Abstract
Although progress in Chlamydia genetics has been rapid, genomic modification has previously been limited to point mutations and group II intron insertions which truncate protein products. The bacterium has thus far been intractable to gene deletion or more-complex genomic integrations such as allelic exchange. Herein, we present a novel suicide vector dependent on inducible expression of a chlamydial gene that renders Chlamydia trachomatis fully genetically tractable and permits rapid reverse genetics by fluorescence-reported allelic exchange mutagenesis (FRAEM). We describe the first available system of targeting chlamydial genes for deletion or allelic exchange as well as curing plasmids from C. trachomatis serovar L2. Furthermore, this approach permits the monitoring of mutagenesis by fluorescence microscopy without disturbing bacterial growth, a significant asset when manipulating obligate intracellular organisms. As proof of principle, trpA was successfully deleted and replaced with a sequence encoding both green fluorescent protein (GFP) and β-lactamase. The trpA-deficient strain was unable to grow in indole-containing medium, and this phenotype was reversed by complementation with trpA expressed in trans. To assess reproducibility at alternate sites, FRAEM was repeated for genes encoding type III secretion effectors CTL0063, CTL0064, and CTL0065. In all four cases, stable mutants were recovered one passage after the observation of transformants, and allelic exchange was limited to the specific target gene, as confirmed by whole-genome sequencing. Deleted sequences were not detected by quantitative real-time PCR (qPCR) from isogenic mutant populations. We demonstrate that utilization of the chlamydial suicide vector with FRAEM renders C. trachomatis highly amenable to versatile and efficient genetic manipulation.
Document Type
Article
Publication Date
1-19-2016
Digital Object Identifier (DOI)
https://doi.org/10.1128/mBio.01817-15
Funding Information
HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) provided funding to Ken Fields under grant number AI065530.
Repository Citation
Mueller, Konrad E.; Wolf, Katerina; and Fields, Kenneth A., "Gene Deletion by Fluorescence-Reported Allelic Exchange Mutagenesis in Chlamydia trachomatis" (2016). Microbiology, Immunology, and Molecular Genetics Faculty Publications. 86.
https://uknowledge.uky.edu/microbio_facpub/86
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mBio 2016 Mar 7(1) e01817-15, FIG 2 .ppt (233 kB)
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mBio 2016 Mar 7(1) e01817-15, FIG 3 .ppt (326 kB)
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mBio 2016 Mar 7(1) e01817-15, FIG 7 .ppt (279 kB)
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mbo001162632st1.pdf (72 kB)
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Notes/Citation Information
Published in mBio, v. 7, issue 1, e01817-15, p.1-9.
Copyright © 2016 Mueller et al.
This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license, which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.