Evidence map›Paper›PMID 24616884›Full record

ReviewFrontiers in cellular and infection microbiology2014

Chlamydia exploit the mammalian tryptophan-depletion defense strategy as a counter-defensive cue to trigger a survival state of persistence.

Carol A Bonner, Gerald I Byrne, Roy A Jensen

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cellular and infection microbiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.4field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Article
  3. A 2-pyridone amide inhibitor of transcriptional activity inAntimicrobial agents and chemotherapy · 2023
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Localized Peptidoglycan Biosynthesis inFrontiers in microbiology · 2021
    Article
  13. Allosteric inhibitors of Mycobacterium tuberculosis tryptophan synthase.Protein science : a publication of the Protein Society · 2020
    Article
  14. Article
  15. Article
  16. Chlamydial Infection From Outside to Inside.Frontiers in microbiology · 2019
    Review
  17. Seventy Years ofFrontiers in microbiology · 2019
    Review
  18. Article
  19. Frontiers in microbiology · 2018
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Carol A BonnerMicrobiology and Cell Science, Emerson Hall, University of Florida Gainesville, FL, USA.
Gerald I ByrneDepartment of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center Memphis, TN, USA.
Roy A JensenMicrobiology and Cell Science, Emerson Hall, University of Florida Gainesville, FL, USA.
University of Florida · USUniversity of Tennessee Health Science Center · US

Funding

IMMUNITY AND LATENCY TO CHLAMYDIAL INFECTIONSR01AI019782 · NIAID · UNIVERSITY OF WISCONSIN MADISON · PI BYRNE, GERALD IRWIN · 1985 to 2014
$4.7M
NIAID NIH HHS HHSN272200900040CNIAID NIH HHS R01 AI019782
6 · The paper itself

Abstract

We previously proposed that in Chlamydiaceae rapid vegetative growth and a quiescent state of survival (persistence) depend upon alternative protein translational profiles dictated by host tryptophan (Trp) availability. These alternative profiles correspond, respectively, with a set of chlamydial proteins having higher-than-predicted contents of Trp ("Up-Trp" selection), or with another set exhibiting lower-than-predicted contents of Trp ("Down-Trp" selection). A comparative evaluation of Chlamydiaceae proteomes for Trp content has now been extended to a number of other taxon families within the Chlamydiales Order. At the Order level, elevated Trp content occurs for transporters of nucleotides, S-adenosylmethionine (SAM), dicarboxylate substrates, and Trp itself. For Trp and nucleotide transporters, this is even more pronounced in other chlamydiae families (Parachlamydiaceae, Waddliaceae, and Simkaniaceae) due to extensive paralog expansion. This suggests that intracellular Trp availability served as an ancient survival cue for enhancement or restraint of chlamydial metabolism in the common Chlamydiales ancestor. The Chlamydiaceae Family further strengthened Up-Trp selection for proteins that function in cell division, lipopolysaccharide biosynthesis, and methyltransferase reactions. Some proteins that exhibit Up-Trp selection are uniquely present in the Chlamydiaceae, e.g., cytotoxin and the paralog families of polymorphic membrane proteins (Pmp's). A striking instance of Down-Trp selection in the Chlamydiaceae is the chorismate biosynthesis pathway and the connecting menaquinone pathway. The newly recognized 1,4-dihydroxy-6-napthoate pathway of menaquinone biosynthesis operates in Chlamydiaceae, whereas the classic 2-napthoate pathway is used in the other Chlamydiales families. Because of the extreme Down-Trp selection, it would appear that menaquinone biosynthesis is particularly important to the integrity of the persistent state maintained under conditions of severe Trp limitation, and may thus be critical for perpetuation of chronic disease states.

Indexed as

Gene Expression Regulation, BacterialHost-Pathogen InteractionsMicrobial ViabilityAnimalsChlamydiaHumansMetabolic Networks and PathwaysTryptophanTryptophanchlamydiaeDown-Trp selectionmenaquinone biosynthesispersistencereductive evolutiontryptophanUp-Trp selection

Identifiers

PMID24616884
PMCPMC3937554
OpenAlexW2115866722

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.