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An Efficient Tetraplex Surveillance Tool for Salmonid Pathogens.

作者信息

von Ammon Ulla, Averink Tessa, Kumanan Karthiga, Brosnahan Cara L, Pochon Xavier, Hutson Kate S, Symonds Jane E

机构信息

Aquaculture & Marine Biosecurity, Cawthron Institute, Nelson, New Zealand.

College of Science and Engineering, James Cook University, Townsville, QLD, Australia.

出版信息

Front Microbiol. 2022 Apr 21;13:885585. doi: 10.3389/fmicb.2022.885585. eCollection 2022.


DOI:10.3389/fmicb.2022.885585
PMID:35531301
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9069008/
Abstract

Fish disease surveillance methods can be complicated and time consuming, which limits their value for timely intervention strategies on aquaculture farms. Novel molecular-based assays using droplet digital Polymerase Chain Reaction (ddPCR) can produce immediate results and enable high sample throughput with the ability to multiplex several targets using different fluorescent dyes. A ddPCR tetraplex assay was developed for priority salmon diseases for farmers in New Zealand including New Zealand -like organism 1 (NZ-RLO1), NZ-RLO2, , and . The limit of detection in singleplex and tetraplex assays was reached for most targets at 10 ng/μl with, respectively, NZ-RLO1 = 0.931 and 0.14 copies/μl, NZ-RLO2 = 0.162 and 0.21 copies/μl, 0.345 and 0.93 copies/μl, while the limit of detection for was 10 with 1.0 copies/μl and 0.7 copies/μl. While specificity of primers was demonstrated in previous studies, we detected cross-reactivity of with some strains of and with , respectively. The tetraplex assay was applied as part of a commercial fish disease surveillance program in New Zealand for 1 year to demonstrate the applicability of tetraplex tools for the salmonid aquaculture industry.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f9f/9069008/824f3fea1f73/fmicb-13-885585-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f9f/9069008/663bd9203f44/fmicb-13-885585-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f9f/9069008/d74cdbc9fa2b/fmicb-13-885585-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f9f/9069008/db2e83fa156f/fmicb-13-885585-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f9f/9069008/824f3fea1f73/fmicb-13-885585-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f9f/9069008/663bd9203f44/fmicb-13-885585-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f9f/9069008/d74cdbc9fa2b/fmicb-13-885585-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f9f/9069008/db2e83fa156f/fmicb-13-885585-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f9f/9069008/824f3fea1f73/fmicb-13-885585-g004.jpg

相似文献

[1]
An Efficient Tetraplex Surveillance Tool for Salmonid Pathogens.

Front Microbiol. 2022-4-21

[2]
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[5]
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[6]
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[8]
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引用本文的文献

[1]
Experimental Challenge of Chinook Salmon (Oncorhynchus tshawytscha) With Tenacibaculum maritimum and Tenacibaculum dicentrarchi Fulfils Koch's Postulates.

J Fish Dis. 2025-6

[2]
A novel ddPCR™ assay for eDNA detection and quantification of Greater Amberjack and three congeners in US waters: challenges and application to fisheries independent surveys.

PeerJ. 2025-1-27

[3]
Development of a Tetraplex Digital PCR Assay for the Detection of Invasive Snake Species in Florida, USA.

Ecol Evol. 2024-11-20

本文引用的文献

[1]
Salmon gut microbiota correlates with disease infection status: potential for monitoring health in farmed animals.

Anim Microbiome. 2021-4-20

[2]
Discovery and surveillance of viruses from salmon in British Columbia using viral immune-response biomarkers, metatranscriptomics, and high-throughput RT-PCR.

Virus Evol. 2020-9-1

[3]
Absolute quantification of priority bacteria in aquaculture using digital PCR.

J Microbiol Methods. 2021-4

[4]
Descriptive multi-agent epidemiology via molecular screening on Atlantic salmon farms in the northeast Pacific Ocean.

Sci Rep. 2021-2-10

[5]
Advances in understanding the impacts of global warming on marine fishes farmed offshore: Sparus aurata as a case study.

J Fish Biol. 2021-6

[6]
Multiplex droplet digital PCR assay for detection of Flavobacterium psychrophilum and Yersinia ruckeri in Norwegian aquaculture.

J Microbiol Methods. 2020-10

[7]
Optimization of Viability Treatment Essential for Accurate Droplet Digital PCR Enumeration of Probiotics.

Front Microbiol. 2020-7-28

[8]
Bayesian estimation of diagnostic sensitivity and specificity of a qPCR and a bacteriological culture method for Piscirickettsia salmonis in farmed Atlantic salmon (Salmo salar L.) in Chile.

J Fish Dis. 2020-10

[9]
Quantifying greenhouse gas emissions from global aquaculture.

Sci Rep. 2020-7-15

[10]
Digital PCR as an Emerging Tool for Monitoring of Microbial Biodegradation.

Molecules. 2020-2-6

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