首页> 外文期刊>World Mycotoxin Journal >Quantitative detection of Fusarium spp. and its correlation with fumonisin content in maize from South African subsistence farmers.
【24h】

Quantitative detection of Fusarium spp. and its correlation with fumonisin content in maize from South African subsistence farmers.

机译:us spp的定量检测。及其与南非自给农民玉米中伏马毒素含量的相关性。

获取原文
获取原文并翻译 | 示例
       

摘要

A quantitative detection tool was developed to enable the monitoring of fumonisin-producing fungi in food and feed commodities. To this end, a quantitative PCR (TaqMan) was developed that targets a conserved region in the polyketide synthase gene fum1, which is involved in the biosynthesis of fumonisin. Hence, this method specifically detected isolates from the fumonisin-producing species Fusarium verticillioides, F. proliferatum, F. nygamai and F. globosum whereas isolates of the fumonisin non-producing species F. equiseti, F. graminearum, F. oxysporum, F. semitectum and F. subglutinans that commonly occur on maize were not detected. Moreover, a few fumonisin non-producing F. verticillioides isolates did not generate any fluorescent signals and were therefore not detected. The correlation between quantitative PCR and mycotoxin content was determined using field samples collected at homestead farms in South Africa. Among 40 samples from the Eastern Cape collected in 2005 a good correlation (R2=0.8303) was found between pg fungal DNA and fumonisin content. A similar correlation (R2=0.8658) was found among 126 samples collected from four provinces in South Africa in 2007. These observations indicate that samples containing >=40 pg fungal DNA/mg sample are suspected of also exceeding the 1 mg/kg total fumonisin level and therefore do not comply with the European Commission limit for fumonisins B1+B2 for maize intended for direct human consumption that applies from 1 October 2007. Combined with the very high maize intake, our results indicate that fumonisin levels in maize from South African homesteads regularly exceed the tolerable daily intake for fumonisins.
机译:开发了一种定量检测工具,以能够监测食品和饲料商品中产生伏马毒素的真菌。为此,开发了针对聚酮化合物合酶基因 fum1 中一个保守区域的定量PCR(TaqMan),该基因参与了伏马菌素的生物合成。因此,该方法专门检测了生产伏马毒素的菌种 verticillioides , F的分离株。 proliferatum , F。 nygamai 和 F。 globosum ,而伏马菌素非生产菌 F的分离株。 Equiseti , F。禾本科, F。 oxysporum , F。 semitectum 和 F。未检测到通常在玉米上发生的次谷蛋白。此外,一些伏马菌素不产生F。拟杆菌属分离物未产生任何荧光信号,因此未检测到。定量PCR和霉菌毒素含量之间的相关性是使用在南非的宅基地农场收集的田间样品确定的。在2005年从东开普省采集的40个样本中,pg真菌DNA和伏马菌素含量之间存在良好的相关性(R 2 = 0.8303)。在2007年从南非四个省收集的126个样品中发现了相似的相关性(R 2 = 0.8658)。这些观察结果表明,怀疑含有> = 40 pg真菌DNA / mg样品的样品也超过伏马菌素总含量超过1 mg / kg的水平,因此不符合欧盟委员会针对直接供人类食用的玉米所用伏马菌素B 1 + B 2 的限制2007年10月1日。结合极高的玉米摄入量,我们的结果表明,来自南非家园的玉米中伏马毒素的含量经常超过伏马毒素的每日容许摄入量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号