Cell and Molecular Biology Program, University of Arkansas, Fayetteville, AR, 72701, USA.
Present address: Department of Microbiology and Immunology, University of Iowa, Iowa City, IA, 52242, USA.
BMC Genom Data. 2022 Jul 22;23(1):55. doi: 10.1186/s12863-022-01069-3.
Iron is a crucial element for bacterial survival and virulence. During Salmonella infection, the host utilizes a variety of mechanisms to starve the pathogen from iron. However, Salmonella activates distinctive defense mechanisms to acquire iron and survive in iron-restricted host environments. Yet, the comprehensive set of the conditionally essential genes that underpin Salmonella survival under iron-restricted niches has not been fully explored.
Here, we employed transposon sequencing (Tn-seq) method for high-resolution elucidation of the genes in Salmonella Typhimurium (S. Typhimurium) 14028S strain required for the growth under the in vitro conditions with four different levels of iron restriction achieved by iron chelator 2,2'-dipyridyl (Dip): mild (100 and 150 μM), moderate (250 μM) and severe iron restriction (400 μM). We found that the fitness of the mutants reduced significantly for 28 genes, suggesting the importance of these genes for the growth under iron restriction. These genes include sufABCDSE, iron transport fepD, siderophore tonB, sigma factor E ropE, phosphate transport pstAB, and zinc exporter zntA. The siderophore gene tonB was required in mild and moderate iron-restricted conditions, but it became dispensable in severe iron-restricted conditions. Remarkably, rpoE was required in moderate and severe iron restrictions, leading to complete attenuation of the mutant under these conditions. We also identified 30 genes for which the deletion of the genes resulted in increased fitness under iron-restricted conditions.
The findings broaden our knowledge of how S. Typhimurium survives in iron-deficient environments, which could be utilized for the development of new therapeutic strategies targeting the pathways vital for iron metabolism, trafficking, and scavenging.
铁是细菌生存和毒力的关键元素。在沙门氏菌感染过程中,宿主利用多种机制使病原体缺铁。然而,沙门氏菌激活了独特的防御机制来获取铁,并在缺铁的宿主环境中存活。然而,尚未充分探索支持沙门氏菌在铁限制生态位中生存的条件必需基因的综合组。
在这里,我们采用转座子测序(Tn-seq)方法,高分辨率地阐明了沙门氏菌 Typhimurium(S. Typhimurium)14028S 菌株在体外条件下生长所需的基因,这些条件通过铁螯合剂 2,2'-二吡啶(Dip)实现了 4 个不同水平的铁限制:轻度(100 和 150 μM)、中度(250 μM)和严重铁限制(400 μM)。我们发现 28 个基因的突变体适应度显著降低,表明这些基因对铁限制下的生长很重要。这些基因包括 sufABCDSE、铁转运 fepD、铁载体 tonB、σ因子 E ropE、磷酸盐转运 pstAB 和锌外排 zntA。铁载体基因 tonB 在轻度和中度铁限制条件下是必需的,但在严重铁限制条件下则不再必需。值得注意的是,rpoE 在中度和严重铁限制下是必需的,导致突变体在这些条件下完全衰减。我们还鉴定了 30 个基因,这些基因的缺失导致在铁限制条件下适应性增加。
这些发现拓宽了我们对沙门氏菌如何在缺铁环境中生存的认识,这可能有助于开发针对铁代谢、运输和清除至关重要的途径的新治疗策略。