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从谷物中分离出的产赭曲霉毒素A的疣孢青霉菌株显示出较大的扩增片段长度多态性(AFLP)指纹图谱变异性。

Ochratoxin A producing Penicillium verrucosum isolates from cereals reveal large AFLP fingerprinting variability.

作者信息

Frisvad J C, Lund F, Elmholt S

机构信息

Center for Microbial Biotechnology, Biocentrum-DTU, Søltofts Plads, Technical University of Denmark, Lyngby, Denmark.

出版信息

J Appl Microbiol. 2005;98(3):684-92. doi: 10.1111/j.1365-2672.2004.02509.x.

Abstract

AIMS

To examine if molecular amplified fragment length polymorphism (AFLP) fingerprinting of the only ochratoxin A-producing species in European cereals, Penicillium verrucosum, can be used as a method in hazard analysis using critical control points (HACCP).

METHODS AND RESULTS

A total of 321 isolates of P. verrucosum were isolated from ochratoxin A-contaminated cereals from Denmark (oats), UK (wheat and barley) and Sweden (wheat). Of these, 236 produced ochratoxin A as determined by thin layer chromatography; 185 ochratoxin A-producing isolates were selected for AFLP fingerprinting. A total of 138 isolates had unique AFLP patterns, whereas 52 isolates could be allocated to small groups containing from two to four isolates with similar AFLP patterns. A total of 155 clones were found among the 185 P. verrucosum isolates, thus 84% of the isolates may represent different genets of P. verrucosum. As the few isolates that were grouped often came from the same farm, and those groups that contained AFLP-identical isolates from different countries were morphotypically different. On single farms up to 35 clones were found. The few groups of ramets from the same genet indicated that a HACCP approach based on clones may require a very large number of AFLP analysis to work in practice, we recommend basing the HACCP approach on the actual species P. verrucosum. A more detailed characterization should rather be based on the profile of species present at different control points, or analysis of the mycotoxins ochratoxin A and citrinin in the isolates. Examination of 86 isolates with HPLC and diode array detection of P. verrucosum showed that 66% produced ochratoxin A, 87% produced citrinin, 92% produced verrucin and 100% produced verrucolone.

CONCLUSIONS

Among 184 ochratoxin A-producing Penicillium verrucosum, 155 clonal lineages were indicated by AFLP fingerprinting, indicating a high genetical diversity, yet the species P. verrucosum is phenotypically distinct and valid.

SIGNIFICANCE AND IMPACT OF THE STUDY

AFLP fingerprinting of Penicillium verrucosum indicates that genetic recombination takes place in this fungus.

摘要

目的

研究欧洲谷物中唯一能产生赭曲霉毒素A的疣孢青霉的分子扩增片段长度多态性(AFLP)指纹图谱能否作为危害分析关键控制点(HACCP)中的一种方法。

方法与结果

从丹麦(燕麦)、英国(小麦和大麦)及瑞典(小麦)受赭曲霉毒素A污染的谷物中总共分离出321株疣孢青霉。其中,通过薄层色谱法测定,有236株能产生赭曲霉毒素A;选取185株产赭曲霉毒素A的分离株进行AFLP指纹图谱分析。共有138株分离株具有独特的AFLP图谱,而52株分离株可归为含有两至四株具有相似AFLP图谱的小群体。在185株疣孢青霉分离株中总共发现了155个克隆,因此84%的分离株可能代表疣孢青霉的不同遗传型。由于少数归为一组的分离株通常来自同一个农场,且那些包含来自不同国家AFLP相同分离株的群体在形态型上存在差异。在单个农场中发现了多达35个克隆。来自同一遗传型的少数分株群体表明,基于克隆的HACCP方法在实际应用中可能需要进行大量的AFLP分析,我们建议HACCP方法基于实际的疣孢青霉物种。更详细的特征描述应基于不同控制点存在的物种概况,或对分离株中赭曲霉毒素A和桔霉素这两种霉菌毒素的分析。用高效液相色谱法和二极管阵列检测法对86株疣孢青霉进行检测,结果显示66%的菌株产生赭曲霉毒素A,87%的菌株产生桔霉素,92%的菌株产生疣孢菌素,100%的菌株产生疣孢酮。

结论

在184株产赭曲霉毒素A的疣孢青霉中,AFLP指纹图谱显示有155个克隆谱系,表明其具有高度的遗传多样性,但疣孢青霉物种在表型上是独特且有效的。

研究的意义和影响

疣孢青霉的AFLP指纹图谱表明该真菌中发生了基因重组。

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