单端孢霉烯族毒素生物脱毒技术研究进展

单端孢霉烯族毒素在粮食和饲料中污染严重,主要是T-2毒素和脱氧雪腐镰刀烯醇(DON)等,其毒性作用强,对人和动物产生严重危害。因此,单端孢霉烯族毒素的脱毒方式逐渐成为研究热点,尤其是生物脱毒。很多微生物被证实能够降解霉菌毒素,包括细菌、真菌和酵母菌,可将毒素降解成低毒或无毒的产物。论文以生物脱毒为出发点,从细菌、真菌和酵母菌三个角度概述了单端孢霉烯族毒素中T-2毒素和DON的脱毒研究现状,以期为后续开发并挖掘更加安全高效的生物脱毒方式提供参考。     

T-2毒素研究进展

T-2毒素是单端孢霉烯族毒素之一,也是毒性最强的真菌毒素,可由多种真菌产生,在自然界中广泛存在,严重危害人畜健康。T-2毒素由Bamburg于1968年首次分离提纯并确认了化学结构。     

T-2毒素毒性作用研究进展

T-2是A类单端孢霉烯族化合物中毒性最强的一种,对动物机体具有较强的危害,可造成多个系统出现中毒效应。作者主要对T-2毒素对动物的广泛毒性作用进行论述,且对下一步的研究方向进行了展望。     

T-2毒素的神经毒性及作用机制研究进展

T-2毒素是最具毒性的单端孢霉烯族化合物,是农产品中常见的污染物之一。饮食摄入是人类接触T-2毒素最常见的途径。T-2毒素暴露导致许多病理状况,如神经紊乱、心血管改变、免疫抑制和皮肤炎症。然而,T-2毒素导致的神经毒性尚不清楚,为了更全面地把握T-2毒素的神经毒性研究现状,本文对T-2毒素诱导神经毒性的可能作用机制进行了探讨。     

T-2毒素毒性分子作用机制与脱毒的研究进展

T-2毒素是一种A类单端孢霉烯族毒素,具有高度致毒作用、毒性较难降解等特点,严重威胁人类和动物安全。目前,用于T-2毒素脱毒的方法有物理吸附法、化学试剂中和法、微生物分解法等。但T-2毒素导致的中毒反应的分子机制还尚未明确,可能涉及多个方面,如线粒体损伤、细胞自噬、免疫逃逸、细胞凋亡等。因此,文章主要探讨了T-2毒素毒性作用分子机制以及T-2毒素脱毒的研究进展,为T-2毒素的深入研究提供参考。     

T-2毒素及其对关节软骨和心肌毒性研究进展

T-2毒素是A族单端孢霉烯族毒素中毒性最强的毒素,也是我国两种地方病,即大骨节病和克山病最可能的致病因素,主要对关节软骨及心肌有毒害作用。T-2毒素可以诱导细胞凋亡,引起家畜、家禽关节超微结构的改变和关节软骨细胞的损伤;还能影响心肌离子通道电活动,影响脂质过氧化物代谢,也能改变心肌超微结构;微量元素硒对T-2毒素致关节软骨和心肌损害有明显的保护作用。大骨节病和克山病的高发地区粮食中T-2毒素含量偏高20%左右,所以大骨节病和克山病可能和T-2毒素中毒有关。     

T-2毒素的毒性作用及其诱导细胞凋亡机制概述

T-2毒素是一种毒性作用很强的霉菌毒素,是以镰刀菌属为主要产毒菌株所产生的一种A类单端孢霉烯族毒素,在多种谷物中的污染水平较高,通过食物摄入后在人类和动物机体内产生一系列毒性作用,严重威胁人类和动物的健康。论文从T-2毒素的理化性质、产毒菌株、毒性作用及对细胞凋亡的作用机制进行了简述,重点介绍了T-2毒素在免疫系统、消化系统和肝脏毒性、神经和皮肤毒性、血液毒性、生殖毒性方面的研究进展,以及T-2毒素通过线粒体信号通路介导细胞凋亡机制的研究进展,为T-2毒素的深入研究提供参考。     

T-2毒素免疫毒性研究现状

T-2毒素的免疫毒性具有矛盾性和复杂性。低剂量T-2毒素可提升动物对病原体的抵抗力,高剂量T-2毒素则大大降低动物的免疫力。T-2毒素暴露时间早于病原体可增加动物免疫抵抗力,反之或毒素与病原体同时暴露,则降低动物对病原体的抵抗力。近期研究发现,细胞凋亡/存活通路维持毒素免疫调控动态平衡,自噬在免疫调控中发挥着关键而复杂的作用,但T-2毒素免疫调控中是否存在类似"免疫逃避"机制亟待研究。论文综述了T-2毒素免疫毒性的矛盾性,并重点讨论了其潜在的分子机制,为单端孢霉烯族毒素的免疫毒性和动物疫病防控研究提供参考。     

呕吐毒素和其他B型单端孢霉烯族毒素对肠道影响研究进展

霉菌毒素被认为是对人类和动物的健康一个重要的危险因子,其中单端孢霉毒素被认为危害最为严重的霉菌毒素之一。呕吐毒素(DON)和其他B型单端孢霉烯族可诱发肠道病理病变,对肠上皮细胞的完整性造成破坏,进而改变肠道屏障功能,并且DON和B型单端孢霉烯族毒素也可影响肠上皮免疫细胞产生免疫因子,抑制肠道上皮的免疫反应。本文在国内外已有的研究基础上,就呕吐毒素和其他B型单端孢霉烯毒素对肠道影响研究进展进行了综述。     

单端孢霉烯族毒素抑制动物生长作用的研究进展

单端孢霉烯族毒素是主要的饲料污染物,包括T-2毒素、脱氧雪腐镰刀菌烯醇(DON)等,具有较强的毒性作用,能引起动物体多种病理变化。其毒性作用能改变真核翻译起始因子2α(EIF2α)、丝裂原激活的蛋白激酶(MAPK)、热休克蛋白90(Hsp90)、胰岛素样生长因子1(IGF-1)等细胞因子的活性,调节多种胺酰tRNA合成酶的活性,进而抑制蛋白质合成,阻滞动物生长。论文从单端孢霉烯族毒素对生长激素影响的角度,综述了该类毒素对动物生长的抑制作用,以期为阐明单端孢霉烯族毒素抑制动物生长的毒性作用机制奠定基础。     

Inhibitory effect of trichothecene mycotoxins on bovine platelets stimulated by platelet activating factor.

Several species of fungi, which infect cereals and grains, can produce a class of compounds, known as trichothecene mycotoxins, which is characterized by a substituted epoxy-trichothecene ring structure. Cattle are susceptible to intoxication from feeds contaminated with T-2 toxin, one of the more potent trichothecene mycotoxins, while swine refuse to ingest feed contaminated with T-2 toxin. The bovine platelet has been used as a model cell system to evaluate the effects of T-2 toxin and its natural metabolites, HT-2 toxin and T-2 tetraol, on cell function in vitro. Due to the lipophilic nature of these mycotoxins, a biologically active phospholipid was used to stimulate the platelets in the presence and absence of the toxins. The mycotoxin T-2 toxin and its major metabolite HT-2 toxin inhibited platelet activating factor-stimulated bovine platelets, suspended in homologous plasma, in a concentration but not time dependent manner. Significant inhibition of platelet function (p less than 0.01) occurred with 135 ng T-2 toxin per 10(6) platelets and with 77 ng HT-2 toxin per 10(6) platelets. These mycotoxins exerted an additive inhibitory effect on the platelet aggregation response. In contrast, the minor metabolite T-2 tetraol had no inhibitory effect on platelet function and had no influence on the responses of T-2 toxin or HT-2 toxin when the mycotoxins were present together in the platelet suspensions.(ABSTRACT TRUNCATED AT 250 WORDS)     

Deoxynivalenol and T-2 Toxin in Raw Feeds for Horses

In all, 72 samples of raw materials for equine feed were collected from farms located in different parts of northern Italy, and the presence of deoxynivalenol (DON) and T-2 toxin was evaluated using enzyme-linked immunosorbent assay. DON was detected in 38.9% of the samples tested, at levels ranging from 0.2 to 1.9 mg/kg. Maize was found to have the highest concentrations of DON, whereas barley was found to be the most commonly contaminated grain (73.3%). T-2 toxin was found in maize and rice bran at levels ranging from 12 to 102 μg/kg, with an overall incidence of 12.3% in the samples analyzed. In almost all the samples, T-2 toxin was found only in combination with DON. The occurrence of contamination observed in this survey, especially the presence of DON, is noteworthy. The levels detected are not very high, but even long-term exposure to low doses of these mycotoxins may represent a threat to horse health.     

The fungal T-2 toxin alters the activation of primary macrophages induced by TLR-agonists resulting in a decrease of the inflammatory response in the pig

T-2 toxin is known to be one of the most toxic trichothecene mycotoxins. Exposure to T-2 toxin induces many hematologic and immunotoxic disorders and is involved in immuno-modulation of the innate immune response. The objective of this work was to evaluate the effects of T-2 toxin on the activation of macrophages by different agonists of Toll-like receptors (TLR) using an in vitro model of primary porcine alveolar macrophages (PAM). Cytotoxic effects of T-2 toxin on PAM were first evaluated. An IC₅₀ of 19.47 ± 0.9753 nM was determined for the cytotoxicity of T-2 toxin. A working concentration of 3 nM of T-2 toxin was chosen to test the effect of T-2 toxin on TLR activation; this dose was not cytotoxic and did not induce apoptosis as demonstrated by Annexin/PI staining. A pre-exposure of macrophages to 3 nM of T-2 toxin decreased the production of inflammatory mediators (IL-1 beta, TNF-alpha, nitric oxide) in response to LPS and FSL1, TLR4 and TLR2/6 agonists respectively. The decrease of the pro-inflammatory response is associated with a decrease of TLR mRNA expression. By contrast, the activation of TLR7 by ssRNA was not modulated by T-2 toxin pre-treatment. In conclusion, our results suggest that ingestion of low concentrations of T-2 toxin affects the TLR activation by decreasing pattern recognition of pathogens and thus interferes with initiation of inflammatory immune response against bacteria and viruses. Consequently, mycotoxins could increase the susceptibility of humans and animals to infectious diseases.     

T-2毒素致猪肾细胞损伤及氧化应激相关机理的研究

试验旨在研究T-2毒素对猪肾细胞(PK15)的毒性作用及其氧化应激反应。用不同浓度的T-2毒素处理细胞,通过MTT法检测细胞活性、测定细胞内乳酸脱氢酶(LDH)释放率及苏木素伊红(HE)染色观察细胞形态变化评估T-2毒素对细胞的毒性作用;通过检测细胞内的活性氧(ROS)水平、丙二醛(MDA)含量及谷胱甘肽(GSH)含量、谷胱甘肽过氧化物酶(GPx)活性,评估不同剂量T-2毒素对细胞氧化应激水平的影响;检测Nrf2-ARE信号通路相关基因Nrf2、Keap1、GPx-1、Nqo1及Hmox1 mRNA的表达水平,分析T-2毒素对该信号通路的影响。结果表明,PK15细胞活性呈毒素剂量依赖性下降(P<0.05),LDH释放率呈毒素剂量依赖性上调(P<0.05);随T-2毒素剂量升高,细胞间隙逐渐增加,细胞固缩,细胞数量也随之减少。细胞内ROS阳性细胞率呈剂量依赖性升高,且T-2毒素为100 nmol/L时,ROS阳性细胞率显著高于其他剂量组(P<0.05);细胞内MDA含量与GPx活性呈毒素剂量依赖性升高(P<0.05),而GSH含量呈毒素剂量依赖性下降(P<0.05)。20、50及100 nmol/L的T-2毒素可显著上调Keap1、Gpx-1及Nqo1基因mRNA的相对表达量(P<0.05),且50 nmol/L的相对表达量最高。T-2毒素对K15细胞有毒性作用,可诱导其氧化损伤,且该氧化应激过程受Nrf2-AER信号通路调控。     

T-2毒素研究进展

T-2毒素是污染我国饲料的主要霉菌毒素,主要危害动物的造血组织和免疫器官,引起出血性综合征,出现白细胞减少、贫血,使胃肠道功能受损等,对畜禽健康和畜牧业生产的危害很大.本文主要从T-2毒素的一般性质、产毒菌株、毒性效应、毒性机制及预防控制等方面作了论述.     

猪肉和鸡肉中脱氧雪腐镰刀菌烯醇和T-2毒素酶联免疫吸附检测方法的建立

为保障动物源性食品安全,本研究建立了分别检测猪肉和鸡肉中脱氧雪腐镰刀菌烯醇(deoxynivalenol,DON)和T-2毒素残留的间接竞争酶联免疫吸附法.结果显示,该方法在猪肉和鸡肉样本中DON的检测限分别为34.9和43.5 μg/kg,添加回收率为72.7%~97.1%,变异系数小于8.7%;T-2毒素的检测限分别为33.7和28.7 μg/kg,添加回收率为72.1%~95.0%,变异系数小于11.3%.该方法灵敏度高、准确、简便,适用于猪肉和鸡肉中DON和T-2毒素残留的快速检测.     

17种植物性饲料原料中伏马毒素(B1+B2)、赭曲霉毒素A、T-2毒素、黄曲霉毒素B1污染状况调查检测分析

为了解掌握伏马毒素（B₁+B₂）、赭曲霉毒素A、T-2毒素、黄曲霉毒素B₁在植物性饲料原料中的污染状况,指导饲料生产企业和养殖企业开展霉菌毒素防控,降低霉菌毒素对饲料产品质量及畜禽养殖危害,减少经济损失,2019年对17种62份植物性饲料原料进行采集,采用液相色谱—串联质谱法、免疫亲和柱净化—高效液相色谱法检测,依据《饲料卫生标准》（GB 13078—2017）判定分析。结果表明：伏马毒素（B₁+B₂）、赭曲霉毒素A、黄曲霉毒素B₁在17种植物性饲料原料中的污染状况差别明显,伏马毒素（B₁+B₂）、赭曲霉毒素A、黄曲霉毒素B₁平均检出率分别为37.09%、8.06%、29.03%,最大检测值分别为15.96 mg/kg、26.60 μg/kg、351.00 μg/kg。从检测结果得出,4种霉菌毒素在17种植物性饲料原料中的污染较重,整体污染率达48.40%,玉米皮、喷浆玉米皮、花生粕3种植物性饲料原料中黄曲霉毒素B₁超标,污染率与超标率不一定呈正比,表明霉菌毒素在植物性饲料原料中污染普遍,对饲料产品及养殖安全造成严重影响。针对该问题,提出控制植物性饲料原料质量建议,为今后控制饲料原料中霉菌毒素含量提供参考。