Department of Clinical Microbiology, IIS- Fundación Jiménez Díaz, UAM, Madrid, 28040 Madrid, Spain.
Laboratory of Pharmaceutical Microbiology, Ghent University, B-9000 Ghent, Belgium.
Pathog Dis. 2018 Jun 1;76(4). doi: 10.1093/femspd/fty034.
Mycobacterium abscessus lung infection is a major health problem for cystic fibrosis (CF) patients. Understanding the in vivo factors that influence the outcome of therapy may help addressing the poor correlation between in vitro and in vivo antibiotic efficacy. We evaluated the influence of interspecies interactions and lung epithelial cells on antibiotic efficacy. Therefore, single and dual-species biofilms of M. abscessus and a major CF pathogen (Pseudomonas aeruginosa) were cultured on a plastic surface or on in vivo-like three-dimensional (3-D) lung epithelial cells, and the activity of antibiotics (colistin, amikacin, clarithromycin, ceftazidime) in inhibiting biofilm formation was evaluated. Using the most physiologically relevant model (dual-species biofilms on 3-D cells), we observed that treatment with antibiotics during biofilm development inhibited P. aeruginosa but not M. abscessus biofilms, resulting in a competitive advantage for the latter. Clarithromycin efficacy against P. aeruginosa was inhibited by 3-D lung cells. In addition, biofilm induction of M. abscessus was observed by certain antibiotics on plastic but not on 3-D cells. Pseudomonas aeruginosa influenced the efficacy of certain antibiotics against M. abscessus, but not vice versa. In conclusion, these results suggest a role of host cells and interspecies interactions in bacterial responses to antimicrobials.
脓肿分枝杆菌肺部感染是囊性纤维化 (CF) 患者的一个主要健康问题。了解影响治疗结果的体内因素可能有助于解决体外和体内抗生素疗效之间的相关性差的问题。我们评估了种间相互作用和肺上皮细胞对抗生素疗效的影响。因此,在塑料表面或类似于体内的三维 (3-D) 肺上皮细胞上培养了脓肿分枝杆菌和主要 CF 病原体 (铜绿假单胞菌) 的单种和双种生物膜,并评估了抗生素(多粘菌素、阿米卡星、克拉霉素、头孢他啶)抑制生物膜形成的活性。使用最具生理相关性的模型(3-D 细胞上的双种生物膜),我们观察到在生物膜形成过程中用抗生素治疗抑制了铜绿假单胞菌但不抑制脓肿分枝杆菌生物膜,导致后者具有竞争优势。克拉霉素对铜绿假单胞菌的疗效被 3-D 肺细胞抑制。此外,在塑料上而不是在 3-D 细胞上观察到某些抗生素诱导脓肿分枝杆菌生物膜的形成。铜绿假单胞菌影响某些抗生素对脓肿分枝杆菌的疗效,但反之则不然。总之,这些结果表明宿主细胞和种间相互作用在细菌对抗微生物药物的反应中起作用。