Entamoeba histolytica, a protozoan parasite, is an important human pathogen. Diseases caused by E. histolytica include dysentery and liver abscesses, and the organism is a leading parasitic cause of death on a global scale. Regulation of gene expression is a key factor that enables the parasite to adapt to the host environment during tissue invasion and to convert to the cyst stage and propagate disease outside the host. One mechanism of gene regulation in Entamoeba is a robust and complex endogenous RNAi pathway. Over the last several years we have made important observations about this pathway including that small RNAs associate with amebic Argonaute protein to mediate transcriptional gene silencing and have highly unusual 5'- polyP termini. However, despite extensive efforts we have not identified which aspects of amebic biology are regulated by small RNAs, although given that the pathway is maintained in related Entamoeba, a strong evolutionary pressure and clear biological role must exist. We have recently identified that ameba secrete extracellular vesicles that contain small RNAs and RNAi effector proteins. We now seek to determine whether these extracellular vesicles containing small RNAs serve as a means of host-parasite or parasite-parasite intercellular communication. Thus, we will (i) identify small RNA repertoire of amebic extracellular vesicles, (ii) determine if they participate in intercellular communication, and (iii) determine protein components of EVs with focus on RNA binding proteins. These data will improve our understanding of the molecular mechanisms of RNAi in Entamoeba and will also broaden our understanding of the roles of small RNAs in intercellular communication. Our work is at the intersection of the basic cellular process of RNA- interference and amebic biology. Data that emerge will contribute to both understanding amebic pathogenesis but also to expanding the knowledge about the fundamental process of RNAi.

Public Health Relevance

Entamoeba histolytica is an important pathogen with an impact on human health on a global scale. This organism contains a robust endogenous RNAi pathway, which regulates virulence pathways. We have recently identified ameba-derived extracellular vesicles, which contain small RNAs and RNAi effector proteins and wish to understand if this is a means of small RNA mediated intercellular communication. Data that emerge will be informative to both amebic biology as well as the fundamental process of RNAi.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AI125764-01
Application #
9165169
Study Section
Pathogenic Eukaryotes Study Section (PTHE)
Program Officer
Mcgugan, Glen C
Project Start
2016-06-10
Project End
2018-05-31
Budget Start
2016-06-10
Budget End
2017-05-31
Support Year
1
Fiscal Year
2016
Total Cost
$197,500
Indirect Cost
$72,500
Name
Stanford University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94304
Sulka, Katherine B; Strle, Klemen; Crowley, Jameson T et al. (2018) Correlation of Lyme Disease-Associated IgG4 Autoantibodies With Synovial Pathology in Antibiotic-Refractory Lyme Arthritis. Arthritis Rheumatol 70:1835-1846