Evidence map›Paper›PMID 24595070›Full record

ArticlePloS one2014

Genomic and metabolomic insights into the natural product biosynthetic diversity of a feral-hog-associated Brevibacillus laterosporus strain.

Christine M Theodore, Blake W Stamps, Jarrod B King, Lauren S L Price, Douglas R Powell, Bradley S Stevenson, Robert H Cichewicz

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

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  12. Role of Proline in Pathogen and Host Interactions.Antioxidants & redox signaling · 2019
    Review
  13. Article
  14. Article
  15. Retrospective analysis of natural products provides insights for future discovery trends.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  16. 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

7 authors.

Christine M TheodoreDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma, United States of America; Natural Products Discovery Group, Institute for Natural Products Applications and Research Technologies, University of Oklahoma, Norman, Oklahoma, United States of America.
Blake W StampsDepartment of Microbiology and Plant Biology, University of Oklahoma, Norman, Oklahoma, United States of America.
Jarrod B KingDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma, United States of America; Natural Products Discovery Group, Institute for Natural Products Applications and Research Technologies, University of Oklahoma, Norman, Oklahoma, United States of America.
Lauren S L PriceDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma, United States of America; Natural Products Discovery Group, Institute for Natural Products Applications and Research Technologies, University of Oklahoma, Norman, Oklahoma, United States of America.
Douglas R PowellDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma, United States of America.
Bradley S StevensonNatural Products Discovery Group, Institute for Natural Products Applications and Research Technologies, University of Oklahoma, Norman, Oklahoma, United States of America; Department of Microbiology and Plant Biology, University of Oklahoma, Norman, Oklahoma, United States of America.
Robert H CichewiczDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma, United States of America; Natural Products Discovery Group, Institute for Natural Products Applications and Research Technologies, University of Oklahoma, Norman, Oklahoma, United States of America.

Funding

Antimicrobials from Mammalian MicrobiomesR21AI101487 · NIAID · UNIVERSITY OF OKLAHOMA · PI CICHEWICZ, ROBERT HENRY, STEVENSON, BRADLEY SCOTT · 2012 to 2013
$391k
NIAID NIH HHS 5R21AI101487NIAID NIH HHS R21 AI101487
6 · The paper itself

Abstract

Bacteria associated with mammals are a rich source of microbial biodiversity; however, little is known concerning the abilities of these microbes to generate secondary metabolites. This report focuses on a bacterium isolated from the ear of a feral hog from southwestern Oklahoma, USA. The bacterium was identified as a new strain (PE36) of Brevibacillus latersporus, which was shown via genomic analysis to contain a large number of gene clusters presumably involved in secondary metabolite biosynthesis. A scale-up culture of B. latersporus PE36 yielded three bioactive compounds that inhibited the growth of methicillin-resistant Staphylococcus aureus (basiliskamides A and B and 12-methyltetradecanoic acid). Further studies of the isolate's secondary metabolome provided both new (auripyrazine) and previously-described pyrazine-containing compounds. In addition, a new peptidic natural product (auriporcine) was purified that was determined to be composed of a polyketide unit, two L-proline residues, two D-leucine residues, one L-leucine residue, and a reduced L-phenylalanine (L-phenylalanol). An examination of the genome revealed two gene clusters that are likely responsible for generating the basiliskamides and auriporcine. These combined genomic and chemical studies confirm that new and unusual secondary metabolites can be obtained from the bacterial associates of wild mammals.

Indexed as

GenomeMetabolomicsAnimalsAnimals, WildBiological ProductsBrevibacillusGenes, BacterialPhylogenySwineBiological Products

Identifiers

PMID24595070
PMCPMC3940840

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.