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Transformation of a plasmid-free, genital tract isolate of Chlamydia trachomatis with a plasmid vector carrying a deletion in CDS6 revealed that this gene regulates inclusion phenotype

Transformation of a plasmid-free, genital tract isolate of Chlamydia trachomatis with a plasmid vector carrying a deletion in CDS6 revealed that this gene regulates inclusion phenotype
Transformation of a plasmid-free, genital tract isolate of Chlamydia trachomatis with a plasmid vector carrying a deletion in CDS6 revealed that this gene regulates inclusion phenotype
The development of a plasmid-based genetic transformation protocol for Chlamydia trachomatis provides the basis for the detailed investigation of the function of the chlamydial plasmid and its individual genes or coding sequences (CDS). In this study we constructed a plasmid vector with CDS6 deleted (pCDS6KO) from the original Escherichia coli/C. trachomatis shuttle vector pGFP::SW2. pCDS6KO was transformed into a clinical isolate of C. trachomatis from Sweden that is plasmidfree(C. trachomatis SWFP–). Penicillin-resistant transformants expressing the green fluorescent protein were selected. These transformants did not stain with iodine, indicating that this property is regulated by CDS6 or its gene product. In addition, mature inclusions of C. trachomatis SWFP– transformed by pCDS6KO displayed an identical morphological phenotype to the untransformed plasmid-free recipient host. In this phenotype the morphology of inclusions was altered with the chlamydiae lining the periphery of the inclusion leaving a ‘hole’ in the centre. These green fluorescent inclusions appear ‘doughnut-shaped’ with an empty centre when examined under blue light, giving rise to a characteristic ‘black hole’ phenotype. Our study demonstrates the power of the new genetic system for investigating chlamydial gene function using gene deletion technology.
chlamydia trachomatis, plasmid, transformation, deletion, cds 6, glycogen biosynthesis
100-103
Wang, Yibing
a4dc0303-7006-411e-9063-c26297fac847
Cutcliffe, Lesley T.
88f242f4-b4f7-46d4-a1dd-c187dd60a773
Skilton, Rachel J.
74a38e2c-d4fb-4ebe-b560-3d335a76feef
Persson, Kenneth
9ecaea9f-c093-4d57-8bf3-99373ab580c7
Bjartling, Carina
b8c0bfea-b7dc-4605-a865-0f1f4d40685b
Clarke, Ian N.
ff6c9324-3547-4039-bb2c-10c0b3327a8b
Wang, Yibing
a4dc0303-7006-411e-9063-c26297fac847
Cutcliffe, Lesley T.
88f242f4-b4f7-46d4-a1dd-c187dd60a773
Skilton, Rachel J.
74a38e2c-d4fb-4ebe-b560-3d335a76feef
Persson, Kenneth
9ecaea9f-c093-4d57-8bf3-99373ab580c7
Bjartling, Carina
b8c0bfea-b7dc-4605-a865-0f1f4d40685b
Clarke, Ian N.
ff6c9324-3547-4039-bb2c-10c0b3327a8b

Wang, Yibing, Cutcliffe, Lesley T., Skilton, Rachel J., Persson, Kenneth, Bjartling, Carina and Clarke, Ian N. (2013) Transformation of a plasmid-free, genital tract isolate of Chlamydia trachomatis with a plasmid vector carrying a deletion in CDS6 revealed that this gene regulates inclusion phenotype. Pathogens and Disease, 67 (2), 100-103. (doi:10.1111/2049-632X.12024).

Record type: Article

Abstract

The development of a plasmid-based genetic transformation protocol for Chlamydia trachomatis provides the basis for the detailed investigation of the function of the chlamydial plasmid and its individual genes or coding sequences (CDS). In this study we constructed a plasmid vector with CDS6 deleted (pCDS6KO) from the original Escherichia coli/C. trachomatis shuttle vector pGFP::SW2. pCDS6KO was transformed into a clinical isolate of C. trachomatis from Sweden that is plasmidfree(C. trachomatis SWFP–). Penicillin-resistant transformants expressing the green fluorescent protein were selected. These transformants did not stain with iodine, indicating that this property is regulated by CDS6 or its gene product. In addition, mature inclusions of C. trachomatis SWFP– transformed by pCDS6KO displayed an identical morphological phenotype to the untransformed plasmid-free recipient host. In this phenotype the morphology of inclusions was altered with the chlamydiae lining the periphery of the inclusion leaving a ‘hole’ in the centre. These green fluorescent inclusions appear ‘doughnut-shaped’ with an empty centre when examined under blue light, giving rise to a characteristic ‘black hole’ phenotype. Our study demonstrates the power of the new genetic system for investigating chlamydial gene function using gene deletion technology.

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More information

Published date: March 2013
Keywords: chlamydia trachomatis, plasmid, transformation, deletion, cds 6, glycogen biosynthesis
Organisations: Clinical & Experimental Sciences

Identifiers

Local EPrints ID: 351307
URI: http://eprints.soton.ac.uk/id/eprint/351307
PURE UUID: 6e7d83ac-fdc3-4699-a778-4dffe928a3d7
ORCID for Ian N. Clarke: ORCID iD orcid.org/0000-0002-4938-1620

Catalogue record

Date deposited: 18 Apr 2013 10:45
Last modified: 15 Mar 2024 02:33

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Contributors

Author: Yibing Wang
Author: Lesley T. Cutcliffe
Author: Rachel J. Skilton
Author: Kenneth Persson
Author: Carina Bjartling
Author: Ian N. Clarke ORCID iD

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