhancement to improve the microscopic diagnosis of falciparum malaria. 2007;6:89.
    doi: 10.1186/1475-2875-6-89pmc: PMC1950880pubmed: 17617912google scholar: lookup
  18. Hall T, Biosciences I, Carlsbad C. BioEdit: an important software for molecular biology. 2011;2:60–61.
  19. Hasyim H, Dhimal M, Bauer J. Does livestock protect from malaria or facilitate malaria prevalence? A cross - sectional study in endemic rural areas of Indonesia. 2018;17:302.
    doi: 10.1186/s12936-018-2447-6pmc: PMC6102806pubmed: 30126462google scholar: lookup
  20. Jongwutiwes S, Putaporntip C, Iwasaki T. Naturally acquired malaria in human, Thailand. 2004;10:2211–2213.
    doi: 10.3201/eid1012.040293pmc: PMC3323387pubmed: 15663864google scholar: lookup
  21. Kaewthamasorn M, Takeda M, Saiwichai T. Genetic homogeneity of goat malaria parasites in Asia and Africa suggests their expansion with domestic goat host. 2018;8(5827):1–7.
  22. Kemenkes R: Infodatin malaria. 2016: p.8.
  23. Knowlesi R. Monkey malaria. 1935;3907:1020.
  24. Krief S, Escalante A, Pacheco M. On the diversity of malaria parasites in African apes and the origin of from Bonobos. 2010;6: e1000765.
  25. Kuris AM, Blaustein AR, Alio JJ. Hosts as islands. 1980;116:570–586.
  26. Lee KS, Divis PCS, Zakaria SK. Reservoir hosts and tracking the emergence in humans and macaques. 2011;7(4):1–11.
  27. Liu W, Li Y, Learn GH. Origin of the human parasite in gorillas. 2010;23(467(7314)):420–425.
    doi: 10.1038/nature09442pmc: PMC2997044pubmed: 20864995google scholar: lookup
  28. Liu W, Li Y, Shaw KS. African origin of the malaria parasite vivax. 2014;5:3346.
    doi: 10.1038/ncomms4346pmc: PMC4089193pubmed: 24557500google scholar: lookup
  29. nMorgan AD, Koskella B:nnnnElsevier;2011: pp.147–171.n10.1016/B978-0-12-384890-1.00006-6n
  30. Mu J, Joy DA, Duan J. Host switch leads to emergence of malaria in humans. 2005;22:1686–1693.
    doi: 10.1093/molbev/msi160pubmed: 15858201google scholar: lookup
  31. Munirah M, Wahyuni S, Hamid F. The discovery of human among domestic animals in West Sumba and Fakfak, Indonesia. 2021.
  32. Ng O, Ooi E, Lee C. Naturally acquired human infection, Singapore. 2008;14:814–816.
    doi: 10.3201/eid1405.070863pmc: PMC2600232pubmed: 18439370google scholar: lookup
  33. Nurhidayah N, Satrija F, Retnani EB. Prevalensi dan faktor risiko infeksi parasit saluran pencernaan pada kerbau lumpur di Kabupaten Brebes, Jawa Tengah. 2019;20:572–582.
  34. Obeagu EI, Obeagu GU. Adapting to the shifting landscape: Implications of climate change for malaria control: A review. 2024;103(29): e39010.
  35. Perandin F, Manca N, Calderaro A. Development of a Real-Time PCR Assay for detection of for routine clinical diagnosis. 2004;42(3):1214–1219.
  36. Perkins S, Schaer J. Modern menagerie of mammalian malaria. 2016;32:772–782.
    doi: 10.1016/j.pt.2016.06.001pubmed: 27492115google scholar: lookup
  37. Prior KF, Rijo-Ferreira F, Assis PA. Periodic Parasites and Daily Host Rhythms. 2020;27(2):176–187.
    doi: 10.1016/j.chom.2020.01.005pmc: PMC7137616pubmed: 32053788google scholar: lookup
  38. Prugnolle F, Rougeron V, Becquart P. Diversity, host switching and evolution of infecting African great apes. 2013;110:8123–8128.
    doi: 10.1073/pnas.1306004110pmc: PMC3657773pubmed: 23637341google scholar: lookup
  39. Public Health Office of Fakfak and West Sumba. Malaria case reports. 2018 and 2019.Unpublished data.
  40. Rahayu N, Hidayat S, Sulasmi S. Kontribusi pekerja hutan terhadap kejadian malaria di Desa Temunih Kecamatan Kusan Hulu Kabupaten Tanah Bumbu Provinsi Kalimantan Selatan. 2016;2:42–51.
  41. Sheather A. Malaria parasite in the blood of a buffalo. 1919;32:223–226.
  42. Shivahare R, Dubey S, McGwire BS. The tug of war between parasites survival and host immunity. 2023;14:1234191.
    doi: 10.3389/fimmu.2023.1234191pmc: PMC10315897pubmed: 37404830google scholar: lookup
  43. Singh B, Daneshvar C. Human infections and detection of. 2013 Apr;26(2):165–184.
    doi: 10.1128/CMR.00079-12pmc: PMC3623376pubmed: 23554413google scholar: lookup
  44. Snounou G, Viriyakosol S, Zhu XP. High sensitivity of detection of human malaria parasites by the use of nested polymerase chain reaction. 1993a;61:315–320.
    doi: 10.1016/0166-6851(93)90077-bpubmed: 8264734google scholar: lookup
  45. Snounou G, Vlrlyakosol S, Jarra W. Identification of the four human malaria parasite species in field samples by the polymerase chain reaction and detection of a high prevalence of mixed infections. 1993b;58:283–292.
    doi: 10.1016/0166-6851(93)90050-8pubmed: 8479452google scholar: lookup
  46. Templeton T, Martinsen E, Kaewthamasorn M. The rediscovery of malaria parasites of ungulates. 2016a;143:1501–1508.
    doi: 10.1017/S0031182016001141pubmed: 27444556google scholar: lookup
  47. Templeton TJ, Asada M, Jiratanh M. Ungulate malaria parasites. 2016b;6:1–8.
    doi: 10.1038/srep23230pmc: PMC4800408pubmed: 26996979google scholar: lookup
  48. Tisgratog R, Tananchai C, Juntarajumnong W. Host feeding patterns and preference of (Diptera: Culicidae) in a malaria endemic area of western Thailand: baseline site description. 2012;5:114.
    doi: 10.1186/1756-3305-5-114pmc: PMC3407501pubmed: 22676415google scholar: lookup
  49. Trung HD, Bortel WV, Sochantha T. Behavioural heterogeneity of species in ecologically different localities in Southeast Asia: a challenge for vector control. 2005;10:251–262.
  50. Vidhya PT, Sunish IP, Maile A. Mosquitoes as Vector for , Andaman and Nicobar Islands, India. 2019;25:817–820.
    doi: 10.3201/eid2504.181668pmc: PMC6433020pubmed: 30882328google scholar: lookup
  51. Vincke I, Lips M. Un nouveau d’un rongeur sauvage du Congo, n.sp.. 1948;28:97–104.
    pubmed: 18874862
  52. Yang Y, Ma C, Zu J. Coevolutionary dynamics of host-pathogen interaction with density-dependent mortality. 2022;85(2):15.
    doi: 10.1007/s00285-022-01782-8pmc: PMC9309463pubmed: 35877051google scholar: lookup
  53. Zhang X, Kadir KA, Quintanilla-Zariñan LF. Distribution and prevalence of malaria parasites among long-tailed macaques ( ) in regional populations across Southeast Asia. 2016 Sep;15(1):450.
    doi: 10.1186/s12936-016-1494-0pmc: PMC5010671pubmed: 27590474google scholar: lookup
  54. . Human-Plasmodium Like in Domestic-goat Blood in Malaria Endemic Areas in Purworejo Indonesia. 2021;53(04):148-152.
    doi: 10.24321/0019.5138.202185google scholar: lookup
  55. . Penularan Penyakit Malaria Oleh Vektor Zoofilik Dengan Sumber Pakan Darah Non Manusia. 2023;1(Oktober):35-43.
  56. . Utilisation and Delivery of Healthcare Services as Factors in Malaria Control in Kolar: A Community-Based Study. 2023;55(03):1-6.
    doi: 10.24321/0019.5138.202329google scholar: lookup

Citations

This article has been cited 1 times.
  1. Hasyim H, Jassey B, Yudhastuti R, Misnaniarti M, Liberty IA, Sunarsih E, Priyanto L, Dalilah D, Yusri Y, Taufiq FH, Maharani FE, Hakim L, Herlinda S. Prevalence of Plasmodium spp. in humans and cattle: Implications for zoonotic malaria transmission in Indonesia.. Vet World 2025 Jul;18(7):1831-1839.