Evidence map›Paper›PMID 22389878›Full record

ArticleAnnals of laboratory medicine2012

Evaluation of DNA extraction methods and their clinical application for direct detection of causative bacteria in continuous ambulatory peritoneal dialysis culture fluids from patients with peritonitis by using broad-range PCR.

Si Hyun Kim, Haeng Soon Jeong, Yeong Hoon Kim, Sae Am Song, Ja Young Lee, Seung Hwan Oh, Hye Ran Kim, Jeong Nyeo Lee, Weon-Gyu Kho, Jeong Hwan Shin

Open access · hybridAbstract readEvaluation Study
In one paragraph

Article in Annals of laboratory medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

16 citing papers in PubMed, 34 citations in OpenAlex.

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  8. Validation of real-time PCR technique for detection of Mycobacterium bovis and Brucella abortus in bovine raw milk.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2020
    Article
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  11. ISPD Peritonitis Recommendations: 2016 Update on Prevention and Treatment.Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis · 2016
    Review
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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

10 authors at 2 institutions in 1 country.

Si Hyun KimDepartment of Laboratory Medicine, Inje University College of Medicine, Busan, Korea.
Haeng Soon Jeong
Yeong Hoon Kim
Sae Am Song
Ja Young Lee
Seung Hwan Oh
Hye Ran Kim
Jeong Nyeo Lee
Weon-Gyu Kho
Jeong Hwan Shin
Inje University · KRInje University Busan Paik Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aims of this study were to compare several DNA extraction methods and 16S rDNA primers and to evaluate the clinical utility of broad-range PCR in continuous ambulatory peritoneal dialysis (CAPD) culture fluids.

methodsSix type strains were used as model organisms in dilutions from 10(8) to 10(0) colony-forming units (CFU)/mL for the evaluation of 5 DNA extraction methods and 5 PCR primer pairs. Broad-range PCR was applied to 100 CAPD culture fluids, and the results were compared with conventional culture results.

resultsThere were some differences between the various DNA extraction methods and primer sets with regard to the detection limits. The InstaGene Matrix (Bio-Rad Laboratories, USA) and Exgene Clinic SV kits (GeneAll Biotechnology Co. Ltd, Korea) seem to have higher sensitivities than the others. The results of broad-range PCR were concordant with the results from culture in 97% of all cases (97/100). Two culture-positive cases that were broad-range PCR-negative were identified as Candida albicans, and 1 PCR-positive but culture-negative sample was identified as Bacillus circulans by sequencing. Two samples among 54 broad-range PCR-positive products could not be sequenced.

conclusionsThere were differences in the analytical sensitivity of various DNA extraction methods and primers for broad-range PCR. The broad-range PCR assay can be used to detect bacterial pathogens in CAPD culture fluid as a supplement to culture methods.

Indexed as

Genetic TechniquesBacillusBacteriaCandida albicansDNA, BacterialDNA PrimersHumansPeritoneal Dialysis, Continuous AmbulatoryPeritonitisPolymerase Chain ReactionReagent Kits, DiagnosticSequence Analysis, DNADNA, BacterialDNA PrimersReagent Kits, DiagnosticBroad-Range PCRCAPD culture fluidDNA extraction

Identifiers

PMID22389878
PMCPMC3289776
OpenAlexW2171294560

What OpenQuestion holds

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LicenceCC BY-NC
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.