Kerenga Bomai K, McKenna James A, Harvey Peta J, Quimbar Pedro, Garcia-Ceron Donovan, Lay Fung T, Phan Thanh Kha, Veneer Prem K, Vasa Shaily, Parisi Kathy, Shafee Thomas M A, van der Weerden Nicole L, Hulett Mark D, Craik David J, Anderson Marilyn A, Bleackley Mark R
Department of Biochemistry and Genetics, La Trobe Institute for Molecular Science, La Trobe University, Bundoora, VIC, Australia.
Division of Chemistry and Structural Biology, Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, Australia.
Front Microbiol. 2019 Apr 12;10:795. doi: 10.3389/fmicb.2019.00795. eCollection 2019.
Pathogenic microbes are developing resistance to established antibiotics, making the development of novel antimicrobial molecules paramount. One major resource for discovery of antimicrobials is the arsenal of innate immunity molecules that are part of the first line of pathogen defense in many organisms. Gene encoded cationic antimicrobial peptides are a major constituent of innate immune arsenals. Many of these peptides exhibit potent antimicrobial activity . However, a major hurdle that has impeded their development for use in the clinic is the loss of activity at physiological salt concentrations, attributed to weakening of the electrostatic interactions between the cationic peptide and anionic surfaces of the microbial cells in the presence of salt. Using plant defensins we have investigated the relationship between the charge of an antimicrobial peptide and its activity in media with elevated salt concentrations. Plant defensins are a large class of antifungal peptides that have remarkable stability at extremes of pH and temperature as well as resistance to protease digestion. A search of a database of over 1200 plant defensins identified ZmD32, a defensin from , with a predicted charge of +10.1 at pH 7, the highest of any defensin in the database. Recombinant ZmD32 retained activity against a range of fungal species in media containing elevated concentrations of salt. In addition, ZmD32 was active against biofilms as well as both Gram negative and Gram-positive bacteria. This broad spectrum antimicrobial activity, combined with a low toxicity on human cells make ZmD32 an attractive lead for development of future antimicrobial molecules.
致病微生物正在对现有的抗生素产生耐药性,因此开发新型抗菌分子至关重要。抗菌药物发现的一个主要资源是先天免疫分子库,这些分子是许多生物体病原体防御第一道防线的一部分。基因编码的阳离子抗菌肽是先天免疫武器库的主要组成部分。这些肽中的许多都表现出强大的抗菌活性。然而,阻碍它们在临床上应用的一个主要障碍是在生理盐浓度下活性丧失,这归因于在盐存在下阳离子肽与微生物细胞阴离子表面之间的静电相互作用减弱。我们利用植物防御素研究了抗菌肽电荷与其在高盐浓度培养基中活性之间的关系。植物防御素是一大类抗真菌肽,在极端的pH值和温度下具有显著的稳定性,并且对蛋白酶消化具有抗性。在一个包含1200多种植物防御素的数据库中搜索,发现了来自玉米的ZmD32防御素,在pH 7时预测电荷为+10.1,是该数据库中所有防御素中电荷最高的。重组ZmD32在含有高浓度盐的培养基中对一系列真菌物种保持活性。此外,ZmD32对生物膜以及革兰氏阴性菌和革兰氏阳性菌均有活性。这种广谱抗菌活性,加上对人类细胞的低毒性,使ZmD32成为未来抗菌分子开发的一个有吸引力的先导物。