Faculty of Biology, University of Freiburg, Schänzlestr. 1, D-79104, Freiburg, Germany.
Evolutionary Genomics Group, División de Microbiología, Universidad Miguel Hernández, Apartado 18, San Juan, 03550, Alicante, Spain.
ISME J. 2018 Apr;12(4):981-996. doi: 10.1038/s41396-017-0034-4. Epub 2018 Jan 15.
Interactions between co-existing microorganisms deeply affect the physiology of the involved organisms and, ultimately, the function of the ecosystem as a whole. Copiotrophic Alteromonas are marine gammaproteobacteria that thrive during the late stages of phytoplankton blooms in the marine environment and in laboratory co-cultures with cyanobacteria such as Trichodesmium. The response of this heterotroph to the sometimes rapid and transient changes in nutrient supply when the phototroph crashes is not well understood. Here, we isolated and sequenced the strain Alteromonas macleodii str. Te101 from a laboratory culture of Trichodesmium erythraeum IMS101, yielding a chromosome of 4.63 Mb and a single plasmid of 237 kb. Increasing salinities to ≥43 ppt inhibited the growth of Trichodesmium but stimulated growth of the associated Alteromonas. We characterized the transcriptomic responses of both microorganisms and identified the complement of active transcriptional start sites in Alteromonas at single-nucleotide resolution. In replicate cultures, a similar set of genes became activated in Alteromonas when growth rates of Trichodesmium declined and mortality was high. The parallel activation of fliA, rpoS and of flagellar assembly and growth-related genes indicated that Alteromonas might have increased cell motility, growth, and multiple biosynthetic activities. Genes with the highest expression in the data set were three small RNAs (Aln1a-c) that were identified as analogs of the small RNAs CsrB-C in E. coli or RsmX-Z in pathogenic bacteria. Together with the carbon storage protein A (CsrA) homolog Te101_05290, these RNAs likely control the expression of numerous genes in responding to changes in the environment.
共存微生物之间的相互作用深刻影响着相关生物的生理学,并最终影响整个生态系统的功能。富营养型交替单胞菌是海洋γ变形菌,在海洋环境中浮游植物大量繁殖的后期以及与蓝细菌(如束毛藻属)的实验室共培养中茁壮成长。当光养生物崩溃时,这种异养生物对营养供应有时快速而短暂变化的反应还不是很清楚。在这里,我们从 Trichodesmium erythraeum IMS101 的实验室培养物中分离并测序了一株 Alteromonas macleodii str. Te101,得到了一个 4.63Mb 的染色体和一个 237kb 的单一质粒。将盐度增加到≥43 ppt 会抑制束毛藻的生长,但会刺激相关的交替单胞菌的生长。我们对这两种微生物的转录组反应进行了表征,并以单核苷酸分辨率确定了 Alteromonas 中活跃转录起始位点的完整组成。在重复培养中,当束毛藻的生长速率下降且死亡率较高时,Alteromonas 中的一组类似基因被激活。 fliA、rpoS 和鞭毛组装及生长相关基因的平行激活表明,Alteromonas 可能增加了细胞的运动性、生长和多种生物合成活性。在数据集表达最高的基因是三个小 RNA(Aln1a-c),它们被鉴定为大肠杆菌中的小 RNA CsrB-C 或致病菌中的 RsmX-Z 的类似物。与碳储存蛋白 A(CsrA)同源物 Te101_05290 一起,这些 RNA 可能在响应环境变化时控制着众多基因的表达。