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. Author manuscript; available in PMC: 2014 May 5.
Published in final edited form as: Future Microbiol. 2013 Sep;8(9):1129–1146. doi: 10.2217/fmb.13.80

Table 1.

Effects of gene diversity in chlamydial proteins on disease severity and tissue tropism.

Gene family Gene name Locus Function/role Effect on tissue tropism Potential effect on disease
severity
Omp family omp A ct681 Most prominent outer membrane protein;
porin; antigen-variants
Classification of Chlamydia trachomatis serovars into A–K
and LGV
No correlation between ompA and
disease severity demonstrated

Pmp family pmp A ct412 Type V secreted proteins: some members
(D, E, G and H) are expressed on the EB
surface. PmpD, D and G elicit a strong
inflammatory response. All of these
proteins likely play a role in phase
variation
Unknown High variability of pmp genes by
SNPs, gene duplication and indel
mutations may be significant in
contributing to disease severity
pmpB ct413 Specific amino acid substitutions distinguish LGV from
non-LGV; difference in C. trachomatis E and F to other
genital serovars
pmpC ct414 Specific amino acid substitutions distinguish LGV from
non-LGV; difference in C. trachomatis E and F to other
genital serovars
pmpD ct812 Specific amino acid substitutions distinguish LGV from
non-LGV
pmpE ct869 Specific nucleotide substitutions segregate ocular from
urogenital and LGV; difference in C. trachomatis E and F to
other genital serovars
pmpF ct870 Specific nucleotide substitutions segregate ocular from
urogenital and LGV
pmpG ct871 Specific amino acid substitutions distinguish LGV from
non-LGV
pmpH ct872 Specific nucleotide substitutions segregate ocular from
urogenital and LGV; difference in C. trachomatis E and F to
other genital serovars
pmpl ct874 Difference in C. trachomatis E and F to other genital serovars
tarp ct456 Binds to actin, phosphorylated by host
kinases; cytoskeleton rearrangement;
involved in internalization
Number of actin-binding sites differentiate LGV and
non-LGV; number of actin-binding sites important for
tropism?
Number of actin-binding sites
important for disease severity?

Inc proteins incD ctll 5 Sphingolipid transport; interacts with
CERT
Mutations in incD specific to ocular and LGV tissue tropism Unknown
incE ct116 Unknown Unknown Unknown
incF ct117 Unknown Unknown Unknown
incG ctll8 Blocks release of cytochrome C and
inhibits apoptosis
Unknown Unknown
incA ct119 Homotypic fusion of intracellular
inclusions
In LGV the genetic variation of incA may reflect tissue
tropism
Nonfusogenic clinical isolates have
less severe clinical signs
ct229f Modulation of inclusion trafficking; binds
to Rab4A
Unknown Unknown
incB ct232 Unknown Unknown Unknown
incC ct233 Unknown Unknown Unknown
aaxB ct373 AAX: arginine decarboxylase proenzyme;
inhibits host cell polyamine synthesis, or
inhibition of nitric oxide synthesis?
Unknown Unknown
aaxC ct374 AAX: cytoplasmic arginine:agmatine
antiporter; inhibits host cell polyamine
synthesis, or inhibition of nitric oxide
synthesis?
Unknown Unknown
trpA ct171 Subunit of Trp synthase, which produces
Trp from indole
Mutations in trpA segregate ocular from genital isolates Unknown
ct166f Toxin-like protein; glycosylates Rac1;
causing actin reorganization
Contains serovar specific loci, missing in LGV strains;
potential role in invasiveness?
Potentially plays a role in disease
severity (LGV strains lack the
cytotoxin)

These loci have not, as yet, been named.

AAX: Arginine:agmatine exchange system; EB: Elementary body; Indel: Insertion and deletion; LGV: Lymphogranuloma venereum; SNP: Single nucleotide polymorphism.