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1.
J Fish Dis ; 40(1): 105-118, 2017 Jan.
Article in English | MEDLINE | ID: mdl-27193445

ABSTRACT

Iridoviridae are known to cause disease in sturgeons in North America. Here, histological and molecular methods were used to screen for this family of virus in sturgeons from various European farms with low-to-high morbidity. Some histological samples revealed basophilic cells in the gill and labial epithelia, strongly suggesting the accumulation of iridovirus particles. Newly developed generic PCR tests targeting the major capsid protein (MCP) gene of sturgeon iridoviruses identified in North America, namely the white sturgeon iridovirus and the Namao virus (NV), produced positive signals in most samples from four sturgeon species: Russian (Acipenser gueldenstaedtii), Siberian (A. baerii), Adriatic (A. naccarii) and beluga (Huso huso). The sequences of the PCR products were generally highly similar one another, with nucleotide identities greater than 98%. They were also related to (74-88%), although distinct from, American sturgeon iridoviruses. These European viruses were thus considered variants of a single new virus, provisionally named Acipenser iridovirus-European (AcIV-E). Moreover, three samples infected with AcIV-E showed genetic heterogeneity, with the co-existence of two sequences differing by five nucleotides. One of our European samples carried a virus distinct from AcIV-E, but closely related to NV identified in Canada (95%). This study demonstrates the presence of two distinct sturgeon iridoviruses in Europe: a new genotype AcIV-E and an NV-related virus.


Subject(s)
Capsid Proteins/genetics , DNA Virus Infections/veterinary , Fish Diseases/diagnosis , Fishes , Iridoviridae/isolation & purification , Polymerase Chain Reaction/veterinary , Animals , DNA Virus Infections/diagnosis , DNA Virus Infections/virology , Europe , Fish Diseases/virology , Polymerase Chain Reaction/methods , Real-Time Polymerase Chain Reaction/veterinary , Sequence Analysis, DNA/veterinary
2.
Syst Parasitol ; 48(2): 141-50, 2001 Feb.
Article in English | MEDLINE | ID: mdl-11252277

ABSTRACT

Molecular and morphological features of Gyrodactylus specimens from Oncorhynchus mykiss, Salmo trutta and Salmo salar were examined. Sequences from variable region V4 of the small subunit ribosomal RNA gene and the ribosomal RNA internal transcribed spacers, produced by the FRS Marine Laboratory, revealed that these were not the same as other well-characterised Gyrodactylus that are common on European salmonids and were in fact a distinct species. Initial morphological examination of the opisthaptor indicated that this species very closely resembles G. salaris Malmberg, 1957. More detailed analysis revealed differences in the shape of the marginal hook sickle of these two species and thus Gyrodactylus teuchis Lautraite, Blanc, Thiery, Daniel & Vigneulle, 1999 was erected. Analysis of the ribosomal RNA gene or spacer sequences remains the most reliable method of identifying this species. This is believed to be the first record of a Gyrodactylus species identified first from molecular data and confirmed by morphological examination; previous molecular analyses had provided alternative methods for identifying species that had already been described using morphological characters.


Subject(s)
DNA, Ribosomal Spacer/genetics , Genes, rRNA , Trematoda/classification , Animals , Base Sequence , DNA Probes , Genes, Helminth , Molecular Sequence Data , Oncorhynchus/parasitology , Polymerase Chain Reaction , RNA, Ribosomal, 5.8S/genetics , Salmo salar/parasitology , Sequence Analysis, DNA , Trematoda/anatomy & histology , Trematoda/genetics , Trout/parasitology
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