Evidence map›Paper›PMID 28599915›Full record

ArticleJournal of microbiological methods2017

Multiplex polymerase chain reaction for identification of Escherichia coli, Escherichia albertii and Escherichia fergusonii.

Rebecca L Lindsey, L Garcia-Toledo, D Fasulo, L M Gladney, N Strockbine

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Journal of microbiological methods, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 92 citations in OpenAlex.

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  12. Emergence and Genomic Features of aAntibiotics (Basel, Switzerland) · 2023
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  13. Characterization of anPathogens (Basel, Switzerland) · 2023
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  16. Efflux Pumps and Different Genetic Contexts ofInternational journal of molecular sciences · 2023
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  17. Identification and Genomic Characterization ofPathogens (Basel, Switzerland) · 2022
    Article
  18. Article
  19. Microbiology and Epidemiology ofMicroorganisms · 2022
    Review
  20. 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 at 2 institutions in 1 country.

Rebecca L LindseyEnteric Diseases Laboratory Branch, Centers for Disease Control and Prevention, Atlanta, Georgia. Electronic address: Rebecca.Lindsey@cdc.hhs.gov.
L Garcia-ToledoEnteric Diseases Laboratory Branch, Centers for Disease Control and Prevention, Atlanta, Georgia; Oak Ridge Institute for Science and Education, TN, USA.
D FasuloPattern Genomics, LLC, CT, USA.
L M GladneyEnteric Diseases Laboratory Branch, Centers for Disease Control and Prevention, Atlanta, Georgia; IHRC, Inc., Atlanta, GA, USA.
N StrockbineEnteric Diseases Laboratory Branch, Centers for Disease Control and Prevention, Atlanta, Georgia.
Centers for Disease Control and Prevention · USOak Ridge Associated Universities · US

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

Escherichia coli, Escherichia albertii, and Escherichia fergusonii are closely related bacteria that can cause illness in humans, such as bacteremia, urinary tract infections and diarrhea. Current identification strategies for these three species vary in complexity and typically rely on the use of multiple phenotypic and genetic tests. To facilitate their rapid identification, we developed a multiplex PCR assay targeting conserved, species-specific genes. We used the Daydreamer™ (Pattern Genomics, USA) software platform to concurrently analyze whole genome sequence assemblies (WGS) from 150 Enterobacteriaceae genomes (107 E. coli, 5 Shigella spp., 21 E. albertii, 12 E. fergusonii and 5 other species) and design primers for the following species-specific regions: a 212bp region of the cyclic di-GMP regulator gene (cdgR, AW869_22935 from genome K-12 MG1655, CP014225) for E. coli/Shigella; a 393bp region of the DNA-binding transcriptional activator of cysteine biosynthesis gene (EAKF1_ch4033 from genome KF1, CP007025) for E. albertii; and a 575bp region of the palmitoleoyl-acyl carrier protein (ACP)-dependent acyltransferase (EFER_0790 from genome ATCC 35469, CU928158) for E. fergusonii. We incorporated the species-specific primers into a conventional multiplex PCR assay and assessed its performance with a collection of 97 Enterobacteriaceae strains. The assay was 100% sensitive and specific for detecting the expected species and offers a quick and accurate strategy for identifying E. coli, E. albertii, and E. fergusonii in either a single reaction or by in silico PCR with sequence assemblies.

Indexed as

Cross InfectionDNA, BacterialDNA PrimersEnterobacteriaceaeEscherichiaEscherichia coliEscherichia coli InfectionsEscherichia coli ProteinsGenome, BacterialHumansMultiplex Polymerase Chain ReactionSensitivity and SpecificityDNA, BacterialDNA PrimersEscherichia coli ProteinsalbertiiEscherichia colifergusoniiMultiplexPCR

Identifiers

PMID28599915
PMCPMC5603207
OpenAlexW2622053644

What OpenQuestion holds

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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.