Evidence map›Paper›PMID 19703979›Full record

ArticleInfection and immunity2009

Branched-chain amino acids are required for the survival and virulence of Actinobacillus pleuropneumoniae in swine.

Sargurunathan Subashchandrabose, Rhiannon M LeVeque, Trevor K Wagner, Roy N Kirkwood, Matti Kiupel, Martha H Mulks

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  9. Comparative Genomics ofInternational journal of genomics · 2020
    Article
  10. AtxA-Controlled Small RNAs ofFrontiers in microbiology · 2020
    Article
  11. Review
  12. Article
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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

6 authors at 1 institution in 1 country.

Sargurunathan SubashchandraboseComparative Medicine and Integrative Biology Program, Department of Microbiology and Molecular Genetics, 5193 BPS Building, Michigan State University, East Lansing, MI 48824, USA.
Rhiannon M LeVeque
Trevor K Wagner
Roy N Kirkwood
Matti Kiupel
Martha H Mulks
Michigan State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In Actinobacillus pleuropneumoniae, which causes porcine pleuropneumonia, ilvI was identified as an in vivo-induced (ivi) gene and encodes the enzyme acetohydroxyacid synthase (AHAS) required for branched-chain amino acid (BCAA) biosynthesis. ilvI and 7 of 32 additional ivi promoters were upregulated in vitro when grown in chemically defined medium (CDM) lacking BCAA. Based on these observations, we hypothesized that BCAA would be found at limiting concentrations in pulmonary secretions and that A. pleuropneumoniae mutants unable to synthesize BCAA would be attenuated in a porcine infection model. Quantitation of free amino acids in porcine pulmonary epithelial lining fluid showed concentrations of BCAA ranging from 8 to 30 micromol/liter, which is 10 to 17% of the concentration in plasma. The expression of both ilvI and lrp, a global regulator that is required for ilvI expression, was strongly upregulated in CDM containing concentrations of BCAA similar to those found in pulmonary secretions. Deletion-disruption mutants of ilvI and lrp were both auxotrophic for BCAA in CDM and attenuated compared to wild-type A. pleuropneumoniae in competitive index experiments in a pig infection model. Wild-type A. pleuropneumoniae grew in CDM+BCAA but not in CDM-BCAA in the presence of sulfonylurea AHAS inhibitors. These results clearly demonstrate that BCAA availability is limited in the lungs and support the hypothesis that A. pleuropneumoniae, and potentially other pulmonary pathogens, uses limitation of BCAA as a cue to regulate the expression of genes required for survival and virulence. These results further suggest a potential role for AHAS inhibitors as antimicrobial agents against pulmonary pathogens.

Indexed as

Gene Expression Regulation, BacterialAcetolactate SynthaseActinobacillus InfectionsActinobacillus pleuropneumoniaeAmino Acids, Branched-ChainAnimalsBacterial ProteinsBronchoalveolar Lavage FluidLeucine-Responsive Regulatory ProteinMutationReverse Transcriptase Polymerase Chain ReactionSwineUp-RegulationVirulenceAcetolactate SynthaseAmino Acids, Branched-ChainBacterial ProteinsIlvI protein, BacteriaLeucine-Responsive Regulatory Protein

Identifiers

PMID19703979
PMCPMC2772520
OpenAlexW2150050125

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.