Sankappa Nithin Muliya, Lange Miles D, Yildirim-Aksoy Mediha, Eljack Rashida, Kucuktas Huseyin, Beck Benjamin H, Abernathy Jason W
Oak Ridge Institute for Science and Education (ORISE), ARS Research Participation Program, Oak Ridge, TN, United States.
United States Department of Agriculture, Agricultural Research Service, Aquatic Animal Health Research Unit (AAHRU), Auburn, AL, United States.
Front Physiol. 2024 Jan 9;14:1330368. doi: 10.3389/fphys.2023.1330368. eCollection 2023.
The larval waste, exoskeleton shedding, and leftover feed components of the black soldier fly and its larvae make up the by-product known as frass. In this study, we subjected channel catfish () to a 10-week feeding trial to assess how different dietary amounts of frass inclusion would affect both systemic and mucosal tissue gene expression, especially in regard to growth and immune-related genes. Fish were divided in quadruplicate aquaria, and five experimental diets comprising 0, 50, 100, 200, and 300 g of frass per kilogram of feed were fed twice daily. At the end of the trial, liver, head kidney, gill, and intestine samples were collected for gene expression analyses. First, liver and intestine samples from fish fed with a no frass inclusion diet (control), low-frass (50 g/kg) inclusion diet, or a high-frass (300 g/kg) inclusion diet were subjected to Illumina RNA sequencing to determine global differential gene expression among diet groups. Differentially expressed genes (DEGs) included the upregulation of growth-related genes such as glucose-6-phosphatase and myostatin, as well as innate immune receptors and effector molecules such as toll-like receptor 5, apolipoprotein A1, C-type lectin, and lysozyme. Based on the initial screenings of low/high frass using RNA sequencing, a more thorough evaluation of immune gene expression of all tissues sampled, and all levels of frass inclusion, was further conducted. Using targeted quantitative PCR panels for both innate and adaptive immune genes from channel catfish, differential expression of genes was identified, which included innate receptors (TLR1, TLR5, TLR9, and TLR20A), proinflammatory cytokines (IL-1β type a, IL-1β type b, IL-17, IFN-γ, and TNFα), chemokines (CFC3 and CFD), and hepcidin in both systemic (liver and head kidney) and mucosal (gill and intestine) tissues. Overall, frass from black soldier fly larvae inclusion in formulated diets was found to alter global gene expression and activate innate and adaptive immunity in channel catfish, which has the potential to support disease resistance in this species in addition to demonstrated growth benefits.
黑水虻及其幼虫的幼虫粪便、蜕皮和剩余饲料成分构成了被称为虫粪的副产品。在本研究中,我们对斑点叉尾鮰进行了为期10周的饲养试验,以评估不同日粮中虫粪添加量如何影响全身和黏膜组织的基因表达,特别是与生长和免疫相关的基因。将鱼分成四组饲养在水族箱中,每天投喂两次五种实验日粮,日粮中每千克饲料分别含有0、50、100、200和300克虫粪。试验结束时,采集肝脏、头肾、鳃和肠道样本进行基因表达分析。首先,对喂食不含虫粪日粮(对照)、低虫粪添加量(50克/千克)日粮或高虫粪添加量(300克/千克)日粮的鱼的肝脏和肠道样本进行Illumina RNA测序,以确定日粮组之间的整体差异基因表达。差异表达基因(DEGs)包括生长相关基因如葡萄糖-6-磷酸酶和肌肉生长抑制素的上调,以及先天免疫受体和效应分子如Toll样受体5、载脂蛋白A1、C型凝集素和溶菌酶的上调。基于使用RNA测序对低/高虫粪添加量的初步筛选,进一步对所有采样组织以及所有虫粪添加水平的免疫基因表达进行了更全面的评估。使用针对斑点叉尾鮰先天和适应性免疫基因的靶向定量PCR板,鉴定出基因的差异表达,其中包括先天受体(TLR1、TLR5、TLR9和TLR20A)、促炎细胞因子(IL-1β a型、IL-1β b型、IL-17、IFN-γ和TNFα)、趋化因子(CFC3和CFD)以及全身组织(肝脏和头肾)和黏膜组织(鳃和肠道)中的铁调素。总体而言,发现配制日粮中添加黑水虻幼虫虫粪会改变整体基因表达并激活斑点叉尾鮰的先天和适应性免疫,这除了已证明的生长益处外,还有可能增强该物种的抗病能力。