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从囊性纤维化分离株,聚集泛菌Tx10 中分离得到的一种广谱抗菌天然产物。

A broad-spectrum antibacterial natural product from the cystic fibrosis isolate, Pantoea agglomerans Tx10.

机构信息

Department of Biology, University of Regina, 3737 Wascana Parkway, Regina, Saskatchewan, S4S0A2, Canada; Pasteur Institute, Paris, France.

Department of Biology, University of Regina, 3737 Wascana Parkway, Regina, Saskatchewan, S4S0A2, Canada.

出版信息

Microbiol Res. 2020 Aug;237:126479. doi: 10.1016/j.micres.2020.126479. Epub 2020 Apr 24.

Abstract

The prevalence of antibiotic-resistant Gram-positive and Gram-negative pathogens has prompted considerable efforts to identify new antibacterials. Here we show that Pantoea agglomerans Tx10-an isolate from the sputum sample of a cystic fibrosis patient-is a strong competitor that inhibits the growth of a wide range of Gram-positive and Gram-negative bacteria through the production of a secreted compound. A genetic screen to identify the genes involved in the production of this compound resulted in the delineation of a 6-gene biosynthetic cluster. We called this compound Pantoea Natural Product 2 (PNP-2). Assays with mutants deficient in PNP-2 production revealed they were still able to inhibit Erwinia amylovora, suggesting the production of a second antibiotic, which we identified as Pantocin A. We generated Pantocin A knockouts, and a PNP-2/Pantocin A double knockout and used these to evaluate the spectrum of activity of both natural products. We show that strains of Enterobacter, E. coli, Klebsiella, Kosakonia, Pseudocitrobacter, Salmonella, Staphylococcus, and Streptococcus as well as the majority of Pantoea strains assayed are susceptible to PNP-2, indicating a broad spectrum of activity, and potential for therapeutic development.

摘要

抗生素耐药性革兰氏阳性和革兰氏阴性病原体的流行促使人们做出了相当大的努力来识别新的抗菌药物。在这里,我们表明,成团泛菌 Tx10-一种从囊性纤维化患者的痰样中分离出来的菌株-是一种通过分泌一种化合物来抑制广泛的革兰氏阳性和革兰氏阴性细菌生长的强竞争者。一个用于鉴定产生这种化合物的基因的基因筛选导致了一个 6 基因生物合成簇的划定。我们将这种化合物称为 Pantoea 天然产物 2(PNP-2)。对缺乏 PNP-2 产生的突变体进行的测定表明,它们仍然能够抑制梨火疫病菌,这表明产生了第二种抗生素,我们将其鉴定为 Pantocin A。我们生成了 Pantocin A 的敲除突变体,以及 PNP-2/Pantocin A 的双敲除突变体,并利用这些突变体来评估这两种天然产物的活性谱。我们表明,肠杆菌、大肠杆菌、克雷伯氏菌、Kosakonia、Pseudocitrobacter、沙门氏菌、葡萄球菌和链球菌以及大多数测试的成团泛菌菌株都对 PNP-2 敏感,表明其具有广谱活性和治疗开发的潜力。

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