In our preliminary studies, we have shown that substantial genetic recombination occurs in C. hominis. The impact and consequences of this is not known. We now plan to study the role of this process in generating parasite intra-host diversity and on the evolution of this parasite within the Mirpur community. Hypothesis: We hypothesize that cryptosporidiosis in humans is influenced by parasite genetic diversity. Human work: C. hominis oocysts will be isolated from asymptomatic and symptomatic children. Significance: Cryptosporidiosis is one of the top causes of diarrhea in the first 2 years of life in low-income countries but very little is known about the degree and impact of parasite genetic diversity on disease. Innovation: This proposal will allow us to study parasite natural evolution at both the community and individual level. Approach: Clinical and demographic information, as well as parasite oocysts, are being collected on Cryptosporidium positive children at an urban study in Bangladesh.
Aim 1 : To measure the rate of C. hominis evolution within the Mirpur community. We have already sequenced 32 C. hominis genomes and have collected DNA from an additional 59 isolates. We will sequence one hundred new isolates during this grant. Comparison of the genomes over time will identify genes under the diversifying selective pressure which underlies host-parasite interactions.
Aim 2 : To identify the changes that occur in the C. hominis genome during the course of an infection in an individual child. The daughter sporozoites arising from the infecting oocysts can have different alleles. We use this heterozygosity to identify genes and allele combinations important to ensuring parasite intra-host survival. The environment: My collaborators Dr. Petri and Dr. Haque are experts in field studies and I have access to genomic services and sequencing core facilities at UVa. Successful completion of this work: From this work we will understand the role of the parasite evolution in disease.

Public Health Relevance

Severe diarrhea kills an estimated 1.3 million children before their 5th birthday. Cryptosporidiosis has recently been identified as one of the major causes of enteric disease in this age group. We wish to understand the role of the parasite genetic diversity on cryptosporidiosis and identify the differences that will allow us to design therapeutic and preventative strategies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AI142656-01
Application #
9652435
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Joy, Deirdre A
Project Start
2018-12-07
Project End
2020-11-30
Budget Start
2018-12-07
Budget End
2019-11-30
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Virginia
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
065391526
City
Charlottesville
State
VA
Country
United States
Zip Code
22904