Shadomy S, Robertson G M, Shadomy H J, Utz J P, Gamble E
J Bacteriol. 1969 Feb;97(2):481-7. doi: 10.1128/jb.97.2.481-487.1969.
Clinical responses of patients with blastomycosis to treatment with hamycin have been variable. An explanation for this was sought in a series of studies in which in vitro and in vivo susceptibilities to hamycin of five strains of Blastomyces dermatitidis were compared. Minimal inhibitory concentrations of hamycin for the five strains indicated uniformly high levels of in vitro susceptibility (0.008 to 0.016 mug/ml). In vivo activity was measured in infected mice treated intraperitoneally for a period of 28 days with doses of the drug ranging from 0.001 to 0.030 mg per mouse. Significant differences in response to treatment among the five strains were noted (P < 0.001), and protective doses were found to vary from 0.001 to >0.030 mg per mouse per day. Further observations of infected mice after treatment revealed marked rates of relapsing infection, and several strains caused death. Persistent inapparent infections were also detected on culture of selected organs. Toxicity due to hamycin alone was not observed. These results suggest that variations in clinical responses to hamycin therapy in treatment of blastomycosis reflect differences in pathogenesis and host response in vivo to the infecting organism rather than differences in susceptibility of B. dermatitidis to hamycin.
芽生菌病患者对哈霉素治疗的临床反应各不相同。在一系列研究中对此进行了探究,这些研究比较了五株皮炎芽生菌对哈霉素的体外和体内敏感性。哈霉素对这五株菌的最低抑菌浓度表明其体外敏感性均较高(0.008至0.016微克/毫升)。在感染小鼠体内进行活性测定,用剂量范围为每只小鼠0.001至0.030毫克的药物腹腔内给药28天。注意到五株菌对治疗的反应存在显著差异(P<0.001),且发现保护剂量为每只小鼠每天0.001至>0.030毫克不等。治疗后对感染小鼠的进一步观察发现复发感染率很高,有几株菌导致了死亡。在所选器官的培养中也检测到了持续的隐性感染。未观察到仅由哈霉素引起的毒性。这些结果表明,芽生菌病治疗中对哈霉素治疗的临床反应差异反映了体内发病机制和宿主对感染生物体反应的差异,而非皮炎芽生菌对哈霉素敏感性的差异。