Cawthron Institute, 98 Halifax Street East, Nelson, 7010, New Zealand.
Cawthron Institute, 98 Halifax Street East, Nelson, 7010, New Zealand.
Fish Shellfish Immunol. 2020 Aug;103:181-189. doi: 10.1016/j.fsi.2020.05.019. Epub 2020 May 13.
Green-lipped mussels (Perna canaliculus) are a commercially and culturally important bivalve species in New Zealand (NZ). As the highest value export aquaculture product in NZ, understanding and safeguarding the health of this species is imperative. The identification and characterization of hemocytes can provide useful information regarding the health of this species. Using flow cytometry (FCM), the present study assessed for the first time the use of different antiaggregant solutions and storage times on the immune-related parameters of hemocytes from cultured adult P. canaliculus. In addition, characterization of the immune-related functions of hemocyte sub-populations within the hemolymph were assessed. The two antiaggregant solutions tested (Modified Alserver's, MAS, A and B) maintained similar numbers of hemocytes in circulation over a 60 min period but, reduced the viability (MAS A) and increased the ROS production (MAS B) of the hemocytes compared to hemocytes diluted in cold filtered seawater (FSW). Hemocytes diluted in FSW and kept on ice showed significant aggregation after 2 h and a reduction in viability from 4 h. Three different hemocyte sub-populations were identified, discernible by their relative size and internal complexity: blast-like cells, hyalinocytes and granulocytes, which accounted for approximately 4, 67 and 29% of the total hemolymph population respectively. Granulocytes showed significantly higher reactive oxygen species production, phagocytic capabilities and neutral lipid content compared to hyalinocytes and blast-like cells. Results indicate that maintaining extracted hemolymph in cold FSW, completing analysis of fresh samples within 2 h of extraction and FCM assay incubation times of no longer than 30 min are best to obtain accurate results. Formalin fixation can also be used for future determination of hemocyte sub-populations and internal structures. Results from this study will allow effective future study of the effects of various stressors on P. canaliculus health and lead to improved management and production strategies in this species.
绿唇贻贝(Perna canaliculus)是新西兰具有商业和文化重要性的双壳贝类物种。作为新西兰价值最高的出口水产养殖产品,了解和保护该物种的健康至关重要。血细胞的鉴定和特征分析可以为了解该物种的健康状况提供有用信息。本研究首次使用流式细胞术(FCM)评估了不同的抗聚集溶液和储存时间对养殖成年绿唇贻贝血细胞免疫相关参数的影响。此外,还评估了血细胞在血淋巴中的免疫相关功能的亚群特征。测试的两种抗聚集溶液(改良 Alsever 溶液,MAS,A 和 B)在 60 分钟内维持了相似数量的循环血细胞,但与冷过滤海水(FSW)稀释的血细胞相比,降低了血细胞的活力(MAS A)并增加了活性氧的产生(MAS B)。在 FSW 中稀释并保持在冰上的血细胞在 2 小时后显示出明显的聚集,并且在 4 小时后活力降低。鉴定出三种不同的血细胞亚群,可通过其相对大小和内部复杂性来区分:类似于原始细胞的细胞、透明细胞和粒细胞,分别占总血淋巴群体的约 4%、67%和 29%。粒细胞与透明细胞和原始细胞相比,表现出更高的活性氧物质产生、吞噬能力和中性脂质含量。结果表明,在冷 FSW 中维持提取的血淋巴,在提取后 2 小时内完成新鲜样品的分析,以及 FCM 分析孵育时间不超过 30 分钟,是获得准确结果的最佳方法。福尔马林固定也可用于未来确定血细胞亚群和内部结构。本研究的结果将允许有效研究各种应激源对绿唇贻贝健康的影响,并为该物种的管理和生产策略提供改进。