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Co-existence of two Yersinia ruckeri biotypes and serotype O1a retrieved from rainbow trout (Oncorhynchus mykiss) farmed in Puno, Peru

  • Carla Fernandez-Espinel
    ,
  • Marco Medina-Morillo
    ,
  • Rute Irgang
    ,
  • Giovanna Sotil
    ,
  • Henry Araya-León
    ,
  • Violeta Flores-Dominick
*Corresponding author for this work
  • Instituto del Mar del Perú
    ,
  • Interdisciplinary Center for Aquaculture Research (INCAR)
    ,
  • Universidad Andrés Bello
    ,
  • Universidad Nacional Mayor de San Marcos
    ,
  • University of Santiago de Compostela
    ,
  • Universidad Andres Bello
Research Output:
Contribution to journal
Article
Peer-review

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 157-163 (7 pages)

Journal (Volume, Issue Number)

Journal of Fish Diseases (Volume 46, Issue 2)

Publication milestones

  • Accepted/In press - 2022
  • Published - 02/2023

Publication status

Published - 02/2023

ISSN

0140-7775

Publication IDs

  • Scopus: 85142285828

Abstract

Yersinia ruckeri causes important economic losses for rainbow trout (Oncorhynchus mykiss) farms worldwide. This bacterial disease is likely the most common among trout in Peru; however, no commercial vaccine is available nationally, which is, in part, due to a lack of information on the bacterium. The aim of the current study was to characterize 29 Y. ruckeri isolates sampled from seven cage-reared farms in the Puno Region, the focal point for aquaculture activities in Peru. For this, samples were taken from fish with clinical signs (i.e. haemorrhages, uni- or bilateral exophthalmia, hyphaemia and/or melanosis). Notable among our findings was the existence of both Y. ruckeri biotype 1 (9 isolates) and biotype 2 (20 isolates; negative for sorbitol and Tween 80). The isolates further differed in API profiles 5307100 (21 isolates), 1307100 (4 isolates), 1305100 (2 isolates), 1307120 (1 isolate) and 5305100 (1 isolate), with the main differences being in the tests for lysine decarboxylase, gelatine hydrolysis and D-saccharose fermentation. Despite these differences, all isolates shared identical ERIC-PCR and REP-PCR profiles and belonged to the O1a serotype. Fingerprints were identical to the reference strain CECT 955 (serotype O1a). The information obtained will be used for epidemiological purposes by health authorities and for the development of a vaccine against Y. ruckeri, a prominent request made by fish farmers in Peru.

Funding Details

The authors acknowledge Dra. Macarena Echeverría‐Bugueño for their technical assistance in protein analysis. In addition, the authors would like to thank to the Continental laboratory of IMARPE – Puno team for the support and logistic assistance during the fish sampling. This work was funded by ‘Ministerio de la Producción – IMARPE – Perú – PpR‐2018 – Meta 03’, FONDAP 15110027 grants from (ANID) from the Chilean Government, project FONDECYT 128‐2020 and project PNIPA‐ACU‐SIADE‐772 from Peruvian Government. Agencia Nacional de Investigación y Desarollo
FundersFunding numbers
IMARPE
-
FONDECYT
PNIPA‐ACU‐SIADE‐772, 128‐2020
FONDAP
15110027
ANID
-
Ministerio de la Producción
-

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Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well