Programa en Genómica Funcional de Procariotes, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, 62210, Mexico.
Unidad de Análisis Bioinformáticos, Centro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, 62210, Mexico.
Microbiology (Reading). 2023 Jan;169(1). doi: 10.1099/mic.0.001293.
We previously showed that specific polyamines (PAs) present in the extracellular environment markedly affect extracellular polysaccharide (EPS) production, biofilm formation and motility in Rm8530. We hypothesized that extracellular PA signals were sensed and transduced by the NspS and MbaA proteins, respectively, which are homologs of the PA-sensing, c-di-GMP modulating NspS-MbaA proteins described in . Here we show that the decrease in biofilm formation and EPS production in the quorum-sensing (QS)-deficient wild-type strain 1021 in cultures containing putrescine or spermine did not occur in a 1021 mutant (1021 nspS). The transcriptional expression of in strain 1021 was significantly increased in cultures containing either of these polyamines, but not by exogenous cadaverine, 1,3-diaminopropane (DAP), spermidine (Spd) or norspermidine (NSpd). Cell aggregation in liquid cultures did not differ markedly between strain 1021 and 1021 nspS in the presence or absence of PAs. The QS-proficient Rm8530 wild-type and mutant (Rm8530 nspS) produced similar levels of biofilm under control conditions and 3.2- and 2.2-fold more biofilm, respectively, in cultures with NSpd, but these changes did not correlate with EPS production. Cells of Rm8530 nspS aggregated from two- to several-fold more than the wild-type in cultures without PAs or in those containing Spm. NSpd, Spd and DAP differently affected swimming and swarming motility in strains 1021 and Rm8530 and their respective mutants. transcription in strain Rm8530 was greatly reduced by exogenous Spm. Bioinformatic analysis revealed similar secondary structures and functional domains in the MbaA proteins of and , while their NspS proteins differed in some residues implicated in polyamine recognition in the latter species. NspS-MbaA homologs occur in a small subset of soil and aquatic bacterial species that commonly interact with eukaryotes. We speculate that the NspS-MbaA system modulates biofilm formation, EPS production and motility in response to environmental or host plant-produced PAs.
我们之前曾表明,细胞外环境中特定的多胺(PAs)会显著影响 Rm8530 中细胞外多糖(EPS)的产生、生物膜形成和运动。我们假设细胞外 PA 信号分别被 NspS 和 MbaA 蛋白感知和转导,NspS 和 MbaA 蛋白分别是在中描述的 PA 感应、c-di-GMP 调节 NspS-MbaA 蛋白的同源物。在这里,我们表明,在含有腐胺或精胺的培养物中,群体感应(QS)缺陷型 1021 野生型菌株生物膜形成和 EPS 产生的减少不会发生在 1021 nspS 突变体中。在含有这些多胺的培养物中,1021 菌株中 的转录表达显著增加,但外源尸胺、1,3-二氨基丙烷(DAP)、亚精胺(Spd)或正亚精胺(NSpd)则没有增加。在有或没有 PA 的情况下,液体培养物中 1021 菌株和 1021 nspS 之间的细胞聚集没有明显差异。在对照条件下,QS 有效的 Rm8530 野生型和突变体(Rm8530 nspS)产生相似水平的生物膜,而在含有 NSpd 的培养物中分别增加了 3.2 倍和 2.2 倍,但这些变化与 EPS 产生无关。与野生型相比,在没有 PAs 或含有 Spm 的培养物中,Rm8530 nspS 细胞聚集的倍数增加了 2 到数倍。NSpd、Spd 和 DAP 对 1021 株和 Rm8530 及其各自的 nspS 突变株的游泳和群集运动有不同的影响。外源 Spm 大大降低了 Rm8530 菌株中的 转录。生物信息学分析显示, 和 的 MbaA 蛋白具有相似的二级结构和功能结构域,而它们的 NspS 蛋白在一些残基上存在差异,这些残基在后者物种中与多胺识别有关。NspS-MbaA 同源物存在于一小部分与真核生物相互作用的土壤和水生细菌物种中。我们推测,NspS-MbaA 系统会根据环境或宿主植物产生的 PAs 来调节生物膜形成、EPS 产生和运动。