M Poornima, Y Seetang-Nun, S V Alavandi, J Syama Dayal
{"title":"莱姆-辛格病毒:一种与养殖黑虎对虾(白对虾)单斑生长缓慢综合征相关的可能病原。","authors":"M Poornima, Y Seetang-Nun, S V Alavandi, J Syama Dayal","doi":"10.1007/s13337-012-0099-7","DOIUrl":null,"url":null,"abstract":"<p><p>Among the emerging diseases in shrimp aquaculture, monodon slow growth syndrome (MSGS) is a major concern in South and Southeast Asia. Shrimp farming in Thailand was severely affected during 2000-2002 due to MSGS, which caused an economic loss, of about US$ 300 million. MSGS is characterized by abnormally slow growth with coefficients of size variation of >35 %, that has impacted P. monodon production in Thailand. A new shrimp virus, Laem-Singh virus (LSNV) was identified to be associated in MSGS affected shrimp. LSNV a RNA virus of about 25 nm diameter is phylogenetically related to the insect-borne viruses in the families Barnaviridae, Tymoviridae and Sobemoviridae an important histopathological observation is exclusively noticed in growth-retarded shrimp. The LSNV infections have been confirmed in various organs of infected shrimp such as lymphoid organ, gills and nervous tissues by various diagnostic techniques such as reverse transcription polymerase chain reaction (RT-PCR), in situ hybridization, quantitative real-time RT-PCR and reverse transcription loop-mediated isothermal amplification combined with a lateral flow dipstick (RT-LAMP-LFD) and these tools are available for the diagnosis of LSNV. Recently, an integrase containing element has been identified in absolute association with LSNV in stunted growth shrimp. The transmission of LSNV through horizontal and vertical routes has been experimentally demonstrated. The known natural host-range of LSNV includes P. monodon and other penaeid shrimp. The putative RdRp gene involved in replication of LSNV was targeted for dsRNA-mediated gene silencing and appeared to be effective in a dose-dependent manner. Since the discovery of LSNV in 2006 in Thailand, it has been added to the list of viruses to be excluded from domesticated specific pathogen-free stocks of P. monodon and it has been recommended that shrimp farmers avoid stocking post larvae positive for LSNV to prevent MSGS in their farms. </p>","PeriodicalId":50370,"journal":{"name":"Indian Journal of Virology","volume":"23 2","pages":"215-25"},"PeriodicalIF":0.0000,"publicationDate":"2012-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s13337-012-0099-7","citationCount":"9","resultStr":"{\"title\":\"Laem-Singh Virus: A Probable Etiological Agent Associated with Monodon Slow Growth Syndrome in Farmed Black Tiger Shrimp (Penaeus monodon).\",\"authors\":\"M Poornima, Y Seetang-Nun, S V Alavandi, J Syama Dayal\",\"doi\":\"10.1007/s13337-012-0099-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Among the emerging diseases in shrimp aquaculture, monodon slow growth syndrome (MSGS) is a major concern in South and Southeast Asia. Shrimp farming in Thailand was severely affected during 2000-2002 due to MSGS, which caused an economic loss, of about US$ 300 million. MSGS is characterized by abnormally slow growth with coefficients of size variation of >35 %, that has impacted P. monodon production in Thailand. A new shrimp virus, Laem-Singh virus (LSNV) was identified to be associated in MSGS affected shrimp. LSNV a RNA virus of about 25 nm diameter is phylogenetically related to the insect-borne viruses in the families Barnaviridae, Tymoviridae and Sobemoviridae an important histopathological observation is exclusively noticed in growth-retarded shrimp. The LSNV infections have been confirmed in various organs of infected shrimp such as lymphoid organ, gills and nervous tissues by various diagnostic techniques such as reverse transcription polymerase chain reaction (RT-PCR), in situ hybridization, quantitative real-time RT-PCR and reverse transcription loop-mediated isothermal amplification combined with a lateral flow dipstick (RT-LAMP-LFD) and these tools are available for the diagnosis of LSNV. Recently, an integrase containing element has been identified in absolute association with LSNV in stunted growth shrimp. The transmission of LSNV through horizontal and vertical routes has been experimentally demonstrated. The known natural host-range of LSNV includes P. monodon and other penaeid shrimp. The putative RdRp gene involved in replication of LSNV was targeted for dsRNA-mediated gene silencing and appeared to be effective in a dose-dependent manner. 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引用次数: 9
摘要
在对虾养殖中出现的新疾病中,单虾生长缓慢综合征(MSGS)是南亚和东南亚的一个主要问题。2000-2002年期间,泰国虾类养殖受到严重影响,造成约3亿美元的经济损失。MSGS的特征是生长异常缓慢,大小变异系数> 35%,这已经影响了泰国单叶假单胞菌的生产。在受MSGS影响的虾中发现了一种新的虾病毒leem - singh病毒(LSNV)。LSNV - a RNA病毒直径约25 nm,与巴纳病毒科、泰莫病毒科和索莫病毒科虫媒病毒在系统发育上有亲缘关系,在生长迟缓虾中有重要的组织病理学观察。通过逆转录聚合酶链式反应(RT-PCR)、原位杂交、实时定量RT-PCR和逆转录环介导等温扩增结合侧流试纸(RT-LAMP-LFD)等多种诊断技术,证实了LSNV在感染对虾淋巴器官、鳃和神经组织等多个器官的感染,这些诊断工具可用于LSNV的诊断。最近,一种含有整合酶的元素在发育不良的虾中被鉴定出与LSNV有绝对关联。LSNV通过水平和垂直途径的传播已被实验证实。已知的LSNV的自然宿主范围包括单螯虾和其他对虾。参与LSNV复制的推定RdRp基因是dsrna介导的基因沉默的靶标,并且似乎以剂量依赖的方式有效。自2006年在泰国发现LSNV以来,它已被列入从驯化的特定无病原体单斑单胞疟原虫种群中排除的病毒清单,并建议虾农避免饲养LSNV阳性的幼虫,以防止其养殖场发生MSGS。
Laem-Singh Virus: A Probable Etiological Agent Associated with Monodon Slow Growth Syndrome in Farmed Black Tiger Shrimp (Penaeus monodon).
Among the emerging diseases in shrimp aquaculture, monodon slow growth syndrome (MSGS) is a major concern in South and Southeast Asia. Shrimp farming in Thailand was severely affected during 2000-2002 due to MSGS, which caused an economic loss, of about US$ 300 million. MSGS is characterized by abnormally slow growth with coefficients of size variation of >35 %, that has impacted P. monodon production in Thailand. A new shrimp virus, Laem-Singh virus (LSNV) was identified to be associated in MSGS affected shrimp. LSNV a RNA virus of about 25 nm diameter is phylogenetically related to the insect-borne viruses in the families Barnaviridae, Tymoviridae and Sobemoviridae an important histopathological observation is exclusively noticed in growth-retarded shrimp. The LSNV infections have been confirmed in various organs of infected shrimp such as lymphoid organ, gills and nervous tissues by various diagnostic techniques such as reverse transcription polymerase chain reaction (RT-PCR), in situ hybridization, quantitative real-time RT-PCR and reverse transcription loop-mediated isothermal amplification combined with a lateral flow dipstick (RT-LAMP-LFD) and these tools are available for the diagnosis of LSNV. Recently, an integrase containing element has been identified in absolute association with LSNV in stunted growth shrimp. The transmission of LSNV through horizontal and vertical routes has been experimentally demonstrated. The known natural host-range of LSNV includes P. monodon and other penaeid shrimp. The putative RdRp gene involved in replication of LSNV was targeted for dsRNA-mediated gene silencing and appeared to be effective in a dose-dependent manner. Since the discovery of LSNV in 2006 in Thailand, it has been added to the list of viruses to be excluded from domesticated specific pathogen-free stocks of P. monodon and it has been recommended that shrimp farmers avoid stocking post larvae positive for LSNV to prevent MSGS in their farms.