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Journal of Bacteriology, March 2008, p. 1822-1830, Vol. 190, No. 5
0021-9193/08/$08.00+0     doi:10.1128/JB.01240-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Competitive Inhibition of Amino Acid Uptake Suppresses Chlamydial Growth: Involvement of the Chlamydial Amino Acid Transporter BrnQ ^,

Department of Molecular Biology, Max Planck Institute for Infection Biology, Berlin, Germany,¹ Department of Biological Sciences, University of Jordan, Amman, Jordan,² Department of Pediatrics, Charité University Medical Center, Berlin, Germany,³ Institute of Biology, Humboldt Universität zu Berlin, Berlin, Germany⁴

Received 1 August 2007/ Accepted 5 November 2007

Chlamydiaceae are obligate intracellular bacterial pathogens that strictly depend on host metabolites, such as nucleotides, lipids, and amino acids. Depletion of amino acids in cell culture media results in abnormal chlamydial development in vitro. Surprisingly, enrichment of certain amino acids also retards chlamydial growth. Our experiments revealed that the antichlamydial effects are largely independent of changes in the host cell transcriptome or proteome and in the major signal transduction pathway modulated by amino acids, the mTOR (mammalian target of rapamycin) pathway. Furthermore, the chlamydial growth inhibition induced by leucine, isoleucine, methionine, or phenylalanine was completely reversed by concomitant addition of valine. In contrast, the growth inhibition induced by serine, glycine, or threonine was not reversed by valine addition. Functional characterization of the only predicted chlamydial transporter for branched-chain amino acids, BrnQ, revealed that it can be blocked by leucine, isoleucine, methionine, or phenylalanine but not by serine, glycine, or threonine. This chlamydial transporter is the only known BrnQ homolog possessing specificity for methionine, suggesting a unique strategy for methionine uptake among gram-negative bacteria. The antichlamydial effects of leucine, isoleucine, methionine, and phenylalanine could be explained as competitive inhibition of the BrnQ transporter and subsequent valine starvation.

Published ahead of print on 16 November 2007.

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