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Simultaneous Detection of Multiple Fish Pathogens Using a Naked-Eye Readable DNA Microarray
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, St...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Molecular Diversity Preservation International (MDPI)
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376613/ https://www.ncbi.nlm.nih.gov/pubmed/22736973 http://dx.doi.org/10.3390/s120302710 |
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author | Chang, Chin-I Hung, Pei-Hsin Wu, Chia-Che Cheng, Ta Chih Tsai, Jyh-Ming Lin, King-Jung Lin, Chung-Yen |
author_facet | Chang, Chin-I Hung, Pei-Hsin Wu, Chia-Che Cheng, Ta Chih Tsai, Jyh-Ming Lin, King-Jung Lin, Chung-Yen |
author_sort | Chang, Chin-I |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3376613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-33766132012-06-25 Simultaneous Detection of Multiple Fish Pathogens Using a Naked-Eye Readable DNA Microarray Chang, Chin-I Hung, Pei-Hsin Wu, Chia-Che Cheng, Ta Chih Tsai, Jyh-Ming Lin, King-Jung Lin, Chung-Yen Sensors (Basel) Article 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. Molecular Diversity Preservation International (MDPI) 2012-02-29 /pmc/articles/PMC3376613/ /pubmed/22736973 http://dx.doi.org/10.3390/s120302710 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Chang, Chin-I Hung, Pei-Hsin Wu, Chia-Che Cheng, Ta Chih Tsai, Jyh-Ming Lin, King-Jung Lin, Chung-Yen Simultaneous Detection of Multiple Fish Pathogens Using a Naked-Eye Readable DNA Microarray |
title | Simultaneous Detection of Multiple Fish Pathogens Using a Naked-Eye Readable DNA Microarray |
title_full | Simultaneous Detection of Multiple Fish Pathogens Using a Naked-Eye Readable DNA Microarray |
title_fullStr | Simultaneous Detection of Multiple Fish Pathogens Using a Naked-Eye Readable DNA Microarray |
title_full_unstemmed | Simultaneous Detection of Multiple Fish Pathogens Using a Naked-Eye Readable DNA Microarray |
title_short | Simultaneous Detection of Multiple Fish Pathogens Using a Naked-Eye Readable DNA Microarray |
title_sort | simultaneous detection of multiple fish pathogens using a naked-eye readable dna microarray |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376613/ https://www.ncbi.nlm.nih.gov/pubmed/22736973 http://dx.doi.org/10.3390/s120302710 |
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