TY - JOUR
T1 - RNA-Seq analysis reveals genes associated with resistance to Taura syndrome virus (TSV) in the Pacific white shrimp Litopenaeus vannamei
AU - Sookruksawong, Suchonma
AU - Sun, Fanyue
AU - Liu, Zhanjiang
AU - Tassanakajon, Anchalee
N1 - Funding Information:
This work was supported by research grants from the Higher Education Research Promotion and National Research University Project of Thailand , Office of the Higher Education Commission (FW643A), the Thailand Research Fund (TRF Senior Scholar number RTA5580008 ) and partially supported by the Japan International Cooperation Agency (JICA) . A Ph.D. student fellowship to Mrs. Suchonma Sookruksawong for the Strategic Scholarships Fellowships Frontier Research Networks from the Commission on Higher Education is greatly appreciated. We are grateful to SyAqua Siam Co. Ltd for the support of L. vannamei samples. Thanks as well to Mr. Chaiwat Bootchai, Biostatistics and Informatics Laboratory, Genome Institute, National Center for Genetic Engineering and Biotechnology for helping to submit the raw read data at the NCBI Sequence Read Archive (SRA) . We also thank Chulalongkorn University for the support under the Ratchadaphisek Somphot Endowment to the Center of Excellence for Molecular Biology and Genomics of Shrimp . We appreciate the high quality sequencing services of HudsonAlpha Genomic Services Lab (Huntsville, AL, USA) . We are also grateful to Alabama Supercomputer Center for providing the computing capacity for the bioinformatics analysis of this study.
Copyright:
Copyright 2013 Elsevier B.V., All rights reserved.
PY - 2013/12
Y1 - 2013/12
N2 - Outbreak of Taura syndrome virus (TSV) is one of the major pathogens of the Pacific white shrimp Litopenaeus vannamei. Although selective breeding for improvement of TSV resistance in L. vannamei has been successfully developed and has led to a great benefit to the shrimp farming industry worldwide. The molecular mechanisms underlying the viral resistance in shrimp remain largely unknown. In the present study, we conducted the first transcriptomic profiling of host responses in hemolymph and hemocytes in order to identify the differentially expressed genes associated with resistance to TSV in L. vannamei. High-throughput RNA-Seq was employed, obtaining 193.6 and 171.2 million high-quality Illumina reads from TSV-resistant and susceptible L. vannamei lines respectively. A total of 61,937 contigs were generated with an average length of 546.26bp. BLASTX-based gene annotation (E-value<10-5) allowed the identification of 12,398 unique proteins against the NCBI non-redundant NR database. In addition, comparison of digital gene expression between resistant and susceptible strains revealed 1374 significantly differentially expressed contigs (representing 697 unigenes). Gene pathway analysis of the differentially expressed gene set highlighted several putative genes involved in the immune response activity including (1) pathogen/antigen recognition including immune regulator, adhesive protein and signal transducer; (2) coagulation; (3) proPO pathway cascade; (4) antioxidation; and (5) protease. The expression patterns of 22 differentially expressed genes involving immune response were validated by quantitative real-time RT-PCR (average correlation coefficients 0.94, p-value<0.001). Our results provide valuable information on gene functions associated with resistance to TSV in L. vannamei.
AB - Outbreak of Taura syndrome virus (TSV) is one of the major pathogens of the Pacific white shrimp Litopenaeus vannamei. Although selective breeding for improvement of TSV resistance in L. vannamei has been successfully developed and has led to a great benefit to the shrimp farming industry worldwide. The molecular mechanisms underlying the viral resistance in shrimp remain largely unknown. In the present study, we conducted the first transcriptomic profiling of host responses in hemolymph and hemocytes in order to identify the differentially expressed genes associated with resistance to TSV in L. vannamei. High-throughput RNA-Seq was employed, obtaining 193.6 and 171.2 million high-quality Illumina reads from TSV-resistant and susceptible L. vannamei lines respectively. A total of 61,937 contigs were generated with an average length of 546.26bp. BLASTX-based gene annotation (E-value<10-5) allowed the identification of 12,398 unique proteins against the NCBI non-redundant NR database. In addition, comparison of digital gene expression between resistant and susceptible strains revealed 1374 significantly differentially expressed contigs (representing 697 unigenes). Gene pathway analysis of the differentially expressed gene set highlighted several putative genes involved in the immune response activity including (1) pathogen/antigen recognition including immune regulator, adhesive protein and signal transducer; (2) coagulation; (3) proPO pathway cascade; (4) antioxidation; and (5) protease. The expression patterns of 22 differentially expressed genes involving immune response were validated by quantitative real-time RT-PCR (average correlation coefficients 0.94, p-value<0.001). Our results provide valuable information on gene functions associated with resistance to TSV in L. vannamei.
KW - Disease resistance
KW - Immune response
KW - L. vannamei
KW - RNA-Seq
KW - TSV infection
KW - Transcriptome
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U2 - 10.1016/j.dci.2013.07.020
DO - 10.1016/j.dci.2013.07.020
M3 - Article
C2 - 23921257
AN - SCOPUS:84883411643
SN - 0145-305X
VL - 41
SP - 523
EP - 533
JO - Developmental and Comparative Immunology
JF - Developmental and Comparative Immunology
IS - 4
ER -