Frisvad J C, Lund F, Elmholt S
Center for Microbial Biotechnology, Biocentrum-DTU, Søltofts Plads, Technical University of Denmark, Lyngby, Denmark.
J Appl Microbiol. 2005;98(3):684-92. doi: 10.1111/j.1365-2672.2004.02509.x.
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).
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.
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.
AFLP fingerprinting of Penicillium verrucosum indicates that genetic recombination takes place in this fungus.
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。
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。
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。
疣孢青霉的AFLP指纹图谱表明该真菌中发生了基因重组。