Tracking of Anopheles stephensi in Ethiopia using mitochondrial DNA reveals pattern of spread

Carter, T. E.; Yared, S.; Getachew, D.; Spear, J.; Choi, S. H.; Samake, J. N.; Mumba, P.; Dengela, D.; Yohannes, G.; Chibsa, S.; Murphy, M.; Dissanayake, G.; Flatley, C.; Lopez, K.; Janies, D.; Zohdy, S.; Irish, S. R.; Balkew, M.

doi:10.1101/2021.04.07.437873

bioRxiv · 10.1101/2021.04.07.437873

Tracking of Anopheles stephensi in Ethiopia using mitochondrial DNA reveals pattern of spread

Carter, T. E.·Yared, S.·Getachew, D.·Spear, J.·Choi, S. H.·Samake, J. N.·Mumba, P.·Dengela, D.·Yohannes, G.·Chibsa, S.·Murphy, M.·Dissanayake, G.·Flatley, C.·Lopez, K.·Janies, D.·Zohdy, S.·Irish, S. R.·Balkew, M.

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Abstract

The recent detection of the South Asian malaria vector Anopheles stephensi in the Horn of Africa (HOA) raises concerns about the impact of this mosquito on malaria transmission in the region. The mode and history of introduction is important for predicting the likelihood of continued introduction and future spread. Analysis of An. stephensi genetic diversity and population structure can provide insight into the history of the mosquito in the HOA. We investigated genetic diversity of An. stephensi in eastern Ethiopia where detection suggests a range expansion to this region to understand the history of this invasive population. We sequenced the cytochrome oxidase subunit I (COI) and cytochrome B gene (CytB) in 187 An. stephensi collected from 10 sites in Ethiopia in 2018. Phylogenetic analyses using a maximum-likelihood approach and minimum spanning network were conducted for Ethiopian sequences. Molecular identification of bloodmeal sources was also performed using universal vertebrate CytB sequencing. Six COI-CytB haplotypes were observed based on five segregating sites, with the highest number of haplotypes in the northeastern sites (Semera, Bati, and Gewana towns) relative to the southeastern sites (Kebridehar, Godey, and Degehabur) in eastern Ethiopia. In the phylogenetic and network analysis, we observed population differentiation based on the distribution of the haplotypes across the northeastern and central sites (Erer Gota, Dire Dawa, and Awash Sebat Kilo) compared to the southeastern sites and evidence of a South Asian origin of the HOA An. stephensi lineages. The presence of the putative South Asian haplotype of origin at sites closest to Ethiopias northeastern borders support route of introductions into Ethiopia from the northeast. Finally, molecular bloodmeal analysis revealed evidence of feeding on bovines, goats, dogs, and humans, as well as evidence of multiple (mixed) blood meals. In conclusion, we find support for the hypothesis for the recent expansion of An. stephensi into southeastern Ethiopia with multiple introductions. We also find evidence that supports the hypothesis that HOA An. stephensi populations originate from South Asia rather than the Arabian Peninsula. The evidence of both zoophagic and anthropophagic feeding support the potential for livestock movement to play a role in vector spread in this region.

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Carter, T. E., Yared, S., Getachew, D., Spear, J., Choi, S. H., Samake, J. N., Mumba, P., Dengela, D., Yohannes, G., Chibsa, S., Murphy, M., Dissanayake, G., Flatley, C., Lopez, K., Janies, D., Zohdy, S., Irish, S. R., Balkew, M.. 2021-04-09. Tracking of Anopheles stephensi in Ethiopia using mitochondrial DNA reveals pattern of spread. https://doi.org/10.1101/2021.04.07.437873

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