4.7 Article

Tilapia lake virus immunoglobulin G (TiLV IgG) antibody: Immunohistochemistry application reveals cellular tropism of TiLV infection

期刊

FISH & SHELLFISH IMMUNOLOGY
卷 116, 期 -, 页码 115-123

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fsi.2021.06.017

关键词

Antibody; Immunoglobulin G; Immunohistochemistry; In situ hybridization; Tilapia lake virus; Tilapia; Tilapia tilapinevirus; Cellular tropism

资金

  1. Ratchadapisek Somphot Fund for Postdoctoral Fellowship, Chulalongkorn University, Thailand
  2. National Research Council of Thailand (NRCT) through the Royal Golden Jubilee Ph.D. Program, Thailand [NRCT5-RGJ63002-037]
  3. National Research Council of Thailand (NRCT), Thailand [NRCT5-RSA63002-04]

向作者/读者索取更多资源

The study developed a novel immunohistochemical procedure for detecting Tilapia lake virus (TiLV) infection, which accurately localized the virus in infected fish tissues. Validation on different samples confirmed that infections mainly occurred in the intestines, gills, and brain, providing new insights for further research on the viral pathogenesis.
Tilapia lake virus (TiLV) is a notable contagious agent that causes massive economic losses in the tilapia industry globally. Evaluations of the histological changes associated with TiLV infection are not only crucial for diagnosis, but also to gain an understanding of the disease. We therefore synthesized a rabbit polyclonal immunoglobulin G antibody against TiLV and developed an immunohistochemical (IHC) procedure to detect TiLV localization in the tissues of infected fish for comparison with in situ hybridization (ISH) testing. A total of four different sample cohorts derived from TiLV-infected fish was used to validate the IHC procedure. The TiLV IHC application was successfully developed and facilitated nuclear and cytoplasmic immunolabelling in the intestines, gills, brain, liver, pancreas, spleen, and kidneys that corresponded with the ISH results. Apart from the ISH results, TiLV-IHC signals were clearly evident in the endothelial cells of various organs, the circulating leukocytes in the blood vessels, and the areas of tissue inflammation. Among the tested sample cohorts, the intestines, gills, and brain had IHC-positive signals, highlighting the possibility of these organs as common TiLV targets. Immunological staining pattern and distribution corresponded with the TiLV viral load but not the inoculation route. The TiLV IHC was also capable of detecting TiLV infection in the experimentally challenged ornamental cichlids, Mozambique tilapia, giant gourami, and naturally infected tilapia, indicating the dynamic range of IHC for TiLV detection. Overall, our study delivers the first IHC platform to detect TiLV infection and provides novel evidence of cellular tropism during TiLV infection. Our findings also reveal the TiLV distribution pattern of infected fish and propose the endotheliotropism and lymphotropism of this virus, which requires further elaboration. Importantly, this new IHC procedure could be applied to study the pathogenesis and interaction of TiLV in future research.

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