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首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Efficacy of several antibiotic combinations against Brucella melitensis Rev 1 experimental infection in BALB/c mice.
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Efficacy of several antibiotic combinations against Brucella melitensis Rev 1 experimental infection in BALB/c mice.

机译:几种抗生素组合对BALB / c小鼠中布鲁氏布鲁氏菌Rev 1实验性感染的功效。

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摘要

OBJECTIVES: The objective of the present study was to compare the efficacy of gentamicin given alone or combined with doxycycline with that of standard combination therapies in BALB/c mice experimentally infected with the Brucella melitensis vaccine strain Rev 1. METHODS: A standard broth microdilution method was applied to determine the susceptibility of strain Rev 1 to the clinically most relevant aminoglycosides. Eight groups of BALB/c mice were inoculated intraperitoneally (ip) with 1 x 10(6) cfu/mouse of strain Rev 1. While one group remained untreated, the other seven groups were treated 10 days later once a day for 14 days with (i) doxycycline given orally at 2 mg/day; (ii) streptomycin given ip at 0.4 mg/day; (iii) gentamicin given ip at 0.4 mg/day; (iv) rifampicin given orally at 0.5 mg/day; (v) doxycycline plus streptomycin; (vi) doxycycline plus gentamicin; and (vii) doxycycline plus rifampicin. The number of cfu per spleen and clearance of Rev 1 were assessed 34 days after inoculation. RESULTS: With the exception of streptomycin, strain Rev 1 was susceptible to all aminoglycosides tested. As expected, the combination doxycycline/streptomycin was ineffective against Rev 1 infection. In contrast, the combinations doxycycline/gentamicin and doxycycline/rifampicin were effective in the clearance of Rev 1 infection, but only the former improved significantly the therapeutic efficacy as compared with that of the antibiotics given alone. CONCLUSIONS: Gentamicin may be used along with doxycycline when the classical combination is considered the first choice in the treatment of patients with brucellosis due to B. melitensis vaccine strain Rev 1.
机译:目的:本研究的目的是比较庆大霉素单独或联合强力霉素与标准联合疗法在经布鲁氏杆菌疫苗菌株Rev 1感染的BALB / c小鼠中的疗效。方法:标准肉汤微量稀释法将其用于确定菌株Rev 1对临床上最相关的氨基糖苷的敏感性。向八组BALB / c小鼠腹膜内(ip)接种1 x 10(6)cfu /小鼠Rev 1品系腹膜内接种。一组仍未接受治疗,其余7组每天10天后接受一次,共14天。 (i)强力霉素每天2 mg口服; (ii)以0.4毫克/天的剂量腹膜内注射链霉素; (iii)庆大霉素,腹腔注射剂量为0.4毫克/天; (iv)利福平口服0.5毫克/天; (v)强力霉素加链霉素; (vi)强力霉素加庆大霉素; (vii)强力霉素加利福平。接种后34天评估每个脾脏的cfu数和Rev 1的清除率。结果:除链霉素外,菌株Rev 1对所有测试的氨基糖苷均敏感。如预期的那样,强力霉素/链霉素的组合对Rev 1感染无效。相反,强力霉素/庆大霉素和强力霉素/利福平的组合在清除Rev 1感染方面是有效的,但与单独使用抗生素相比,只有前者能显着提高治疗效果。结论:庆大霉素可与强力霉素同时使用,当经典组合被认为是治疗由布鲁氏杆菌疫苗菌株Rev 1引起的布鲁氏菌病患者的首选药物时。

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