期刊论文详细信息
Virology Journal
Complete genome sequence of acute viral necrosis virus associated with massive mortality outbreaks in the Chinese scallop, Chlamys farreri
Jie Huang2  Chongming Wang2  Changming Bai2  Yuyong Cai2  Tristan Renault3  Haixia Chen1  Weicheng Ren4 
[1] Department of Biological and Environmental Sciences, University of Gothenburg, Gothenburg, 40530, Sweden;Maricultural Organism Disease Control and Pathogenic Molecular Biology Laboratory, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Science, Qingdao, 266071, China;Ifremer, Unité Santé, Génétique et Microgiologie des Mollusques, Laboratoire de Génétique et Pathologie des Mollusques Marins, La Tremblade, 17390, France;Department of Rheumatology and Inflammation, University of Gothenburg, Gothenburg, 40530, Sweden
关键词: Genome;    OsHV-1;    Herpesvirus;    Acute viral necrosis virus (AVNV);   
Others  :  1150928
DOI  :  10.1186/1743-422X-10-110
 received in 2012-06-30, accepted in 2013-03-28,  发布年份 2013
PDF
【 摘 要 】

Background

Acute viral necrosis virus (AVNV) is the causative agent of a serious disease resulting in high mortality in cultured Chinese scallops, Chlamys farreri. We have sequenced and analyzed the complete genome of AVNV.

Results

The AVNV genome is a linear, double-stranded DNA molecule of 210,993 bp with a nucleotide composition of 38.5% G + C. A total of 123 open reading frames were predicted to encode functional proteins, ranging from 41 to 1,878 amino acid residues. The DNA sequence of AVNV is 97% identical to that of ostreid herpesvirus 1 (OsHV-1), and the amino acid sequences of the encoded proteins of these two viruses are 94-100% identical. The genomic organization of AVNV is similar to that of OsHV-1, and consists of two unique regions (170.4 kb and 3.4 kb, respectively), each flanked by two inverted repeats (7.6 kb and 10.2 kb, respectively), with a third unique region (1.5 kb) situated between the two internal repeats.

Conclusions

Our results indicate that AVNV is a variant of OsHV-1. The AVNV genome sequence provides information useful for understanding the evolution and divergence of OsHV-1 in marine molluscs.

【 授权许可】

   
2013 Ren et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150406004313410.pdf 1210KB PDF download
Figure 2. 175KB Image download
Figure 1. 115KB Image download
【 图 表 】

Figure 1.

Figure 2.

【 参考文献 】
  • [1]Comps M, Bonami JR: Infection virale associée à des mortalités chez l’huître Crassostrea angulata. Th C r Acad Sci D 1997, 285:1139-1140.
  • [2]Comps M, Duthoit JL: Infection virale associé à la maladie des branchies de l'huître portugaise portugaise Crassostrea angulata Lmk. C R Acad Sci Hebd Seances Acad Sci D 1996, 283:1595-1597.
  • [3]Farley CA, Banfield W, Kasnic G, Foster WS: Oyster herpes-type virus. Sciense 1972, 178:759-760.
  • [4]Farley CA: Proliferative disorders in bivalve molluscs. Mar Fish Rev 1976, 38:30-33.
  • [5]Farley CA: Viruses and virus-like lesions in marine molluscs. Mar Fish Rev 1978, 40:18-20.
  • [6]Ramussen LPD: Occurrence, prevalence and seasonality of neoplasia in the marine mussel Mytilus edulis from three sites in Denmark. Mar Biol 1986, 92:59-64.
  • [7]Miyazaki T, Goto K, Kobayashi T, Kageyama T, Miyata M: Mass mortalities associated with a virus disease in Japanese pearl oysters Pinctada fucata martensii. Dis Aquat Org 1999, 37:1-12.
  • [8]Bower SM: Synopsis of infectious diseases and parasites of commercially exploited shellfish: Assorted viruses detected in oysters and of unknown significance. 2001. http://www-sci.pac.dfo-mpo.gc.ca/shelldis/assortvirusoy_e.htm webcite
  • [9]Renault T, Novoa B: Viral infection among bivalves. Aquat Living Res 2004, 17:397-409.
  • [10]Oprandry JJ, Chang PW, Pronovost AD, Cooper KR, Brown CW, Yates VJ: Isolation of a viral agent causing hematopoietic neoplasia in the soft-shell clam, Mya arenaria. J Invertebr Pathol 1981, 38:45-51.
  • [11]King AMQ, Adams MJ, Carstens EB, Lefkowitz EJ: Virus taxonomy: classification and nomenclature of viruses: Ninth Report of the International Committee on Taxonomy of Viruses. San Diego: Elsevier Academic Press; 2012.
  • [12]Hine PM, Wesney B, Hay BE: Herpesvirus associated with mortalities among hatchery-reared larval Pacific oysters Crassostrea gigas. Dis Aquat Org 1992, 12:135-142.
  • [13]Nicolas JL, Comps M, Cochennec N: Herpes-like virus infecting Pacific-oyster larvae, Crassostrea gigas. Bull Eur Assoc Fish Pathol 1992, 12:11-13.
  • [14]Comps M, Cochennec N: A herpes-like virus from the European oyster Ostrea edulis L. J Invertebr Pathol 1993, 62:201-203.
  • [15]Renault T, Le Deuff RM, Cochennec N, Maffart P: Herpesviruses associated with mortalities among Pacific oyster, Crassostrea gigas, in France-comparative study. Rev Med Vet 1994, 145:735-742.
  • [16]Hine PM, Thorne T: Replication of herpes-like viruses in haemocytes of adult flat oysters Ostrea angasi: an ultrastructural study. Dis Aquat Org 1997, 29:189-196.
  • [17]Hine PM, Wesney B, Besant P: Replication of a herpes-like virus in larvae of the flat oyster Tiostrea chilensis at ambient temperatures. Dis Aquat Org 1998, 32:161-171.
  • [18]Vásquez-Yeomans R, Cáceres-Martínez J, Huerta AF: Herpes-like virus associated with eroded gills of the Pacific oyster Crassostrea gigas in Mexico. J Shellfish Res 2004, 23:417-419.
  • [19]Friedman CS, Estes RM, Stokes NA, Burge CA, Hargove JS, Barber BJ, Elston RA, Burreson EM, Reece KS: Herpes virus in juvenile Pacific oysters Crassostrea gigas from Tomales Bay, California, coincides with summer mortality episodes. Dis Aquat Org 2005, 63:33-41.
  • [20]Chang PH, Kuo ST, Lai SH, Yang HS, Ting YY, Hsu CL, Chen HC: Herpes-like virus infection causing mortality of cultured abalone Haliotis diversicolor supertexta in Taiwan. Dis Aquat Org 2005, 65:23-27.
  • [21]Hooper C, Hardy-Smith P, Handlinger J: Ganglioneuritis causing high mortalities in farmed Australian abalone (Haliotis laevigata and Haliotis rubra). Australian Vet J 2007, 85:188-193.
  • [22]Tan J, Lancaster M, Hyatt A, van Driel R, Wong F, Warner S: Purification of a herpes-like virus from abalone (Haliotis spp) with ganglioneuritis and detection by transmission electron microscopy. J Virol Methods 2008, 149:338-341.
  • [23]Renault T, Le Deuff RM, Chollet B, Cochennec N, Gérard A: Concomitant herpes-like virus infections in hatchery-reared larvae and nursery-cultured spat Crassostrea gigas and Ostrea edulis. Dis Aquat Org 2000, 42:173-183.
  • [24]Renault T, Lipart C, Arzul I: A herpes-like virus infects a non-ostreid bivalve species: virus replication in Ruditapes philippinarum larvae. Dis Aquat Org 2001, 45:1-7.
  • [25]Davison AJ, Trus BL, Cheng N, Steven AC, Watson MS, Cunningham C, Le Deuff RM, Renault T: A novel class of herpesvirus with bivalve hosts. J Gen Virol 2005, 86:41-53.
  • [26]Renault T, Lipart C, Arzul I: A herpes-like virus infecting Crassostrea gigas and Ruditapes philippinarum larvae in France. J Fish Dis 2001, 24:369-376.
  • [27]Arzul I, Renault T, Lipart C, Davison AJ: Evidence for interspecies transmission of oyster herpesvirus in marine bivalves. J Gen Virol 2001, 82:865-870.
  • [28]Arzul I, Nicolas JL, Davison AJ, Renault T: French scallops: a new host for ostreid herpesvirus-1. Virol 2001, 290:342-349.
  • [29]Segarra A, Pépin JF, Arzul I, Morga B, Faury N, Renault T: Detection and description of a particular Ostreid herpesvirus 1 genotype associated with massive mortality outbreaks of Pacific oysters Crassostrea gigas in France in 2008. Virus Res 2010, 153:92-99.
  • [30]Yu RH, Wang RC, Tian CY, Wang ZP: Discussion on the high mortality and its prevention in scallop Chlamys farreri. Trans Oceanol Limnol 1998, 71:69-72.
  • [31]Guo XM, Ford SE, Zhang FS: Molluscan aquaculture in China. J Shellfish Res 1999, 18:19-31.
  • [32]Song WB, Wang CM, Wang XH, Li Y: New research progress on massive mortality of cultured scallop Chlamys farreri. Mar Sci 2001, 25:23-27.
  • [33]Wang CM, Wang XH, Song XL, Huang J, Song WB: Purification and ultrastructure of a spherical virus in cultured scallop Chlamys farreri. J Fish China 2002, 26:180-184.
  • [34]Liu YJ, Wu XZ, Zhu MZ, Wang C, Zhang QZ, Pan JP: Ultrastructural observation and cytopathology of spherical virus in Chlamys farreri (Jones and Preston). J Tropical Oceanography 2002, 21:76-79.
  • [35]Fu C, Song W, Li Y: Monoclonal antibodies developed for detection of an epizootic virus associated with mass mortalities of cultured scallop Chlamys farreri. Dis Aquat Organ 2005, 65:17-22.
  • [36]Wang XH, Wang CM, Li J, Wang XH, Zheng GL, Hu XZ, Gong J, Song WB: Epidemiological study on massive death of the cultured scallop Chlamys farreri in the Jiaozhou Bay. J Fish China 2002, 26:149-155.
  • [37]Stow ND, McMonagle EC: Characterization of the TRS/IRS origin of DNA replication of herpes simplex virus type 1. Virol 1983, 130:427-438.
  • [38]Weller SK, Spadaro A, Schaffer JE, Murray AW, Maxam AM, Schaffer PA: Cloning sequencing and functional analysis of oriL a herpes simplex virus type 1 origin of DNA synthesis. Mol Cell Biol 1985, 5:930-942.
  • [39]Inoue N, Dambaugh TR, Rapp JC, Pellett PE: Alphaherpesvirus origin-binding protein homolog encoded by human herpesvirus 6B a beta-herpesvirus binds to nucleotide sequences that are similar to ori regions of alphaherpesviruses. J Virol 1994, 68:4126-4136.
  • [40]McGeoch DJ, Rixon FJ, Davison AJ: Topics in herpesvirus genomics and evolution. Virus Res 2006, 117:90-104.
  • [41]Do JW, Moon CH, Kim HJ, Ko MS, Kim SB, Son JH, Kim JS, An EJ, Kim MK, Lee SK, Han MS, Cha SJ, Park M, Park MA, Kim YC, Kim JW, Park JW: Complete genomic DNA sequence of rock bream iridovirus. Virol 2004, 325:351-363.
  • [42]Zhou SY, Chen C, Weng SP, Chan SM, He JG, Lü L: Complete genome sequence analysis of an iridovirus isolated from the orange-spotted grouper Epinephelus coioides. Virol 2005, 339:81-100.
  • [43]Shi CY, Jia KT, Yang B, Huang J: Complete genome sequence of a Megalocytivirus (family Iridoviridae) associated with turbot mortality in China. Virol J 2010, 7:159. BioMed Central Full Text
  • [44]McGeoch DJ, Dalrymple MA, Davison AJ, Dolan A, Frame MC, McNab D, Perry LJ, Scott JE, Taylor P: The complete DNA sequence of the long unique region in the genome of herpes simplex virus type 1. J Gen Virol 1998, 69:1531-1574.
  • [45]Davison AJ, Dolan A, Akter P, Addison C, Dargan DJ, Alcendor DJ, McGeoch DJ, Hayward GS: The human cytomegalovirus genome revisited: comparison with the chimpanzee cytomegalovirus genome. J Gen Virol 2003, 84:17-22.
  • [46]Renault T, Le Deuff RM, Cochennec N, Chollet B, Maffart P: Herpesviruses associated with high mortality levels in larvae and spat of Pacific oysters Crassostrea gigas: a comparative study the thermal effects on virus detection in hatchery-reared larvae reproduction of the disease in axenic larvae. Vet Res 1995, 26:539-543.
  • [47]Le Deuff RM, Renault T, Gerard A: Effects of temperature on herpes-like virus detection among hatchery-reared larval Pacific oyster Crassostrea gigas. Dis Aquat Org 1996, 24:149-157.
  • [48]Le Deuff RM, Renault T: Purification and partial genome characterization of a herpes-like virus infecting the Japanese oyster Crassostrea gigas. J Gen Virol 1999, 80:1317-1322.
  • [49]Martenot C, Oden E, Travaillé E, Malas JP, Houssin M: Detection of different variants of Ostreid Herpesvirus 1 in the Pacific oyster Crassostrea gigas between 2008 and 2010. Virus Res 2011, 160:25-31.
  • [50]Renault T, Moreau P, Faury N, Pepin JF, Segarra A, Webb S: Analysis of clinical ostreid herpesvirus 1 (Malacoherpesviridae) specimens by sequencing amplified fragments from three virus genome areas. J Virol 2012, 86:5942-7.
  • [51]Walzek TB, Kelley GO, Alfaro ME, Kurobe T, Davison AJ, Hedrick RP: Phylogenetic relationships in the family Alloherpesviridae. Dis Aquat Organ 2009, 84:179-194.
  • [52]Webby R, Hoffmann E, Webster R: Molecular constraints to interspecies transmission of viral pathogens. Nat Med 2004, 10:S77-S81.
  • [53]Qu XX, Hao P, Song XJ, Jiang SM, Liu YX, Wang PG, Rao X, Song HD, Wang SY, Zuo Y, Zheng AH, Luo M, Wang HL, Deng F, Wang HZ, Hu ZH, Ding MX, Zhao GP, Deng HK: Identification of two critical amino acidresidues of the severe acute respiratory syndrome coronavirus spike protein for this variation in zoonotic tropism transition via a double substitution strategy. J Biol Chem 2005, 280:29588-29595.
  • [54]Bandin I, Dopazo C: Host range host specificity and hypothesized host shift events among viruses of lower vertebrates. Vet Res 2011, 42:67-81. BioMed Central Full Text
  • [55]Connor RJ, Kawaoka Y, Webster RG, Paulson JC: Receptor specificity in human avian and equine H2 and H3 Influenza virus isolates. Virol 1994, 205:17-23.
  • [56]Matrosovich M, Tuzikov A, Bovin N, Gamabaryan A, Klimov A, Castrucci MR, Donatelli I, Kawaoka Y: Early alterations of the receptor-binding properties of H1 H2 and H3 avian influenza virus hemagglutinins after their introduction into mammals. J Virol 2000, 74:8502-8512.
  • [57]Moss JA, Burreson EM, Cordes JF, Dungan CF, Brown GD, Wang A, Wu X, Reece KS: Pathogens in Crassostrea ariakensis and other Asian oyster species: implications for non-native oyster introduction to Chesapeake Bay. Dis Aquat Org 2007, 77:207-223.
  文献评价指标  
  下载次数:13次 浏览次数:15次