Balado Miguel, Puentes Beatriz, Couceiro Lucía, Fuentes-Monteverde Juan C, Rodríguez Jaime, Osorio Carlos R, Jiménez Carlos, Lemos Manuel L
Department of Microbiology and Parasitology, Institute of Aquaculture, University of Santiago de CompostelaSantiago de Compostela, Spain.
Department of Chemistry, Faculty of Sciences and Center for Advanced Scientific Research (CICA), University of A CoruñaA Coruña, Spain.
Front Cell Infect Microbiol. 2017 Aug 8;7:361. doi: 10.3389/fcimb.2017.00361. eCollection 2017.
subsp () is a that has a wide pathogenic potential against many marine animals and also against humans. Some strains of this bacterium acquire iron through the siderophore vibrioferrin. However, there are virulent strains that do not produce vibrioferrin, but they still give a strong positive reaction in the CAS test for siderophore production. In an search on the genome sequences of this type of strains we could not find any ORF which could be related to a siderophore system. To identify genes that could encode a siderophore-mediated iron acquisition system we used a mini-Tn transposon random mutagenesis approach. From more than 1,400 mutants examined, we could isolate a mutant (BP53) that showed a strong CAS reaction independently of the iron levels of the medium. In this mutant the transposon was inserted into the gene, which encodes an isocitrate dehydrogenase that participates in the tricarboxylic acid cycle. The mutant did not show any growth impairment in rich or minimal media, but it accumulated a noticeable amount of citrate (around 7 mM) in the culture medium, irrespective of the iron levels. The parental strain accumulated citrate, but in an iron-regulated fashion, being citrate levels 5-6 times higher under iron restricted conditions. In addition, a null mutant deficient in citrate synthase showed an impairment for growth at high concentrations of iron chelators, and showed almost no reaction in the CAS test. Chemical analysis by liquid chromatography of the iron-restricted culture supernatants resulted in a CAS-positive fraction with biological activity as siderophore. HPLC purification of that fraction yielded a pure compound which was identified as citrate from its MS and NMR spectral data. Although the production of another citrate-based compound with siderophore activity cannot be ruled out, our results suggest that secretes endogenous citrate and use it for iron scavenging from the cell environment.
亚种()是一种对许多海洋动物以及人类都具有广泛致病潜力的细菌。该细菌的一些菌株通过铁载体弧菌素获取铁。然而,存在一些不产生弧菌素的有毒菌株,但它们在铁载体产生的CAS试验中仍给出强阳性反应。在对这类菌株的基因组序列进行搜索时,我们未能找到任何与铁载体系统相关的开放阅读框。为了鉴定可能编码铁载体介导的铁获取系统的基因,我们采用了mini-Tn转座子随机诱变方法。从检测的1400多个突变体中,我们分离出一个突变体(BP53),该突变体无论培养基中铁的水平如何都显示出强烈的CAS反应。在这个突变体中,转座子插入到基因中,该基因编码参与三羧酸循环的异柠檬酸脱氢酶。该突变体在丰富或基本培养基中均未表现出任何生长受损,但无论铁水平如何,它在培养基中积累了大量的柠檬酸盐(约7 mM)。亲本菌株积累柠檬酸盐,但以铁调节的方式,在铁限制条件下柠檬酸盐水平高5-6倍。此外,柠檬酸合酶缺陷的无义突变体在高浓度铁螯合剂存在下生长受损,并且在CAS试验中几乎没有反应。对铁限制培养上清液进行液相色谱化学分析,得到一个具有铁载体生物活性的CAS阳性部分。对该部分进行HPLC纯化,得到一种纯化合物,根据其质谱和核磁共振光谱数据鉴定为柠檬酸盐。尽管不能排除产生另一种具有铁载体活性的基于柠檬酸盐的化合物的可能性,但我们的结果表明,分泌内源性柠檬酸盐并将其用于从细胞环境中清除铁。