C. trachomatis within-host genomic diversity and transmission between female anatomic sites

NIH RePORTER · NIH · R21 · $207,016 · view on reporter.nih.gov ↗

Abstract

Project Summary Understanding the patterns of within-host genetic variation of pathogens is a new frontier in molecular epidemiology and infectious disease biology. By tracing the relationship of closely-related clonal strains using mutations that have occurred after introduction of a bacterium to its human host, we can detect spatial structuring, adaptive evolution and recombination, leading to a deeper picture of the infection process. Our focus in this project is to determine whether Chlamydia trachomatis (Ct), an important obligate intracellular bacterium that is responsible for over 131 million cases of sexually-transmitted infections globally each year, disseminates between the rectum and endocervix of infected women. Understanding within-host movement of Ct will be important for designing future strategies to study transmission and, importantly, will provide initial knowledge of the cycle of transmission within the host and whether rectal infections are being spread to the endocervix. This is important because treatment of endocervical infections has been shown to be inadequate for eliminating infection in the rectum. In addition, this cycle of transmission would be detrimental in terms of the increased risk of upper genital tract sequelae and transmission to partners. We will use samples from a study site in Fiji that has a population of young women with an unusually high rate of Ct infection (up to 38%) allowing us access to a relatively large number the subjects with multiple body site infections. In Aim 1 we will select 25 women with viable Ct infections in the endocervix, vagina and rectum for genomic sequencing to determine Ct genomic strain type composition at each anatomic site. Based on these results, in Aim 2 we will sequence 10 clones from each site for 20 women simultaneously infected in the rectum and genital tract, reconstruct whether admixture of Ct between the sites occurred, and estimate relative bottleneck sizes. This innovative study will provide the first data of its kind on elucidating within-host Ct transmission dynamics that will be important for selecting optimal body sites for diagnostic screening and for determining appropriate therapeutic regimens.

Key facts

NIH application ID
9879680
Project number
5R21AI138079-02
Recipient
EMORY UNIVERSITY
Principal Investigator
DEBORAH Anne DEAN
Activity code
R21
Funding institute
NIH
Fiscal year
2020
Award amount
$207,016
Award type
5
Project period
2019-02-25 → 2023-01-31