Laboratório de Pesquisa em Ciências da Saúde, Universidade Federal da Grande Dourados-UFGD, Dourados, Mato Grosso do Sul, Brazil.
Centro Universitário da Grande Dourados-UNIGRAN, Dourados, Mato Grosso do Sul, Brazil.
PLoS One. 2021 Feb 22;16(2):e0246003. doi: 10.1371/journal.pone.0246003. eCollection 2021.
Dissemination of carbapenem-resistant Klebsiella pneumoniae poses a threat to the successful treatment of bacterial diseases and increases the need for new antibacterial agents development. The objective of this study was to determine the antimicrobial activity of carvacrol against multidrug-resistant K. pneumoniae. Carbapenemase production was detected by MALDI-TOF. The PCR and sequencing showed that the blaKPC-2, blaOXA-48, blaNDM-1, blaCTX-M-8 genes were present in carbapenem-resistant K. pneumoniae strains. The polymyxin-resistant K. pneumoniae strain exhibited alterations in mgrB gene. The antimicrobial activity of carvacrol was evaluated in vitro using broth microdilution and time-kill methods. For this, carbapenem-resistant K. pneumoniae and polymyxin-resistant strains, were evaluated. The in vitro results showed that carvacrol had antimicrobial activity against all isolates evaluated. The survival curves showed that carvacrol eradicated all of the bacterial cells within 4 h. The antimicrobial effect of carvacrol in vivo was determined using a mouse model of infection with Klebsiella pneumoniae carbapenemase (KPC). The treatment with carvacrol was associated with increased survival, and significantly reduced bacterial load in peritoneal lavage. In addition, groups treated with carvacrol, had a significant reduction in the total numbers of white cell and significantly increased of platelets when compared to the untreated group. In vivo and in vitro studies showed that carvacrol regimens exhibited significant antimicrobial activity against KPC-producing K. pneumoniae, making it an interesting candidate for development of alternative treatments.
碳青霉烯类耐药肺炎克雷伯菌的传播对细菌性疾病的成功治疗构成威胁,并增加了对抗菌药物开发的需求。本研究旨在确定香芹酚对多药耐药肺炎克雷伯菌的抗菌活性。采用 MALDI-TOF 检测碳青霉烯酶的产生。PCR 和测序结果表明,碳青霉烯耐药肺炎克雷伯菌菌株中存在 blaKPC-2、blaOXA-48、blaNDM-1、blaCTX-M-8 基因。多黏菌素耐药肺炎克雷伯菌菌株 mgrB 基因发生改变。采用肉汤微量稀释法和时间杀伤法评估香芹酚的体外抗菌活性。为此,评估了碳青霉烯类耐药肺炎克雷伯菌和多黏菌素耐药菌株。体外结果表明,香芹酚对所有评估的分离株均具有抗菌活性。存活曲线表明,香芹酚在 4 小时内可消灭所有细菌细胞。采用肺炎克雷伯菌碳青霉烯酶(KPC)感染小鼠模型测定香芹酚的体内抗菌作用。香芹酚治疗与存活率增加相关,并显著降低腹腔灌洗液中的细菌负荷。此外,与未治疗组相比,用香芹酚治疗的组的白细胞总数显著减少,血小板显著增加。体内和体外研究表明,香芹酚方案对产 KPC 的肺炎克雷伯菌具有显著的抗菌活性,使其成为开发替代治疗方法的有前途的候选药物。