Mohamed Hams M A, Haziri Imer, Saied AbdulRahman A, Dhama Kuldeep, Al-Said Amal A, Abdou Suzan E, Kamaly Heba F, Abd-Elhafeez Hanan H
Department of Microbiology, Faculty of Veterinary Medicine, South Valley University, Qena, 83523, Egypt.
Department of Veterinary Medicine, Faculty of Agriculture and Veterinary, University of Prishtina "Hasan Prishtina", 10000 Pristina, Kosovo.
Vet World. 2023 Aug;16(8):1636-1646. doi: 10.14202/vetworld.2023.1636-1646. Epub 2023 Aug 17.
Several strains of produce mycotoxins that affect the health and productivity of dairy cattle, and their presence in dairy cattle feed is a serious concern. This study aimed to determine the densities of and gliotoxin in commercial dairy feed.
More than 60 dairy feed samples were examined for fungal contamination, specifically for , using phenotypic approaches and DNA sequencing of the () and β-tubulin regions. Thin-layer chromatography and high-performance liquid chromatography (HPLC) were used to assess gliotoxin production in . Real-time polymerase chain reaction (RT-PCR) was used to investigate the expression of Z, which was responsible for gliotoxin production. High-performance liquid chromatography was used to detect gliotoxin in feed samples.
was the most commonly identified genus (68.3%). was isolated from 18.3% of dairy feed samples. Only four of the 11 isolates yielded detectable gliotoxins by HPLC. In total, 7/11 (43.7%) feed samples tested had gliotoxin contamination above the threshold known to induce immunosuppressive and apoptotic effects . The HPLC-based classification of isolates as high, moderate, or non-producers of gliotoxin was confirmed by RT-PCR, and the evaluation of Z expression levels corroborated this classification.
The identification of from animal feed greatly depended on and β-tubulin sequencing. Significant concentrations of gliotoxin were found in dairy cattle feed, and its presence may affect dairy cow productivity and health. Furthermore, workers face contamination risks when handling and storing animal feed.
几种菌株会产生影响奶牛健康和生产力的霉菌毒素,它们在奶牛饲料中的存在是一个严重问题。本研究旨在测定商业奶牛饲料中[具体菌株名称]和胶毒素的密度。
使用表型方法以及对[具体基因名称]和β - 微管蛋白区域进行DNA测序,对60多个奶牛饲料样本进行真菌污染检测,特别是针对[具体菌株名称]。采用薄层色谱法和高效液相色谱法(HPLC)评估[具体菌株名称]中胶毒素的产生情况。使用实时聚合酶链反应(RT - PCR)研究负责胶毒素产生的Z基因的表达。采用高效液相色谱法检测饲料样本中的胶毒素。
[具体菌株名称]是最常鉴定出的属(68.3%)。从18.3%的奶牛饲料样本中分离出[具体菌株名称]。11株[具体菌株名称]分离株中只有4株通过HPLC产生了可检测到的胶毒素。总共,11个测试饲料样本中有7个(43.7%)的胶毒素污染高于已知会诱导免疫抑制和凋亡作用的阈值。通过RT - PCR证实了基于HPLC将分离株分类为胶毒素高产、中产或不产的情况,并且对Z表达水平的评估证实了这一分类。
从动物饲料中鉴定[具体菌株名称]很大程度上依赖于[具体基因名称]和β - 微管蛋白测序。在奶牛饲料中发现了显著浓度的胶毒素,其存在可能会影响奶牛的生产力和健康。此外,工人在处理和储存动物饲料时面临污染风险。