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Catching the fish with the worm: a case study on eDNA detection of the monogenean parasite Gyrodactylus salaris and two of its hosts, Atlantic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss)
by
Hansen, Haakon
, Hytterød, Sigurd
, Markussen, Turhan
, Vrålstad, Trude
, Rusch, Johannes C.
, Strand, David A.
in
Animals
/ Aquatic environment
/ Assaying
/ Biomedical and Life Sciences
/ Biomedicine
/ Case studies
/ Cestode Infections - parasitology
/ Cestode Infections - veterinary
/ Cytochrome
/ Cytochrome b
/ Cytochromes
/ Deoxyribonucleic acid
/ Detection
/ DNA
/ DNA - genetics
/ DNA - isolation & purification
/ Droplet digital PCR (ddPCR)
/ droplets
/ Ectoparasites
/ Electric fishing
/ Entomology
/ Environmental DNA
/ Environmental monitoring
/ Farms
/ Fish
/ Fish Diseases - parasitology
/ Fish migration
/ Fish parasites
/ Fish populations
/ Fisheries
/ Freshwater fishes
/ Glass fibers
/ Gyrodactylus salaris
/ Infectious Diseases
/ Internal transcribed spacer (ITS)
/ Invasive species
/ Marine fishes
/ Methods
/ Migration
/ Mitochondria
/ Mitochondrial DNA (mtDNA)
/ monitoring
/ Monogenea
/ Multiplex PCR
/ NADH
/ Nicotinamide adenine dinucleotide
/ Norway
/ Nucleotide sequence
/ Oncorhynchus mykiss
/ Oncorhynchus mykiss - parasitology
/ Parasites
/ Parasitology
/ Parasitology - methods
/ PCR
/ Platyhelminths - genetics
/ Platyhelminths - isolation & purification
/ Platyhelminths - physiology
/ River systems
/ Rivers
/ Rivers - chemistry
/ Rivers - parasitology
/ Salmo salar
/ Salmo salar - parasitology
/ Salmo trutta
/ Salmon
/ Salmonidae
/ Salvelinus alpinus
/ Specificity
/ Surveillance
/ Tissue
/ Tropical Medicine
/ Trout
/ Veterinary Medicine/Veterinary Science
/ Virology
/ Water analysis
/ Water purification
/ Water sampling
2018
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Catching the fish with the worm: a case study on eDNA detection of the monogenean parasite Gyrodactylus salaris and two of its hosts, Atlantic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss)
by
Hansen, Haakon
, Hytterød, Sigurd
, Markussen, Turhan
, Vrålstad, Trude
, Rusch, Johannes C.
, Strand, David A.
in
Animals
/ Aquatic environment
/ Assaying
/ Biomedical and Life Sciences
/ Biomedicine
/ Case studies
/ Cestode Infections - parasitology
/ Cestode Infections - veterinary
/ Cytochrome
/ Cytochrome b
/ Cytochromes
/ Deoxyribonucleic acid
/ Detection
/ DNA
/ DNA - genetics
/ DNA - isolation & purification
/ Droplet digital PCR (ddPCR)
/ droplets
/ Ectoparasites
/ Electric fishing
/ Entomology
/ Environmental DNA
/ Environmental monitoring
/ Farms
/ Fish
/ Fish Diseases - parasitology
/ Fish migration
/ Fish parasites
/ Fish populations
/ Fisheries
/ Freshwater fishes
/ Glass fibers
/ Gyrodactylus salaris
/ Infectious Diseases
/ Internal transcribed spacer (ITS)
/ Invasive species
/ Marine fishes
/ Methods
/ Migration
/ Mitochondria
/ Mitochondrial DNA (mtDNA)
/ monitoring
/ Monogenea
/ Multiplex PCR
/ NADH
/ Nicotinamide adenine dinucleotide
/ Norway
/ Nucleotide sequence
/ Oncorhynchus mykiss
/ Oncorhynchus mykiss - parasitology
/ Parasites
/ Parasitology
/ Parasitology - methods
/ PCR
/ Platyhelminths - genetics
/ Platyhelminths - isolation & purification
/ Platyhelminths - physiology
/ River systems
/ Rivers
/ Rivers - chemistry
/ Rivers - parasitology
/ Salmo salar
/ Salmo salar - parasitology
/ Salmo trutta
/ Salmon
/ Salmonidae
/ Salvelinus alpinus
/ Specificity
/ Surveillance
/ Tissue
/ Tropical Medicine
/ Trout
/ Veterinary Medicine/Veterinary Science
/ Virology
/ Water analysis
/ Water purification
/ Water sampling
2018
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Catching the fish with the worm: a case study on eDNA detection of the monogenean parasite Gyrodactylus salaris and two of its hosts, Atlantic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss)
by
Hansen, Haakon
, Hytterød, Sigurd
, Markussen, Turhan
, Vrålstad, Trude
, Rusch, Johannes C.
, Strand, David A.
in
Animals
/ Aquatic environment
/ Assaying
/ Biomedical and Life Sciences
/ Biomedicine
/ Case studies
/ Cestode Infections - parasitology
/ Cestode Infections - veterinary
/ Cytochrome
/ Cytochrome b
/ Cytochromes
/ Deoxyribonucleic acid
/ Detection
/ DNA
/ DNA - genetics
/ DNA - isolation & purification
/ Droplet digital PCR (ddPCR)
/ droplets
/ Ectoparasites
/ Electric fishing
/ Entomology
/ Environmental DNA
/ Environmental monitoring
/ Farms
/ Fish
/ Fish Diseases - parasitology
/ Fish migration
/ Fish parasites
/ Fish populations
/ Fisheries
/ Freshwater fishes
/ Glass fibers
/ Gyrodactylus salaris
/ Infectious Diseases
/ Internal transcribed spacer (ITS)
/ Invasive species
/ Marine fishes
/ Methods
/ Migration
/ Mitochondria
/ Mitochondrial DNA (mtDNA)
/ monitoring
/ Monogenea
/ Multiplex PCR
/ NADH
/ Nicotinamide adenine dinucleotide
/ Norway
/ Nucleotide sequence
/ Oncorhynchus mykiss
/ Oncorhynchus mykiss - parasitology
/ Parasites
/ Parasitology
/ Parasitology - methods
/ PCR
/ Platyhelminths - genetics
/ Platyhelminths - isolation & purification
/ Platyhelminths - physiology
/ River systems
/ Rivers
/ Rivers - chemistry
/ Rivers - parasitology
/ Salmo salar
/ Salmo salar - parasitology
/ Salmo trutta
/ Salmon
/ Salmonidae
/ Salvelinus alpinus
/ Specificity
/ Surveillance
/ Tissue
/ Tropical Medicine
/ Trout
/ Veterinary Medicine/Veterinary Science
/ Virology
/ Water analysis
/ Water purification
/ Water sampling
2018
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Catching the fish with the worm: a case study on eDNA detection of the monogenean parasite Gyrodactylus salaris and two of its hosts, Atlantic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss)
Journal Article
Catching the fish with the worm: a case study on eDNA detection of the monogenean parasite Gyrodactylus salaris and two of its hosts, Atlantic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss)
2018
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Overview
Background
Environmental DNA (eDNA) monitoring is growing increasingly popular in aquatic systems as a valuable complementary method to conventional monitoring. However, such tools have not yet been extensively applied for metazoan fish parasite monitoring. The fish ectoparasite
Gyrodactylus salaris
, introduced into Norway in 1975, has caused severe damage to Atlantic salmon populations and fisheries. Successful eradication of the parasite has been carried out in several river systems in Norway, and Atlantic salmon remain infected in only seven rivers, including three in the Drammen region. In this particular infection region, a prerequisite for treatment is to establish whether
G. salaris
is also present on rainbow trout upstream of the salmon migration barrier. Here, we developed and tested eDNA approaches to complement conventional surveillance methods.
Methods
Water samples (2 × 5 l) were filtered on-site through glass fibre filters from nine locations in the Drammen watercourse, and DNA was extracted with a CTAB protocol. We developed a qPCR assay for
G. salaris
targeting the nuclear ribosomal ITS1 region, and we implemented published assays targeting the mitochondrial cytochrome-b and NADH-regions for Atlantic salmon and rainbow trout, respectively. All assays were transferred successfully to droplet digital PCR (ddPCR).
Results
All qPCR/ddPCR assays performed well both on tissue samples and on field samples, demonstrating the applicability of eDNA detection for
G. salaris
, rainbow trout and Atlantic salmon in natural water systems. With ddPCR we eliminated a low cross-amplification of
Gyrodactylus derjavinoides
observed using qPCR, thus increasing specificity and sensitivity substantially. Duplex ddPCR for
G. salaris
and Atlantic salmon was successfully implemented and can be used as a method in future surveillance programs. The presence of
G. salaris
eDNA in the infected River Lierelva was documented, while not elsewhere. Rainbow trout eDNA was only detected at localities where the positives could be attributed to eDNA release from upstream land-based rainbow trout farms. Electrofishing supported the absence of rainbow trout in all of the localities.
Conclusions
We provide a reliable field and laboratory protocol for eDNA detection of
G. salaris
, Atlantic salmon and rainbow trout, that can complement conventional surveillance programs and substantially reduce the sacrifice of live fish. We also show that ddPCR outperforms qPCR with respect to the specific detection of
G. salaris
.
Publisher
BioMed Central,Springer Nature B.V,BMC
Subject
/ Assaying
/ Biomedical and Life Sciences
/ Cestode Infections - parasitology
/ Cestode Infections - veterinary
/ DNA
/ DNA - isolation & purification
/ droplets
/ Farms
/ Fish
/ Fish Diseases - parasitology
/ Internal transcribed spacer (ITS)
/ Methods
/ NADH
/ Nicotinamide adenine dinucleotide
/ Norway
/ Oncorhynchus mykiss - parasitology
/ PCR
/ Platyhelminths - isolation & purification
/ Rivers
/ Salmon
/ Tissue
/ Trout
/ Veterinary Medicine/Veterinary Science
/ Virology
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