Briers Yves, Lavigne Rob
Laboratory of Gene Technology, Department Biosystems, University of Leuven, Kasteelpark Arenberg 21, box 2462, B-3001 Leuven, Belgium.
Future Microbiol. 2015;10(3):377-90. doi: 10.2217/fmb.15.8.
The emergence and spread of antibiotic-resistant bacteria drives the search for novel classes of antibiotics to replenish our armamentarium against bacterial infections. This is particularly critical for Gram-negative pathogens, which are intrinsically resistant to many existing classes of antibiotics due to the presence of a protective outer membrane. In addition, the antibiotics development pipeline is mainly oriented to Gram-positive pathogens such as methicillin-resistant Staphylococcus aureus. A promising novel class of antibacterials is endolysins. These enzymes encoded by bacterial viruses hydrolyze the peptidoglycan layer with high efficiency, resulting in abrupt osmotic lysis and cell death. Their potential as novel antibacterials to treat Gram-positive bacteria has been extensively demonstrated; however, the Gram-negative outer membrane has presented a formidable barrier for the use of endolysins against Gram-negatives until recently. This review reports on the most recent advances in the development of endolysins to kill Gram-negative species with a special focus on endolysin-engineered Artilysins(®).
抗生素耐药菌的出现和传播促使人们寻找新型抗生素,以补充我们对抗细菌感染的武器库。这对于革兰氏阴性病原体尤为关键,由于其存在保护性外膜,这些病原体对许多现有类别的抗生素具有内在抗性。此外,抗生素研发渠道主要针对革兰氏阳性病原体,如耐甲氧西林金黄色葡萄球菌。一类有前景的新型抗菌剂是内溶素。这些由细菌病毒编码的酶高效水解肽聚糖层,导致突然的渗透裂解和细胞死亡。它们作为治疗革兰氏阳性菌的新型抗菌剂的潜力已得到广泛证明;然而,直到最近,革兰氏阴性外膜一直是使用内溶素对抗革兰氏阴性菌的巨大障碍。本综述报告了内溶素用于杀死革兰氏阴性菌的最新进展,特别关注经工程改造的内溶素Artilysins(®)。