Authors
T S Champion3; S Connelly1; C Smith1; C Rowel4; M Adriko4; P H Lamberton2;
1 Infrastructure and Environment,School of Engineering, University of Glasgow, UK; 2 Institute of Biodiversity, Animal Health and comparative Medicine, and Wellcome Centre for Parasitology, University of Glasgow, UK; 3 Institute of Biodiversity, Animal Health and comparative Medicine, University of Glasgow, UK; 4 Vector Control Division, Ministry of Health, Republic of Uganda, Uganda
Discussion
Preventative chemotherapy with praziquantel is the mainstay
of control programs for schistosomiasis and has proved to be cost-effective for
morbidity control. However, integrating additional interventions that can
affect the free-living stages of the schistosome’s lifecycle, could help
interrupt parasite transmission. Environmental contamination by human excreta
facilitates contamination of freshwater sources and the subsequent hatching of
miracidia and their invasion of susceptible snail hosts. Similarly, human
exposure to cercariae-contaminated freshwater enables the progression of the schistosome
to the next stage of its lifecycle.
The aims of my PhD are to characterise the level and
distribution of Schistosoma mansoni (S. mansoni ) environmental contamination
and, assess the potential for environmental engineering interventions to reduce
this contamination. Environmental DNA (eDNA) methodology will be used to
examine the distribution of S. mansoni
in soil proximal to pit latrines and open defecation sites. The contamination
of water contact sites will also be investigated, and PCR will be used to
detect eDNA from these soil and freshwater samples. Following the
characterisation of the eDNA distribution, site appropriate engineering
interventions will be assessed for their potential to reduce the survival of
the free-living stages of S. mansoni lifecycle.
I will present the key aims, methods and preliminary results of this work.