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The establishment of a stable in\u00a0vitro culture system is imperative for the effective isolation, identification, and study of fish viruses.\n                    <jats:styled-content style=\"fixed-case\">CAMsp<\/jats:styled-content>\n                    , generated through trypsin digestion, had successfully undergone over 80 passages since its initial culture. This cell line exhibited rapid proliferation in Leibovitz's\u201015 medium (L\u201015) supplemented with 10% fetal bovine serum at 28\u00b0C, achieving monolayer formation within 24\u2009h at a passage ratio of 1:3. Chromosomal analysis of\n                    <jats:styled-content style=\"fixed-case\">CAMsp<\/jats:styled-content>\n                    at the 60th passage identified a chromosome count of 42; the chromosome number in hybrid snakehead somatic cells is 44, 45, or 46, suggesting chromosomal alterations. Inoculation of\n                    <jats:styled-content style=\"fixed-case\">CAMsp<\/jats:styled-content>\n                    monolayers with\n                    <jats:styled-content style=\"fixed-case\">HSHRV<\/jats:styled-content>\n                    ,\n                    <jats:styled-content style=\"fixed-case\">LMBV<\/jats:styled-content>\n                    , and\n                    <jats:styled-content style=\"fixed-case\">ISKNV<\/jats:styled-content>\n                    resulted in characteristic cytopathic effects (\n                    <jats:styled-content style=\"fixed-case\">CPE<\/jats:styled-content>\n                    ), including cell rounding, aggregation, and eventual detachment. Transmission electron microscopy (\n                    <jats:styled-content style=\"fixed-case\">TEM<\/jats:styled-content>\n                    ) confirmed viral replication and revealed extensive cytopathological changes within the infected cells, demonstrating the susceptibility of the\n                    <jats:styled-content style=\"fixed-case\">CAMsp<\/jats:styled-content>\n                    cell line to all three viruses. Viral titers, determined by\n                    <jats:styled-content style=\"fixed-case\">TCID<\/jats:styled-content>\n                    <jats:sub>50<\/jats:sub>\n                    assay at 7\u2009days post\u2010infection (dpi), reached 10\n                    <jats:sup>9.25<\/jats:sup>\n                    \u2009\u00b1\u200910\n                    <jats:sup>0.36<\/jats:sup>\n                    <jats:styled-content style=\"fixed-case\">TCID<\/jats:styled-content>\n                    <jats:sub>50<\/jats:sub>\n                    \/\n                    <jats:styled-content style=\"fixed-case\">mL<\/jats:styled-content>\n                    for\n                    <jats:styled-content style=\"fixed-case\">LMBV<\/jats:styled-content>\n                    , 10\n                    <jats:sup>6<\/jats:sup>\n                    \u00b7\n                    <jats:sup>15<\/jats:sup>\n                    \u2009\u00b1\u200910\n                    <jats:sup>0.25<\/jats:sup>\n                    <jats:styled-content style=\"fixed-case\">TCID<\/jats:styled-content>\n                    <jats:sub>50<\/jats:sub>\n                    \/\n                    <jats:styled-content style=\"fixed-case\">mL<\/jats:styled-content>\n                    for\n                    <jats:styled-content style=\"fixed-case\">ISKNV<\/jats:styled-content>\n                    , and 10\n                    <jats:sup>8<\/jats:sup>\n                    \u00b7\n                    <jats:sup>33<\/jats:sup>\n                    \u2009\u00b1\u200910\n                    <jats:sup>0.12<\/jats:sup>\n                    <jats:styled-content style=\"fixed-case\">TCID<\/jats:styled-content>\n                    <jats:sub>50<\/jats:sub>\n                    \/\n                    <jats:styled-content style=\"fixed-case\">mL<\/jats:styled-content>\n                    for\n                    <jats:styled-content style=\"fixed-case\">HSHRV<\/jats:styled-content>\n                    , indicating efficient viral propagation in this cell line. The\n                    <jats:styled-content style=\"fixed-case\">CAMsp<\/jats:styled-content>\n                    cell line serves as a valuable model for studying certain fish viruses, virus\u2010host interactions, and disease prevention strategies.\n                  <\/jats:p>","DOI":"10.1111\/jfd.70096","type":"journal-article","created":{"date-parts":[[2025,12,6]],"date-time":"2025-12-06T12:50:30Z","timestamp":1765025430000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Establishment of a Hybrid Snakehead Spleen Cell Line for Viral Studies"],"prefix":"10.1111","volume":"49","author":[{"given":"Xuanming","family":"Liu","sequence":"first","affiliation":[{"name":"Key Laboratory of Fishery Drug Development, Ministry of Agriculture and Rural Affairs, Guangdong Provincial Key Laboratory of Aquatic Animal Immunology and Sustainable Aquaculture Pearl River Fisheries Research Institute, Chinese Academy of Fishery 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