Hatziioanou Diane, Gherghisan-Filip Cristina, Saalbach Gerhard, Horn Nikki, Wegmann Udo, Duncan Sylvia H, Flint Harry J, Mayer Melinda J, Narbad Arjan
Gut Health and Food Safety Institute Strategic Programme, Quadram Institute Bioscience, Colney, Norwich, NR4 7UA, UK.
John Innes Centre, Norwich Research Park, Norwich, NR4 7UA, UK.
Microbiology (Reading). 2017 Sep;163(9):1292-1305. doi: 10.1099/mic.0.000515. Epub 2017 Aug 31.
A novel lanC-like sequence was identified from the dominant human gut bacterium Blautia obeum strain A2-162. This sequence was extended to reveal a putative lantibiotic operon with biosynthetic and transport genes, two sets of regulatory genes, immunity genes, three identical copies of a nisin-like lanA gene with an unusual leader peptide, and a fourth putative lanA gene. Comparison with other nisin clusters showed that the closest relationship was to nisin U. B. obeum A2-162 demonstrated antimicrobial activity against Clostridium perfringens when grown on solid medium in the presence of trypsin. Fusions of predicted nsoA structural sequences with the nisin A leader were expressed in Lactococcus lactis containing the nisin A operon without nisA. Expression of the nisA leader sequence fused to the predicted structural nsoA1 produced a growth defect in L. lactis that was dependent upon the presence of biosynthetic genes, but failed to produce antimicrobial activity. Insertion of the nso cluster into L. lactis MG1614 gave an increased immunity to nisin A, but this was not replicated by the expression of nsoI. Nisin A induction of L. lactis containing the nso cluster and nisRK genes allowed detection of the NsoA1 pre-peptide by Western hybridization. When this heterologous producer was grown with nisin induction on solid medium, antimicrobial activity was demonstrated in the presence of trypsin against C. perfringens, Clostridium difficile and L. lactis. This research adds to evidence that lantibiotic production may be an important trait of gut bacteria and could lead to the development of novel treatments for intestinal diseases.
从占主导地位的人体肠道细菌奥氏布劳特氏菌A2-162菌株中鉴定出一种新的类lanC序列。该序列经扩展后揭示了一个假定的羊毛硫抗生素操纵子,其含有生物合成和转运基因、两组调控基因、免疫基因、三个带有异常前导肽的类乳链菌肽lanA基因的相同拷贝,以及第四个假定的lanA基因。与其他乳链菌肽簇比较表明,其与乳链菌肽U的关系最为密切。当在胰蛋白酶存在的情况下于固体培养基上生长时,奥氏布劳特氏菌A2-162对产气荚膜梭菌表现出抗菌活性。预测的nsoA结构序列与乳链菌肽A前导肽的融合体在不含nisA的含有乳链菌肽A操纵子的乳酸乳球菌中表达。与预测的结构nsoA1融合的乳链菌肽A前导序列的表达在乳酸乳球菌中产生了生长缺陷,该缺陷依赖于生物合成基因的存在,但未能产生抗菌活性。将nso簇插入乳酸乳球菌MG1614可增强对乳链菌肽A的免疫力,但nsoI的表达并未重现这一现象。对含有nso簇和nisRK基因的乳酸乳球菌进行乳链菌肽A诱导,可通过蛋白质免疫印迹杂交检测到NsoA1前体肽。当这种异源生产菌在乳链菌肽诱导下于固体培养基上生长时,在胰蛋白酶存在的情况下对产气荚膜梭菌、艰难梭菌和乳酸乳球菌表现出抗菌活性。这项研究进一步证明羊毛硫抗生素的产生可能是肠道细菌的一个重要特性,并可能导致肠道疾病新疗法的开发。