Melhus A, Janson H, Westman E, Hermansson A, Forsgren A, Prellner K
Department of Medical Microbiology, Lund University, Malmö General Hospital, Sweden.
Antimicrob Agents Chemother. 1997 Sep;41(9):1979-84. doi: 10.1128/AAC.41.9.1979.
Through alterations primarily in the penicillin-binding proteins, a non-beta-lactamase-mediated resistance to beta-lactams has evolved in Haemophilus influenzae. The virulence of these chromosomally changed strains has been questioned. To ascertain whether these alterations involve a reduction in virulence of H. influenzae and whether they could be advantageous for the bacterium during amoxicillin treatment of acute otitis media, a total of 70 Sprague-Dawley rats were challenged with a susceptible recipient strain or a genetically similar resistant transformant strain. Antibiotic therapy was started on day 3 after inoculation, and the animals were monitored by daily otomicroscopy and analysis of bacterial samples from middle ear effusions obtained on day 8, the last day of observation. The animals were also sacrificed on days 4 and 8 and after 2 months for morphological examination. Compared with the susceptible recipient strain, recovery from infections caused by the resistant transformant strain was delayed, and the late structural changes were more severe in the animals challenged with the latter strain. The results of the study indicate that chromosomal alterations mediating a relatively low level of resistance to beta-lactams may be advantageous for H. influenzae during antibiotic treatment of a local infection in the rat, and the alterations may occur without any significant loss of virulence.
通过主要在青霉素结合蛋白方面的改变,流感嗜血杆菌已进化出对β-内酰胺类药物的非β-内酰胺酶介导的耐药性。这些染色体改变菌株的毒力受到了质疑。为了确定这些改变是否涉及流感嗜血杆菌毒力的降低,以及在阿莫西林治疗急性中耳炎期间它们对该细菌是否有利,总共70只Sprague-Dawley大鼠分别用敏感受体菌株或基因相似的耐药转化菌株进行攻击。接种后第3天开始抗生素治疗,并通过每日耳显微镜检查以及对观察最后一天(第8天)获得的中耳积液细菌样本进行分析来监测动物。在第4天、第8天以及2个月后处死动物进行形态学检查。与敏感受体菌株相比,耐药转化菌株引起的感染恢复延迟,并且在后一种菌株攻击的动物中晚期结构变化更严重。研究结果表明,介导对β-内酰胺类药物相对低水平耐药性的染色体改变在大鼠局部感染的抗生素治疗期间可能对流感嗜血杆菌有利,并且这些改变可能在没有任何明显毒力丧失的情况下发生。