Plasmodium falciparum transmission in the highlands of Ethiopia is driven by closely related and clonal parasites

Author:

Holzschuh Aurel1ORCID,Ewnetu Yalemwork2,Carlier Lise34,Lerch Anita1ORCID,Gerlovina Inna5,Baker Sarah Cate3,Yewhalaw Delenasaw6,Haileselassie Werissaw7,Berhane Nega2,Lemma Wossenseged2,Koepfli Cristian1

Affiliation:

1. Department of Biological Sciences, Eck Institute for Global Health University of Notre Dame Notre Dame Indiana USA

2. Department of Medical Biotechnology University of Gondar Gondar Ethiopia

3. Trinity Centre for Global Health Trinity College Dublin Dublin Ireland

4. Noul Inc. Seoul Republic of Korea

5. Department of Medicine, Division of HIV, ID and Global Medicine, EPPIcenter Research Program University of California San Francisco California USA

6. Tropical and Infectious Disease Research Center Jimma University Jimma Ethiopia

7. School of Public Health Addis Ababa University Addis Ababa Ethiopia

Abstract

AbstractMalaria cases are frequently recorded in the Ethiopian highlands even at altitudes above 2000 m. The epidemiology of malaria in the Ethiopian highlands, and, in particular, the role of importation by human migration from the highly endemic lowlands is not well understood. We sequenced 187 Plasmodium falciparum samples from two sites in the Ethiopian highlands, Gondar (n = 159) and Ziway (n = 28), using a multiplexed droplet digital PCR (ddPCR)‐based amplicon sequencing method targeting 35 microhaplotypes and drug resistance loci. Here, we characterize the parasite population structure and genetic relatedness. We identify moderate parasite diversity (mean HE: 0.54) and low infection complexity (74.9% monoclonal). A significant percentage of infections share microhaplotypes, even across transmission seasons and sites, indicating persistent local transmission. We identify multiple clusters of clonal or near‐clonal infections, highlighting high genetic relatedness. Only 6.3% of individuals diagnosed with P. falciparum reported recent travel. Yet, in clonal or near‐clonal clusters, infections of travellers were frequently observed first in time, suggesting that parasites may have been imported and then transmitted locally. 31.1% of infections are pfhrp2‐deleted and 84.4% pfhrp3‐deleted, and 28.7% have pfhrp2/3 double deletions. Parasites with pfhrp2/3 deletions and wild‐type parasites are genetically distinct. Mutations associated with resistance to sulphadoxine–pyrimethamine or suggested to reduce sensitivity to lumefantrine are observed at near‐fixation. In conclusion, genomic data corroborate local transmission and the importance of intensified control in the Ethiopian highlands.

Publisher

Wiley

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