Majzoub Marwan E, McElroy Kerensa, Maczka Michael, Thomas Torsten, Egan Suhelen
Centre for Marine Bio-Innovation, School of Biotechnology and Biomolecular Sciences, The University of New South Wales, Sydney, NSW, Australia.
Agriculture and Food, Commonwealth Scientific and Industrial Research Organisation, Canberra, ACT, Australia.
Front Microbiol. 2018 Nov 2;9:2601. doi: 10.3389/fmicb.2018.02601. eCollection 2018.
2.10 is an effective biofilm former and colonizer of marine surfaces and has the ability to outcompete other microbiota. During biofilm dispersal 2.10 produces heritable phenotypic variants, including those that have a reduced ability to inhibit the co-occurring bacterium . However, the genetic changes that underpin the phenotypic variation and what the ecological consequences are for variants within the population are unclear. To answer these questions we sequenced the genomes of strain NCV12a1, a biofilm variant of 2.10 with reduced inhibitory activity and the 2.10 WT parental strain. Genome wide analysis revealed point mutations in genes involved in synthesis of the antibacterial compound tropodithietic acid (TDA) and indirectly in extracellular polymeric substances (EPS) production. However, confocal laser scanning microscopy analyses found little differences in biofilm growth between 2.10 WT (parental) and NCV12a1. NCV12a1 was also not outcompeted in co-cultured biofilms with , despite its reduced inhibitory activity, rather these biofilms were thicker than those produced when the WT strain was co-cultured with . Notably, dispersal populations from biofilms of NCV12a1 had a higher proportion of WT-like morphotypes when co-cultured with . These observations may explain why the otherwise non-inhibiting variant persists in the presence of a natural competitor, adding to our understanding of the relative importance of genetic diversification in microbial biofilms.
2.10是一种有效的生物膜形成者和海洋表面的定殖者,有能力胜过其他微生物群。在生物膜扩散过程中,2.10产生可遗传的表型变体,包括那些抑制同时存在的细菌的能力降低的变体。然而,导致表型变异的基因变化以及种群内变体的生态后果尚不清楚。为了回答这些问题,我们对菌株NCV12a1(2.10的具有降低抑制活性的生物膜变体)和2.10野生型亲本菌株的基因组进行了测序。全基因组分析揭示了参与抗菌化合物 tropodithietic acid(TDA)合成以及间接参与细胞外聚合物(EPS)产生的基因中的点突变。然而,共聚焦激光扫描显微镜分析发现2.10野生型(亲本)和NCV12a1之间的生物膜生长几乎没有差异。尽管NCV12a1的抑制活性降低,但在与……的共培养生物膜中它也没有被胜过,相反,这些生物膜比野生型菌株与……共培养时产生的生物膜更厚。值得注意的是,当与……共培养时,来自NCV12a1生物膜的扩散群体中具有更高比例的野生型样形态型。这些观察结果可能解释了为什么原本无抑制作用的变体在存在天然竞争者的情况下仍然存在,这增加了我们对微生物生物膜中基因多样化相对重要性的理解。