Evidence map›Paper›PMID 34260309›Full record

ArticleApplied and environmental microbiology2021

Fluorescent Protein Expression as a Proxy for Bacterial Fitness in a High-Throughput Assay.

Rudolf O Schlechter, Evan J Kear, Daniela M Remus, Mitja N P Remus-Emsermann

Open access · hybridAbstract read
In one paragraph

Article in Applied and environmental microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 19 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

4 authors at 2 institutions in 2 countries.

Rudolf O SchlechterSchool of Biological Sciences, University of Canterbury, Christchurch, New Zealand.
Evan J KearSchool of Biological Sciences, University of Canterbury, Christchurch, New Zealand.
Daniela M RemusProtein Science and Engineering, Callaghan Innovationgrid.418016.a, School of Biological Sciences, University of Canterbury, Christchurch, New Zealand.
Mitja N P Remus-EmsermannSchool of Biological Sciences, University of Canterbury, Christchurch, New Zealand.
University of Canterbury · NZCallaghan Innovation · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial growth is classically assessed by measuring the increases in optical density of pure cultures in shaken liquid media. Measuring growth using optical density has severe limitations when studying multistrain interactions, as it is not possible to measure the growth of individual strains within mixed cultures. Here, we demonstrated that constitutively expressed fluorescent proteins can be used to track the growth of individual strains in different liquid media. Fluorescence measurements were highly correlated with optical density measurements and cell counts. This allowed us to assess bacterial growth not only in pure cultures but also in mixed bacterial cultures and determine the impact of a competitor on a focal strain, thereby assessing relative fitness. Furthermore, we were able to track the growth of two different strains simultaneously by using fluorescent proteins with differential excitation and emission wavelengths. Bacterial densities measured by fluorescence yielded more consistent data between technical replicates than optical density measurements. Our setup employs fluorescence microplate readers that allow high throughput and replication.

Indexed as

Bacterial ProteinsFluorescenceHigh-Throughput Screening AssaysLuminescent ProteinsPantoeaRed Fluorescent ProteinBacterial ProteinsLuminescent ProteinsRed Fluorescent ProteincompetitionmScarletoptical densitysYFP2

Identifiers

PMID34260309
PMCPMC8388834
OpenAlexW3180988223

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.