The potential risk of coexistence of mixed heavy metals in the aquatic environment has increased with the development of technology. Lead (Pb) and arsenic (As) are among the most widely applied heavy metals, whose single toxicity has been extensively investigated, but their combined toxicity has been reported relatively rarely. In this study, different concentrations of Pb (40 μg/L, 4 mg/L), As (32 μg/L, 3.2 mg/L) and their combinations (40 μg/L + 32 μg/L, 4 mg/L + 3.2 mg/L) were set up for 30 days to establish a heavy metal exposure model in zebrafish. Pathological sections, biochemical parameters and gene expression analysis were used to assess the toxicity effects of oxidative damage and lipid metabolism in the liver. Our results showed that combined exposure of As and Pb resulted in elevated ROS and MDA levels and upregulated expression of genes related to the Nrf2-Keap1/Are signaling pathway in female zebrafish, causing enhanced oxidative stress. Moreover, mixture of As and Pb was able to cause abnormal upregulation of lipid metabolism-related genes and reduced activity of fatty acid synthase (FAS) in the liver of female zebrafish. The abnormal decrease of carnitine palmitoyl transferase (CPT-1) and gene cpt1a in males were also observed. These results contributed to hepatic Triglyceride (TG) excessive accumulation, ultimately triggering a disturbance of lipid metabolism. These findings indicated that chronic exposure to As and Pb was capable of producing adverse effects on oxidative stress and lipid metabolism in fish in a sex-specific manner. This study provides new perspective for evaluating the combined effects of heavy metals in the aquatic environment.

The increasing emergence and dissemination of bacterial pathogens in largemouth bass culture accelerate the desire for new treatment measures. Antimicrobial peptides as the host's antimicrobial source dominate the preferred molecules for discovering antibacterial agents. Here, the potential of Hepcidin-1 from largemouth bass (Micropterus salmoides) (MsHep-1) against bacterial infection is demonstrated. MsHep-1 not only improved the survival rate in infection experiments involving Nocardia seriolae (12 %) and Aeromonas hydrophila (18 %) but also coped with iron overload conditions in vivo. Moreover, the antibacterial activity of MsHep-1 in vitro was identified against both gram-negative and gram-positive bacteria. Mechanistic studies show MsHep-1 leads to bacterial death by changing the bacterial membrane potential and disrupting the bacterial membrane structure. These findings demonstrate that MsHep-1 may play an important role in the host response to bacterial infection. It provides promising strategies in the application of immunosuppression prevention and control in fish. AMPs may be a promising and available reservoir for treating the current bacterial diseases.

Soybean meal, excessively used in place of fish meal (FM) in aquaculture, has a detrimental impact on fish. In this study, the nanopeptide C-I20, which was created by conjugating antimicrobial peptide gcIFN-20H and CMCS, were evaluated the feeding effect in mandarin fish (Siniperca chuatsi). Compared with the control group, 150 mg/ kg C-I20-fed fish showed the second highest growth performance with no significant changes in body composition. C-I20-fed fish showed more goblet cells and thicker mucin after feeding. The 150 mg/kg C-I20 diet boosted the antioxidant capacity, immunity, and digestive enzymes. After Aeromonas hydrophila and infection spleen and kidney necrosis virus infection, the survival rates in the 150 mg/kg C-I20 group were highest. Meanwhile, many tissues in the 150 mg/kg C-I20 group had significantly lower pathogen loads than the other groups. Treatment with 150 mg/kg C-I20 was effective in increasing antioxidant capacity and immunity. The minimum tissue lesions were observed in the 150 mg/kg C-I20 group. The goblet cell number and mucin thickness were significantly increased by C-I20 treatment after infection. The study results herein showed that a reasonable dietary concentration of C-I20 feed promoted growth performance and disease resistances in fish, suggesting a prospective nano antimicrobial peptide for the aquaculture.

The immunosuppression hazard of fish brought by intensive aquaculture needs to be addressed urgently, while chitooligosaccharide (COS) shows the potential application in the prevention the immunosuppression of fish due to its superior biological properties. In this study, COS reversed the cortisol-induced immunosuppression of macrophages and improved the immune activity of macrophages in vitro, promoting the expression of inflammatory genes (TNF-α, IL-1β, iNOS) and NO production, and increasing the phagocytic activity of macrophages. In vivo, the oral COS was absorbed directly through the intestine, significantly ameliorating the innate immunity of cortisol-induced immunosuppression of blunt snout bream (Megalobrama amblycephala). Such as facilitated the gene expression of inflammatory cytokines (TNF-α, IL-1β, IL-6) and pattern recognition receptors (TLR4, MR) and potentiated bacterial clearance, resulting in an effective improvement in survival and tissue damage. Altogether, this study demonstrates that COS offers potential strategies in the application of immunosuppression prevention and control in fish.

为了探究草鱼防御素的免疫调节作用,研究通过Clustal Omega多序列比对和I-TASSER二级结构预测,发现草鱼β-防御素1(Ctenopharyngodon idellaβ-defensin 1,CiBD1)是一类具有两亲性的富含半胱氨酸的小分子阳离子肽,其结构在硬骨鱼类中高度保守;通过构建pET-32a-CiBD1原核表达载体,IPTG诱导表达后经过Ni2+亲和层析法纯化和肠激酶酶切获得CiBD1重组蛋白,通过CFU平板法验证了CiBD1的抑菌活性,当蛋白浓度达到200μg/mL时,对革兰氏阴性菌(G+)及革兰氏阳性菌(G–)都具有显著的抑制活性;趋化实验表明CiBD1在50 ng/mL时对草鱼原代白细胞趋化活性最佳;通过个体实验探究了CiBD1重组蛋白对嗜水气单胞菌灭活疫苗的免疫佐剂效应,发现添加CiBD1佐剂组死亡率显著低于单独疫苗组,且该组IgM和MHCⅡ转录水平及血清中补体3(C3)和溶菌酶含量都显著高于对照组.研究表明CiBD1重组蛋白在细菌抗感染免疫中发挥着重要作用,在水产养殖中具有一定的应用前景.

Hybrid sturgeon is the main species of sturgeon cultured in China, with the advantages of a fast growth rate, early sexual maturity, fertile offspring, and more stable genetic traits. In May 2021, a large number of deaths characterized by superficial hemorrhage and liver damage occurred in a sturgeon farm in Yichang, Hubei Province, which posed a significant risk to hybrid sturgeon captive breeding. We isolated a pathogenic bacterium named D-59 from the diseased sturgeon with apparent symptoms. The pathogen was identified as Staphylococcus sciuri using 16S rRNA gene phylogenetic analysis combined with biochemical identification. Regression experiments showed that D-59 exhibited clinical signs similar to those of diseased sturgeon in the farm after intraperitoneal injection into hybrid sturgeon. High-throughput sequencing of gut microbes in D-59-infected sturgeon showed that the number of gut microbial species decreased in infected sturgeon, the number of some intestinal commensal bacteria decreased, and the balance of the intestinal microorganisms was disrupted. Histopathological sections indicated many inflammatory cells, congestion, and even necrosis in the tissue of diseased sturgeon. Analysis of blood indexes revealed an increase in the proportion of mononuclear cells and a decrease in the proportion of lymphocytes in the peripheral blood of diseased sturgeon. Significantly elevated serum levels of aspartate aminotransferase and alanine aminotransferase, whereas alkaline phosphatase, total protein, albumin, and globulin were decreased in diseased sturgeon. Antimicrobial susceptibility tests demonstrated that D-59 is susceptible to florfenicol, enrofloxacin, and neomycin sulfate. This study aimed to highlight the dangers of Staphylococcus sciuri infection during hybrid sturgeon culture and to provide recommendations for diagnosis and treatment.

Grass carp reovirus (GCRV) is a severe virus that causes great losses to grass carp culture every year, and GCRV-II is the current popular and fatal strain. VP56, fibrin on the outer surface of GCRV-II, mediates cell attachment. In this study, we firstly divided the VP56 gene into four fragments to screen the optimal antigen by enzyme-linked immunosorbent assay and neutralizing antibody methods. The second fragment VP56-2 demonstrates the optimal efficiency and was employed as an antigen in the following experiments. Bacillus subtilis were used as a carrier, and VP56-2 was expressed on the surface of the spores. Then, we performed the oral immunization for grass carp and the challenge with GCRV-II. The survival rate was remarkably raised, and mRNA expressions of IgM were significantly up-regulated in spleen and head kidney tissues in the B. s-CotC-VP56-2 group. Three crucial immune indexes (complement C3, lysozyme and total superoxide dismutase) in the sera were also significantly enhanced. mRNA expressions of four important genes (TNF-α, IL-1β, IFN1 and MHC-II) were significantly strengthened. Tissue lesions were obviously attenuated by histopathological slide examination in trunk kidney and spleen tissues. Tissue viral burdens were significantly reduced post-viral challenge. These results indicated that the oral recombinant B. subtilis VP56-2 subunit vaccine is effective for controlling GCRV infection and provides a feasible strategy for the control of fish virus diseases.

CSF-1 and CSF-1R have been well demonstrated in humans, regulating the differentiation, proliferation and survival of the mononuclear phagocyte system. However, the functional study on MaCSF-1 and MaCSF-1R from blunt snout bream (Megalobrama amblycephala) is still unknown. In the present study, we cloned and functionally characterized MaCSF-1 and MaCSF-1R. Multiple sequence alignment and phylogenetic tree analysis showed that both MaCSF-1 and MaCSF-1R were mostly close to the grass carp counterparts. Tissue distribution analysis showed that both MaCSF-1 and MaCSF-1R were widely distributed in all examined tissues, dominantly distributed in spleen, blood and head kidney tissues. Furthermore, confocal microscopy assay and flow cytometry assay showed that MaCSF-1R was the marker on the surface of macrophages. Recombinant MaCSF-1 promoted macrophage proliferation, phagocytosis and the production of IL-10. Through the pull-down experiments and indirect immunofluorescence experiments, the interaction between MaCSF-1 and MaCSF-1R was confirmed. To explore the relationship between MaCSF-1 and its receptor, MaCSF-1R and MaCSF-1R antibody was prepared. Then the MaCSF-1R blockage assay indicated that the role of MaCSF-1 on the macrophages proliferation and phagocytosis was weakened, leading the reduction of IL-10 expression level. In conclusion, MaCSF-1R is the marker on the surface of macrophage membrane; and MaCSF-1 promotes macrophage proliferation, phagocytosis, and significantly increased the expression levels of IL-10 depended on the interacting with MaCSF-1R. This study provides basal data for the biological function of MaCSF-1 and MaCSF-1R, and is valuable for the exploration of MaCSF-1 and MaCSF-1R molecular interactions.

Chitooligosaccharide (COS) is an important immune enhancer and has been proven to have a variety of biological activities. Our previous research has established an M1 polarization mode by COS in blunt snout bream (Megalobrama amblycephala) macrophages, but the mechanism of COS activation of blunt snout bream macrophages remains unclear. In this study, we further explored the internalization mechanism and signal transduction pathway of chitooligosaccharide hexamer (COS6) in blunt snout bream macrophages. The results showed that mannose receptor C-type lectin-like domain 4-8 of M. amblycephala (MaMR CTLD4-8) could recognize and bind to COS6 and mediate COS6 into macrophages by both clathrin-dependent and caveolin-dependent pathways. In the inflammatory response of macrophages activated by COS6, the gene expression of tumor necrosis factor (TNF)-α, interleukin (IL)-1β, and nitric oxide synthase 2 (NOS2) was significantly inhibited after MaMR CTLD4-8-specific antibody blockade. However, even if it was blocked, the expression of these inflammation-related genes was still relatively upregulated, which suggested that there are other receptors involved in immune regulation. Further studies indicated that MaMR CTLD4-8 and Toll-like receptor 4 (TLR4) cooperated to regulate the pro-inflammatory response of macrophages caused by COS6. Taken together, these results revealed that mannose receptor (MR) CTLD4-8 is indispensable in the process of recognition, binding, internalization, and immunoregulation of COS in macrophages of blunt snout bream.

Aeromonas veronii (A. veronii) is one of the main pathogens causing bacterial diseases in aquaculture. Although previous studies have shown that hepcidin as an antimicrobial peptide can promote fish resistance to pathogenic bacterial infections, but the mechanisms remain unclear. Here, we expressed and purified recombinant yellow catfish (Pelteobagrus fulvidraco) hepcidin protein (rPfHep). rPfHep can up-regulate the expression of ferritin and enhance the antibacterial activity in primary hepatocytes of yellow catfish. We employed berberine hydrochloride (BBR) and Fursultiamine (FSL) as agonists and antagonists for hepcidin, respectively. The results indicated that agonist BBR can inhibit the proliferation of pathogenic bacteria, and the antagonist FSL shows the opposite effect. After gavage administration, rPfHep and the agonist BBR can enhance the accumulation of iron in liver, which may hinder the iron transport and limit the amount of iron available to pathogenic bacteria. Moreover, rPfHep and the agonist BBR can also reduce the mortality rate, bacterial load and histological lesions in yellow catfish infected with A. veronii. Therefore, hepcidin is an important mediator of iron metabolism, and it can be used as a candidate target for prevent bacterial infections in yellow catfish. Hepcidin and BBR have potential application value in preventing anti-bacterial infection.

Yellow-head catfish, Pelteobagrus fulvidraco, is an economically important specific species in aquaculture in China. However, at present disease has become a major concern of this fish. In this study, a bivalent vaccine was generated, containing two formalin-inactivated bacteria at different mixing ratio of 3:7, 5:5 and 7:3 of A. veronii and E. ictaluri in volume with a concentration at 1.0 x 10(8) CFU mL(-1) for each.The immunization efficacies were evaluated by measuring lysozyme activity, serum total protein, serum C3, specific antibodies, expression of immune-related genes and survival rate against A. veronii or E. ictaluri. The results showed that the bivalent vaccine with a mixing ratio of 3:7 of A. veronii and E. ictaluri in volume presented the highest immunization efficacy. In this immunization group, the lysozyme activity, serum total protein and serum C3 had a noticeable increase at 7 dpi. IgM gene was significantly up-regulated to the peak at 7 dpi in the spleen and at 14 dpi in the kidney after immunization. MR (Mannose receptor) and Ctl (C-type lectin) genes significantly increased and reached their maximum at 24 h after immunization in both spleen and head kidney. Higher antibody levels were observed in vaccinated fish at day 21 post immunization. The challenge test showed that the relative survival percent in the immunized group with the mixing ratio of 3:7 of A. veronii and E. ictaluri in volume was 50.61% +/- 2.64 and 62.82% +/- 2.22 against A. veronii and E. ictaluri infection respectively. These results indicated that the bivalent vaccine of inactivated A. veronii and E. ictaluri can effectively induce immune responses and protect yellow-head catfish against A. veronii and E. ictaluri infection.

Hepcidin is an antimicrobial peptide and regulator of iron homeostasis which has two isoforms in most fishes and some mammals. Previous studies have reported that the two hepcidin isoforms have different roles. Hamp type-1 plays a regulatory role in iron metabolism and hamp type-2 mostly performs an antimicrobial role. In this study, we found thatCtenopharyngodon idella(C. idella) have only one hepcidin isoform (hamp type-1), which showed both broad-spectrum antibacterial and iron regulatory functions.C. idellahepcidin mature peptide (hepcidin-25) and truncated peptide (hepcidin-20) exhibited bactericidal activities against both Gram-positive and Gram-negative bacteria in a dose-dependent manner in part through membrane rupture and binding to bacterial genomic DNA. The data from challenge tests demonstrated that the administration of hepcidin-25 significantly reduced mortality rates ofC. idellabyA. hydrophilainfection, probably due to direct bactericidal activities of the peptide and a reduction of iron content in the fish serum. In addition, a comparison between hepcidin-20 and -25 suggests that the N terminal 5 amino acids play a critical role in reducing iron content in fish serum. Our findings revealed an important role of hamp type-1 in maintaining iron homeostasis and fighting against bacterial infections, suggesting the hepcidin has implications for the prevention and control of bacterial infection in aquaculture.

为探究树种的防火能力,科学选择防火林带树种,提高生物防火林带的树种多样性,对28种防火林带树种的理化指标进行测定,应用因子分析和聚类分析方法对其抗火性能进行综合排序与分类.结果表明,树叶热值与灰分、挥发分与固定碳之间呈极显著相关关系,热值与挥发分之间、灰分与挥发分之间呈显著相关关系;综合排序表明鸭脚木、夹竹桃、米老排、大叶相思、深山含笑、黧蒴、木荷、红花油茶、铁冬青、台湾相思、醉香含笑、凤凰木为抗火性较好的12个树种.聚类分析结果表明,抗火性强的树种有4种,夹竹桃、鸭脚木、大叶相思、铁冬青;抗火性较强的树种有7种,黧蒴、米老排、醉香含笑、台湾相思、深山含笑、木荷、山杜英;抗火性中等的树种有6种,西南木荷、乌桕、凤凰木、红花油茶、土沉香、樟树;抗火性较弱的树种有8种,枫香、柠檬桉、黄葛榕、马占相思、观光木、红苞木、红锥、山乌桕;抗火性弱的树种有3种,多花山竹子、蝴蝶果、假苹婆.

Edwardsiella ictaluri (E. ictaluri) causes severe infections in yellow catfish (Pelteobagrus fulvidraco), which leads to a massive loss in the aquaculture industry especially in catfish commercial production. Previous studies have confirmed that vitamin D3 is essential in immune regulation in mammals. Based on next-generation sequencing, this study explored the immunomodulatory effects of dietary vitamin D3 on the head kidney of yellow catfish after E. ictaluri challenge. Current results showed that increasing the content of dietary vitamin D3 within the experimental concentration range (1120IU/kg-16600IU/kg) could reduce the mortality of the yellow catfish after E. ictaluri challenge. Results of the next-generation sequencing showed that dietary vitamin D3 regulates the immune mechanism of the head kidney mainly through three pathways i.e. negative regulation of interferon-β production, negative regulation of interleukin-6 production and neutrophil chemotaxis. Proteins HSPA8, MAP4K4 and MRC1 may be involved in vitamin D3-mediated immunoregulation in the head kidney. qPCR results showed that increasing the content of dietary vitamin D3 can improve the immune function of the yellow catfish by down-regulating ifn-β and pro-inflammatory factors tnf-α, il1-β, il-6, il-8 and up-regulating the anti-inflammatory factor il-10. The above results indicated that dietary addition of vitamin D3 regulated the immune response in head kidney of yellow catfish and helped the fish to resist the negative effects of infection by E. ictaluri in a dose-dependent manner.

Hepcidin links iron metabolism with innate immunity during the inhibition of bacterial infection. Our previous studies had shown that recombinant hepcidin can significantly reduce the mortality rate of Ctenopharyngodon idella infected with Flavobacterium columnare under laboratory conditions. Here, we studied the preventive and therapeutic effects of feed supplemented with different doses of recombinant hepcidin on F. columnare-challenged C. idella reared in a cage culture environment. The results showed that in the prevention groups, 30 and 90 mg/kg of added purified and unpurified hepcidin respectively resulted in a higher survival rate in the early post-infection period, while 60 mg/kg of purified hepcidin significantly improved the survival rate in the therapy group (all compared to the control group). In the hepatopancreas, the expression of hepcidin and ferritin was significantly up-regulated, and the levels of ferroportin and serum iron were significantly decreased, especially in the therapy group. In addition, the expression of iron-related genes in spleen and intestine exhibited a similar trend to that in hepatopancreas. Meanwhile, immune genes were up-regulated to varying degrees, and the therapy group exhibited a significantly improved expression of pro-inflammatory cytokines and specific immunity. In summary, our study shows that different doses of recombinant hepcidin had protective effects against bacterial infection by regulating the iron distribution and immune gene expression, which provides a strong foundation for the application of recombinant hepcidin in aquaculture.

为研究罗非鱼湖病毒在吉富罗非鱼体内和敏感细胞E-11中的感染特性,实验首先从人工感染罗非鱼湖病毒的吉富罗非鱼脾脏中获得罗非鱼湖病毒第4片段基因组,其cDNA全长1250 bp,开放读码框长度为1065 bp,编码354个氨基酸.通过进化树分析,该蛋白是罗非鱼湖病毒血凝素—酯酶融合蛋白(HEF).随后通过在大肠杆菌大量表达和提纯GST融合HEF蛋白,免疫新西兰大白兔,制备了兔抗TiLV-HEF多克隆抗体.ELISA结果显示获得的抗血清效价高于1:51200,并且获得的抗体可以特异性识别病毒的TiLV-HEF蛋白.人工感染实验结果显示,TiLV的感染造成鱼体表面溃疡、全身性出血以及眼晶状体混浊等症状.H.E染色结果显示,肝脏形成合胞体,脾脏中含铁血黄素增加和部分细胞空泡变性.头肾出现淋巴细胞坏死,体肾蛋白质沉淀和肾小球坏死等病理症状.Western blot和免疫组织化学结果显示该病毒在所有组织中均有分布,其中脾脏、头肾和鳃中的病毒丰度高于肝脏、体肾和脑组织.通过细胞间接免疫荧光实验,发现TiLV感染E-11细胞后,HEF蛋白在细胞质中.TiLV可以通过感染吉富罗非鱼幼鱼的肝脏、脾脏、头肾、体肾、鳃和脑等组织而引起疾病.

Siniperca chuatsi is an economically important fish in China, but infectious spleen and kidney necrosis virus (ISKNV) causes high mortality and significant economic losses. Currently, vaccination is the most promising strategy to prevent infectious diseases, while adjuvant can effectively enhance immune responses. In this study, inactivated ISKNV vaccine was prepared, then poly (I:C), chitosan, anisodamine and ims1312 were used as adjuvants to evaluate the effect on the immune responses and ISKNV replication. Chitosan could strongly boost the protection of liver and spleen tissues by pathological sections. In serum, poly (I:C) and chitosan group had protective effect on catalase, acid phosphatase, blood urea nitrogen. mRNA expressions showed these adjuvants induced the cytokines of early immune responses (TNF-alpha, Viperin) in both spleen and mesonephron by real time quantitative RT-PCR assays. Meanwhile, poly (I:C), chitosan and anisodamine were significantly improved the antiviral function and inhibited ISKNV replication. Chitosan and anisodamine played a significantly protective role in the immune protective rate test. The results indicated that all the four adjuvants are valid in the inactivated ISKNV vaccine, and chitosan is recommended preferentially. The present study provides reference for other animal vaccine adjuvants.

The grass carp (Ctenopharyngodon idella), blunt snout bream (Megalobrama amblycephala) and yellow catfish (Pelteobagrus fulvidraco) are economically important fishes in China. Fish hematological features, especially the type and number of peripheral blood cells, are crucial for the evaluation of fish health and the diagnosis of fish diseases. Since the automatic blood cell count equipment for human is not suitable for fishes, the manual method is critical in the quantification of fish blood cells. To make sense of the comparison and interpretation of the blood cell count studies in different articles, the standardization of blood cell classification is necessary. In this study, erythrocytes (red blood cell, RBC), thrombocytes (TC) and leucocytes (i.e. white blood cells, WBC, including lymphocytes, neutrophils and monocytes) were well distinguished in blood smears with Giemsa staining and confirmed by transmission electron microscopy. RBC, TC and WBC were directly counted with an improved Neubauer counting chamber in a modified diluting solution. The differential leucocyte count (DLC) was carried out in blood smears. In view of the labeling characteristics of peroxidase (PO) positivity in neutrophils and non-specific esterase (α-ANAE) positivity in monocytes, PO positive cell percentage and α-ANAE positive cell percentage were also determined in cytochemistry staining smears. No difference was found for the percentages of neutrophils and monocytes between Giemsa staining and cytochemistry staining. The standardized classification, normal count ranges and sizes of the peripheral blood cells by the present systemic studies will provide useful references for monitoring the health status of grass carp, blunt snout bream and yellow catfish.

MicroRNAs are non-coding RNAs, which widely participate in biological processes. In recent years, Siniperca chuatsi rhabdovirus (SCRV) has caused mass mortality in Chinese perch (Siniperca chuatsi). To identify specific miRNAs involved in SCRV infection, deep sequencing of microRNA on Chinese perch brain cell line (CPB) with or without SCRV infection were performed at 6 and 12 h post of infection (hpi). Totally 382 miRNAs were identified, including 217 known miRNA aligned with zebrafish miRNAs and 165 novel miRNAs by MiRDeep2 program. Of which 15 and 35 differentially-expressed miRNAs were determined respectively to 6 and 12 hpi. Nine miRNAs were selected randomly from the differentially-expressed miRNAs and validated by quantitative real-time PCR (qRT-PCR). These results were consistent with the microRNA sequencing results. Besides, target genes of 98 differentially-expressed miRNAs were predicted. Three of miRNAs (miR-122, miR-214, miR-135a) were selected, and its effects were analyzed in CPC cells transfected with appropriate miRNA mimics/inhibitors to evaluate its regulation effects by qRT-PCR and western blot. The results demonstrated that miR-214 inhibited the replication of SCRV, while miR-122 promoted the replication of SCRV and there was no correlation between the miR-135a and SCRV replication. These results will pave a new way for the development of effective strategies against the SCRV infection.

The yellow catfish (Pelteobagrus fulvidraco) is an economically important fish in China, but Edwardsiella ictaluri, an intracellular pathogenic bacterium, causes great losses to the culture industry. Currently, vaccination is the most promising strategy to combat the infectious diseases, while adjuvant can provide effective assistant for vaccines to enhance immune responses. In the present study, inactivated E. ictaluri vaccine was prepared, then Astragalus polysaccharides (APS), chitosan and poly(I:C) were employed as adjuvants to evaluate the effect on boosting immune responses and protecting yellow catfish against E. ictaluri. The survival rate was obviously improved after vaccination with APS, chitosan or poly(I:C) respectively, in addition, these three adjuvants could clearly protect the target tissue (intestine) by pathological sections in infectious experiments. In sera, total protein levels increased throughout the immunization stages, total superoxide dismutase levels continued to raise after vaccination, and lysozyme activity levels improved at different periods, examining by the commercial kits. Moreover, checking by real time quantitative RT-PCR assays, in both spleen and head kidney tissues which were the major immune organs, mRNA expressions of inflammatory cytokine IL-1β increased in the early stage of immunity, typical Th1 immune response cytokines IL-2 and IFN-γ2 rose up in the whole immune period, and IgM significantly enhanced in the adjuvant supplementation groups. The results demonstrated the good efficiency of APS, chitosan or poly(I:C) as adjuvant, and provided more options for the fish adjuvants.