Evidence map›Paper›PMID 36734186›Full record

ArticleChembiochem : a European journal of chemical biology2023

Whole-Cell MALDI-ToF MS Coupled with Untargeted Metabolomics Facilitates Investigations of Microbial Chemical Interactions.

Nicole Aiosa, Anupama Sinha, Hanan Albataineh, Ashlee M Phillips, Catherine M Mageeney, Delaney S Wilde, Kelly P Williams, Nicole M Collette, Steven S Branda, Neha Garg

Open access · greenAbstract read
In one paragraph

Article in Chembiochem : a European journal of chemical biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 47% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

10 authors at 4 institutions in 1 country.

Nicole AiosaSchool of Chemistry and Biochemistry, Georgia Institute of Technology, 950 Atlantic Drive, Atlanta, GA 30332, USA.ORCID 0000-0002-4219-5470
Anupama SinhaBiotechnology & Bioengineering, Sandia National Laboratories, 7011 East Avenue, Livermore, CA 94550, USA.ORCID 0000-0001-5381-7370
Hanan AlbatainehSchool of Chemistry and Biochemistry, Georgia Institute of Technology, 950 Atlantic Drive, Atlanta, GA 30332, USA.
Ashlee M PhillipsBiosciences and Biotechnology Division, Lawrence Livermore National Laboratory, 7000 East Avenue, Livermore, CA 94550, USA.ORCID 0000-0002-5494-7916
Catherine M MageeneyBiotechnology & Bioengineering, Sandia National Laboratories, 7011 East Avenue, Livermore, CA 94550, USA.ORCID 0000-0001-7969-1622
Delaney S WildeDepartment of Bioengineering, University of Pennsylvania, 210 South 33rd Street, Philadelphia, PA 19104, USA.ORCID 0000-0001-5115-3208
Kelly P WilliamsSystems Biology, Sandia National Laboratories, 7011 East Avenue, Livermore, CA 94550, USA.ORCID 0000-0002-2606-9562
Nicole M ColletteBiosciences and Biotechnology Division, Lawrence Livermore National Laboratory, 7000 East Avenue, Livermore, CA 94550, USA.ORCID 0000-0002-9068-8712
Steven S BrandaSystems Biology, Sandia National Laboratories, 7011 East Avenue, Livermore, CA 94550, USA.ORCID 0000-0001-8763-1013
Neha GargSchool of Chemistry and Biochemistry, Georgia Institute of Technology, 950 Atlantic Drive, Atlanta, GA 30332, USA.ORCID 0000-0002-2760-7123
Sandia National Laboratories California · USGeorgia Institute of Technology · USLawrence Livermore National Laboratory · USUniversity of Pennsylvania · US

Funding

Molecular analysis of bacterial interactionsR35GM150870 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI Neha Garg · 2023 to 2026
$1.5M
NIGMS NIH HHS R35 GM150870
6 · The paper itself

Abstract

The emergence of drug-resistant pathogens necessitates the development of new countermeasures. In this regard, the introduction of probiotics to directly attack or competitively exclude pathogens presents a useful strategy. Application of this approach requires an understanding of how a probiotic and its target pathogen interact. A key means of probiotic-pathogen interaction involves the production of small molecules called natural products (NPs). Here, we report the use of whole-cell matrix-assisted laser desorption/ionization time-of-flight (MALDI-ToF) mass spectrometry to characterize NP production by candidate probiotics (mouse airway microbiome isolates) when co-cultured with the respiratory pathogen Burkholderia. We found that a Bacillus velezensis strain inhibits growth of and elicits NP production by Burkholderia thailandensis. Dereplication of known NPs detected in the metabolome of this B. velezensis strain suggests that a previously unannotated bioactive compound is involved. Thus, we present the use of whole-cell MALDI as a broadly applicable method for screening the NP composition of microbial co-cultures; this can be combined with other -omics methods to characterize probiotic-pathogen and other microbe-microbe interactions.

Indexed as

MetabolomicsAnimalsMiceSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationBacillus sp.Burkholderia thailandensismass spectrometrymass spectrometry imagingmetabolomicsmolecular networkingnatural productswhole-cell MALDI-ToF

Identifiers

PMID36734186
PMCPMC13505854
OpenAlexW4319063325

What Socratic 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 Socratic graph.