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“Viral diseases restrict the development of the world shrimp industry and there are few studies on cell response to the presence of viral infections. We performed immunohistochemistry assays https://www.selleckchem.com/products/jq1.html to characterize hemocytes subpopulations involved in the immune process occurring in the LO of Litopenaeus vannamei shrimp. Tissue sections of animals that increased their LO spheroids and hemocytes infiltration after WSSV induced infection, were used. Three MABs namely, 40E10 (recognizing small granule hemocytes), 40E2 (recognizing

large granule hemocytes), and 41B12, which recognize α2-macroglobulin were used. Additionally one polyclonal antibody was used against the penaeidins antimicrobial peptides, and to detect WSSV a commercial immunohistochemistry kit (DiagXotics) was used. Numerous small granule hemocytes were detected in the stromal matrix of LO tubules, whereas large granule hemocytes were less numerous and located

mainly in hemal sinuses. The exocytosis of two molecules, which have been related to the phagocytosis process, i.e. penaeidins, and α2-macroglobulin, was detected in the external stromal matrix and the outer tubule walls. α2-macroglobulin inhibits phenoloxidase activity and its strong release in LO tissue may explain the absence of melanization in the immune processes occurring in it. The immunolabeling of vesicles within the LO spheroids with MABs 41B12 40E10 and antipenaedin antibody suggests that LOS are formed by phagocytic cells derived find more from small granule and hyaline hemocytes, with a possible role of peneidins and α2-macroglobulin acting as opsonines. Viral diseases represent the major constraint to shrimp culture development in the world. Despite the progress in knowledge of shrimp immune defense, few studies focus on the cell response to viral infection. Phagocytosis has been reported as a useful mechanism of viral clearance in penaeid shrimp and its suppression by inhibitors increases susceptibility Janus kinase (JAK) to WSSV (1). Molecular events involved in shrimp phagocytosis begin to be characterized. A phagocytosis

activating protein was isolated in Penaeus monodon and Marsupenaeus japonicus shrimp (2), its expression being induced by immunostimulation with WSSV, increasing the phagocyte index in P. monodon (2). This protein has sequence similarity with the ribosomal protein RPL26, which is upregulated in activated murine macrophages. During the process of phagocytosis it is found that the small G protein superfamily is necessarily required. Thus, Wu et al. (3) determined that a Rab GTPase could regulate the hemocytic phagocytosis in M. japonicus, forming a four protein complex consisting of Rab, β-actin, tropomiosin and WSSV envelop protein and Liu et al. (4) found that RanGTPase regulates the phagocytosis in the WSSV-resistant shrimp by interacting with myosin. Clearance of foreign material from the hemocoel of decapod crustaceans involves several distinct kinds of cells and tissues (5).