Morck D W, Merrill J K, Gard M S, Olson M E, Nation P N
Department of Biological Sciences, University of Calgary, Alberta.
Can J Vet Res. 1997 Jul;61(3):187-92.
Twenty four (24) healthy male Holstein calves (< 70 kg) were each experimentally infected by intrabronchial inoculation of 4.0 x 10(9) viable cells of Pasteurella haemolytica-AI (B122) at Time = 0 h. At 1 h following inoculation animals received either: 1) Sham treatment with sterile 0.85% saline SC (n = 12); or 2) a single injection of 10 mg tilmicosin per kg body weight (n = 12). Calves that were non-infected and tilmicosin-treated were also included for determining tilmicosin concentrations in serum and lung tissue at 1, 2, 4, 6, 8, 24, 48, and 72 h (n = 3-per time). In the infected calves, response to therapy was monitored clinically. Serum samples were collected for determination of tilmicosin concentrations using HPLC. Any animal becoming seriously ill was humanely killed. Complete necropsy examinations were performed on all animals and included gross pathologic changes, bacteriologic analysis, histopathology, and determination of pulmonary concentrations of tilmicosin. Tilmicosin treated animals responded significantly better to therapy than saline-treated control calves. Clinical assessment of calves during the study indicated that tilmicosin-treated calves had significantly improved by T = 8 h compared to satine-treated animals (P < 0.05). At necropsy tilmicosin-treated calves had significantly less severe gross and histological lesions (P < 0.05) of the pulmonary tissue. Of the 12 saline-treated calves, 92% (11/12) had Pasteurella haemolytica-A1 in lung tissue, while of the tilmicosin-treated calves 0% (0/12) cultured positive for P. haemolytica. Mean (+/- standard error) serum tilmicosin concentrations in infected calves peaked at 1 h post-injection (1.10 +/- 0.06 micrograms/mL) and rapidly decreased to 0.20 +/- 0.03 microgram/mL, well below the MIC of 0.50 microgram/mL for P. haemolytica-A1 (B122), by 12 h. These serum concentrations were very similar to serum concentrations of tilmicosin in non-infected tilmicosin-treated calves. Lung tissue concentrations of the antibiotic were comparatively high, even at 72 h post-infection (6.50 +/- 0.75 ppm). Lung tissue concentrations at 72 h were significantly higher in experimentally infected calves than in non-infected tilmicosin-treated animals (P < 0.05). These data demonstrate that tilmicosin was effective in treating experimentally-induced pneumonic pasteurellosis as determined by alleviation of clinical signs, pathological findings at post mortem, and presence of viable bacteria from the lung. Concentrations substantially above MIC for P. haemolytica were present in lung tissue even at 72 h following a single subcutaneous injection of 10 mg tilmicosin per kg body weight.
24头健康的雄性荷斯坦犊牛(体重<70千克)在时间为0小时时,通过支气管内接种4.0×10⁹个溶血性巴氏杆菌-AI(B122)活细胞进行实验性感染。接种后1小时,动物被分为两组:1)用无菌0.85%生理盐水皮下注射进行假处理(n = 12);2)每千克体重单次注射10毫克替米考星(n = 12)。未感染且接受替米考星治疗的犊牛也被纳入,用于在1、2、4、6、8、24、48和72小时测定血清和肺组织中的替米考星浓度(每个时间点n = 3)。对感染的犊牛进行临床治疗反应监测。采集血清样本,使用高效液相色谱法测定替米考星浓度。任何病情严重的动物均被人道处死。对所有动物进行完整的尸检,包括大体病理变化、细菌学分析、组织病理学以及测定肺组织中替米考星的浓度。与生理盐水处理的对照犊牛相比,替米考星治疗的动物对治疗反应明显更好。研究期间对犊牛的临床评估表明,与生理盐水处理的动物相比,替米考星治疗的犊牛在T = 8小时时病情显著改善(P < 0.05)。尸检时,替米考星治疗的犊牛肺组织的大体和组织学病变明显较轻(P < 0.05)。在12头生理盐水处理的犊牛中,92%(11/12)的肺组织中检测到溶血性巴氏杆菌-A1,而替米考星治疗的犊牛中0%(0/12)培养出溶血性巴氏杆菌阳性。感染犊牛血清中替米考星浓度平均值(±标准误差)在注射后1小时达到峰值(1.10±0.06微克/毫升),并迅速下降至0.20±0.03微克/毫升,到12小时时远低于溶血性巴氏杆菌-A1(B122)的最低抑菌浓度0.50微克/毫升。这些血清浓度与未感染且接受替米考星治疗的犊牛血清中的替米考星浓度非常相似。即使在感染后72小时,抗生素在肺组织中的浓度相对较高(6.50±0.75 ppm)。实验感染犊牛在72小时时的肺组织浓度显著高于未感染且接受替米考星治疗的动物(P < 0.05)。这些数据表明,通过临床症状的缓解、死后病理检查结果以及肺中活菌的存在来判断,替米考星在治疗实验性诱导的肺炎型巴氏杆菌病方面是有效的。即使在每千克体重单次皮下注射10毫克替米考星72小时后,肺组织中替米考星的浓度仍大大高于溶血性巴氏杆菌的最低抑菌浓度。