Cristin-resultat-ID: 1701477
Sist endret: 14. januar 2020, 09:31
Resultat
Vitenskapelig foredrag
2019

Update on environmental DNA (eDNA) monitoring of Aphanomyces astaci and freshwater crayfish

Bidragsytere:
  • Trude Vrålstad
  • David Strand
  • Stein Ivar Johnsen
  • Johannes Rusch
  • Sune Agersnap
  • William Brenner Larsen
  • mfl.

Presentasjon

Navn på arrangementet: The 10th Annual Workshop of the National Reference Laboratories for Crustacean Diseases
Sted: Technical University of Denmark
Dato fra: 29. mai 2019

Arrangør:

Arrangørnavn: Technical University of Denmark

Om resultatet

Vitenskapelig foredrag
Publiseringsår: 2019

Klassifisering

Vitenskapsdisipliner

Molekylærbiologi

Emneord

Krepsdyr • Krepsepest • Miljø DNA • Tifotkreps

Beskrivelse Beskrivelse

Tittel

Update on environmental DNA (eDNA) monitoring of Aphanomyces astaci and freshwater crayfish

Sammendrag

Environmental DNA (eDNA) methodology has become an important non-invasive tool to monitor freshwater micro- and macro-organisms. From a single water sample, it is possible to detect several species of interest or even whole communities. eDNA can be used to reveal elusive targets, such as alien invasive species at an early stage or rare and endangered species. eDNA can also be used to investigate presence/absence and relative quantities of pathogens in water. Over years, we have developed and used eDNA monitoring tools for Aphanomyces astaci, the causative agent of crayfish plague, in combination with eDNA monitoring of susceptible- and tolerant freshwater crayfish. In a recently published study, we used eDNA monitoring to follow a crayfish plague outbreak in a large water course, and compared it to traditional crayfish plague monitoring that uses cages with live crayfish as “canaries in a coalmine”. We show that eDNA‐monitoring corresponds well with the biological status measured in terms of crayfish mortality and trapping results. It reveals the presence of A. astaci in the water up to 2.5 weeks in advance of the cage‐method. eDNA estimates of A. astaci concentration and noble crayfish numbers increased markedly during mortality, and vanished quickly thereafter, demonstrating the dynamics during an outbreak of crayfish plague. The eDNA monitoring also provided a snapshot of the presence, absence or disappearance of crayfish regardless of season, and constitutes a valuable supplement to the trapping‐method that relies on season and legislation. One of the main benefits of eDNA monitoring is the possibility for temporal and spatial monitoring of several organisms from the same water samples. The simultaneous eDNA monitoring of A. astaci and relevant native and invasive freshwater crayfish species is well-suited for early-warning of invasion or infection, risk assessments, habitat evaluation and surveillance regarding pathogen and invasive/native crayfish status. In Norway, eDNA monitoring have replaced the traditional cage dependent crayfish plague monitoring in the national surveillance program of crayfish plague, and was recently also implanted as a supplement method in the national surveillance program for noble crayfish and spread of signal crayfish.

Bidragsytere

Aktiv cristin-person

Trude Vrålstad

  • Tilknyttet:
    Forfatter
    ved Forskningsgruppe fiskehelse ved Veterinærinstituttet

David Strand

  • Tilknyttet:
    Forfatter
    ved Forskningsgruppe fiskehelse ved Veterinærinstituttet
Aktiv cristin-person

Stein Ivar Johnsen

  • Tilknyttet:
    Forfatter
    ved NINA Lillehammer ved Norsk institutt for naturforskning

Johannes Rusch

  • Tilknyttet:
    Forfatter
    ved Forskningsgruppe fiskehelse ved Veterinærinstituttet

Sune Agersnap

  • Tilknyttet:
    Forfatter
    ved Københavns Universitet
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