Life Sciences College of Nanjing Agricultural University, Nanjing 210095, Jiangsu, China.
Gene. 2012 Jan 25;492(2):368-74. doi: 10.1016/j.gene.2011.11.009. Epub 2011 Nov 10.
A novel cathelicidin-like antimicrobial peptide was identified by mining genome of panda. This peptide (cathelicidin-AM) was synthesized. It showed potential antimicrobial activities against wide spectrum of microorganisms including Gram-negative and -positive bacteria, and fungi. It had similar antimicrobial abilities against both standard and clinically isolated drug-resistant strains. Cathelicidin-AM could rapidly exert its antibacterial activities. It just took less than 1h to kill all Staphylococcus sciuri at the concentration of 2, 4 or 10 times of minimal inhibitory concentration (MIC) while clindamycin took 6h. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) analysis indicated that cathelicidin-AM killed bacteria by directly affecting bacterial cell wall and membrane. Phylogenetic analysis revealed that the panda cathelicidin had the nearest evolution relationship with dog cathelicidin. The current work provides a novel cathelicidin-like peptide with strong antimicrobial abilities.
通过挖掘大熊猫基因组,鉴定出一种新型的抗菌肽 cathelicidin-AM。该肽被合成后,显示出对革兰氏阴性菌和革兰氏阳性菌以及真菌等多种微生物的潜在抗菌活性。它对标准菌株和临床分离的耐药菌株均具有相似的抗菌能力。cathelicidin-AM 能够迅速发挥其抗菌作用,在浓度为 2、4 或 10 倍最小抑菌浓度(MIC)时,只需不到 1 小时即可杀死所有屎肠球菌,而克林霉素则需要 6 小时。透射电子显微镜(TEM)和扫描电子显微镜(SEM)分析表明,cathelicidin-AM 通过直接影响细菌细胞壁和细胞膜来杀死细菌。系统发育分析表明,大熊猫 cathelicidin 与犬科 cathelicidin 具有最接近的进化关系。本研究提供了一种具有强抗菌能力的新型抗菌肽。