Nota Técnica Tilapias

Total Page:16

File Type:pdf, Size:1020Kb

Nota Técnica Tilapias Viral Diseases in Tilapias Dr. Marco Rozas-Serri DVM, MSc, PhD 2020 VIRAL DISEASES IN TILAPIAS The viral infections have the potential to cause relatively high mortalities of up to 90% in some affected populations. The actual impact and geographical distribution of the viruses are not known so there is a potential danger of the viruses being introduced to new countries or regions unintentionally through movement of sub-clinically infected fish that are destined for aquaculture farms lacking appropriate control measures (Table 1). The priority focus of the Brazilian tilapia industry As outlined by the OIE Guide for aquatic animal, surveillance may be should be on the active relatively simple in the form of passive surveillance or highly sophisticated in surveillance of two important the form of active surveillance that implements specific sampling strategies exotic viruses: Infectious and that may target specific disease agents. In all the viral diseases that spleen kidney necrosis virus affect tilapia, the correlation between virulence, genetic type, survival outside host as well as environmental factors, is an area of research requiring infection and Tilapia lake virus attention. Table 1. Summary of viral diseases affecting tilapines. Infectious spleen kidney necrosis virus - ISKNV The first DNA viruses discovered in tilapia were iridoviruses. Although the family Iridoviridae is composed of 5 genera, only members of the genera Megalocytivirus, Lymphocystivirus, and Ranavirus infect fish. The ISKNV is the only formally accepted into the Megalocytivirus genus. The ISKNV virus has been isolated from both marine and freshwater fish: rock bream iridovirus (RBIV), red seabream iridovirus (RSIV), orange spotted grouper iridovirus (OSGIV), turbot reddish body iridovirus (TRBIV), large yellow croaker iridovirus (LYCIV), giant seaperch The disease was described in tilapia after a US Midwestern iridovirus (GSIV-K1), scale drop disease virus aquaculture tilapia facility experienced heavy mortalities of 50– (SDDV). 75% from November to December 2012. The moribund fish The ISKNV contains naked double-stranded DNA genome displayed lethargy, branchial pallor, and distension of the encapsulated by an outer nucleocapsid layer, forming an coelomic cavity due to a clear ascitic coelomic fluid (Table 2) icosahedral shape with a diameter of 140–200 nm (Table 1). (Figure 2). Table 2. Diagnosis and characterization of etiological agent. Tilapia lake virus - TiLV Tilapia lake virus (TiLV) affected wild and farmed tilapines (Table 1). It has been reported in Asia, Africa and South America, and the number of countries where the agent has been detected is likely to increase rapidly as a result of increased awareness, surveillance and availability of diagnostic methods (Table 2). There are currently severe knowledge gaps relating to TiLV and no effective, affordable vaccines are yet available. The virus is an enveloped, negative-sense, single-stranded RNA virus with 10 segments and a diameter between 55 and 100 nm. A taxonomic proposal is a new genus Tilapinevirus, specie Tilapia tilapinevirus. The reported clinical signs and gross pathological lesions associated with TiLV infections are somewhat variable, depending on geographical origin (Figure 2). Based on the available information, it seems that a list of pathognomonic signs, to allow a reliable diagnosis based on clinical signs alone, is not currently feasible. Figure 2. Tilapia lake virus (TiLV). (A) Naturally diseased red tilapia showing skin haemorrhages. (B) Experimentally diseased Nile tilapia showing exophthalmia, abdominal swelling and scale protrusion. (C) The infected liver tissue showed syncytial hepatocytes and foamy cytoplasm, intracytoplasmic inclusion bodies. Jansen et al. 2018 Figure 1. Infectious spleen kidney necrosis virus (ISKNV). (A) Broodstock with microphthalmia (left arrow head), skin haemorrhages (middle arrow head) and skin ulcers (right arrow head). (B) Juvenile with exophthalmia (left arrow head), ascites Pathovet Chile is carrying out PCR and RT-PCR tests (arrow) and loss of scales, excess of mucus and haemorrhages to detect all exotic and enzootic viruses and bacteria (right arrow head). (C) Ventral view of juvenile fish showing for the tilapia industry in Brazil. An active severe ascites black arrow and skin haemorrhages (arrow head). Bar= 1cm. (D) Spleen. Affected cells show pronounced epidemiological surveillance program based on eosinophilia and are distributed throughout the section (*). regular sampling to detect specific disease agents is Numerous vacuolated macrophage aggregates are also present the technical basis from which it must to build the (M). Bar = 50μm. (E) Pronephros showing extensive distribution comprehensive health management strategy for of megalocytes without associated tissue necrosis (*). disease prevention and control in aquaculture. Bar=100μm. Inset shows pale staining of DNA in the cytoplasm of Histological diagnosis and histoscores are also affected cells (arrows). Feulgen stain. Bar=25μm. Ramirez- available to complement the health surveillance plan Paredes et al. 2019. Palena 280, Puerto Montt, CHILE / www.pathovet.cl / +56 65 2 77 31 75.
Recommended publications
  • Artemia Spp., a Susceptible Host and Vector for Lymphocystis Disease Virus
    viruses Article Artemia spp., a Susceptible Host and Vector for Lymphocystis Disease Virus Estefania J. Valverde, Alejandro M. Labella, Juan J. Borrego and Dolores Castro * Departamento de Microbiología, Facultad de Ciencias, Universidad de Málaga, 29017 Málaga, Spain; [email protected] (E.J.V.); [email protected] (A.M.L.); [email protected] (J.J.B.) * Correspondence: [email protected]; Tel.: +34-952134214 Received: 8 May 2019; Accepted: 30 May 2019; Published: 1 June 2019 Abstract: Different developmental stages of Artemia spp. (metanauplii, juveniles and adults) were bath-challenged with two isolates of the Lymphocystis disease virus (LCDV), namely, LCDV SA25 (belonging to the species Lymphocystis disease virus 3) and ATCC VR-342 (an unclassified member of the genus Lymphocystivirus). Viral quantification and gene expression were analyzed by qPCR at different times post-inoculation (pi). In addition, infectious titres were determined at 8 dpi by integrated cell culture (ICC)-RT-PCR, an assay that detects viral mRNA in inoculated cell cultures. In LCDV-challenged Artemia, the viral load increased by 2–3 orders of magnitude (depending on developmental stage and viral isolate) during the first 8–12 dpi, with viral titres up to 2.3 102 × Most Probable Number of Infectious Units (MPNIU)/mg. Viral transcripts were detected in the infected Artemia, relative expression values showed a similar temporal evolution in the different experimental groups. Moreover, gilthead seabream (Sparus aurata) fingerlings were challenged by feeding on LCDV-infected metanauplii. Although no Lymphocystis symptoms were observed in the fish, the number of viral DNA copies was significantly higher at the end of the experimental trial and major capsid protein (mcp) gene expression was consistently detected.
    [Show full text]
  • Megalocytivirus Induces Complicated Fish Immune Response at Multiple RNA Levels Involving Mrna, Mirna, and Circrna
    International Journal of Molecular Sciences Article Megalocytivirus Induces Complicated Fish Immune Response at Multiple RNA Levels Involving mRNA, miRNA, and circRNA Qian Wu 1,2,3, Xianhui Ning 1 and Li Sun 1,2,3,* 1 CAS and Shandong Province Key Laboratory of Experimental Marine Biology, CAS Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, 7 Nanhai Road, Qingdao 266071, China; [email protected] (Q.W.); [email protected] (X.N.) 2 Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, 1 Wenhai Road, Qingdao 266237, China 3 College of Earth and Planetary Sciences, University of Chinese Academy of Sciences, 19 Yuquan Road, Beijing 100049, China * Correspondence: [email protected]; Tel.: +86-532-82898829 Abstract: Megalocytivirus is an important viral pathogen to many farmed fishes, including Japanese flounder (Paralichthys olivaceus). In this study, we examined megalocytivirus-induced RNA responses in the spleen of flounder by high-throughput sequencing and integrative analysis of various RNA- seq data. A total of 1327 microRNAs (miRNAs), including 368 novel miRNAs, were identified, among which, 171 (named DEmiRs) exhibited significantly differential expressions during viral infection in a time-dependent manner. For these DEmiRs, 805 differentially expressed target mRNAs (DETmRs) were predicted, whose expressions not only significantly changed after megalocytivirus infection but were also negatively correlated with their paired DEmiRs. Integrative analysis of Citation: Wu, Q.; Ning, X.; Sun, L. Megalocytivirus Induces immune-related DETmRs and their target DEmiRs identified 12 hub DEmiRs, which, together with Complicated Fish Immune Response their corresponding DETmRs, formed an interaction network containing 84 pairs of DEmiR and at Multiple RNA Levels Involving DETmR.
    [Show full text]
  • Aquatic Emergency Preparedness and Response Systems for Effective Management of Transboundary Disease Outbreaks in Southeast Asia
    AQUATIC EMERGENCY PREPAREDNESS AND RESPONSE SYSTEMS FOR EFFECTIVE MANAGEMENT OF TRANSBOUNDARY DISEASE OUTBREAKS IN SOUTHEAST ASIA Proceedings of ASEAN Regional Technical Consultation on Aquatic Emergency Preparedness and Response Systems for Effective Management of Transboundary Disease Outbreaks in Southeast Asia 20-22 August 2018 Centara Grand Central Ladprao, Bangkok, Thailand Eleonor A. Tendencia Leobert D. de la Peña Joesyl Marie V. de la Cruz Editors AQUATIC EMERGENCY PREPAREDNESS AND RESPONSE SYSTEMS FOR EFFECTIVE MANAGEMENT OF TRANSBOUNDARY DISEASE OUTBREAKS IN SOUTHEAST ASIA ISBN 978-971-9931-08-9 Published and printed by Southeast Asian Fisheries Development Center Aquaculture Department Tigbauan, Iloilo, Philippines Copyright © 2019 Southeast Asian Fisheries Development Center Aquaculture Department Tigbauan, Iloilo, Philippines All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopy, recording, or any information storage and retrieval system, without permission in writing from the publisher. SEAFDEC Aquaculture Department Library Cataloging-in-Publication Data ASEAN Regional Technical Consultation on Aquatic Emergency Preparedness and Response Systems for Effective Management of Transboundary Disease Outbreaks in Southeast Asia (2018 : Bangkok, Thailand). Aquatic emergency preparedness and response systems for effective management of transboundary disease outbreaks in Southeast Asia : proceedings of ASEAN Regional Technical Consultation, 20-22 August 2018, Centara Grand Central, Ladprao, Bangkok, Thailand / Eleonor A. Tendencia, Leobert D. de la Peña, Joesyl Marie V. de la Cruz, editors. -- Tigbauan, Iloilo, Philippines : Aquaculture Dept., Southeast Asian Fisheries Development Center, 2019, ©2019. xii, 122 pages : illustrations (chiefly color), maps (chiefly color). Includes bibliographical references. 1. Fish -- Diseases -- Southeast Asia -- Congresses.
    [Show full text]
  • Genome Analysis of Ranavirus Frog Virus 3Isolated from American Bullfrog
    www.nature.com/scientificreports OPEN Genome analysis of Ranavirus frog virus 3 isolated from American Bullfrog (Lithobates catesbeianus) in South America Marcelo Candido 1*, Loiane Sampaio Tavares1, Anna Luiza Farias Alencar2, Cláudia Maris Ferreira3, Sabrina Ribeiro de Almeida Queiroz1, Andrezza Maria Fernandes1 & Ricardo Luiz Moro de Sousa1 Ranaviruses (family Iridoviridae) cause important diseases in cold-blooded vertebrates. In addition, some occurrences indicate that, in this genus, the same virus can infect animals from diferent taxonomic groups. A strain isolated from a Ranavirus outbreak (2012) in the state of Sao Paulo, Brazil, had its genome sequenced and presented 99.26% and 36.85% identity with samples of Frog virus 3 (FV3) and Singapore grouper iridovirus (SGIV) ranaviruses, respectively. Eight potential recombination events among the analyzed sample and reference FV3 samples were identifed, including a recombination with Bohle iridovirus (BIV) sample from Oceania. The analyzed sample presented several rearrangements compared to FV3 reference samples from North America and European continent. We report for the frst time the complete genome of Ranavirus FV3 isolated from South America, these results contribute to a greater knowledge related to evolutionary events of potentially lethal infectious agent for cold-blooded animals. Among the major viral pathogens, worldwide distributed and recent history, Ranavirus (Rv) is highlighted, on which, studies in South America remain limited. Rv are part of the family Iridoviridae that is divided into fve genera, of which three are considered more relevant by infectious severity in aquatic and semi-aquatic animals: Lymphocystivirus, Megalocytivirus and Rv. Tey are enveloped and unenveloped viruses, showing double-stranded DNA whose genome ranges from 103 to 220 kbp.
    [Show full text]
  • The Lymphocystis Diseases in the Olive Flounder, Paralichthys Olivaceus
    Univ. j. zool. Rajshahi Univ. Vol. 26, 2007. pp. 59-62 ISSN 1023-6104 http://journals.sfu.ca/bd/index.php/UJZRU © Rajshahi University Zoological Society The lymphocystis diseases in the Olive flounder, Paralichthys olivaceus Mosharrof Hossain, Seok Ryel Kim and Myung Joo Oh* Division of Food Science and Aqualife Medicine, Chonnam National University Yeosu-550-749, Korea. Abstract: Lymphocystis disease virus (LCDV) is the causative agent of lymphocystis disease, affecting more than 100 teleost species worldwide. Characteristically, LCD is chronic, self limiting and species specific. The greatly hypertrophied cells, called lymphocystis tumor cells, typically occur on the skin, fins and oral region. Lymphocystis cells were ovoid to circular and varied in sizes ranging from 200-250 mm. The lymphocystis disease infected flounder have unsightly appearances that discourage the commercial values. A PCR detection technique was developed to amplify a fragment of LCDV major capsid protein gene (1347bp) which is shortcoming and useful. The PCR result proved that the LCD-virus replicated in the epidermis (fins and skin) not in the spleen, kidney, intestine or brain of Paralichthys olivaceus. Keyword: Lymphocystis disease, LCDV, PCR, Paralichthys olivaceus Introduction diseases have been isolated from more than 100 teleost Lymphocystis disease (LCD) is a chronic, self-limiting, species (Anders, 1989), however the infections and viral disease affecting many species of teleosts virus replication is unknown. LCDV has been studied worldwide. Freshwater, estuarine, and marine fish in for the different isolation and characterization warm-water, and cold-water environments are techniques (Iwamoto et al., 2002; Alonso et al., 2005; susceptible to this disease. In general, lymphocystis is a Cano et al., 2006) that helping shortcoming detection disease of more evolutionarily advanced species of of the disease and to take initiatives to a disease free teleosts, like perches, seabreams and flounders.
    [Show full text]
  • The Megalocytivirus RBIV Induces Apoptosis and MHC Class I Presentation in Rock Bream (Oplegnathus Fasciatus) Red Blood Cells
    ORIGINAL RESEARCH published: 04 March 2019 doi: 10.3389/fimmu.2019.00160 The Megalocytivirus RBIV Induces Apoptosis and MHC Class I Presentation in Rock Bream (Oplegnathus fasciatus) Red Blood Cells Myung-Hwa Jung 1, Verónica Chico 2, Sergio Ciordia 3, Maria Carmen Mena 3, Sung-Ju Jung 1 and Maria Del Mar Ortega-Villaizan 2* 1 Department of Aqualife Medicine, Chonnam National University, Gwangju, South Korea, 2 IBMC-IDiBE, Universidad Miguel Hernandez, Elche, Spain, 3 Unidad de Proteómica, Centro Nacional de Biotecnología (CSIC), Madrid, Spain Rock bream iridovirus (RBIV) causes severe mass mortality in Korean rock bream (Oplegnathus fasciatus) populations. To date, immune defense mechanisms of rock bream against RBIV are unclear. While red blood cells (RBCs) are known to be involved in the immune response against viral infections, the participation of rock bream RBCs in the immune response against RBIV has not been studied yet. In this study, we examined induction of the immune response in rock bream RBCs Edited by: Brian Dixon, after RBIV infection. Each fish was injected with RBIV, and virus copy number in University of Waterloo, Canada RBCs gradually increased from 4 days post-infection (dpi), peaking at 10 dpi. A total Reviewed by: of 318 proteins were significantly regulated in RBCs from RBIV-infected individuals, Stephanie DeWitte-Orr, 183 proteins were upregulated and 135 proteins were downregulated. Differentially Wilfrid Laurier University, Canada Magdalena Chadzinska, upregulated proteins included those involved in cellular amino acid metabolic processes, Jagiellonian University, Poland cellular detoxification, snRNP assembly, and the spliceosome. Remarkably, the MHC *Correspondence: class I-related protein pathway was upregulated during RBIV infection.
    [Show full text]
  • First Report of Megalocytivirus (Iridoviridae) in Grouper Culture in Sabah, Malaysia
    Int.J.Curr.Microbiol.App.Sci (2014) 3(3): 896-909 ISSN: 2319-7706 Volume 3 Number 3 (2014) pp. 896-909 http://www.ijcmas.com Original Research Article First report of Megalocytivirus (Iridoviridae) in grouper culture in Sabah, Malaysia Asrazitah Abd Razak1, Julian Ransangan1* and Ahemad Sade2 1Microbiology and Fish Disease Laboratory, Borneo Marine Research Institute, Universiti Malaysia Sabah, Jalan UMS, 88400, Kota Kinabalu, Sabah, Malaysia 2Fisheries Department Sabah, Wisma Pertanian, Jalan Tasek, 88628 Kota Kinabalu, Sabah, Malaysia *Corresponding author A B S T R A C T Groupers are popular aquaculture species in Sabah, Malaysia. However, its aquaculture production is often limited by disease outbreaks. Although many diseases are known to affect groupers, iridovirus infection is a major concern because it causes high mortality within a short period of time. Recently, a disease resembled to iridovirus occurred and caused heavy losses to grouper aquaculture in K e y w o r d s Sabah. This has prompted us to conduct a study with the aim to determine if iridovirus present in the culture groupers. In this study, we examined 212 fish Grouper; specimens, which represented all the major culture grouper species in Malaysia. Megalo- The examination was carried out using single- and nested-PCR methods and cytivirus; followed by DNA sequencing. Two genes (major capsid protein and ATPase) were ISKNV; targeted for the PCR amplification and DNA sequencing. The finding showed nested-PCR; 15.6% (33/212) of the grouper specimens were severely infected by iridovirus. Sabah; Meanwhile, 17.4% of the specimens exhibited latent infection or asymptomatic Malaysia carriers.
    [Show full text]
  • Comparative Analysis of Transcriptional Regulation Patterns: Understanding the Gene Expression Profile in Nucleocytoviricota
    pathogens Review Comparative Analysis of Transcriptional Regulation Patterns: Understanding the Gene Expression Profile in Nucleocytoviricota Fernanda Gil de Souza †,Jônatas Santos Abrahão * and Rodrigo Araújo Lima Rodrigues *,† Laboratório de Vírus, Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais 31270-901, Brazil; [email protected] * Correspondence: [email protected] (J.S.A.); [email protected] (R.A.L.R.) † These authors contributed equally to this work. Abstract: The nucleocytoplasmic large DNA viruses (NCLDV) possess unique characteristics that have drawn the attention of the scientific community, and they are now classified in the phylum Nucleocytoviricota. They are characterized by sharing many genes and have their own transcriptional apparatus, which provides certain independence from their host’s machinery. Thus, the presence of a robust transcriptional apparatus has raised much discussion about the evolutionary aspects of these viruses and their genomes. Understanding the transcriptional process in NCLDV would provide information regarding their evolutionary history and a better comprehension of the biology of these viruses and their interaction with hosts. In this work, we reviewed NCLDV transcription and performed a comparative functional analysis of the groups of genes expressed at different times of infection of representatives of six different viral families of giant viruses. With this analysis, it was possible to observe
    [Show full text]
  • D:\Publikasi-Kumpulan Iaj-Pdf\I
    Distribution analysis of enlarged cells derived from ... (Indah Mastuti) DISTRIBUTION ANALYSIS OF ENLARGED CELLS DERIVED FROM GROUPER SLEEPY DISEASE IRIDOVIRUS (GSDIV) INFECTED HUMPBACK GROUPER Cromileptes altivelis Indah Mastuti# and Ketut Mahardika Research and Development Institute for Mariculture, Gondol, Bali (Received 5 December 2011 ; Accepted 12 April 2012) ABSTRACT Characteristic of Megalocytivirus infection has been known to produce formation of inclusion body bearing cells (IBCs) on internals organs of fish predominantly on spleen and kidney. Megalocytivirus that infected grouper is known as Grouper Sleepy Disease Iridovirus (GSDIV). This study was conducted to answer the effect of entry sites of GSDIV on distribution of enlarged cells formed on the internal organs of humpback grouper Cromileptes altivelis. Enlarged cells were observed histologically under the light microscope on spleen, head kidney, trunk kidney, liver, gill, heart, stomach, intestine, muscle and brain. Entry sites were designated to intramuscularly injection, intraperitoneally injection, dipped gill and inoculum added feed. Enlarged cells were formed on spleen, head kidney, trunk kidney, liver, gill, heart, stomach, muscle, except on intestine and brain. All the entry sites resulted in formation of enlarged cells on spleen, head kidney, trunk kidney, liver, heart. Spleen and head kidney were the most frequent observed organ. These results suggested that distribution of enlarged cells were not affected by the entry site of GSDIV. KEYWORDS: Megalocytivirus, enlarged cells, distribution, internal organs INTRODUCTION The ultrastructure study of enlarged cells on GSDIV infected fish revealed that IBCs con- Megalocytivirus which infect grouper is tained replication site of the virus (Mahardika known as Grouper Sleepy Disease Iridovirus et al., 2004; 2008; Sudthongkong et al., 2002).
    [Show full text]
  • Cell Culture-Derived Tilapia Lake Virus-Inactivated Vaccine Containing Montanide Adjuvant Provides High Protection Against Viral Challenge for Tilapia
    Article Cell Culture-Derived Tilapia Lake Virus-Inactivated Vaccine Containing Montanide Adjuvant Provides High Protection against Viral Challenge for Tilapia Weiwei Zeng 1,2,*, Yingying Wang 2, Huzi Hu 2, Qing Wang 2,*, Sven M. Bergmann 3 , Yahui Wang 2, Bo Li 2, Yuefeng Lv 2, Hua Li 1, Jiyuan Yin 1 and Yingying Li 2 1 Guangdong Provincial Key Laboratory of Animal Molecular Design and Precise Breeding, School of Life Science and Engineering, Foshan University, Foshan 528000, China; [email protected] (H.L.); [email protected] (J.Y.) 2 Key Laboratory of Aquatic Animal Immune Technology, Key Laboratory of Fishery Drug Development, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Ministry of Agriculture, Guangzhou 510380, China; [email protected] (Y.W.); [email protected] (H.H.); [email protected] (Y.W.); [email protected] (B.L.); [email protected] (Y.L.); [email protected] (Y.L.) 3 Institute of Infectology, Friedrich-Loffler-Institut (FLI), Federal Research Institute for Animal Health, Greifswald-Insel Riems, 17493 Greifswald, Germany; Sven.Bergmann@fli.de * Correspondence: [email protected] (W.Z.); [email protected] (Q.W.) Abstract: Tilapia lake virus (TiLV) is a newly emerging pathogen responsible for high mortality and economic losses in the global tilapia industry. Currently, no antiviral therapy or vaccines are available for the control of this disease. The goal of the present study was to evaluate the immunological effects and protective efficacy of formaldehyde- and β-propiolactone-inactivated vaccines against Citation: Zeng, W.; Wang, Y.; Hu, H.; TiLV in the presence and absence of the Montanide IMS 1312 VG adjuvant in tilapia.
    [Show full text]
  • Ultrastructural Morphogenesis of a Virus Associated with Lymphocystis-Like Lesions in Parore Girella Tricuspidata (Kyphosidae: Perciformes)
    Vol. 121: 129–139, 2016 DISEASES OF AQUATIC ORGANISMS Published September 26 doi: 10.3354/dao03050 Dis Aquat Org OPENPEN ACCESSCCESS Ultrastructural morphogenesis of a virus associated with lymphocystis-like lesions in parore Girella tricuspidata (Kyphosidae: Perciformes) P. M. Hine1,3,*, St. J. Wakefield2, G. Mackereth1, R. Morrison1 1National Centre for Disease Investigation, MAF Operations, Ministry of Agriculture and Forestry, PO Box 40-742, Upper Hutt, New Zealand 2School of Medicine, University of Otago, PO Box 7343, Newtown, Wellington, New Zealand 3Present address: 73, rue de la Fée au Bois, Fouras 17450, France ABSTRACT: The morphogenesis of large icosahedral viruses associated with lymphocystis-like lesions in the skin of parore Girella tricuspidata is described. The electron-lucent perinuclear viro- matrix comprised putative DNA with open capsids at the periphery, very large arrays of smooth endoplasmic reticulum (sER), much of it with a reticulated appearance (rsER) or occurring as rows of vesicles. Lysosomes, degenerating mitochondria and virions in various stages of assembly, and paracrystalline arrays were also present. Long electron-dense inclusions (EDIs) with 15 nm repeating units split terminally and curled to form tubular structures internalising the 15 nm repeating structures. These tubular structures appeared to form the virion capsids. Large parallel arrays of sER sometimes alternated with aligned arrays of crinkled cisternae along which passed a uniformly wide (20 nm) thread-like structure. Strings of small vesicles near open capsids may also have been involved in formation of an inner lipid layer. Granules with a fine fibrillar appear- ance also occurred in the viromatrix, and from the presence of a halo around mature virions it appeared that the fibrils may form a layer around the capsid.
    [Show full text]
  • Complete Genome Sequence Analysis of an Iridovirus Isolated from the Orange-Spotted Grouper, Epinephelus Coioides
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Virology 339 (2005) 81 – 100 www.elsevier.com/locate/yviro Complete genome sequence analysis of an iridovirus isolated from the orange-spotted grouper, Epinephelus coioides Ling Lu¨ a,1, Song Y. Zhoua,1, Cheng Chena, Shao P. Wenga,b, Siu-Ming Chanb, Jian G. Hea,* aState Key Laboratory for Biocontrol, School of Life Sciences, Zhongshan University, Guangzhou 510275, P. R. China bDepartment of Zoology, The University of Hong Kong, Hong Kong, P. R. China Received 25 February 2005; returned to author for revision 9 March 2005; accepted 11 May 2005 Available online 20 June 2005 Abstract Orange-spotted grouper iridovirus (OSGIV) was the causative agent of serious systemic diseases with high mortality in the cultured orange-spotted grouper, Epinephelus coioides. Here we report the complete genome sequence of OSGIV. The OSGIV genome consists of 112,636 bp with a G + C content of 54%. 121 putative open reading frames (ORF) were identified with coding capacities for polypeptides varying from 40 to 1168 amino acids. The majority of OSGIV shared homologies to other iridovirus genes. Phylogenetic analysis of the major capsid protein, ATPase, cytosine DNA methyl transferase and DNA polymerase indicated that OSGIV was closely related to infectious spleen and kidney necrosis virus (ISKNV) and rock bream iridovirus (RBIV), but differed from lymphocytisvirus and ranavirus. The determination of the genome of OSGIV will facilitate a better understanding of the molecular mechanism underlying the pathogenesis of the OSGIV and may provide useful information to develop diagnosis method and strategies to control outbreak of OSGIV.
    [Show full text]