Oliveri C, Torta L, Catara V
Dipartimento di Scienze e Tecnologie Fitosanitarie, Università degli Studi di Catania, via S. Sofia, 100, 95123 Catania, Italy.
Int J Food Microbiol. 2008 Sep 30;127(1-2):147-54. doi: 10.1016/j.ijfoodmicro.2008.06.021. Epub 2008 Jun 29.
Aspergillus strains belonging to section Nigri isolated during a two year survey in eight Sicilian vineyards located on the slopes of Mount Etna (Sicily, Italy) were analysed analyzed in order to characterize species responsible for ochratoxin A (OTA) contamination of grapes. The polyphasic approach permitted analysis of biodiversity of Aspergillus isolates in relation to their morphology, ochratoxigenicity and genetic variability. We assessed OTA production by A. carbonarius, A. niger, A. tubingensis and A. japonicus using an enzyme-linked immunosorbent assay. A. carbonarius isolates were the strongest OTA producers. A subset of 66 representative strains was selected for further DNA-based characterization. PCR assays using species-specific primers discriminated between A. niger, A. carbonarius and A. japonicus on the basis of the target sequences for each species. The PCR-based methods matched morphological characterization in identifying all the black aspergilli (BA) isolates tested, whereas RFLP analysis with RsaI of isolates positive to PCRs with A. niger specific primers identified three A. tubingensis isolates. The identification of thirteen isolates was further confirmed by ITS analysis. By this method, each of the isolates was identified and assigned to an Aspergillus species. The fAFLP analysis of 40 isolates highlighted the power of this technique to discriminate different species and single strains, to verify the presence of mixed populations in the same vineyard, through homogeneous species clusters. No correlation was observed between the clusters and OTA production level or origin.
为了鉴定导致葡萄中赭曲霉毒素A(OTA)污染的菌种,对在意大利西西里岛埃特纳火山山坡上八个西西里葡萄园进行的为期两年的调查中分离出的属于黑曲霉组的曲霉菌株进行了分析。多相方法允许分析曲霉分离株的生物多样性与其形态、产赭曲霉毒素能力和遗传变异性之间的关系。我们使用酶联免疫吸附测定法评估了碳黑曲霉、黑曲霉、管囊曲霉和日本曲霉的OTA产量。碳黑曲霉分离株是最强的OTA生产者。选择了66个代表性菌株的子集进行进一步的基于DNA的鉴定。使用物种特异性引物的PCR分析根据每个物种的靶序列区分黑曲霉、碳黑曲霉和日本曲霉。基于PCR的方法在鉴定所有测试的黑曲霉(BA)分离株时与形态学鉴定相匹配,而对用黑曲霉特异性引物进行PCR呈阳性的分离株用RsaI进行RFLP分析鉴定出三个管囊曲霉分离株。通过ITS分析进一步确认了13个分离株的鉴定。通过这种方法,每个分离株都被鉴定并归为一个曲霉物种。对40个分离株的fAFLP分析突出了该技术区分不同物种和单个菌株、通过同质物种簇验证同一葡萄园混合种群存在的能力。在簇与OTA产量水平或来源之间未观察到相关性。
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