Document Type

Article

Publication Date

8-12-2025

Publication Title

Journal of Bacteriology

Abstract

Chlamydia trachomatis has a DNA topoisomerase I with a unique C-terminal domain (CTD) homologous to eukaryotic SWIB domains. This study focused on determining the function of the SWIB domain-containing TopA from C. trachomatis (CtTopA). We demonstrated that, despite the lack of sequence similarity at the CTDs between CtTopA and TopA from Escherichia coli (EcTopA), full-length CtTopA removed negative DNA supercoils in vitro and complemented the growth defect of a topA mutant of E. coli. CtTopA is less processive in DNA relaxation than EcTopA in dose-response and time course studies. An antibody generated against the SWIB domain of CtTopA specifically recognized CtTopA but not EcTopA or Mycobacterium tuberculosis TopA, consistent with the sequence differences in their CTDs. The endogenous CtTopA protein is expressed at a relatively high level during the middle and late developmental stages of C. trachomatis. Overexpressing a topA mutant allele lacking the SWIB domain in C. trachomatis resulted in slow growth when host protein synthesis was inhibited. These data suggest that productive infection of C. trachomatis requires functional SWIB domain-containing CtTopA and de novo host protein synthesis. Because SWIB domain-containing CtTopAs are not found in prokaryotes beyond Chlamydia spp., our work suggests an important function of the SWIB domain on CtTopA activity during C. trachomatis infection.

PubMed ID

40793755

Volume

207

Issue

9

Creative Commons License

Creative Commons Attribution 4.0 International License
This work is licensed under a Creative Commons Attribution 4.0 International License.

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