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Golassa, L.

Publications and source records attributed to Golassa, L..

3 recordsLinked to original sources

Genomic connectivity and the spread of adaptive insecticide resistance alleles in Anopheles arabiensis from East Africa

Population connectivity and adaptive gene flow in disease vectors can shape the emergence and spread of insecticide resistance, with direct implications for control strategies such as insecticide spraying or the use of bed nets for malaria control. Using whole-genome sequencing, we first resolved the geographic population structure of the major but understudied malaria vector, Anopheles arabiensis, across the East African region, including the geographically diverse country of Ethiopia. We then assessed evidence for adaptive gene flow of insecticide resistance alleles across the region. Within Ethiopia, Central Rift Valley populations flanked by mountainous terrain were subject to restricted gene flow, although higher connectivity with the southwestern populations suggests an intermediate point of genetic exchange with the rest of Ethiopia. Anopheles arabiensis from western and northernmost Ethiopia were connected to populations from a similarly arid environment in Turkana - Kenya. Furthermore, broad-scale analysis revealed that populations from the rest of Kenya were connected with those from Uganda and Tanzania, but finer-scale analysis revealed more subtle structuring along the Rift Valley flanks, underscoring the role of landscape features in shaping patterns of gene flow. Adaptive gene flow analyses of diplotype clustering revealed that resistance alleles such as Cyp6aa/p and Gste2 copy number variants (CNV) were widely spread across East Africa despite the geographical population structuring we observed. At the Gste2 locus, An. arabiensis from Ethiopia and Kenya carried a newly annotated CNV spanning chromosome position 3R:28,596,832-28,606,222 linked to the non-synonymous SNP V47L, which was only at a low frequency in Kenya. Collectively, our findings demonstrate that An. arabiensis is subject to transboundary movement of resistance alleles, highlighting the need for coordinated cross-country vector management. Although areas of high connectivity may challenge genetic control technologies such as gene drives, more isolated populations may provide opportunities for targeted deployment. SignificanceMosquitoes movement across landscapes determines how insecticide resistance spreads, yet the genomic connectivity of Anopheles arabiensis populations in East Africa is understudied. Using whole genome data, we show that geographic features such as the Rift Valley restrict gene flow in Ethiopia, with western and northernmost Ethiopia connecting to Turkana, while Kenyan populations outside Turkana connect further south with Tanzania and Uganda. Despite these geographic barriers, resistance variants at genes such as Cyp6aa/p and Gste2 spread widely through adaptive gene flow, including a newly annotated CNV allele at Gste2 in Ethiopia and Kenya. These findings demonstrate that resistance alleles move across national borders, underscoring the need for coordinated regional vector management. They also highlight that while broader connectivity may limit genetic control tools such as gene drive, more isolated populations offer opportunities for targeted deployment.

genomics↗

Regional Plasmodium falciparum subpopulations and malaria transmission connectivity in Africa were detected with an enlarged panel of genome-wide microsatellite loci

Unravelling the genetic diversity of Plasmodium falciparum malaria parasite provides critical information on how populations are affected by interventions and the environment, especially the evolution of molecular markers associated with parasite fitness and adaptation to drugs and vaccines. This study expands previous studies based on small sets of microsatellite loci, which often showed limited substructure in African populations of P. falciparum. Combining several short tandem repeat detection algorithms, we genotyped and analysed 2329 polymorphic microsatellite loci from next-generation sequences of 992 low-complexity P. falciparum isolates from 15 sub-Saharan African countries. Based on pairwise relatedness, we identified seven subpopulations and gene flow between the Central and Eastern African populations. The most divergent subpopulation was from Ethiopia, while unexpected unique subpopulations from Gabon and Malawi were resolved. Isolates from the Democratic Republic of Congo shared ancestry with multiple regional populations, suggesting a possible founder population of P. falciparum from the Congo basin, where there was stronger geneflow eastwards to Tanzania, and Kenya. and Malawi. The most differentiated microsatellite loci were those around the P. falciparum dihydropteroate synthase (Pfdhps) gene associated with sulphadoxine resistance. Haplotypes around the Pfdhps gene separated the West, Central, and East Africa parasite populations into distinct clusters, suggesting independent local evolution of Pfdhps-associated sulphadoxine resistance alleles in each African region. Overall, this study presents genome-wide microsatellites as markers for resolving P. falciparum population diversity, structure, and evolution in populations like Africa, where there is high gene flow.

genomics↗

Genome-Wide Association Studies of malaria susceptibility and resistance: progress, pitfalls and prospects

P. falciparum malaria is still among the leading causes of child mortality in sub-Saharan Africa; killing hundreds of thousands of children each year. Malaria has been recognized as one of the prominent evolutionary selective forces of human genome that led to the emergence of multiple host protective polymorphisms associated with minimizing the risk of developing severe malaria in endemic areas. A comprehensive understanding of the genetic bases of malaria resistance can shed light to the molecular mechanisms of host-parasite interactions that can potentially pave ways to the development of new therapeutics and vaccines. Genome-wide association studies (GWASs) have recently been implemented in malaria endemic areas and identified a number of novel association genetic variants. Despite this success, only few variants did replicate across the studies and the underlying biology is yet to be understood for the majority of the novel variants. Besides, there are several open questions around heritability, polygenic effects, epistatic interactions, genetic correlations and associated molecular pathways among others. In this review, we first assess the progress and pitfalls of malaria susceptibility GWASs. We then, provide an overview of the current progress in post-GWAS approaches and discuss how these approaches can potentially be implemented in malaria susceptibility GWASs to extract further functional information. We conclude by highlighting the importance of multi-step and multidimensional integrative studies for unravelling the genetic basis of malaria susceptibility and resistance at systems biology level.

genomics↗