Molecular Characterization of the Myxosporean Associated with Parasitic Encephalitis of Farmed Atlantic Salmon (Salmo salar) in Ireland
Abstract
In the summers of 1992, 1993, and 1994, epizootics of encephalitis and mass mortality
occurred in Atlantic salmon (Salmo salar) smolts at a sea-farm in Ireland.5 In 1993
neurologic signs were observed within 6 to 8 weeks of transfer to the sea, and mortalities exceeded 90
percent of the total smolt stocks within 4 weeks of the onset.4
Seasonally variable mortalities of smolts at this sea-farm have been associated with
variations in the prevalence and density of encephalitis and infection by a neurotropic
parasite.4,2 This parasite was detected in histologic sections of the central nervous system of
affected and unaffected smolts.4,2 In smolts from 1995, the distribution of the parasite in the
brain was non-random, and parasites were detected with significantly greater frequency in the optic tectum of
the mesencephalon than in other neuroanatomic subdivisions.2 Encephalitis was non-suppurative,
multifocal, and also non-randomly distributed, with significantly greater frequency of encephalitic foci in
the myelencephalon. Based on ultrastructural studies, this neurotropic parasite has been identified as an
intercellular presporogonic multicellular developmental stage of a histozoic myxosporean, displaying distinct
cortical zones of pinocytotic channels, cytoplasmic partitioning into ectoplasm and endoplasm, and large
numbers of generative cells arranged singly or in cell doublets. Such morphologic features are characteristic
of developmental stages of members of Family Myxobolidae, which includes the genera
Myxobolus, Henneguya, Thelohanellus, and
Neothelohanellus.3 No mature spores were detected. Of these genera, neurotropic species of
Myxobolus have been identified in salmonid hosts in other European locations. A few species of
Thelohanellus and Neothelohanellus are neurotropic, although they have been identified in
non-salmonid hosts. On the basis of ultrastructure and the detection of the parasite only in histologic
sections of the central nervous system, it has been proposed that this parasite is a proliferative stage of a
neurotropic myxosporean, possibly a Myxobolus species.2 In order to substantiate the
morphological classification of this myxosporean in the absence of detectable sporogony and to generate
genomic sequence data for phylogenetic comparisons, polymerase chain reaction (PCR), Southern blot
hybridization, and dideoxynucleotide-chain termination DNA sequencing were used in concert to characterize
segments of the small subunit ribosomal RNA (SSU rRNA) gene. Oligonucleotide primers were created from
sequences of the SSU rRNA gene of Myxobolus cerebralis and were employed in PCR experiments using DNA
extracted from formalin-fixed paraffin-embedded tissue sections of infected brains. Five separate fragments
of the SSU rRNA gene from the myxosporean were amplified. Amplicons were separated by agarose gel
electrophoresis and detected by Southern blot hybridization using digoxigenin-labeled DNA probes generated
from specific sequences of the SSU rRNA gene of M. cerebralis. Fragments ranged in size from 228 bases
to 306 bases. Alignments to sequences of the SSU rRNA genes of M. cerebralis, M. squamalis, and
M. insidiosus1 demonstrated 99% homology to that of M. cerebralis. These results are
indicative of SSU rRNA sequence homologies which support the morphologic assertion that the myxosporean
associated with parasitic encephalitis of farmed Atlantic salmon smolts is a neurotropic myxobolid. The
amplification and sequencing of fragments of the SSU rRNA gene from a proliferative stage of this myxosporean
provides a reliable and reproducible means of identification of some myxosporean developmental stages in the
absence of detectable sporogony. The genetic information from this and similar studies will be useful in the
development of probes for the identification of intermediate hosts and the elucidation of life cycles.
Acknowledgements
The assistance of the technical manager and staff of the fish farm is gratefully
acknowledged. Timothy S. Gorton of the Department of Pathobiology, University of Connecticut, is acknowledged
for his assistance with the creation of primers and the alignments of sequences. Karl B. Andree and Delores
B. Antonio of the Fish Health Laboratory, University of California Davis, are acknowledged for their
assistance with the initial experiments. This research was partially funded by grants from the Storrs
Agricultural Experiment Station, College of Agriculture and Natural Resources, University of Connecticut, and
from a private aquaculture company in Ireland.
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