Evidence map›Paper›PMID 22736973›Full record

ArticleSensors (Basel, Switzerland)2012

Simultaneous detection of multiple fish pathogens using a naked-eye readable DNA microarray.

Chin-I Chang, Pei-Hsin Hung, Chia-Che Wu, Ta Chih Cheng, Jyh-Ming Tsai, King-Jung Lin, Chung-Yen Lin

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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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

5 citing papers in PubMed.

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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

7 authors.

Chin-I ChangAquaculture Division, Fisheries Research Institute, Ministry of Agriculture, Keelung 20246, Taiwan. cichang@mail.tfrin.gov.tw
Pei-Hsin Hung
Chia-Che Wu
Ta Chih Cheng
Jyh-Ming Tsai
King-Jung Lin
Chung-Yen Lin

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We coupled 16S rDNA PCR and DNA hybridization technology to construct a microarray for simultaneous detection and discrimination of eight fish pathogens (Aeromonas hydrophila, Edwardsiella tarda, Flavobacterium columnare, Lactococcus garvieae, Photobacterium damselae, Pseudomonas anguilliseptica, Streptococcus iniae and Vibrio anguillarum) commonly encountered in aquaculture. The array comprised short oligonucleotide probes (30 mer) complementary to the polymorphic regions of 16S rRNA genes for the target pathogens. Targets annealed to the microarray probes were reacted with streptavidin-conjugated alkaline phosphatase and nitro blue tetrazolium/5-bromo-4-chloro-3'-indolylphosphate, p-toluidine salt (NBT/BCIP), resulting in blue spots that are easily visualized by the naked eye. Testing was performed against a total of 168 bacterial strains, i.e., 26 representative collection strains, 81 isolates of target fish pathogens, and 61 ecologically or phylogenetically related strains. The results showed that each probe consistently identified its corresponding target strain with 100% specificity. The detection limit of the microarray was estimated to be in the range of 1 pg for genomic DNA and 10(3) CFU/mL for pure pathogen cultures. These high specificity and sensitivity results demonstrate the feasibility of using DNA microarrays in the diagnostic detection of fish pathogens.

Indexed as

ColorimetryOligonucleotide Array Sequence AnalysisAlkaline PhosphataseAnimalsBacteriaDNA PrimersDNA ProbesFish DiseasesFishesGenome, BacterialNucleic Acid HybridizationPolymerase Chain ReactionRNA, Ribosomal, 16SStreptavidinTetrazolium Salts4-anisyltetrazolium blueAlkaline PhosphataseDNA PrimersDNA ProbesRNA, Ribosomal, 16SStreptavidinTetrazolium Salts16S rDNAfish pathogen detectionnaked-eye reading microarray

Identifiers

PMID22736973
PMCPMC3376613

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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.