Abstract
Ookinete invasion of Anopheles midgut is a critical step for malaria transmission; the parasite numbers drop drastically and practically reach a minimum during the parasite's whole life cycle. At this stage, the parasite as well as the vector undergoes immense oxidative stress. Thereafter, the vector undergoes oxidative stress at different time points as the parasite invades its tissues during the parasite development. The present study was undertaken to reconstruct the network of differentially expressed genes involved in oxidative stress in Anopheles stephensi during Plasmodium development and maturation in the midgut. Using high throughput next generation sequencing methods, we generated the transcriptome of the An. stephensi midgut during Plasmodium vinckei petteri oocyst invasion of the midgut epithelium. Further, we utilized large datasets available on public domain on Anopheles during Plasmodium ookinete invasion and Drosophila datasets and arrived upon clusters of genes that may play a role in oxidative stress. Finally, we used support vector machines for the functional prediction of the un-annotated genes of An. stephensi. Integrating the results from all the different data analyses, we identified a total of 516 genes that were involved in oxidative stress in An. stephensi during Plasmodium development. The significantly regulated genes were further extracted from this gene cluster and used to infer an oxidative stress network of An. stephensi. Using system biology approaches, we have been able to ascertain the role of several putative genes in An. stephensi with respect to oxidative stress. Further experimental validations of these genes are underway.
Highlights
Maintenance of redox homeostasis is critical for proper functioning of cellular processes and disruption of this prooxidant-antioxidant balance in a cell results in oxidative stress
We inferred gene-gene interaction network of oxidative stress in An. stephensi during P. vinckei petteri development by integrating datasets originating from Illumina RNA-seq technology and gene expression microarrays
Anopheles stephensi midgut transcriptome during blood feed and P. vinckei petteri infection
Summary
Maintenance of redox homeostasis is critical for proper functioning of cellular processes and disruption of this prooxidant-antioxidant balance in a cell results in oxidative stress. Oxidative stress may be caused by the normal functioning of the cell (mitochondrial respiration) or as an immune response to pathogens [1, 2] and is manifested by an increase in reactive oxygen species (ROS) and reactive nitrogen species (RNS) in the cells. These reactive species are capable of modifying DNA and proteins, inactivating biological activity and causing oxidative injury [3, 4]. It has been shown that Plasmodium overcomes this obstacle by using its defense mechanisms to protect against oxidative damage [10, 14, 15]
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