Vaz Marcia Soares Mattos, de Almeida de Souza Gleyce Hellen, Radai Joyce Alencar Dos Santos, Fraga Thiago Leite, Simionatto Simone
Health Sciences Research Laboratory, Federal University of Grande Dourados - UFGD, Rodovia Dourados - Itahum, km 12, Cidade Universitária, Dourados, Mato Grosso do Sul, CEP: 79804970, Brazil.
University Center of Grande Dourados - UNIGRAN, Dourados, Mato Grosso do Sul, Brazil.
Braz J Microbiol. 2025 Aug 18. doi: 10.1007/s42770-025-01677-y.
The global spread of multi-drug-resistant bacteria, including strains resistant to both polymyxin and carbapenems, poses a significant threat to public health, highlighting the need to develop new antimicrobial agents. This study assessed the antimicrobial potential of cinnamaldehyde, alone and in combination with antibiotics, against carbapenem-polymyxin-resistant K. pneumoniae strains (CPR-Kp). The antimicrobial activity was assessed through minimum inhibitory concentration (MIC), checkerboard assay, and survival curve analysis. Cinnamaldehyde showed inhibitory effects (MIC 281 µg/mL), and when combined with polymyxin B, resulted in synergistic effects, effectively overcoming resistance to both polymyxin and carbapenem. Notably, cinnamaldehyde (70 µg/mL) combined with polymyxin B (1 µg/mL) led to a significant reduction in the MIC of polymyxin B, from 64 µg/mL to 1 µg/mL, with a fractional inhibitory concentration index (FICI) of 0.26, indicating synergy. The ZIP synergy score analysis further corroborated these findings, revealing a global synergy score of 32.728, with the highest values observed at cinnamaldehyde concentrations of 70-140 µg/mL in combination with polymyxin B. Similarly, in vivo the combination of cinnamaldehyde (30 or 100 mg/kg) with polymyxin B (2 mg/kg) significantly reduced bacterial loads in blood and peritoneal lavage (p < 0.0001) and improved survival rates. These findings underscore the efficacy of cinnamaldehyde as an adjuvant to polymyxin B in treating infections caused by CPR-Kp. The observed synergistic effect suggests that cinnamaldehyde as a pivotal component in future therapeutic formulations, providing a promising avenue for further research in combating antimicrobial resistance.
包括对多粘菌素和碳青霉烯类均耐药的菌株在内的多重耐药细菌在全球范围内的传播,对公共卫生构成了重大威胁,凸显了开发新型抗菌药物的必要性。本研究评估了肉桂醛单独及与抗生素联合使用时,对耐碳青霉烯-多粘菌素的肺炎克雷伯菌菌株(CPR-Kp)的抗菌潜力。通过最低抑菌浓度(MIC)、棋盘法和生存曲线分析来评估抗菌活性。肉桂醛显示出抑制作用(MIC为281µg/mL),当与多粘菌素B联合使用时,产生协同作用,有效克服了对多粘菌素和碳青霉烯类的耐药性。值得注意的是,肉桂醛(70µg/mL)与多粘菌素B(1µg/mL)联合使用导致多粘菌素B的MIC显著降低,从64µg/mL降至1µg/mL,部分抑菌浓度指数(FICI)为0.26,表明存在协同作用。ZIP协同评分分析进一步证实了这些结果,显示全球协同评分为32.728,在肉桂醛浓度为70-140µg/mL与多粘菌素B联合使用时观察到最高值。同样,在体内,肉桂醛(30或100mg/kg)与多粘菌素B(2mg/kg)联合使用显著降低了血液和腹腔灌洗液中的细菌载量(p<0.0001),并提高了生存率。这些发现强调了肉桂醛作为多粘菌素B治疗CPR-Kp引起的感染的佐剂的有效性。观察到的协同作用表明,肉桂醛作为未来治疗制剂的关键成分,为对抗抗菌药物耐药性的进一步研究提供了一条有前景的途径。