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. Author manuscript; available in PMC: 2014 Aug 27.
Published in final edited form as: Nature. 2013 Dec 11;506(7489):507–510. doi: 10.1038/nature12892

Table 1. DCS Chlamydia trachomatis plaque assay in the presence of natural and modified D-amino acids.

C. trachomatis serovar L2 strain 434/Bu was grown in the plaque assay as previously described4 in the presence of D-cycloserine (DCS) and varying molar equivalent concentrations of D-alanine (D-ala), D-alanine-D-alanine (DA-DA), EDA, DA-EDA, and EDA-DA.

DCS (µM) Amino acid, amino acid to DCS
ratio
Plaque formation
0 ++++
294 No amino acid
Dipeptides
DA-DA, 1:1 ++
DA-DA, 10:1 +++
DA-EDA, 1:1
DA-EDA, 10:1 +++
EDA-DA, 1:1
EDA-DA, 10:1 ++
Single amino acids
D-ala, 1:1 ++++
D-ala, 1:10 +++
EDA, 1:1
EDA, 10:1

++++ complete infection, bacterial growth, and lysis of the monolayer; +++ numerous large plaques but less than complete lysis of the monolayer; ++ numerous small plaques; + few (~10–20) small plaques; −, no plaque formation (no bacterial growth). Data represent the average of three biological replicates and each experiment was conducted with technical duplicates.