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Analysis of the genetic diversity of the lymphocystis virus and its evolutionary relationship with its hosts
Lymphocystis disease virus (LCDV) is the causative agent of lymphocystis disease. In this study, the mcp gene of LCDV and the cyt b gene of the host fish were selected as molecular markers, and the phylogenetic relationships between LCDV and its host were analyzed. The 25 LCDV isolates examined in t...
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Published in: | Virus genes 2011-12, Vol.43 (3), p.358-366 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Lymphocystis disease virus (LCDV) is the causative agent of lymphocystis disease. In this study, the
mcp
gene of LCDV and the
cyt
b gene of the host fish were selected as molecular markers, and the phylogenetic relationships between LCDV and its host were analyzed. The 25 LCDV isolates examined in this study were attributed to seven LCDV genotypes: genotype I (LCDV-1), genotype II (LCDV-cn, etc.), genotype III (LCDV-rf), genotype IV (LCDV-rc and LCDV-sb), genotype V (LCDV-cb), genotype VI (LCDV-tl), and genotype VII (LCDV-sa). Genotype VII is a new genotype. LCDV1 was found to have differentiated first, followed by LCDV-rf; then LCDV-tl; LCDV-cb; and then LCDV-sa; and by LCDV-rc and LCDV-sb; and finally by LCDV-cn, LCDV-C, and LCDV-jf. From the host evolutionary perspective,
Rachycentron canadum
was found to have differentiated first, followed by
Trichogaster leeri
,
Chanda baculis
, and
Sebastes schlegeli
,
Lateolabrax
sp.,
Sparus aurata
,
Platichthys flesus
, and
Paralichthys olivaceus
. Comparison of the phylogenies of the host fish species and LCDVs revealed no significant evidence of cospeciation between LCDVs and their host fish. In-depth studies of the genetic variation in LCDVs can enhance our understanding of the mechanism of LCDV infection, which may provide important insights into the prevention and treatment of lymphocystis disease. |
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ISSN: | 0920-8569 1572-994X |
DOI: | 10.1007/s11262-011-0646-0 |