Literature DB >> 16772415

Naturally occurring amino acids differentially influence the development of Chlamydia trachomatis and Chlamydia (Chlamydophila) pneumoniae.

Hesham M Al-Younes, Joscha Gussmann, Peter R Braun, Volker Brinkmann, Thomas F Meyer.   

Abstract

The differential influence of individual amino acids on the growth of Chlamydia trachomatis versus Chlamydia (Chlamydophila) pneumoniae was investigated. Certain essential amino acids added in excess at the middle of the infection course resulted in varying degrees of abnormality in the development of the two species. If amino acids were added as early as 2 h post-infection, these effects were even more pronounced. The most effective amino acids in terms of C. trachomatis growth inhibition were leucine, isoleucine, methionine and phenylalanine. These amino acids elicited similar effects against C. pneumoniae, except methionine, which, surprisingly, showed a lower inhibitory activity. Tryptophan and valine marginally inhibited C. trachomatis growth and, paradoxically, led to a considerable enhancement of C. pneumoniae growth. On the other hand, some non-essential amino acids administered at the middle of or throughout the infection course differentially affected the development of the two species. For example, C. trachomatis growth was efficiently inhibited by glycine and serine, whereas C. pneumoniae was relatively less sensitive to these agents. Another difference was apparent for glutamate, glutamine and aspartate, which stimulated C. pneumoniae growth more than that of C. trachomatis. Overall, several distinctive patterns of susceptibility to excess amino acid levels were revealed for two representative C. trachomatis and C. pneumoniae isolates. Perturbation of amino acid levels, e.g. of leucine and isoleucine, might form a basis for the development of novel treatment or preventive regimens for chlamydial diseases.

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Year:  2006        PMID: 16772415     DOI: 10.1099/jmm.0.46445-0

Source DB:  PubMed          Journal:  J Med Microbiol        ISSN: 0022-2615            Impact factor:   2.472


  8 in total

Review 1.  Evolution to a chronic disease niche correlates with increased sensitivity to tryptophan availability for the obligate intracellular bacterium Chlamydia pneumoniae.

Authors:  Wilhelmina M Huston; Christopher J Barker; Anu Chacko; Peter Timms
Journal:  J Bacteriol       Date:  2014-03-28       Impact factor: 3.490

2.  Chlamydia trachomatis Oligopeptide Transporter Performs Dual Functions of Oligopeptide Transport and Peptidoglycan Recycling.

Authors:  Raghuveer Singh; George Liechti; Jessica A Slade; Anthony T Maurelli
Journal:  Infect Immun       Date:  2020-04-20       Impact factor: 3.441

3.  Competitive inhibition of amino acid uptake suppresses chlamydial growth: involvement of the chlamydial amino acid transporter BrnQ.

Authors:  Peter R Braun; Hesham Al-Younes; Joscha Gussmann; Jeannette Klein; Erwin Schneider; Thomas F Meyer
Journal:  J Bacteriol       Date:  2007-11-16       Impact factor: 3.490

4.  Characterization of an acid-dependent arginine decarboxylase enzyme from Chlamydophila pneumoniae.

Authors:  Teresa N Giles; David E Graham
Journal:  J Bacteriol       Date:  2007-08-10       Impact factor: 3.490

5.  Genomic factors related to tissue tropism in Chlamydia pneumoniae infection.

Authors:  Thomas Weinmaier; Jonathan Hoser; Sebastian Eck; Inga Kaufhold; Kensuke Shima; Tim M Strom; Thomas Rattei; Jan Rupp
Journal:  BMC Genomics       Date:  2015-04-07       Impact factor: 3.969

6.  Human enteroendocrine cell responses to infection with Chlamydia trachomatis: a microarray study.

Authors:  Aldona Dlugosz; Sandra Muschiol; Katherina Zakikhany; Ghazaleh Assadi; Mauro D'Amato; Greger Lindberg
Journal:  Gut Pathog       Date:  2014-06-16       Impact factor: 4.181

7.  Genomewide Transcriptional Responses of Iron-Starved Chlamydia trachomatis Reveal Prioritization of Metabolic Precursor Synthesis over Protein Translation.

Authors:  Amanda J Brinkworth; Mark R Wildung; Rey A Carabeo
Journal:  mSystems       Date:  2018-02-13       Impact factor: 6.496

8.  De novo histidine biosynthesis protects Mycobacterium tuberculosis from host IFN-γ mediated histidine starvation.

Authors:  Abhisek Dwivedy; Anam Ashraf; Bhavya Jha; Deepak Kumar; Nisheeth Agarwal; Bichitra K Biswal
Journal:  Commun Biol       Date:  2021-03-25
  8 in total

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