Application of polyphasic approach for identification of epiphytic fungi isolated from wheat grains

Nevin Emin, K. Dimitrova, Y. Kartalska
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Abstract

In this study, epiphytic fungi were isolated from wheat seeds (Triticum aestivum L) and a polyphasic approach for their identification was applied. The initial morphological characterisation was done on selected twenty-tree strains and continued with their identification based on the carbon utilisation pattern according to the Biolog OmniLog system protocol (Hayward, CA, USA). Throughout the isolated strains, the Biolog data indicated predominance of the genera Aspergillus, Penicillium and Fusarium. The carbon utilisation pattern of five strains assigned them to several different from aforementioned genera and due to their scarcity they were not included in the current study. The indicated by the Biolog genus designation of the strains was used as a guideline for the further molecular identification of seventeen strains from the predominant genera. Molecular identification was based on a polymerase chain reaction (PCR) with universal primers, which targeted the internal transcribed spacer (ITS) region of rDNA gene. The PCR fragments were sequenced and after applying a BLAST algorithm, a high percentage of similarity was found for eleven strains. At the species level, the Biolog and molecular technique showed a discrepancy in the identification of two strains. The procedure of identification was unsuccessful for six strains either due to insufficient quantity of the PCR product or the lack of sufficient similarity of the fragments to the GenBank database. Current study showed that the unbiased identification of epiphytic fungi requires a polyphasic approach, which applies morphological, physiological and molecular techniques.
多相法在小麦附生真菌鉴定中的应用
本研究从小麦种子(Triticum aestivum L)中分离得到附生真菌,并采用多相法对其进行鉴定。对选定的20株菌株进行了初始形态表征,并根据Biolog OmniLog系统协议(Hayward, CA, USA)的碳利用模式继续进行鉴定。在所有分离菌株中,生物学数据显示曲霉属、青霉属和镰刀菌属占优势。5个菌株的碳利用模式将它们划分为与上述属不同的几个属,由于它们的稀缺性,它们未被纳入本研究。该菌株的Biolog属标记可作为优势属中17株菌株进一步分子鉴定的指导。分子鉴定基于rDNA基因内部转录间隔区(ITS)的聚合酶链反应(PCR)和通用引物。采用BLAST算法对PCR片段进行测序,发现11株菌株具有较高的相似性。在种水平上,两种菌株的生物学和分子鉴定存在差异。由于PCR产物数量不足或片段与GenBank数据库缺乏足够的相似性,6株菌株的鉴定过程失败。目前的研究表明,附生真菌的公正鉴定需要多相方法,包括形态学、生理学和分子技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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