Walsh Catherine J, Sherwood Tracy A, Tarnecki Andrea M, Rhody Nicole R, Main Kevan L, Restivo Jessica
Marine Immunology Program, Mote Marine Laboratory, 1600 Ken Thompson Parkway, Sarasota, FL, 34236, USA.
Environmental Laboratory for Forensics, Mote Marine Laboratory, Sarasota, FL, USA.
In Vitro Cell Dev Biol Anim. 2025 Jan 22. doi: 10.1007/s11626-024-01011-0.
The overall goal of this research was to develop an embryonic stem cell (ESC) line from the Pacific white shrimp, Litopenaeus vannamei, to support production of cell-based cultivated seafood products towards meeting a growing global demand for sustainable seafood. It was hypothesized that characteristics of ESCs, such as high proliferation and pluripotency, would facilitate development of a continuous cell line that could be triggered to differentiate into a muscle cell phenotype. The targeted approach was based on collection of ESCs from fertilized shrimp eggs at the blastomere stage. Various media, supplements, growth factors, and plate coatings were tested to achieve growth of the shrimp ESCs. Although successful in early culture, this manuscript describes substantial challenges encountered as cultures grew over time. The cell cultures were initially dominated by shrimp as indicated by 18S rDNA community analysis, but after multiple passages, thraustochytrids, a common contaminant of invertebrate cell culture, became the predominant cell type. Presence of shrimp cells was confirmed through species-specific primers for the cytochrome C oxidase subunit 1 gene. Presence of thraustochytrids was also confirmed using species-specific primers, morphological features, growth properties, and acriflavine staining. Unsuccessful attempts to eradicate thraustochytrid contamination prevented shrimp cells from thriving. The future of shrimp cell culture depends on eliminating culture contaminants while encouraging growth of shrimp ESCs.
本研究的总体目标是从南美白对虾(Litopenaeus vannamei)中培育出一种胚胎干细胞(ESC)系,以支持基于细胞的养殖海产品生产,从而满足全球对可持续海产品不断增长的需求。研究假设胚胎干细胞的特性,如高增殖能力和多能性,将有助于建立一个连续的细胞系,该细胞系可被诱导分化为肌肉细胞表型。目标方法是基于在卵裂球阶段从受精虾卵中收集胚胎干细胞。对各种培养基、添加剂、生长因子和平板包被物进行了测试,以实现虾胚胎干细胞的生长。尽管在早期培养中取得了成功,但本文描述了随着培养时间的推移所遇到的重大挑战。18S rDNA群落分析表明,细胞培养最初以虾细胞为主,但经过多次传代后,破囊壶菌(一种无脊椎动物细胞培养中常见的污染物)成为主要的细胞类型。通过细胞色素C氧化酶亚基1基因的物种特异性引物确认了虾细胞的存在。还使用物种特异性引物、形态特征、生长特性和吖啶黄染色确认了破囊壶菌的存在。根除破囊壶菌污染的尝试未成功,阻碍了虾细胞的茁壮成长。虾细胞培养的未来取决于消除培养污染物,同时促进虾胚胎干细胞的生长。