CBR Division, Defence Science and Technology Laboratory (Dstl), Porton Down, Salisbury, Wiltshire, United Kingdom.
Q3 Analytical Ltd., Porton Science Park, Porton Down, Salisbury, United Kingdom.
Antimicrob Agents Chemother. 2022 Nov 15;66(11):e0070822. doi: 10.1128/aac.00708-22. Epub 2022 Oct 13.
Burkholderia pseudomallei is the causative agent of melioidosis and presents with diverse clinical manifestations. Naturally occurring infection occurs following contamination of cuts or skin abrasions, or ingestion of contaminated water, and occasionally through inhalational of infected soil or water particles. The influence of the route of disease acquisition on the efficacy of medical countermeasures has not been explored in humans or in appropriate animal models. The efficacy of co-trimoxazole against melioidosis acquired by different routes of exposure was assessed in postexposure prophylaxis (PEP) and treatment studies in marmoset models of melioidosis. Following challenge with B. pseudomallei by the inhalational, subcutaneous, or ingestion routes of administration, animals were given co-trimoxazole at 12 hourly intervals for 14 days, starting either 6 h postchallenge or at the onset of fever. Animals were then observed for 28 days. All animals that received antibiotic 6 h postchallenge survived the duration of dosing. All animals that received antibiotics at the onset of fever completed the treatment, but 10%, 57%, and 60% of those with ingestion, subcutaneous, and inhalation challenge relapsed, respectively. Bacteriological and histological differences were observed between placebo-control animals and those that relapsed. Immunological profiles indicate difference between animals given placebo and those that relapsed or survived the duration of the study. A broad T-cell activation was observed in animals that survived. Overall, these data suggest the efficacy of co-trimoxazole, as measured in the incidence of relapse, differs depending on the disease-acquisition route. Therefore, there are implications in treating this disease in regions of endemicity.
类鼻疽伯克霍尔德菌是类鼻疽病的病原体,具有多种临床表现。自然感染是通过污染的切口或皮肤擦伤,或摄入受污染的水,偶尔通过吸入受感染的土壤或水颗粒而发生的。疾病获取途径对医疗对策疗效的影响尚未在人类或适当的动物模型中进行探索。在类鼻疽猴模型的暴露后预防(PEP)和治疗研究中,评估了复方新诺明对不同暴露途径获得的类鼻疽病的疗效。通过吸入、皮下或口服途径用 B. pseudomallei 进行攻击后,动物在挑战后 6 小时或发热开始时每 12 小时接受复方新诺明治疗 14 天。然后观察动物 28 天。所有在接受抗生素治疗后 6 小时接受挑战的动物都存活了整个治疗过程。所有在发热时接受抗生素治疗的动物都完成了治疗,但接受口服、皮下和吸入挑战的动物中分别有 10%、57%和 60%复发。在安慰剂对照动物和复发动物之间观察到细菌学和组织学差异。免疫谱表明,接受安慰剂的动物与复发或完成研究持续时间的动物之间存在差异。存活的动物观察到广泛的 T 细胞激活。总体而言,这些数据表明,复方新诺明的疗效(以复发率衡量)因疾病获取途径而异。因此,在流行地区治疗这种疾病存在影响。