• Eugenia Lo’s Lab
  • Research
  • Publications
  • Teaching
  • Lab members
  • Photo gallery
  • Latest News

Contact Me

Office: Woodward 381C
Phone: 704.687.8532
Email: Eugenia.Lo@uncc.edu
Twitter: https://twitter.com/UNCC_Lo_Lab

Links

  • Genome wide assessment of gene copy number and SNP variation in Plasmodium vivax from Ethiopia
  • Population structure and diversity of Plasmodium falciparum parasites in children with asymptomatic malaria living in different ecological zones of Ghana
  • Plasmodium falciparum genetic diversity and antimalarial drug resistance prevalence across different transmission zones in Ghana

RSS Latest Malaria News

  • Impact of dhps mutations on sulfadoxine-pyrimethamine protective efficacy and implications for malaria chemoprevention
  • Elicitation of liver-stage immunity by nanoparticle immunogens displaying P. falciparum CSP-derived antigens
  • A noninferiority cluster randomised evaluation of a broflanilide indoor residual spraying insecticide, VECTRON T500, for malaria vector control in Tanzania

Research

Study Sites

I. Transmission dynamics of malaria parasites

+++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++

Human movements and dispersal of vector mosquitoes allow spread of malaria and impact genetic structure of the parasite populations. Understanding the relatedness among Plasmodium populations and how such influenced by geographical and environmental features is vital. The combined approach of population genomics and landscape genetics allows us to examine the role of spatial variation and local adaptation in disease transmission. Knowledge of the source/sink of infections and the magnitude of disease spread are keys to make decision and implement control measures effectively in the most malarious areas.

Landscape genetic plot showing the level of gene flow among P. vivax populations in the Myanmar-China border area.

Bayesian inferences of genetic clusters by STRUCTURE among P. vivax samples in Myanmar.

Migratory pathways and rates of Plasmodium falciparum and P. vivax in Ethiopia based on Migrate-N and BayesAss.

 

 

++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++

II. Molecular epidemiology of malaria

++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++

Emergence of antimalarial drug resistance and persistence of submicroscopic parasite reservoirs are apparent hurdles to malaria reduction and elimination in many African countries. These issues require close monitoring and effective resolution. One aspect of my research is to examine demographic factors of malaria prevalence, transmission intensity, disease severity, as well as bio-markers related to antimalarial drug resistance. This information will contribute to assessing and monitoring the disease burden in places where people are still battling or at high risk of malaria.

Antimalarial treatment policy in Ethiopia and mutation prevalence of antimalarial resistance genes in Plasmodium falciparum.

Plasmodium malariae prevalence and circumsporozoite protein gene diversity in Kenya, 2014 and 2015.

Histogram showing the mean malaria prevalence rate of the three age groups (under 5, aged 5–14, and over 14) in the lowlands and highlands of Western Kenya.

 

 

++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++

III. Evolution of parasite-host interactions

++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++

Malaria is caused by the invasion of Plasmodium into human red blood cell and subsequently disrupts its normal function. RBC invasion involves multiple interactions between parasite ligand and host receptor proteins. Although a number of invasion ligands have been recently documented, in very few cases have their functional significance and red blood cell receptors been identified, especially in P. vivax. It is always possible that parasites evolve novel RBC invasion pathways. This could influence the efficacy of existing preventive vaccines and elevate malaria burden at a global level. My research explores molecular mechanisms of parasite invasion with the goal to identify key RBC binding proteins.

Detection of P. vivax infection in Duffy-negative Ethiopians by microscopy and PCR method.

High copy number of PvDBP observed in Plasmodium vivax from Duffy negative patients in Ethiopia based on quantitative real-time PCR.

Maximum likelihood tree of Plasmodium vivax isolates that have different PvDBP copy number.

 

 

++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++

IV. Phylogeny of malaria parasites and vectors

++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++

Genetic relationships among biological organisms take into account the mutational changes occurred over time as well as migration rates. My research examines mutational and genotypic variation within parasite species and explores genetic relatedness at the spatial and temporal scales to elucidate ancestral origins and character changes. This involves the use of geo-reference tools to model geological changes with respect to species movement and distribution over time. This information sheds light on the role and impact of long-distance migration and adaptive radiation on species diversity and population structure.

Maximum-likelihood analyses of circumsporozoite protein gene (csp) sequences of Plasmodium malariae and global distribution of the samples.

Neighbor-joining trees showing the genetic relatedness among Plasmodium falciparum and P. vivax samples in Ethiopia.
Phylogenetic network of mitochondrial haplotypes of CO1 gene in Aedes albopictus around the world.

 

Skip to toolbar
  • Log In