Cross-kingdom communications via small non-coding RNAs. This project aims to determine the role of small non-coding RNAs in mosquito-Wolbachia interactions, including Wolbachia microRNAs, concentrating on exchanged microRNAs between the two organisms and explore microRNAs effect on Wolbachia maintenance and its anti-viral property. Small non-coding RNAs play significant roles in various biological processes, including host-microorganism interactions. Recent evidence suggests that small RNAs can ....Cross-kingdom communications via small non-coding RNAs. This project aims to determine the role of small non-coding RNAs in mosquito-Wolbachia interactions, including Wolbachia microRNAs, concentrating on exchanged microRNAs between the two organisms and explore microRNAs effect on Wolbachia maintenance and its anti-viral property. Small non-coding RNAs play significant roles in various biological processes, including host-microorganism interactions. Recent evidence suggests that small RNAs can be exchanged between microorganisms and their hosts and regulate gene expression in the other organism. The endosymbiotic bacterium, Wolbachia, has attracted worldwide attention due to inhibiting replication of various vector-borne pathogens in mosquito vectors.Read moreRead less
SNARE-mediated perforin and cytokine release in natural killer cells. Cytotoxic cells release toxic granules and cytokine messengers to kill pathogen infected and cancerous cells and to mount immune responses. This project will investigate different SNARE molecules that regulate the secretion of perforin from granules and cytokines from other carriers, assisting in the understanding of complex but essential cellular pathways.
Formation of the Chlamydial Inclusion Requires Host Trafficking Pathways. Using cellular and biochemical approaches this project aims to examine the membrane trafficking pathways hijacked by the pathogen Chlamydia and to define the key components of these pathways. Chlamydia are obligate intracellular pathogens responsible for a range of human and animal diseases. In order to survive within the host cell, the pathogen hijacks the host's membrane trafficking pathways to engineer an intracellular ....Formation of the Chlamydial Inclusion Requires Host Trafficking Pathways. Using cellular and biochemical approaches this project aims to examine the membrane trafficking pathways hijacked by the pathogen Chlamydia and to define the key components of these pathways. Chlamydia are obligate intracellular pathogens responsible for a range of human and animal diseases. In order to survive within the host cell, the pathogen hijacks the host's membrane trafficking pathways to engineer an intracellular niche called an inclusion. In addition to providing a permissive environment, this strategy also shields the pathogen from the host's immune system.Read moreRead less
Regulation of human immunodeficiency virus type 1 (HIV-1) replication by viral and cellular proteins. Using a mouse model, human cells will be treated with a very powerful antiviral protein using a gene therapy approach so as to block the human immunodeficiency virus (HIV) from growing. By learning how this antiviral protein works, this project will assist in the development of new strategies to treat HIV infection.