Molecular Characterization of Fungi Associated with Dump Site Soil

N. Ogbuji, A. Ataga, P. Tari-Ukuta, C. J. Olisedeme
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Abstract

Aims: A study was conducted to identify fungal species isolated from dumpsite soil in University of Port Harcourt using molecular techniques. Methodology: Molecular methods for determining the species of a fungus based on the amplification and sequencing of the internal subscribed spacer (ITS) region of the fungal rRNA operon using molecular markers was applied. Soil sample was collected from a dumpsite in the University of Port Harcourt, Rivers State, Nigeria. Isolation of fungi associated with the dumpsite soil was carried out using spread plate method. Fungal genomic DNA was extracted using Quick-DNA Fungal/Bacterial Miniprep kit. The ITS1-2 gene of the isolates was amplified by Polymerase Chain Reaction (PCR) using the primer pair; ITS4 and ITS5. Results: The sequences of the amplified ITS region were blasted against known sequences on the National Centre for Biotechnology Information (NCBI) database. Nucleotide sequence analysis revealed the species identity of the fungal isolates to be: Aspergillus fumigatus, Trichoderma harzianum, Aspergillus felis, Aspergillus templicola, Aspergillus flavipes, Aspergillus fumigatus and Cunninghamella binariae. Phylogenetic analysis was carried out to ascertain the relationship between the isolates and other closely-related isolates on GenBank. Isolates 2 (Trichoderma harzianum) and 7 (Cunninghamella binariae), 3 (Aspergillus felis) and 6 (Aspergillus fumigatus), and 4 (Aspergillus templicola) and 5 (Aspergillus flavipes) were found to be more closely related to each other. Conclusion: The molecular techniques employed successfully identified the organisms to the species level as these techniques are based on the genetic constitution of organisms. The result obtained from this study will complement the information on the fungal organisms associated with dumpsite soil.
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垃圾场土壤真菌的分子特性研究
目的:利用分子技术对哈科特港大学垃圾场土壤中分离的真菌进行鉴定。方法:利用分子标记对真菌rRNA操纵子的内部预定间隔区(ITS)进行扩增和测序,采用分子方法确定真菌种类。土壤样本是从尼日利亚河流州哈科特港大学的一个垃圾场收集的。采用铺板法对垃圾场土壤真菌进行了分离。使用Quick-DNA真菌/细菌Miniprep试剂盒提取真菌基因组DNA。利用该引物对,聚合酶链反应(PCR)扩增出菌株的ITS1-2基因;ITS4和ITS5。结果:扩增的ITS区域序列与NCBI数据库中的已知序列进行比对。核苷酸序列分析表明,分离真菌为烟曲霉、哈茨木霉、狐曲霉、天曲霉、黄曲霉、烟曲霉和双生坎宁哈默氏菌。系统发育分析确定该分离株与GenBank上其他近缘分离株的关系。分离菌株2(哈茨木霉)和7(双生坎宁哈默氏菌)、3 (felis曲霉)和6(烟曲霉)、4 (templicola曲霉)和5 (flavavipes曲霉)亲缘关系较近。结论:基于生物遗传结构的分子技术在物种水平上成功地鉴定了生物。这项研究的结果将补充与垃圾场土壤有关的真菌生物的信息。
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