Using High-throughput Sequencing to Study the Development of Fungal Community in Stored Wheat

被引:1
作者
Yue X. [1 ]
Zhang H. [1 ]
Chen W. [1 ]
Xu W. [2 ]
Guo M. [2 ]
机构
[1] College of Food Engineering, Henan University of Animal Husbandry and Economy, Zhengzhou
[2] College of Food Science and Nutritional Engineering, China Agricultural University, Beijing
来源
Shipin Kexue/Food Science | 2020年 / 41卷 / 14期
关键词
Fungal community; High throughput sequencing; Wheat;
D O I
10.7506/spkx1002-6630-20190526-309
中图分类号
学科分类号
摘要
In this paper, high-throughput sequencing technology was used to study the development of the fungal community in stored wheat and the factors inf l uencing it, aiming to provide useful information for optimizing the storage conditions of wheat. The results showed that Alternaria, Aspergillus, and Cladosporium were the most abundant fungal contaminants in stored wheat. Aspergillus was the genus with the highest diversity at the species level, including 11 species. Storage period of wheat had a great influence on the fungal community. The fungal communities in wheat stored for one, two and three years had their own characteristic fungi. The location of wheat in the warehouse had little relationship with the fungal community, while the depth of the warehouse affected the fungal community, and the abundance of Sordariomycetes decreased with the increase in storage depth. The fungal communities of stored wheat in different provinces were quite different. This study can provide basic data for the establishment of a model for describing the development of the fungal community in stored wheat, and also provide feasible schemes for fungal control in stored wheat in the future. © 2020, China Food Publishing Company. All right reserved.
引用
收藏
页码:109 / 115
页数:6
相关论文
共 18 条
  • [1] AHMAD A, YU JAE-HYUK, Occurrence, toxicity, and analysis of major mycotoxins in food[J], International Journal of Environmental Research and Public Health, 14, 6, (2017)
  • [2] FREIRE L, ANDERSON S., Modified mycotoxins: an updated review on their formation, detection, occurrence, and toxic effects, Food and Chemical Toxicology, 111, pp. 189-205, (2018)
  • [3] 3, pp. 28-30
  • [4] 5, pp. 51-54
  • [5] AYDIN S, SHAHI A, OZBAYRAM E G, Et al., Use of PCR-DGGE based molecular methods to assessment of microbial diversity during anaerobic treatment of antibiotic combinations, Bioresource Technology, 192, pp. 735-740, (2015)
  • [6] KERMANI F, SHAMS-GHAHFAROKHI M, GHOLAMI-SHABANI M, Et al., Diversity, molecular phylogeny and fingerprint profiles of airborne Aspergillus species using random amplified polymorphic DNA, World Journal of Microbiology & Biotechnology, 32, 6, (2016)
  • [7] CAMARINHASILVA A, WOSOXLEY M L, JAUREGUI R, Et al., Validating T-RFLP as a sensitive and high-throughput approach to assess bacterial diversity patterns in human anterior nares[J], Fems Microbiology Ecology, 79, 1, pp. 98-108, (2015)
  • [8] 5
  • [9] MELO S C, PUNGARTNIK C, CASCARDO J C, Et al., Rapid and efficient protocol for DNA extraction and molecular identification of the basidiomycete Crinipellis perniciosa, Genetics and Molecular Research, 5, 4, pp. 851-855, (2006)
  • [10] TAPIA-TUSSELL R, LAPPE P, ULLOA M, Et al., A rapid and simple method for DNA extraction from yeasts and fungi isolated from Agave fourcroydes, Molecular Biotechnology, 33, 1, pp. 67-70, (2006)