Kemler Martin, Garnas Jeff, Wingfield Michael J, Gryzenhout Marieka, Pillay Kerry-Anne, Slippers Bernard
Department of Genetics, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, South Africa.
Department of Zoology and Entomology, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, South Africa.
PLoS One. 2013 Dec 16;8(12):e81718. doi: 10.1371/journal.pone.0081718. eCollection 2013.
The Kingdom Fungi adds substantially to the diversity of life, but due to their cryptic morphology and lifestyle, tremendous diversity, paucity of formally described specimens, and the difficulty in isolating environmental strains into culture, fungal communities are difficult to characterize. This is especially true for endophytic communities of fungi living in healthy plant tissue. The developments in next generation sequencing technologies are, however, starting to reveal the true extent of fungal diversity. One of the promising new technologies, namely semiconductor sequencing, has thus far not been used in fungal diversity assessments. In this study we sequenced the internal transcribed spacer 1 (ITS1) nuclear encoded ribosomal RNA of the endophytic community of the economically important tree, Eucalyptus grandis, from South Africa using the Ion Torrent Personal Genome Machine (PGM). We determined the impact of various analysis parameters on the interpretation of the results, namely different sequence quality parameter settings, different sequence similarity cutoffs for clustering and filtering of databases for removal of sequences with incomplete taxonomy. Sequence similarity cutoff values only had a marginal effect on the identified family numbers, whereas different sequence quality filters had a large effect (89 vs. 48 families between least and most stringent filters). Database filtering had a small, but statistically significant, effect on the assignment of sequences to reference sequences. The community was dominated by Ascomycota, and particularly by families in the Dothidiomycetes that harbor well-known plant pathogens. The study demonstrates that semiconductor sequencing is an ideal strategy for environmental sequencing of fungal communities. It also highlights some potential pitfalls in subsequent data analyses when using a technology with relatively short read lengths.
真菌界极大地丰富了生命的多样性,但由于其隐秘的形态和生活方式、巨大的多样性、正式描述的标本稀缺以及将环境菌株分离培养的困难,真菌群落难以被表征。对于生活在健康植物组织中的内生真菌群落而言尤其如此。然而,新一代测序技术的发展开始揭示真菌多样性的真实程度。其中一项有前景的新技术,即半导体测序,迄今尚未用于真菌多样性评估。在本研究中,我们使用离子激流个人基因组测序仪(PGM)对来自南非的经济重要树种巨桉的内生真菌群落的内部转录间隔区1(ITS1)核编码核糖体RNA进行了测序。我们确定了各种分析参数对结果解读的影响,即不同的序列质量参数设置、用于聚类的不同序列相似性截止值以及为去除分类不完整的序列而对数据库进行过滤。序列相似性截止值对鉴定出的科数量仅有微小影响,而不同的序列质量过滤器则有很大影响(最宽松和最严格的过滤器之间分别为89个科和48个科)。数据库过滤对序列与参考序列的比对有较小但具有统计学意义的影响。该群落以子囊菌门为主,尤其是座囊菌纲中包含著名植物病原体的科。该研究表明,半导体测序是真菌群落环境测序的理想策略。它还凸显了在使用读长相对较短的技术进行后续数据分析时的一些潜在陷阱。