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A MarR family transcriptional regulator and subinhibitory antibiotics regulate type VI secretion gene clusters in Burkholderia pseudomallei

机译:MarR家族的转录调节因子和亚抑制性抗生素调节假伯克霍尔德氏菌中的VI型分泌基因簇

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摘要

Burkholderia pseudomallei, the aetiological agent of melioidosis, is an inhabitant of soil and water in many tropical and subtropical regions worldwide. It possesses six distinct type VI secretion systems (T6SS-1 to T6SS-6), but little is known about most of them, as they are poorly expressed in laboratory culture media. A genetic screen was devised to locate a putative repressor of the T6SS-2 gene cluster and a MarR family transcriptional regulator, termed TctR, was identified. The inactivation of tctR resulted in a 50-fold increase in the expression of an hcp2–lacZ transcriptional fusion, indicating that TctR is a negative regulator of the T6SS-2 gene cluster. Surprisingly, the tctR mutation resulted in a significant decrease in the expression of an hcp6–lacZ transcriptional fusion. B. pseudomallei K96243 and a tctR mutant were grown to logarithmic phase in rich culture medium and RNA was isolated and sequenced in order to identify other genes regulated by TctR. The results identified seven gene clusters that were repressed by TctR, including T6SS-2, and three gene clusters that were significantly activated. A small molecule library consisting of 1120 structurally defined compounds was screened to identify a putative ligand (or ligands) that might bind TctR and derepress transcription of the T6SS-2 gene cluster. Seven compounds, six fluoroquinolones and one quinolone, activated the expression of hcp2–lacZ. Subinhibitory ciprofloxacin also increased the expression of the T6SS-3, T6SS-4 and T6SS-6 gene clusters. This study highlights the complex layers of regulatory control that B. pseudomallei utilizes to ensure that T6SS expression only occurs under very defined environmental conditions.
机译:类鼻疽病的病原体伯克霍尔德菌(Burkholderia pseudomallei)是全世界许多热带和亚热带地区土壤和水的栖息地。它拥有六个不同的VI型分泌系统(T6SS-1至T6SS-6),但由于它们在实验室培养基中的表达较差,因此对它们的了解很少。设计了遗传筛选来定位推定的T6SS-2基因簇的阻遏物,并鉴定了称为TctR的MarR家族转录调节子。 tctR的失活导致hcp2-lacZ转录融合体表达增加50倍,表明TctR是T6SS-2基因簇的负调控子。令人惊讶的是,tctR突变导致hcp6-lacZ转录融合蛋白的表达显着降低。假芽孢杆菌K96243和tctR突变体在丰富的培养基中生长至对数期,分离RNA并测序以鉴定受TctR调控的其他基因。结果确定了七个受TctR抑制的基因簇,包括T6SS-2,以及三个被显着激活的基因簇。筛选了由1120个结构定义的化合物组成的小分子文库,以鉴定可能结合TctR并抑制T6SS-2基因簇转录的推定配体。七种化合物(六种氟喹诺酮和一种喹诺酮)激活了hcp2-lacZ的表达。亚抑制环丙沙星还增加了T6SS-3,T6SS-4和T6SS-6基因簇的表达。这项研究强调了假苹果芽孢杆菌利用复杂的调控层来确保T6SS表达仅在非常明确的环境条件下发生。

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