Ladjouzi Rabia, Dussert Elodie, Teiar Radja, Belguesmia Yanath, Drider Djamel
UMR Transfrontalière BioEcoAgro, INRAe 1158, ICV-Institut Charles Viollette, University Lille, INRAE, University Liège, UPJV, YNCREA, University Artois, University Littoral Côte d'Opale, F-59000 Lille, France.
Antibiotics (Basel). 2023 Jul 14;12(7):1188. doi: 10.3390/antibiotics12071188.
Enterocin DD14 (EntDD14) is a two-peptide leaderless bacteriocin (LLB) produced by 14, a human strain isolated from meconium. Studies performed on EntDD14 enabled it to show its activity against Gram-positive bacteria such as , , , and . EntDD14 was also shown to potentiate the activity of different antibiotics such as erythromycin, kanamycin, and methicillin when assessed against methicillin-resistant (MRSA) in vitro and in vivo in the NMRI-F holoxenic mouse model. Additionally, EntDD14 has an antiviral activity and decreased the secretion of pro-inflammatory IL-6 and IL-8 in inflamed human intestinal Caco-2 cells. The genome of 14 was sequenced and annotated. Molecular tools such as Bagel4 software enabled us to locate a 6.7kb-EntDD14 cluster. Transport of EntDD14 outside of the cytoplasm was shown to be performed synergistically by a channel composed of two pleckstrin-homology-domain-containing proteins, namely DdE/DdF and the ABC transporter DdGHIJ. This latter could also protect the bacteriocinogenic strain against extracellular EntDD14. Here, we focus on academic data and potential therapeutic issues of EntDD14, as a model of two-peptide LLB.
肠球菌素DD14(EntDD14)是一种由从胎粪中分离出的人源菌株14产生的双肽无领导肽细菌素(LLB)。对EntDD14进行的研究表明,它对革兰氏阳性菌如[具体菌株1]、[具体菌株2]、[具体菌株3]和[具体菌株4]具有活性。在NMRI-F无菌小鼠模型中进行体外和体内实验时,EntDD14还被证明能增强不同抗生素如红霉素、卡那霉素和甲氧西林对耐甲氧西林金黄色葡萄球菌(MRSA)的活性。此外,EntDD14具有抗病毒活性,并能减少炎症人肠Caco-2细胞中促炎细胞因子IL-6和IL-8的分泌。对菌株14的基因组进行了测序和注释。诸如Bagel4软件等分子工具使我们能够定位一个6.7kb的EntDD14基因簇。EntDD14在细胞质外的转运被证明是由一种由两种含pleckstrin同源结构域的蛋白质组成的通道协同完成的,即DdE/DdF和ABC转运蛋白DdGHIJ。后者还可以保护产细菌素的菌株免受细胞外EntDD14的影响。在这里,我们将重点关注EntDD14作为双肽LLB模型的学术数据和潜在治疗问题。