Westman Eva, Lundin Susanne, Hermansson Ann, Melhus Asa
Department of Oto-Rhino-Laryngology, Umeå University Hospital, Umeå, Sweden.
Antimicrob Agents Chemother. 2004 Sep;48(9):3536-42. doi: 10.1128/AAC.48.9.3536-3542.2004.
Acute otitis media (AOM) is the most common reason for outpatient antimicrobial therapy. Mixed infections pose a potential problem, since the first-line drug used for the treatment of AOM, amoxicillin, can be neutralized by beta-lactamase-producing pathogens of the upper respiratory tract. To study the effects of a 5-day course of amoxicillin on a mixed middle ear infection, rats were challenged with Streptococcus pneumoniae alone or in combination with beta-lactamase-producing nontypeable Haemophilus influenzae. Amoxicillin was introduced at the clinical peak of the infection. Local and systemic changes were monitored by otomicroscopy, bacterial culture, and analysis of histological changes and the expression of the transforming growth factor beta (TGF-beta) gene. beta-Lactamase-producing H. influenzae did not demonstrate an ability to protect S. pneumoniae. Amoxicillin eradicated the pneumococci in all treated animals but increased to some degree the ability of H. influenzae to persist at the site of infection. Thus, only an insignificant acceleration of the resolution of the AOM caused by a mixture of pathogens was observed during treatment. Moderate to major morphological changes could not be avoided by treatment of the mixed infections, but a slight downregulation of TGF-beta expression was observed. In contrast to infections caused by a single pathogen, the mixed infections induced white plaques in the tympanic membrane at a remarkably high frequency independent of treatment. These experimental findings constitute support for further studies of antimicrobial drugs and AOM caused by bacteria with and without mechanisms of antibiotic resistance.
急性中耳炎(AOM)是门诊抗菌治疗最常见的原因。混合感染是一个潜在问题,因为用于治疗AOM的一线药物阿莫西林可被上呼吸道产生β-内酰胺酶的病原体中和。为研究阿莫西林5天疗程对中耳混合感染的影响,将大鼠单独用肺炎链球菌或与产生β-内酰胺酶的非分型流感嗜血杆菌联合进行攻击。在感染的临床高峰期给予阿莫西林。通过耳显微镜检查、细菌培养以及组织学变化分析和转化生长因子β(TGF-β)基因表达监测局部和全身变化。产生β-内酰胺酶的流感嗜血杆菌未表现出保护肺炎链球菌的能力。阿莫西林根除了所有治疗动物体内的肺炎球菌,但在一定程度上增加了流感嗜血杆菌在感染部位持续存在的能力。因此,治疗期间仅观察到由病原体混合物引起的AOM消退有微不足道的加速。治疗混合感染无法避免中度至重度形态学变化,但观察到TGF-β表达有轻微下调。与单一病原体引起的感染不同,混合感染无论是否治疗均以极高频率在鼓膜诱导产生白色斑块。这些实验结果为进一步研究抗菌药物以及由有或无抗生素耐药机制的细菌引起的AOM提供了支持。