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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...

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Autores principales: Chang, Chin-I, Hung, Pei-Hsin, Wu, Chia-Che, Cheng, Ta Chih, Tsai, Jyh-Ming, Lin, King-Jung, Lin, Chung-Yen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2012
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.
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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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