TitleDemonstration of Persistent Infections and Genome Stability by Whole-Genome Sequencing of Repeat-Positive, Same-Serovar Chlamydia trachomatis Collected From the Female Genital Tract.
Publication TypeJournal Article
Year of Publication2017
AuthorsSuchland, RJ, Dimond, ZE, Putman, TE, Rockey, DD
JournalJ Infect Dis
Volume215
Issue11
Pagination1657-1665
Date Published2017 06 01
ISSN1537-6613
KeywordsChlamydia Infections, Chlamydia trachomatis, Cohort Studies, DNA, Bacterial, Female, Genitalia, Female, Genome, Bacterial, Genomics, Humans, Mutation, Phylogeny
Abstract

Background: The biology of recurrent or long-term infections of humans by Chlamydia trachomatis is poorly understood. Because repeated or persistent infections are correlated with serious complications in humans, understanding these processes may improve clinical management and public health disease control.

Methods: We conducted whole-genome sequence analysis on C. trachomatis isolates collected from a previously described patient set in which individuals were shown to be infected with a single serovar over a lengthy period.

Results: Data from 5 of 7 patients showed compelling evidence for the ability of these patients to harbor the same strain for 3-5 years. Mutations in these strains were cumulative, very uncommon, and not linked to any single protein or pathway. Serovar J strains isolated from 1 patient 3 years apart did not accumulate a single base change across the genome. In contrast, the sequence results of 2 patients, each infected only with serovar Ia strains, revealed multiple same-serovar infections over 1-5 years.

Conclusions: These data demonstrate examples of long-term persistence in patients in the face of repeated antibiotic therapy and show that pathogen mutational strategies are not important in persistence of this pathogen in patients.

DOI10.1093/infdis/jix155
Alternate JournalJ Infect Dis
PubMed ID28368459
PubMed Central IDPMC6543881
Grant ListR21 AI088540 / AI / NIAID NIH HHS / United States
R01 AI099278 / AI / NIAID NIH HHS / United States
R01 AI126785 / AI / NIAID NIH HHS / United States