Zeidner Nordin S, Massung Robert F, Dolan Marc C, Dadey Eric, Gabitzsch Elizabeth, Dietrich Gabrielle, Levin Michael L
Division of Vector-Borne Infectious Diseases, Centers for Disease Control and Prevention, Fort Collins, CO 80522, USA.
Division of Viral and Rickettsial Diseases, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
J Med Microbiol. 2008 Apr;57(Pt 4):463-468. doi: 10.1099/jmm.0.47535-0.
Current prophylaxis for infected tick bites consists of personal protective measures directed towards ticks. This study compared the efficacy of a single oral dose of doxycycline with that of a single injection of sustained-release doxycycline in a model of Lyme borreliosis and Anaplasma phagocytophilum infection. Dosages of doxycycline were equilibrated based on previously determined peak plasma levels in mice [oral, 2.4 microg (ml plasma)(-1); sustained release, 1.9 microg (ml plasma)(-1)] determined 8 h after inoculation. In challenge experiments where five Borrelia burgdorferi-infected and five A. phagocytophilum-infected nymphs were used per mouse, only 20 and 30 % of mice were protected from B. burgdorferi and A. phagocytophilum infection, respectively, using oral doxycycline. In contrast, 100 % of mice receiving sustained-release doxycycline were protected from A. phagocytophilum infection, as indicated by real-time PCR of blood samples, quantitative PCR and culture isolation of spleen samples, and protected against B. burgdorferi infection as demonstrated by culture of ear, heart and bladder. Although 15-40 copies of A. phagocytophilum could be amplified from the spleens of mice treated with sustained-release doxycycline, no viable A. phagocytophilum from these spleens could be cultured in HL-60 cells. In contrast, 7/10 mice receiving oral doxycycline were PCR- and culture-positive for A. phagocytophilum, with copy numbers ranging from 800 to 10 000 within the spleen, as determined by quantitative PCR. Other correlates with A. phagocytophilum infection included a significant difference in spleen mass (mean of 110 mg for sustained-release treatment versus a mean of 230 mg for oral treatment) and the number of splenic lymphoid nodules (mean of 8 for sustained-release treatment versus mean of 12.5 for oral doxycycline) as determined by histopathology. These studies indicate that a single injection of a sustained-release formulation antibiotic may offer a viable prophylactic treatment option for multiple infectious agents in patients presenting with tick bites.
目前针对蜱虫叮咬感染的预防措施包括针对蜱虫的个人防护措施。本研究在莱姆病螺旋体和嗜吞噬细胞无形体感染模型中,比较了单次口服多西环素与单次注射缓释多西环素的疗效。根据先前测定的小鼠接种8小时后的血浆峰值水平(口服,2.4微克/毫升血浆;缓释,1.9微克/毫升血浆)平衡多西环素的剂量。在每只小鼠使用5只感染伯氏疏螺旋体和5只感染嗜吞噬细胞无形体若虫的攻毒实验中,使用口服多西环素时,分别只有20%和30%的小鼠免受伯氏疏螺旋体和嗜吞噬细胞无形体感染。相比之下,通过血液样本的实时PCR、脾脏样本的定量PCR和培养分离表明,接受缓释多西环素的小鼠中有100%免受嗜吞噬细胞无形体感染,并且通过耳部、心脏和膀胱培养证明可免受伯氏疏螺旋体感染。尽管在用缓释多西环素治疗的小鼠脾脏中可扩增出15 - 40拷贝的嗜吞噬细胞无形体,但这些脾脏中没有活的嗜吞噬细胞无形体能够在HL - 60细胞中培养。相比之下,接受口服多西环素的10只小鼠中有7只嗜吞噬细胞无形体PCR和培养呈阳性,通过定量PCR测定,脾脏中的拷贝数在800至10000之间。与嗜吞噬细胞无形体感染相关的其他因素包括脾脏质量的显著差异(缓释治疗的平均值为110毫克,口服治疗的平均值为230毫克)以及通过组织病理学确定的脾脏淋巴小结数量(缓释治疗的平均值为8个,口服多西环素的平均值为12.5个)。这些研究表明,对于出现蜱虫叮咬的患者,单次注射缓释制剂抗生素可能为多种感染病原体提供一种可行的预防性治疗选择。