Steinberg D A, Hurst M A, Fujii C A, Kung A H, Ho J F, Cheng F C, Loury D J, Fiddes J C
IntraBiotics Pharmaceuticals, Inc., Sunnyvale, California 94086, USA.
Antimicrob Agents Chemother. 1997 Aug;41(8):1738-42. doi: 10.1128/AAC.41.8.1738.
Protegrin-1 (PG-1) is a cysteine-rich, 18-residue beta-sheet peptide isolated from porcine leukocytes with antimicrobial activity against a broad range of microorganisms. The MICs of PG-1 against representative gram-positive and gram-negative bacteria ranged from 0.12 to 2 microg/ml. At these levels, PG-1 was rapidly bactericidal in vitro, reducing the number of viable CFU of either methicillin-resistant Staphylococcus aureus (MRSA) or Pseudomonas aeruginosa by more than three log units in less than 15 min. Resistance to PG-1 did not develop after 11 subculturings of P. aeruginosa or 18 subcultures of MRSA in Mueller-Hinton broth containing PG-1 at one-half the MIC. Under similar conditions of serial passage, the MICs of norfloxacin and gentamicin against P. aeruginosa increased 10 and 190 times, respectively. Similarly, the MIC of norfloxacin against MRSA increased 85 times. Immunocompetent mice inoculated intraperitoneally (i.p.) with P. aeruginosa or S. aureus exhibited 93 to 100% mortality in the vehicle control group compared with 0 to 27% mortality in animals that received a single i.p. injection of PG-1 (0.5 mg/kg of body weight). Mice inoculated with S. aureus by intravenous (i.v.) injection and dosed 0 to 60 min later with a single i.v. injection of PG-1 (5 mg/kg) had a mortality of 7 to 33%, compared to a mortality of 73 to 93% in the vehicle controls. In leukopenic mice inoculated i.v. with vancomycin-resistant Enterococcus faecium, mortality was 87% in the vehicle control group and 33% in animals that received a single i.v. injection of PG-1 (2.5 mg/kg). Taken together, these data indicate that PG-1 has potential for use as an antimicrobial agent in the treatment of local or systemic infections caused by clinically relevant pathogens.
防御素-1(PG-1)是一种富含半胱氨酸的、由18个氨基酸残基组成的β-折叠肽,从猪白细胞中分离得到,对多种微生物具有抗菌活性。PG-1对代表性革兰氏阳性菌和革兰氏阴性菌的最低抑菌浓度(MIC)范围为0.12至2微克/毫升。在这些浓度下,PG-1在体外具有快速杀菌作用,在不到15分钟内可使耐甲氧西林金黄色葡萄球菌(MRSA)或铜绿假单胞菌的活菌菌落形成单位(CFU)数量减少超过三个对数单位。在含有PG-1且浓度为MIC一半的穆勒-欣顿肉汤中,铜绿假单胞菌传代11次或MRSA传代18次后均未产生对PG-1的耐药性。在类似的连续传代条件下,诺氟沙星和庆大霉素对铜绿假单胞菌的MIC分别增加了10倍和190倍。同样,诺氟沙星对MRSA的MIC增加了85倍。经腹腔注射(i.p.)接种铜绿假单胞菌或金黄色葡萄球菌的免疫活性小鼠,在溶剂对照组中的死亡率为93%至100%,而接受单次腹腔注射PG-1(0.5毫克/千克体重)的动物死亡率为0至27%。通过静脉注射(i.v.)接种金黄色葡萄球菌并在0至60分钟后单次静脉注射PG-1(5毫克/千克)的小鼠,死亡率为7%至33%,而溶剂对照组的死亡率为73%至93%。在经静脉注射接种耐万古霉素屎肠球菌的白细胞减少小鼠中,溶剂对照组的死亡率为87%,接受单次静脉注射PG-1(2.5毫克/千克)的动物死亡率为33%。综上所述,这些数据表明PG-1有潜力作为抗菌剂用于治疗由临床相关病原体引起的局部或全身感染。