Evidence map›Paper›PMID 35408437›Full record

ArticleMolecules (Basel, Switzerland)2022

Automated Microbial Library Generation Using the Bioinformatics Platform IDBac.

Chase M Clark, Linh Nguyen, Van Cuong Pham, Laura M Sanchez, Brian T Murphy

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Rationally Minimizing Natural Product Libraries Using Mass Spectrometry.bioRxiv : the preprint server for biology · 2024
    Article
  8. 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

5 authors.

Chase M ClarkDepartment of Pharmaceutical Sciences, Center for Biomolecular Sciences, College of Pharmacy, University of Illinois at Chicago, 833 S. Wood St., Chicago, IL 60612, USA.ORCID 0000-0001-6439-9397
Linh NguyenInstitute of Marine Biochemistry, Vietnam Academy of Science and Technology, Nghiado, Caugiay, Hanoi 10000, Vietnam.
Van Cuong PhamInstitute of Marine Biochemistry, Vietnam Academy of Science and Technology, Nghiado, Caugiay, Hanoi 10000, Vietnam.
Laura M SanchezDepartment of Chemistry and Biochemistry, University of California Santa Cruz, 1156 High Street, Santa Cruz, CA 95064, USA.ORCID 0000-0001-9223-7977
Brian T MurphyDepartment of Pharmaceutical Sciences, Center for Biomolecular Sciences, College of Pharmacy, University of Illinois at Chicago, 833 S. Wood St., Chicago, IL 60612, USA.ORCID 0000-0002-1372-3887

Funding

MALDI-TOF MS/IDBac to discover antibiotics from the Great Lakes sponge microbiomeR01GM125943 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MURPHY, BRIAN THACHER, SANCHEZ, LAURA MARGARET · 2018 to 2021
$2.1M
Enhancing basic and translational TB research in northern VietnamD43TW010530 · FIC · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MURPHY, BRIAN THACHER, PHAM, CUONG VAN · 2017 to 2021
$1.1M
Identification of antimicrobial reagents against TB and ESKAPE pathogens from bacteria collected in VietnamR01AI160696 · NIAID · --INSTITUTE OF MARINE BIOCHEMISTRY · PI NGUYEN, LINH THUY, TRAN, TUAN ANH · 2021 to 2021
$130k
A New Paradigm in Developing Microbial Libraries for Drug DiscoveryF31AT010419 · NCCIH · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CLARK, CHASE MADISON · 2019 to 2020
$91k
NIAID NIH HHS R01 AI160696NIGMS NIH HHS R01 GM125943NIH HHS D43TW010530NIH HHS F31AT010419NIH HHS R01AI160696-01NIH HHS R01GM125943
6 · The paper itself

Abstract

Libraries of microorganisms have served as a cornerstone of therapeutic drug discovery, though the continued re-isolation of known natural product chemical entities has remained a significant obstacle to discovery efforts. A major contributing factor to this redundancy is the duplication of bacterial taxa in a library, which can be mitigated through the use of a variety of DNA sequencing strategies and/or mass spectrometry-informed bioinformatics platforms so that the library is created with minimal phylogenetic, and thus minimal natural product overlap. IDBac is a MALDI-TOF mass spectrometry-based bioinformatics platform used to assess overlap within collections of environmental bacterial isolates. It allows environmental isolate redundancy to be reduced while considering both phylogeny and natural product production. However, manually selecting isolates for addition to a library during this process was time intensive and left to the researcher's discretion. Here, we developed an algorithm that automates the prioritization of hundreds to thousands of environmental microorganisms in IDBac. The algorithm performs iterative reduction of natural product mass feature overlap within groups of isolates that share high homology of protein mass features. Employing this automation serves to minimize human bias and greatly increase efficiency in the microbial strain prioritization process.

Indexed as

Biological ProductsComputational BiologyBacteriaGene LibraryHumansPhylogenySpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationBiological Productsbioinformaticsdrug discoveryIDBacMALDImicroorganismsnatural products

Identifiers

PMID35408437
PMCPMC9000433

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.