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    无水芽孢杆菌MC2-1对急性盐碱胁迫下大口黑鲈组织损伤、抗氧化能力及肠道菌群组成的影响

    BACILLUS INAQUOSORUM MC2-1 ON TISUUE DAMAGE, ANTIOXIDANT CAPACITY, AND INTESTINAL FLORA COMPOSITION OF MICROPTERUS SALMOIDES UNDER ACUTE SALT-ALKALINE STRESS

    • 摘要: 本研究旨在探讨无水芽孢杆菌MC2-1 (Bacillus inaquosorum MC2-1, 简称MC2-1)对急性盐碱胁迫下大口黑鲈(Micropterus salmoides)的组织损伤、抗氧化能力、离子转运和肠道菌群等的影响。实验设置盐度6 psu和碱度4.5 mmol/L的盐碱水体, 随机选取初始体重为(8.56±0.04) g的大口黑鲈幼鱼, 分为5组: 淡水对照组(CK)、盐碱水胁迫组(SC)及SC + 2×106、2×107、2×108 CFU/尾 MC2-1 (LT、MT和HT组)3个浓度, 连续灌喂1周。结果显示, 与CK组相比, SC组的肠道肌层厚度显著降低(P<0.05), 次级鳃小弓直径变短、鳃片层间隔变大及短径变宽, 呈现次级鳃弓肿胀、肝脏空泡化和细胞核偏移等病变; 与SC组相比, 灌喂MC2-1组的肠道肌层厚度均显著升高(P<0.05), 肝脏病变程度明显减轻, MT组和HT组次级鳃弓直径和短径恢复至对照组水平。与CK组相比, SC组肝脏T-AOC显著升高, 肾脏SOD活性和鳃丝T-AOC水平显著降低(P<0.05), MT组鳃SOD、肠道AKP和ACP活性均显著提高(P<0.05); 与SC组相比, HT组肝脏CAT和鳃SOD活性显著增加, 且肠道AMS和LPS活性较其他组也显著升高(P<0.05)。与CK组相比, SC组血清中TP、Ca2+含量显著增加, HT组可逆转血清Cl和Ca2+含量至对照组水平(P<0.05)。与CK组相比, MT组肠道副球菌属的相对丰度较其他组显著升高(P<0.05); 与SC组相比, HT组显著提高微杆菌属、Hyphomicrobiales及芽孢杆菌的相对丰度, 但条件致病菌邻单胞菌的相对丰度也显著升高(P<0.05)。综上, 在急性盐碱胁迫下, 灌喂MC2-1可减轻大口黑鲈的鳃、肝脏和肠道组织损伤, 2×107—2×108 CFU/尾 MC2-1可显著改善肝脏和鳃组织的抗氧化酶系统、提高肠道免疫力和菌群多样性, 进而增强机体的耐盐碱能力。

       

      Abstract: To investigate the mitigating effects of Bacillus inaquosorum MC2-1 (hereinafter referred to as MC2-1) on tissue damage, antioxidant capacity, ion transport, and intestinal flora under acute salt-alkaline stress in largemouth bass (Micropterus salmoides), a one-week oral administration trial was conducted. Largemouth bass juveniles mean initial weight (8.56±0.04) g were randomly divided into five treatments: a freshwater control (CK), a saline-alkaline stress group (SC; 6 psu salinity, 4.5 mmol/L alkalinity), and three probiotic-supplemented groups receiving SC water plus MC2-1 at 2×106, 2×107 and 2×108 CFU/tail (LT, MT, and HT, respectively). The results revealed that compared to the CK group, the SC group exhibited a significantly thinner intestinal muscle layer (P<0.05), shorter the secondary gill arch, larger gill lamella interval and wider short diameter, and increased severity of hepatic lesions including vacuolization and nuclear shift. Conversely, MC2-1 administration significantly restored intestinal muscle thickness and markedly mitigated liver damage induced by saline-alkaline stress, and the diameter and short diameter of the secondary gill arch in the MT and HT groups were restored (P<0.05). Regarding antioxidant and immune responses, the SC group significantly elevated hepatic T-AOC but decreased renal SOD activity and branchial T-AOC (P<0.05). Notably, the MT group significantly enhanced branchial SOD activity, and intestinal AKP and ACP activities compared to the CK group. Furthermore, compared to the SC group, the HT group significantly increased liver CAT and branchial SOD activities, with intestinal AMS and LPS activities being significantly higher in the HT group than that in all other groups (P<0.05). In terms of serum biochemistry, salt-alkaline stress led to a significant increase in TP and Ca2+ levels (P<0.05). Importantly, supplementation in the HT group successfully restored serum Cl- and Ca2+ concentrations to levels comparable to those in the control group (P<0.05). Analysis of the gut microbiota showed that the relative abundance of Paracoccus was significantly higher in the CK group than that in other groups (P<0.05). Compared to the SC group, the HT group showed increased relative abundances of Aurantimicrobium, Hyphomicrobiales, and Bacillus; however, the relative abundance of the pathogenic bacterium Plesiomonas was also significantly elevated in this group (P<0.05). In conclusion, oral administration of MC2-1 can effectively alleviate histological damage to the gills, liver, and intestines of largemouth bass under acute salt-alkaline stress. Specifically, supplementation at 2×107—2×108 CFU/tail significantly improves the liver and branchial antioxidant systems, enhances intestinal immune parameters, and modulates the gut microbiota, thereby collectively enhancing the salt-alkaline tolerance of the fish.

       

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