Genomic and phenotypic insights into Serratia interaction with plants from an ecological perspective.

IF 1.9 4区 生物学 Q3 MICROBIOLOGY Brazilian Journal of Microbiology Pub Date : 2025-06-01 Epub Date: 2025-03-25 DOI:10.1007/s42770-025-01652-7
Ubiana C Mourão Silva, Daliane R C da Silva, Sara Cuadros-Orellana, Leandro M Moreira, Laura R Leite, Julliane D Medeiros, Erica B Felestrino, Washington L Caneschi, Nalvo F Almeida, Robson S Silva, Christiane A Oliveira-Paiva, Vera Lúcia Dos Santos
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Abstract

We investigated the plant growth-promoting potential of two endophytic strains of Serratia marcescens, namely SmCNPMS2112 and SmUFMG85, which were isolated from the roots of the same maize (Zea mays) plant. The strains were evaluated in vitro for their ability to produce siderophores and indoleacetic acid, form biofilm, solubilize iron phosphate (Fe-P) and Araxá rock phosphate (RP), mineralize phytate, and for their ability to adhere and colonize host roots. Additionally, their plant growth-promoting potential was tested in vivo under greenhouse conditions using millet grown in soil under two fertilization schemes (triple superphosphate, TSP, or commercial rock phosphate, cRP). Both strains improved at least five physiological traits of millet or P content in soil. In order to elucidate the genetic basis of the plant growth-promoting ability of these strains, their genomes were compared. While both genomes exhibited a similar overall functional profile, each strain had unique features. SmCNPMS2112 contained genes related to arsenic and aromatic hydrocarbons degradation, whereas SmUFMG85 harbored genes related to rhamnolipid biosynthesis and chromium bioremediation. Also, we observe a unique repertoire of genes related to plant growth-promotion (PGP) in the SmUFMG85 genome, including oxalate decarboxylase (OxdC), associated with the catabolism of oxalic acid, and aerobactin siderophore (lucD) in the genome of SmCNPMS2112. The alkaline phosphatase was observed on two strains, but acid phosphatase was exclusive to SmUFMG85. Eighteen secondary metabolic gene clusters, such as those involved in the biosynthesis of macrolides and bacillomycin, among others, occur in both strains. Moreover, both genomes contained prophages, suggesting that viral-mediated horizontal gene transfer may be a key mechanism driving genomic variability in the endophytic environment. Indeed, the most genes unique and accessory of SmUFMG85 and SmCNPMS2112 were localized in genomic islands, highlighting genome plasticity and its underlying drivers. To investigate the ecological distribution of plant-interaction traits in the genus Serratia, the genomes of SmUFMG85 and SmCNPMS2112 strains were compared with those of other 19 Serratia strains of different species, which were isolated from different environments. We observe that many features for PGP are present in all genomes, regardless of niche, for instance: formation of flagella, fimbriae and pili, chemotaxis, biosynthesis of siderophores, indole-3-acetic acid (IAA) and volatile organic (VOC) and inorganic (VIC) compounds, such as acetoin and HCN. Also, all the analyzed genomes show an antimicrobial resistance repertoire of genes that confer resistance to several antibiotics belonging to the groups of aminoglycosides and quinolones, for instance. Also, from a niche partitioning perspective, secretion system preference and the ability to produce exopolysaccharides involved in biofilm formation are among the features that vary the most among strains, and most likely influence niche adaptation in Serratia spp., even though only the latter seems to be a feature specifically associated with virulence in the analyzed strains. Our results show that populations of bacteria sharing the same niche can present significant physiological and genomic differences, and reveal the intraspecific metabolic plasticity that underlie plant-bacteria interactions. Also, this study reveals the potential of two Serratia marcescens strains as bioinoculants in agriculture. Considering that Serratia spp. are regarded as low risk biological agents, despite the fact that they can be associated with human disease, we suggest that strain biosafety be evaluated using a combination of genome and phenotypic analyses, as presented herein.

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从生态学角度研究沙雷菌与植物相互作用的基因组和表型。
研究了从同一株玉米(Zea mays)根中分离得到的粘质沙雷菌内生菌株SmCNPMS2112和SmUFMG85对植物生长的促进作用。研究人员在体外对这些菌株的产铁载体和吲哚乙酸、形成生物膜、溶解磷酸铁(Fe-P)和磷酸arax岩(RP)、矿化植酸的能力以及对寄主根系的粘附和定植能力进行了评估。此外,在温室条件下,利用谷子在土壤中生长,在两种施肥方案(三重过磷酸钙,TSP或商业磷矿粉,cRP)下测试了它们的植物生长促进潜力。两个品系至少改善了谷子的5个生理性状或土壤磷含量。为了阐明这些菌株促进植物生长能力的遗传基础,对它们的基因组进行了比较。虽然两个基因组显示出相似的整体功能概况,但每个菌株都有独特的特征。SmCNPMS2112含有与砷和芳烃降解相关的基因,而SmUFMG85含有与鼠李糖脂生物合成和铬生物修复相关的基因。此外,我们还观察到SmUFMG85基因组中与植物生长促进(PGP)相关的独特基因库,包括与草酸分解代谢相关的草酸脱羧酶(OxdC)和SmCNPMS2112基因组中的有氧肌动蛋白铁载体(lucD)。两株菌株均有碱性磷酸酶,而SmUFMG85只具有酸性磷酸酶。18个次级代谢基因簇,如参与大环内酯类和芽孢杆菌素等生物合成的基因簇,在这两种菌株中都存在。此外,这两个基因组都含有前噬菌体,这表明病毒介导的水平基因转移可能是内生环境中驱动基因组变异的关键机制。事实上,SmUFMG85和SmCNPMS2112的大多数独特和辅助基因都定位在基因组岛中,这突出了基因组可塑性及其潜在驱动因素。为研究沙雷氏菌属植物互作性状的生态分布,将SmUFMG85和SmCNPMS2112菌株与其他19株不同种类、不同环境分离的沙雷氏菌进行了基因组比较。我们观察到,PGP的许多特征存在于所有基因组中,无论其生态位如何,例如:鞭毛,毛和毛的形成,趋化性,铁载体,吲哚-3-乙酸(IAA)和挥发性有机(VOC)和无机(VIC)化合物的生物合成,如乙酰胆碱和HCN。此外,所有分析的基因组都显示出抗微生物药物耐药性的基因库,例如,这些基因赋予了对氨基糖苷类和喹诺酮类抗生素的耐药性。此外,从生态位分配的角度来看,分泌系统偏好和产生参与生物膜形成的外多糖的能力是菌株之间差异最大的特征之一,最有可能影响沙雷氏菌的生态位适应,尽管在所分析的菌株中,只有后者似乎是与毒力特异性相关的特征。我们的研究结果表明,共享同一生态位的细菌群体可以呈现显着的生理和基因组差异,并揭示了植物-细菌相互作用背后的种内代谢可塑性。此外,本研究还揭示了两种粘质沙雷菌菌株作为农业生物接种剂的潜力。考虑到沙雷氏菌被认为是低风险的生物制剂,尽管它们可能与人类疾病有关,我们建议使用基因组和表型分析相结合的方法来评估菌株的生物安全性,如本文所述。
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来源期刊
Brazilian Journal of Microbiology
Brazilian Journal of Microbiology 生物-微生物学
CiteScore
4.10
自引率
4.50%
发文量
216
审稿时长
1.0 months
期刊介绍: The Brazilian Journal of Microbiology is an international peer reviewed journal that covers a wide-range of research on fundamental and applied aspects of microbiology. The journal considers for publication original research articles, short communications, reviews, and letters to the editor, that may be submitted to the following sections: Biotechnology and Industrial Microbiology, Food Microbiology, Bacterial and Fungal Pathogenesis, Clinical Microbiology, Environmental Microbiology, Veterinary Microbiology, Fungal and Bacterial Physiology, Bacterial, Fungal and Virus Molecular Biology, Education in Microbiology. For more details on each section, please check out the instructions for authors. The journal is the official publication of the Brazilian Society of Microbiology and currently publishes 4 issues per year.
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