Marter Pia, Freese Heike M, Ringel Victoria, Brinkmann Henner, Pradella Silke, Rohde Manfred, Jarek Michal, Spröer Cathrin, Wagner-Döbler Irene, Overmann Jörg, Bunk Boyke, Petersen Jörn
Leibniz Institute DSMZ - German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Helmholtz Centre for Infection Research, Braunschweig, Germany.
Environ Microbiol Rep. 2025 Feb;17(1):e70066. doi: 10.1111/1758-2229.70066.
The filamentous cyanobacterium Coleofasciculus chthonoplastes is the key primary producer of marine microbial mats. We elucidated the microbiomes of 32 non-axenic Coleofasciculus isolates using PacBio-based amplicon sequencing of the complete 16S rRNA gene and the internally transcribed spacer (16S-ITS). The length of authentic amplicon sequence variants (ASVs) ranged from 1827 to 3044 nucleotides (median: 2267 nt). The results, which were complemented by metagenome analyses and cultivation approaches, revealed the presence of more than 70 associated heterotrophs in the culture of Coleofasciculus sp. WW12. The great bacterial diversity in the cyanosphere is dominated by Pseudomonadota (59%) and Bacteroidota (23%). Allelic ribosomal operon variants were detected in 18 Coleofasciculus strains and our analyses proposed the presence of at least four different species. A comparative analysis of cyanobacterial microbiomes documented complementary advantages of amplicon sequencing versus metagenomics with an individual strength of the 16S-ITS approach in terms of (i) ribosomal target sequence quality, (ii) contaminant detection and (iii) identification of rare bacteria. The characterisation of the Coleofasciculus microbiome showed that long-read amplicon sequencing of the 16S-ITS region is the method of choice for rapid profiling of non-axenic cyanobacteria. Its superior resolution allows a reliable differentiation of even very closely related strains.
丝状蓝细菌Chthonoplastes鞘丝藻是海洋微生物席的关键初级生产者。我们使用基于PacBio的完整16S rRNA基因和内部转录间隔区(16S-ITS)的扩增子测序,阐明了32株非无菌鞘丝藻分离株的微生物群落。真实扩增子序列变体(ASV)的长度范围为1827至3044个核苷酸(中位数:2267 nt)。宏基因组分析和培养方法补充了这些结果,揭示了鞘丝藻WW12培养物中存在70多种相关异养生物。蓝细菌周围的细菌多样性主要由假单胞菌门(59%)和拟杆菌门(23%)主导。在18株鞘丝藻菌株中检测到等位核糖体操纵子变体,我们的分析表明至少存在四个不同的物种。蓝细菌微生物群落的比较分析记录了扩增子测序与宏基因组学的互补优势,以及16S-ITS方法在(i)核糖体靶序列质量、(ii)污染物检测和(iii)稀有细菌鉴定方面的独特优势。鞘丝藻微生物群落的表征表明,16S-ITS区域的长读长扩增子测序是快速分析非无菌蓝细菌的首选方法。其卓越的分辨率甚至可以可靠地区分非常密切相关的菌株。