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Journal Article

Ultrastructural and biomolecular detection of Rickettsiales‐like organisms in tissues of rainbow trout with Red Mark Syndrome

M Galeotti; M Manzano; P Beraldo; C Bulfon; G Rossi; D Volpatti; G E Magi
Journal of Fish Diseases · Vol. 40, Issue 7 · pp. 907-917 · 2017

Abstract

Red mark syndrome ( RMS ) and US strawberry disease ( US SD ) are skin disorders affecting rainbow trout farmed in Europe and USA . The disease etiology has not yet been established. In spite of specific investigations, identifying Rickettsia ‐like organism ( RLO )‐ and Midichloria ‐like organism ( MLO )‐related DNA in affected individuals, these pathogens have never been observed. We performed histological, ultrastructural and biomolecular analysis on skin and spleen samples of trout with RMS . Examination by TEM revealed the presence of intracytoplasmic microorganisms resembling Rickettsiales within macrophages, fibroblasts and erythrocytes. The microorganisms were oval or short rod shaped (400–800 nm in length and 100–200 nm in width) and often showed a cell wall similar to Gram‐negative bacteria. PCR analysis for Rickettsiales supported these findings: 53% of affected trout were positive by both PCR and TEM The primers Ri FC fw‐Ri FC rev were used to anneal both the RLO 16S DNA sequence and the MLO 16S DNA sequence. For this reason, and in agreement with previous studies confirming the presence of Rickettsiales‐related DNA in trout with RMS , we assume that TEM detected microorganisms morphologically consistent with bacteria belonging to Rickettsiales order and could be considered as possible causative agents of RMS .

Bibliographic Information

JournalJournal of Fish Diseases
PublisherWiley
Publication Date2017-07-01
Publication Year2017
Volume40
Issue7
Pages907-917
Document TypeJournal Article
Print ISSN0140-7775
eISSN1365-2761
DOI10.1111/jfd.12571
SubjectGeneral Aquaculture, Fisheries & Fish Science

Access Information

NARA Access Coverage1997-01-01~Current
Journal Homepagehttps://onlinelibrary.wiley.com/loi/13652761
Publisher PageOpen Publisher Page
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