Evidence map›Paper›PMID 25437334›Full record

ArticlePathogens (Basel, Switzerland)2013

Comprehensive analysis of prokaryotes in environmental water using DNA microarray analysis and whole genome amplification.

Takeshi Akama, Akira Kawashima, Kazunari Tanigawa, Moyuru Hayashi, Yuko Ishido, Yuqian Luo, Akihisa Hata, Noboru Fujitani, Norihisa Ishii, Koichi Suzuki

Abstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Takeshi AkamaLaboratory of Molecular Diagnostics, Department of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases, Tokyo 189-0002, Japan. akama@umich.edu.
Akira KawashimaLaboratory of Molecular Diagnostics, Department of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases, Tokyo 189-0002, Japan. akirak@jichi.ac.jp.
Kazunari TanigawaLaboratory of Molecular Diagnostics, Department of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases, Tokyo 189-0002, Japan. tanigawa@pharm.teikyo-u.ac.jp.
Moyuru HayashiLaboratory of Molecular Diagnostics, Department of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases, Tokyo 189-0002, Japan. mhayashi@rs.kagu.tus.ac.jp.
Yuko IshidoLaboratory of Molecular Diagnostics, Department of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases, Tokyo 189-0002, Japan. yishido@nih.go.jp.
Yuqian LuoLaboratory of Molecular Diagnostics, Department of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases, Tokyo 189-0002, Japan. yuqianluo31@gmail.com.
Akihisa HataDepartment of Medical Risk Management, Faculty of Risk Management, Chiba Institute of Science, Faculty of Risk and Crisis Management, Choshi, Chiba 288-0025, Japan. ahata@cis.ac.jp.
Noboru FujitaniDepartment of Medical Risk Management, Faculty of Risk Management, Chiba Institute of Science, Faculty of Risk and Crisis Management, Choshi, Chiba 288-0025, Japan. nfujitani@cis.ac.jp.
Norihisa IshiiLeprosy Research Center, National Institute of Infectious Diseases, Tokyo 189-0002, Japan. norishii@nih.go.jp.
Koichi SuzukiLaboratory of Molecular Diagnostics, Department of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases, Tokyo 189-0002, Japan. koichis@nih.go.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The microflora in environmental water consists of a high density and diversity of bacterial species that form the foundation of the water ecosystem. Because the majority of these species cannot be cultured in vitro, a different approach is needed to identify prokaryotes in environmental water. A novel DNA microarray was developed as a simplified detection protocol. Multiple DNA probes were designed against each of the 97,927 sequences in the DNA Data Bank of Japan and mounted on a glass chip in duplicate. Evaluation of the microarray was performed using the DNA extracted from one liter of environmental water samples collected from seven sites in Japan. The extracted DNA was uniformly amplified using whole genome amplification (WGA), labeled with Cy3-conjugated 16S rRNA specific primers and hybridized to the microarray. The microarray successfully identified soil bacteria and environment-specific bacteria clusters. The DNA microarray described herein can be a useful tool in evaluating the diversity of prokaryotes and assessing environmental changes such as global warming.

Identifiers

PMID25437334
PMCPMC4235703

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.