Strong isolation by distance and evidence of population microstructure reflect ongoing Plasmodium falciparum transmission in Zanzibar

Author:

Connelly Sean V.1ORCID,Brazeau Nicholas F.1ORCID,Msellem Mwinyi2,Ngasala Billy E.34ORCID,Aydemir Özkan5ORCID,Goel Varun6ORCID,Niaré Karamoko7ORCID,Giesbrecht David J.7ORCID,Popkin-Hall Zachary R.8ORCID,Hennelly Christopher M.8ORCID,Park Zackary9ORCID,Moormann Ann M.5ORCID,Ong’echa John Michael10ORCID,Verity Robert11ORCID,Mohammed Safia12,Shija Shija J.12,Mhamilawa Lwidiko E.34,Morris Ulrika13ORCID,Mårtensson Andreas4,Lin Jessica T.9ORCID,Björkman Anders1314ORCID,Juliano Jonathan J.91516ORCID,Bailey Jeffrey A.7ORCID

Affiliation:

1. MD-PhD Program, University of North Carolina

2. Research Division, Ministry of Health

3. Department of Parasitology and Medical Entomology, Muhimbili University of Health and Allied Sciences

4. Global Health and Migration Unit, Department of Women’s and Children’s Health, Uppsala University

5. Department of Medicine, University of Massachusetts Chan Medical School

6. Carolina Population Center, University of North Carolina

7. Department of Pathology and Laboratory Medicine, Brown University

8. Institute for Global Health and Infectious Diseases, School of Medicine, University of North Carolina at Chapel Hill

9. Division of Infectious Diseases, Department of Medicine, School of Medicine, University of North Carolina at Chapel Hill

10. Center for Global Health Research, Kenyan Medical Research Institute

11. MRC Centre for Global Infectious Disease Analysis, Imperial College

12. Zanzibar Malaria Elimination Program (ZAMEP)

13. Department of Microbiology

14. Department of Global Public Health, Karolinska Institutet

15. Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina

16. Curriculum in Genetics and Molecular Biology, University of North Carolina

Abstract

The Zanzibar archipelago of Tanzania has become a low-transmission area for Plasmodium falciparum. Despite being considered an area of pre-elimination for years, achieving elimination has been difficult, likely due to a combination of imported infections from mainland Tanzania, and continued local transmission. To shed light on these sources of transmission, we applied highly multiplexed genotyping utilizing molecular inversion probes to characterize the genetic relatedness of 282 P. falciparum isolates collected across Zanzibar and in Bagamoyo District on the coastal mainland from 2016-2018. Overall, parasite populations on the coastal mainland and Zanzibar archipelago remain highly related. However, parasite isolates from Zanzibar exhibit population microstructure due to rapid decay of parasite relatedness over very short distances. This, along with highly related pairs within shehias , suggests ongoing low level local transmission. We also identified highly related parasites across shehias that reflect human mobility on the main island of Unguja and identified a cluster of highly related parasites, suggestive of an outbreak, in the Micheweni district on Pemba island. Parasites in asymptomatic infections demonstrated higher complexity of infection than those in symptomatic infections, but have similar core genomes. Our data support importation as a main source of genetic diversity and contribution to the parasite population on Zanzibar, but they also show local outbreak clusters where targeted interventions are essential to block local transmission. These results highlight the need for preventive measures against imported malaria and enhanced control measures in areas that remain receptive for malaria reemergence due to susceptible hosts and competent vectors.

Publisher

eLife Sciences Publications, Ltd

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