Evidence map›Paper›PMID 35350846›Full record

ArticlemSphere2022

The Stickland Reaction Precursor

A D Reed, J R Fletcher, Y Y Huang, R Thanissery, A J Rivera, R J Parsons, A K Stewart, D J Kountz, A Shen, E P Balskus and 1 more

Open access · goldAbstract read
In one paragraph

Article in mSphere, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 27 citations in OpenAlex.

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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

11 authors at 3 institutions in 1 country.

A D Reed *Department of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State Universitygrid.40803.3f, Raleigh, North Carolina, USA.
J R Fletcher *Department of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State Universitygrid.40803.3f, Raleigh, North Carolina, USA.
Y Y HuangDepartment of Chemistry and Chemical Biology, Harvard Universitygrid.38142.3c, Cambridge, Massachusetts, USA.ORCID 0000-0003-1263-1515
R ThanisseryDepartment of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State Universitygrid.40803.3f, Raleigh, North Carolina, USA.
A J RiveraDepartment of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State Universitygrid.40803.3f, Raleigh, North Carolina, USA.
R J ParsonsDepartment of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State Universitygrid.40803.3f, Raleigh, North Carolina, USA.
A K StewartMolecular Education, Technology and Research Innovation Center, North Carolina State Universitygrid.40803.3f, Raleigh, North Carolina, USA.
D J KountzDepartment of Chemistry and Chemical Biology, Harvard Universitygrid.38142.3c, Cambridge, Massachusetts, USA.
A ShenDepartment of Molecular Biology and Microbiology, Tufts Universitygrid.429997.8 School of Medicine, Boston, Massachusetts, USA.ORCID 0000-0002-9786-5742
E P BalskusDepartment of Chemistry and Chemical Biology, Harvard Universitygrid.38142.3c, Cambridge, Massachusetts, USA.
C M TheriotDepartment of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State Universitygrid.40803.3f, Raleigh, North Carolina, USA.ORCID 0000-0002-1895-8941
North Carolina State University · USHarvard University · USTufts University · US

Funding

Targeted bacterial restoration of colonization resistance against C. difficileR35GM119438 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI THERIOT, CASEY MICHELLE · 2016 to 2020
$1.6M
NIGMS NIH HHS R35 GM119438
6 · The paper itself

Abstract

An intact gut microbiota confers colonization resistance against Clostridioides difficile through a variety of mechanisms, likely including competition for nutrients. Recently, proline was identified as an important environmental amino acid that C. difficile uses to support growth and cause significant disease. A posttranslationally modified form, trans-4-hydroxyproline, is highly abundant in collagen, which is degraded by host proteases in response to C. difficile toxin activity. The ability to dehydrate trans-4-hydroxyproline via the HypD glycyl radical enzyme is widespread among gut microbiota, including C. difficile and members of the commensal

Indexed as

Clostridioides difficileClostridium InfectionsAnimalsClostridioidesClostridiumHydroxyprolineMicePeptide HydrolasesProlineHydroxyprolinePeptide HydrolasesProlinetrans-4-hydroxy-L-prolineamino acidsClostridiaClostridioides difficilecolonization resistancehydroxyprolineStickland fermentationStickland reaction

Identifiers

PMID35350846
PMCPMC9044972
OpenAlexW4220715588

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.