L'Hériteau F, Entenza J M, Lacassin F, Leport C, Glauser M P, Moreillon P
Service des Maladies Infectieuses et Tropicales, Hôpital Bichat-Claude Bernard, Paris, France.
Antimicrob Agents Chemother. 1995 Jul;39(7):1425-9. doi: 10.1128/AAC.39.7.1425.
RP 59500 is a new injectable streptogramin composed of two synergistic components (quinupristin and dalfopristin) which are active against a number of erythromycin-susceptible and -resistant gram-positive bacteria. The following experiments investigate the ability of RP 59500 to prevent experimental endocarditis due to either of two erythromycin-susceptible streptococcal isolates or their constitutively erythromycin-resistant Tn916 delta E transconjugants. RP 59500 had low MICs (0.125 to 0.5 mg/liter) for all four test organisms and was substantially bactericidal in vitro. Rats with catheter-induced aortic vegetations were given single-dose antibiotic prophylaxis 30 to 60 min before bacterial inoculation through a computerized pump system which permitted the simulation of drug kinetics for humans produced by either 7 mg of RP 59500 per kg of body weight or 1 g of vancomycin. Single-dose RP 59500 prophylaxis successfully prevented endocarditis due to both the erythromycin-susceptible parent strains and their erythromycin-resistant derivatives in rats challenged with the minimal inoculum infecting 90% of controls. In addition, RP 59500 also prevented infection in animals challenged with fivefold-larger inocula of the erythromycin-susceptible parent strains. Vancomycin successfully prevented endocarditis due to any of the four test organisms. These results underline the in vivo efficacy of RP 59500 against both erythromycin-susceptible and -resistant streptococci. Such good results against the resistant strains would not be expected with erythromycin or clindamycin, which are the standard macrolidelincosamide-streptogramin antibiotics used for endocarditis prophylaxis in humans. An oral form of RP 59500 which might advantageously replace some of the older prophylactic regimens is currently being developed.
RP 59500是一种新型注射用链阳菌素,由两种具有协同作用的成分(奎奴普丁和达福普汀)组成,对多种对红霉素敏感和耐药的革兰氏阳性菌具有活性。以下实验研究了RP 59500预防由两种对红霉素敏感的链球菌分离株或其组成型耐红霉素的Tn916 ΔE转接合子引起的实验性心内膜炎的能力。RP 59500对所有四种测试菌株的最低抑菌浓度(MIC)较低(0.125至0.5毫克/升),且在体外具有显著的杀菌作用。通过计算机泵系统在细菌接种前30至60分钟给予导管诱导主动脉赘生物的大鼠单剂量抗生素预防,该系统可模拟每千克体重7毫克RP 59500或1克万古霉素在人体内产生的药代动力学。单剂量RP 59500预防成功地预防了用最低接种量攻击大鼠时由对红霉素敏感的亲本菌株及其耐红霉素衍生物引起的心内膜炎,该接种量感染了90%的对照大鼠。此外,RP 59500还预防了用五倍量更大接种量的对红霉素敏感亲本菌株攻击的动物的感染。万古霉素成功地预防了由四种测试菌株中的任何一种引起的心内膜炎。这些结果强调了RP 59500对耐红霉素和敏感链球菌的体内疗效。对于红霉素或克林霉素来说,不会预期对耐药菌株有如此好的结果,而红霉素和克林霉素是用于人类心内膜炎预防的标准大环内酯-林可酰胺-链阳菌素类抗生素。目前正在研发一种口服形式的RP 59500,它可能会有利地取代一些较老的预防方案。