Merrigan Michelle M, Sambol Susan P, Johnson Stuart, Gerding Dale N
Research Service, Edward Hines Jr. Veterans Affairs Hospital, Hines, IL 60141, USA.
Int J Antimicrob Agents. 2009 Mar;33 Suppl 1:S46-50. doi: 10.1016/S0924-8579(09)70017-2.
Non-toxigenic strains of Clostridium difficile are highly effective in preventing toxigenic C. difficile infection in hamsters when given following a single dose of an antimicrobial agent. The goal of this study was to determine the ability of non-toxigenic C. difficile to colonise hamsters during administration of an antibiotic to which the organisms are resistant - ceftriaxone - and an antibiotic to which they are susceptible - ampicillin - and to determine if non-toxigenic colonisation is protective against toxigenic strain challenge. Groups of four or five hamsters were administered daily ceftriaxone 60 mg/kg/d intraperitoneally or ampicillin 60 mg/kg/d orally for 5 days. Three non-toxigenic strains of C. difficile, M3, M23, and T7 (MICs 96-128 mg/L) were each given orally at a dose of 1 x 10(6) spores to groups of five animals 3h after the first dose of ceftriaxone. All animals were colonised successfully by day 3 of the study and when challenged with 1 x 10(6) spores of toxigenic strain J9 (MIC >256 mg/L) on day 3 all animals survived, whereas the control animal given ceftriaxone, but not non-toxigenic C. difficile, died within 48h of challenge. When groups of four hamsters were given ampicillin, administration of non-toxigenic strain M3 (MIC 2 mg/L) or toxigenic strain J9 (MIC 0.75 mg/L) at 1 x 10(6) spores did not result in any colonisation or infection of the animals until day 8, 3 days after the last ampicillin dose. A protection study was designed by giving M3 spores to groups of five animals daily for 5 days beginning on day 1, 3, or 5 of ampicillin. Toxigenic challenge was given with J9 spores on day 3 of each M3 regimen. M3 colonised all animals by day 8 and none became infected with J9. Colonisation by non-toxigenic C. difficile is an effective prevention strategy during antibiotic administration of ceftriaxone or ampicillin, but multiple-day administration is required for ampicillin and colonisation does not occur until several days after the drug is discontinued.
在单次给予抗菌药物后给予艰难梭菌非产毒菌株,对预防仓鼠产毒艰难梭菌感染非常有效。本研究的目的是确定非产毒艰难梭菌在给予该菌耐药的抗生素(头孢曲松)和敏感的抗生素(氨苄西林)期间在仓鼠体内定殖的能力,并确定非产毒菌株定殖是否能保护仓鼠免受产毒菌株的攻击。将四五只仓鼠分为一组,每天腹腔注射头孢曲松60mg/kg/d或口服氨苄西林60mg/kg/d,持续5天。在首次给予头孢曲松3小时后,将三株非产毒艰难梭菌菌株M3、M23和T7(最低抑菌浓度为96 - 128mg/L)分别以1×10(6)个孢子的剂量口服给予五组动物。在研究的第3天,所有动物均成功定殖,并且在第3天用1×10(6)个产毒菌株J9(最低抑菌浓度>256mg/L)的孢子进行攻击时,所有动物均存活,而仅给予头孢曲松但未给予非产毒艰难梭菌的对照动物在攻击后48小时内死亡。当给四组仓鼠给予氨苄西林时,以1×10(6)个孢子的剂量给予非产毒菌株M3(最低抑菌浓度2mg/L)或产毒菌株J9(最低抑菌浓度0.75mg/L),直到最后一剂氨苄西林给药3天后的第8天才导致动物出现任何定殖或感染。设计了一项保护研究,从氨苄西林给药的第1天、第3天或第5天开始,连续5天每天给五组动物给予M3孢子。在每种M3给药方案的第3天用J9孢子进行产毒攻击。到第8天,M3定殖了所有动物,且没有动物感染J9。在给予头孢曲松或氨苄西林抗生素期间,非产毒艰难梭菌定殖是一种有效的预防策略,但氨苄西林需要多天给药,并且在停药几天后才会发生定殖。