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Journal articles on the topic 'Taura syndrome virus'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 February 2022

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1

Luo, Peng, Chao-Qun Hu, Chun-Hua Ren, and Zhao-Feng Sun. "Taura Syndrome Virus and Mammalian Cell Lines." Emerging Infectious Diseases 10, no. 12 (2004): 2260–61. http://dx.doi.org/10.3201/eid1012.040537.

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2

Pantoja, Carlos R., Solangel A. Navarro, Jaime Naranjo, Donald V. Lightner, and Charles P. Gerba. "Nonsusceptibility of Primate Cells to Taura Syndrome Virus." Emerging Infectious Diseases 10, no. 12 (2004): 2106–12. http://dx.doi.org/10.3201/eid1012.040419.

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3

Erickson, HS, BT Poulos, KFJ Tang, D. Bradley-Dunlop, and DV Lightner. "Taura syndrome virus from Belize represents a unique variant." Diseases of Aquatic Organisms 64 (2005): 91–98. http://dx.doi.org/10.3354/dao064091.

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4

Wertheim, Joel O., Kathy F. J. Tang, Solangel A. Navarro, and Donald V. Lightner. "A quick fuse and the emergence of Taura syndrome virus." Virology 390, no. 2 (2009): 324–29. http://dx.doi.org/10.1016/j.virol.2009.05.010.

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5

Srisuvan, T., KFJ Tang, and DV Lightner. "Experimental infection of Penaeus monodon with Taura syndrome virus (TSV)." Diseases of Aquatic Organisms 67 (2005): 1–8. http://dx.doi.org/10.3354/dao067001.

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6

Do, JW, SJ Cha, NS Lee, et al. "Taura syndrome virus from Penaeus vannamei shrimp cultured in Korea." Diseases of Aquatic Organisms 70 (2006): 171–74. http://dx.doi.org/10.3354/dao070171.

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7

Do, JW, SJ Cha, NS Lee, et al. "Taura syndrome virus in Penaeus vannamei shrimp originating from Hawaii." Diseases of Aquatic Organisms 74, no. 1 (2007): 81–83. http://dx.doi.org/10.3354/dao077081.

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8

Côté, I., S. Navarro, K. F. J. Tang, B. Noble, and D. V. Lightner. "Taura syndrome virus from Venezuela is a new genetic variant." Aquaculture 284, no. 1-4 (2008): 62–67. http://dx.doi.org/10.1016/j.aquaculture.2008.07.059.

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9

Lotz, Jeffrey M., Anne Marie Flowers, and Verlee Breland. "A model of Taura syndrome virus (TSV) epidemics in Litopenaeus vannamei." Journal of Invertebrate Pathology 83, no. 2 (2003): 168–76. http://dx.doi.org/10.1016/s0022-2011(03)00083-1.

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10

Boube, I., J. M. Lotz, A. E. Pozhitkov, S. Li, and R. J. Griffitt. "Identification of Genes Involved in Taura Syndrome Virus Resistance inLitopenaeus Vannamei." Journal of Aquatic Animal Health 26, no. 3 (2014): 137–43. http://dx.doi.org/10.1080/08997659.2013.860058.

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11

Côté, I., B. T. Poulos, R. M. Redman, and D. V. Lightner. "Development and characterization of a monoclonal antibody against Taura syndrome virus." Journal of Fish Diseases 32, no. 12 (2009): 989–96. http://dx.doi.org/10.1111/j.1365-2761.2009.01082.x.

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12

Yulia Kartika, Hari Suprapto,. "Pemantauan Virus Dengan Metode PCR (Polymerase Chain Reaction) Di Pantai Utara Jawa Timur [Monitoring Virus By PCR Method (Polymerase Chain Reaction) In North Coast, East Java]." Jurnal Ilmiah Perikanan dan Kelautan 4, no. 1 (2019): 65. http://dx.doi.org/10.20473/jipk.v4i1.11587.

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Abstract The disease most dangerous for the cultivation activity is virus. Viruses are organisms subseluler that contain only nucleic acid (RNA or DNA) as genetic material. Koi Herpes Virus is one type of virus that causes mortality in cultured Cyprinids. KHV disease in Indonesia started in Blitar, East Java on March 2002 because the entry of imported koi fish that carry the virus KHV, while mortality prosentase could reach 80% - 85%, which causes loss of about 5 billion rupiah. In addition of KHV, there are several types of viral diseases in shrimp is White Spot Syndrome Virus (WSSV), Taura S

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13

Phalitakul, Sukanya, Janenuj Wongtawatchai, Meena Sarikaputi, and Nareerat Viseshakul. "The molecular detection of Taura syndrome virus emerging with White spot syndrome virus in penaeid shrimps of Thailand." Aquaculture 260, no. 1-4 (2006): 77–85. http://dx.doi.org/10.1016/j.aquaculture.2006.05.040.

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14

Srisuvan, T., CR Pantoja, RM Redman, and DV Lightner. "Ultrastructure of the replication site in Taura syndrome virus (TSV)-infected cells." Diseases of Aquatic Organisms 73 (December 14, 2006): 89–101. http://dx.doi.org/10.3354/dao073089.

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15

Vergel, Joseph Carlo, Lara Denise Cabawatan, Vivien Alexandra Madrona, et al. "Detection of Taura Syndrome Virus (TSV) in Litopenaeus vannamei in the Philippines." Philippine Journal of Fisheries 26, no. 1 (2019): 8–14. http://dx.doi.org/10.31398/tpjf/25.2.2018-0003.

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16

Navarro, Solangel A., Kathy F. J. Tang, and Donald V. Lightner. "An improved Taura syndrome virus (TSV) RT-PCR using newly designed primers." Aquaculture 293, no. 3-4 (2009): 290–92. http://dx.doi.org/10.1016/j.aquaculture.2009.05.003.

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17

Tang, KFJ, SA Navarro, CR Pantoja, FL Aranguren, and DV Lightner. "New genotypes of white spot syndrome virus (WSSV) and Taura syndrome virus (TSV) from the Kingdom of Saudi Arabia." Diseases of Aquatic Organisms 99, no. 3 (2012): 179–85. http://dx.doi.org/10.3354/dao02470.

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18

Ochoa, Lauren Marie, Roberto Cruz-Flores, and Arun K. Dhar. "Detection and Phylogenetic Analyses of Taura Syndrome Virus from Archived Davidson’s-Fixed Paraffin-Embedded Shrimp Tissue." Viruses 12, no. 9 (2020): 1030. http://dx.doi.org/10.3390/v12091030.

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Taura syndrome is a World Organization for Animal Health (OIE)-listed disease of marine shrimp that is caused by Taura syndrome virus (TSV), a single-stranded RNA virus. Here we demonstrate the utility of using 15-year-old archived Davidson’s-fixed paraffin-embedded (DFPE) shrimp tissues for TSV detection and phylogenetic analyses. Total RNA was isolated from known TSV-infected DFPE tissues using three commercially available kits and the purity and ability to detect TSV in the isolated RNA were compared. TSV was successfully detected through RT-qPCR in all the tested samples. Among the TSV-spe

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19

Lien, Tzu-Wen, Hann-Chang Hsiung, Chih-Cheng Huang, and Yen-Ling Song. "Genomic Similarity of Taura Syndrome Virus (TSV) between Taiwan and Western Hemisphere Isolates." Fish Pathology 37, no. 2 (2002): 71–75. http://dx.doi.org/10.3147/jsfp.37.71.

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20

George, Sunil K., Krista N. Kaizer, Yelena M. Betz, and Arun K. Dhar. "Multiplication of Taura syndrome virus in primary hemocyte culture of shrimp (Penaeus vannamei)." Journal of Virological Methods 172, no. 1-2 (2011): 54–59. http://dx.doi.org/10.1016/j.jviromet.2010.12.020.

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21

Lotz, JM, L. Salazar Anton, and MA Soto. "Effect of chronic Taura syndrome virus infection on salinity tolerance of Litopenaeus vannamei." Diseases of Aquatic Organisms 65 (2005): 75–78. http://dx.doi.org/10.3354/dao065075.

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22

Teng, PH, CL Chen, CN Wu, SY Wu, BR Ou, and PY Lee. "Rapid and sensitive detection of Taura syndrome virus using nucleic acid-based amplification." Diseases of Aquatic Organisms 73 (November 21, 2006): 13–22. http://dx.doi.org/10.3354/dao073013.

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23

Song, Yen-Ling, Chun-I. Yu, Tzu-Wen Lien, Chih-Cheng Huang, and Min-Nan Lin. "Haemolymph parameters of Pacific white shrimp (Litopenaeus vannamei) infected with Taura syndrome virus." Fish & Shellfish Immunology 14, no. 4 (2003): 317–31. http://dx.doi.org/10.1006/fsim.2002.0440.

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24

Aranguren, LF, KFJ Tang, and DV Lightner. "Protection from yellow head virus (YHV) infection in Penaeus vannamei pre-infected with Taura syndrome virus (TSV)." Diseases of Aquatic Organisms 98, no. 3 (2012): 185–92. http://dx.doi.org/10.3354/dao02448.

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25

Soto, M. Andres, and Jeffrey M. Lotz. "Transmission, Virulence, and Recovery Coefficients of White Spot Syndrome Virus (WSSV) and Taura Syndrome Virus (TSV) Infections in Kona StockLitopenaeus vannamei." Journal of Aquatic Animal Health 15, no. 1 (2003): 48–54. http://dx.doi.org/10.1577/1548-8667(2003)015<0048:tvarco>2.0.co;2.

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26

Tang, Kathy F. J., Jun Wang, and Donald V. Lightner. "Quantitation of Taura syndrome virus by real-time RT-PCR with a TaqMan assay." Journal of Virological Methods 115, no. 1 (2004): 109–14. http://dx.doi.org/10.1016/j.jviromet.2003.09.021.

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27

LU, Y., and P. SUN. "Viral resistance in shrimp that express an antisense Taura syndrome virus coat protein gene." Antiviral Research 67, no. 3 (2005): 141–46. http://dx.doi.org/10.1016/j.antiviral.2005.06.007.

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28

Robalino, Javier, Craig L. Browdy, Sarah Prior, et al. "Induction of Antiviral Immunity by Double-Stranded RNA in a Marine Invertebrate." Journal of Virology 78, no. 19 (2004): 10442–48. http://dx.doi.org/10.1128/jvi.78.19.10442-10448.2004.

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ABSTRACT Vertebrates mount a strong innate immune response against viruses, largely by activating the interferon system. Double-stranded RNA (dsRNA), a common intermediate formed during the life cycle of many viruses, is a potent trigger of this response. In contrast, no general inducible antiviral defense mechanism has been reported in any invertebrate. Here we show that dsRNA induces antiviral protection in the marine crustacean Litopenaeus vannamei. When treated with dsRNA, shrimp showed increased resistance to infection by two unrelated viruses, white spot syndrome virus and Taura syndrome

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29

Robles-Sikisaka, Refugio, Kenneth W. Hasson, Denise K. Garcia, et al. "Genetic variation and immunohistochemical differences among geographic isolates of Taura syndrome virus of penaeid shrimp." Journal of General Virology 83, no. 12 (2002): 3123–30. http://dx.doi.org/10.1099/0022-1317-83-12-3123.

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Taura syndrome virus (TSV) is an important virus infecting penaeid shrimp in the western hemisphere. Genetic variation and immunohistochemical differences of 20 TSV isolates collected from the USA, Taiwan, Mexico and Nicaragua were compared. Capsid protein genes CP1 (546 bp) and CP2 (584 bp) were amplified by RT–PCR and the cDNAs were sequenced. Pairwise comparison of nucleotide sequences showed a 0–2·4% difference in CP1 and a 0–3·5% difference in CP2. Phylogenetic analyses clustered the TSV isolates into two groups: one contained USA, Taiwan and some Mexican isolates, the other contained Mex

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30

Kiatpathomchai, Wansika, Wansadaj Jareonram, Sarawut Jitrapakdee, and T. W. Flegel. "Rapid and sensitive detection of Taura syndrome virus by reverse transcription loop-mediated isothermal amplification." Journal of Virological Methods 146, no. 1-2 (2007): 125–28. http://dx.doi.org/10.1016/j.jviromet.2007.06.007.

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31

Poulos, BT, R. Kibler, D. Bradley-Dunlop, LL Mohney, and DV Lightner. "Production and use of antibodies for the detection of Taura syndrome virus in penaeid shrimp." Diseases of Aquatic Organisms 37 (1999): 99–106. http://dx.doi.org/10.3354/dao037099.

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32

Hasson, KW, DV Lightner, LL Mohney, RM Redman, and B. White. "Role of lymphoid organ spheroids in chronic Taura syndrome virus (TSV) infections in Penaeus vannamei." Diseases of Aquatic Organisms 38 (1999): 93–105. http://dx.doi.org/10.3354/dao038093.

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33

Chongsatja, Phattara-orn, Apichai Bourchookarn, Chu Fang Lo, Visith Thongboonkerd, and Chartchai Krittanai. "Proteomic analysis of differentially expressed proteins in Penaeus vannamei hemocytes upon Taura syndrome virus infection." PROTEOMICS 7, no. 19 (2007): 3592–601. http://dx.doi.org/10.1002/pmic.200700281.

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34

Poulos, BT, BW Noble, and DV Lightner. "Comparison of Taura syndrome virus (TSV) detection methods during chronic-phase infection in Penaeus vannamei." Diseases of Aquatic Organisms 82 (December 22, 2008): 179–85. http://dx.doi.org/10.3354/dao01996.

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35

Cao, Z., SY Wang, V. Breeland, AM Moore, and JM Lotz. "Taura syndrome virus loads in Litopenaeus vannamei hemolymph following infection are related to differential mortality." Diseases of Aquatic Organisms 91, no. 2 (2010): 97–103. http://dx.doi.org/10.3354/dao02258.

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36

Chang, Yun-Shiang, Shao-En Peng, Hon-Tsen Yu, et al. "Genetic and phenotypic variations of isolates of shrimp Taura syndrome virus found in Penaeus monodon and Metapenaeus ensis in Taiwan." Journal of General Virology 85, no. 10 (2004): 2963–68. http://dx.doi.org/10.1099/vir.0.80132-0.

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Distinct Taura syndrome virus (TSV) isolates were found in Metapenaeus ensis (isolate Tw2KMeTSV), Penaeus monodon (isolate Tw2KPmTSV) and Litopenaeus vannamei (isolate Tw02LvTSV). Nucleotide sequence analysis of these three isolates revealed differences in the TSV structural protein (capsid protein precursor) gene orf2. TSV ORF2 amino acid sequence comparison and phylogenetic analysis suggested a comparatively close relationship between these three Taiwanese isolates and the Hawaiian isolate HI94TSV. In P. monodon specimens that were naturally and experimentally infected with the Tw2KPmTSV iso

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37

Dwinanti, S. H., and Munti Yuhana. "Existing of White Spot Syndrome Virus (WSSV), Taura Syndrome Virus (TSV) and Infectious Hypodermal Haematopoitic Necrosis Virus (IHHNV) in White Shrimp Litopenaeus vannamei Reared at Intensive Tambak System in Bakauheni, Lampung Selatan." Jurnal Akuakultur Indonesia 8, no. 2 (2009): 109. http://dx.doi.org/10.19027/jai.8.109-116.

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<p>Development of white shrimp, <em>Litopenaeus vannamei</em> culture to increase production yield should take attention in prevention of viral outbreak which is a main factor caused harvesting failure. Viruses that usually infect shrimp are <em>white spo</em><em>t </em><em>syndrome </em><em>vi</em><em>r</em><em>u</em><em>s</em> (WSSV), <em>taura syndrome virus</em> (TSV) dan <em>infectious</em><em> </em><em>hypodermal hematopoietic necrosis v</em&g

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38

Argue, Brad J., Steve M. Arce, Jeffrey M. Lotz, and Shaun M. Moss. "Selective breeding of Pacific white shrimp (Litopenaeus vannamei) for growth and resistance to Taura Syndrome Virus." Aquaculture 204, no. 3-4 (2002): 447–60. http://dx.doi.org/10.1016/s0044-8486(01)00830-4.

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39

Phromjai, Jurairat, Thitima Mathuros, Ditsayuth Phokharatkul, et al. "RT-LAMP detection of shrimp Taura syndrome virus (TSV) by combination with a nanogold-oligo probe." Aquaculture Research 46, no. 8 (2013): 1902–13. http://dx.doi.org/10.1111/are.12345.

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40

Nielsen, L., W. Sang-oum, S. Cheevadhanarak, and TW Flegel. "Taura syndrome virus (TSV) in Thailand and its relationship to TSV in China and the Americas." Diseases of Aquatic Organisms 63 (2005): 101–6. http://dx.doi.org/10.3354/dao063101.

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41

Arunrut, N., J. Phromjai, W. Gangnonngiw, N. Kanthong, S. Sriurairatana, and W. Kiatpathomchai. "In vitro cultivation of shrimp Taura syndrome virus (TSV) in a C6/36 mosquito cell line." Journal of Fish Diseases 34, no. 10 (2011): 805–10. http://dx.doi.org/10.1111/j.1365-2761.2011.01286.x.

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42

Dhar, Arun K., Dilip K. Lakshman, Keenan Amundsen, et al. "Characterization of a Taura syndrome virus isolate originating from the 2004 Texas epizootic in cultured shrimp." Archives of Virology 155, no. 3 (2010): 315–27. http://dx.doi.org/10.1007/s00705-009-0584-5.

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43

Mari, Jocelyne, Bonnie T. Poulos, Donald V. Lightner, and Jean-Robert Bonami. "Shrimp Taura syndrome virus: genomic characterization and similarity with members of the genus Cricket paralysis-like viruses." Journal of General Virology 83, no. 4 (2002): 915–26. http://dx.doi.org/10.1099/0022-1317-83-4-915.

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The single-stranded genomic RNA of Taura syndrome virus (TSV) is 10205 nucleotides in length, excluding the 3′ poly(A) tail, and contains two large open reading frames (ORFs) that are separated by an intergenic region of 207 nucleotides. The ORFs are flanked by a 377 nucleotide 5′ untranslated region (UTR) and a 226 nucleotide 3′ UTR followed by a poly(A) tail. The predicted amino acid sequence of ORF1 revealed sequence motifs characteristic of a helicase, a protease and an RNA-dependent RNA polymerase, similar to the non-structural proteins of several plant and animal RNA viruses. In addition

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44

Zhang, Cong, Jun-fa Yuan, and Zheng-li Shi. "Molecular epidemiological investigation of infectious hypodermal and hematopoietic necrosis virus and Taura syndrome virus in Penaeus Vannamei cultured in China." Virologica Sinica 22, no. 5 (2007): 380–88. http://dx.doi.org/10.1007/s12250-007-0036-x.

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45

Prior, S., CL Browdy, EF Shepard, R. Laramore, and PG Parnell. "Controlled bioassay systems for determination of lethal infective doses of tissue homogenates containing Taura syndrome or white spot syndrome virus." Diseases of Aquatic Organisms 54 (2003): 89–96. http://dx.doi.org/10.3354/dao054089.

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46

Zeng, Digang, Min Peng, Xiuli Chen, et al. "Molecular cloning, characterization, and immune response against white spot syndrome virus and Taura syndrome virus infections of peroxiredoxin in Litopenaeus vannamei and its antioxidant activity." Crustaceana 88, no. 10-11 (2015): 1149–61. http://dx.doi.org/10.1163/15685403-00003476.

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Peroxiredoxin (Prx) is an important peroxidase that can protect organisms against various oxidative stresses. In this study, a member of Prx family, designated LvPrx, was cloned fromLitopenaeus vannamei. Sequence and phylogenetic analyses indicated that LvPrx belongs to the 2-Cys Prx (Prx IV) isoform. The recombinant LvPrx protein was constructed and expressed inEscherichia coli, and the purified LvPrx proteins were shown to reduce H2O2in vitro in the presence of dithiothreitol, indicating that LvPrx is a functional peroxiredoxin. Using qRT-PCR, the mRNA expression levels of LvPrx were determi

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47

Longyant, S., P. Poyoi, P. Chaivisuthangkura, et al. "Specific monoclonal antibodies raised against Taura syndrome virus (TSV) capsid protein VP3 detect TSV in single and dual infections with white spot syndrome virus (WSSV)." Diseases of Aquatic Organisms 79 (March 3, 2008): 75–81. http://dx.doi.org/10.3354/dao01885.

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48

Garza, J. R., K. W. Hasson, B. T. Poulos, R. M. Redman, B. L. White, and D. V. Lightner. "Demonstration of Infectious Taura Syndrome Virus in the Feces of Seagulls Collected during an Epizootic in Texas." Journal of Aquatic Animal Health 9, no. 2 (1997): 156–59. http://dx.doi.org/10.1577/1548-8667(1997)009<0156:doitsv>2.3.co;2.

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49

Chaivisuthangkura, Parin, Siwaporn Longyant, Warunee Hajimasalaeh, Pattarin Sridulyakul, Sombat Rukpratanporn, and Paisarn Sithigorngul. "Improved sensitivity of Taura syndrome virus immunodetection with a monoclonal antibody against the recombinant VP2 capsid protein." Journal of Virological Methods 163, no. 2 (2010): 433–39. http://dx.doi.org/10.1016/j.jviromet.2009.11.007.

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50

Hasson, KW, DV Lightner, LL Mohney, RM Redman, BT Poulos, and BM White. "Taura syndrome virus (TSV) lesion development and the disease cycle in the Pacific white shrimp Penaeus vannamei." Diseases of Aquatic Organisms 36 (1999): 81–93. http://dx.doi.org/10.3354/dao036081.

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