Lianshen Zhang, Yingzhang Zhang, Lijie Tian, Qiang Shen, Xiaolong Ma
{"title":"多西氟脲苷可有效杀灭慢性阻塞性肺病患者体内的耐抗生素金黄色葡萄球菌。","authors":"Lianshen Zhang, Yingzhang Zhang, Lijie Tian, Qiang Shen, Xiaolong Ma","doi":"10.1128/spectrum.01805-24","DOIUrl":null,"url":null,"abstract":"<p><p>Chronic obstructive pulmonary disease (COPD) is a leading cause of morbidity and mortality globally, often exacerbated by infections such as methicillin-resistant <i>Staphylococcus aureus</i> (MRSA). The rise in antibiotic-resistant strains complicates treatment and underscores the need for novel therapeutic drugs. In this paper, we further investigated the antimicrobial potential of a fluoropyrimidine anticancer drug doxifluridine against multidrug-resistant <i>S. aureus</i>. Determination of minimum inhibitory concentration (MIC) or minimum bactericidal concentration (MBC), monitoring of growth curve, time-kill assays, biofilm bactericidal assays, and chequerboard studies were conducted to evaluate the antibacterial efficacy of doxifluridine. Safety was assessed via hemolysis and cytotoxicity assays, and an <i>in vivo Galleria mellonella</i> larvae model was employed to test protective effects. Doxifluridine demonstrated significant antibacterial activity against clinical multidrug resistance (MDR) <i>S. aureus</i> isolates, with MIC and MBC values ranging from 0.5 to 2 µg/mL and 1 to 4 µg/mL, respectively. The results revealed doxifluridine's potent bactericidal effects within 8 hours. Moreover, doxifluridine-treated bacteria showed a substantial reduction in biofilm mass and viability. Furthermore, chequerboard assays indicated synergistic interactions between doxifluridine and other antibiotics, reducing MIC values by two- to eightfold. More importantly, safety evaluations confirmed that doxifluridine did not exhibit hemolytic toxicity or cytotoxicity. Finally, doxifluridine significantly increased the survival rate of MRSA-infected <i>G. mellonella</i> larvae <i>in vivo</i>. In brief, doxifluridine exhibited promising <i>in vitro</i> and <i>in vivo</i> antibacterial activity against MRSA, suggesting its potential as a repurposed drug for treating resistant bacterial infections in COPD patients.IMPORTANCEThe study provides robust evidence for the antibacterial efficacy of doxifluridine against Methicillin-resistant <i>Staphylococcus aureus</i> in chronic obstructive pulmonary disease (COPD) patients. Its rapid action, ability to disrupt biofilms, and synergistic effects with other antibiotics, combined with a favorable safety profile, highlight its potential as a repurposed therapeutic agent. Future clinical trials will be essential to confirm these findings and pave the way for its integration into clinical practice. 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The rise in antibiotic-resistant strains complicates treatment and underscores the need for novel therapeutic drugs. In this paper, we further investigated the antimicrobial potential of a fluoropyrimidine anticancer drug doxifluridine against multidrug-resistant <i>S. aureus</i>. Determination of minimum inhibitory concentration (MIC) or minimum bactericidal concentration (MBC), monitoring of growth curve, time-kill assays, biofilm bactericidal assays, and chequerboard studies were conducted to evaluate the antibacterial efficacy of doxifluridine. Safety was assessed via hemolysis and cytotoxicity assays, and an <i>in vivo Galleria mellonella</i> larvae model was employed to test protective effects. Doxifluridine demonstrated significant antibacterial activity against clinical multidrug resistance (MDR) <i>S. aureus</i> isolates, with MIC and MBC values ranging from 0.5 to 2 µg/mL and 1 to 4 µg/mL, respectively. The results revealed doxifluridine's potent bactericidal effects within 8 hours. Moreover, doxifluridine-treated bacteria showed a substantial reduction in biofilm mass and viability. Furthermore, chequerboard assays indicated synergistic interactions between doxifluridine and other antibiotics, reducing MIC values by two- to eightfold. More importantly, safety evaluations confirmed that doxifluridine did not exhibit hemolytic toxicity or cytotoxicity. Finally, doxifluridine significantly increased the survival rate of MRSA-infected <i>G. mellonella</i> larvae <i>in vivo</i>. In brief, doxifluridine exhibited promising <i>in vitro</i> and <i>in vivo</i> antibacterial activity against MRSA, suggesting its potential as a repurposed drug for treating resistant bacterial infections in COPD patients.IMPORTANCEThe study provides robust evidence for the antibacterial efficacy of doxifluridine against Methicillin-resistant <i>Staphylococcus aureus</i> in chronic obstructive pulmonary disease (COPD) patients. Its rapid action, ability to disrupt biofilms, and synergistic effects with other antibiotics, combined with a favorable safety profile, highlight its potential as a repurposed therapeutic agent. Future clinical trials will be essential to confirm these findings and pave the way for its integration into clinical practice. 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引用次数: 0
摘要
慢性阻塞性肺病(COPD)是全球发病率和死亡率的主要原因,感染(如耐甲氧西林金黄色葡萄球菌(MRSA))往往会加重病情。抗生素耐药菌株的增加使治疗变得更加复杂,也凸显了对新型治疗药物的需求。本文进一步研究了氟嘧啶类抗癌药物多西氟脲对耐多药金黄色葡萄球菌的抗菌潜力。通过测定最低抑菌浓度(MIC)或最低杀菌浓度(MBC)、监测生长曲线、时间杀伤试验、生物膜杀菌试验和棋盘式研究来评估多西氟脲的抗菌效力。安全性通过溶血和细胞毒性实验进行了评估,并采用了一种体内灰飞虱幼虫模型来测试其保护作用。多西氟脲对临床多药耐药性(MDR)金黄色葡萄球菌分离株具有显著的抗菌活性,MIC 和 MBC 值分别为 0.5 至 2 µg/mL 和 1 至 4 µg/mL。研究结果表明,多西氟脲在 8 小时内就能发挥强大的杀菌作用。此外,经多西氟脲处理的细菌的生物膜质量和存活率均大幅降低。此外,棋盘试验表明多西氟脲与其他抗生素之间存在协同作用,可将 MIC 值降低 2 到 8 倍。更重要的是,安全性评估证实多西氟脲苷不会产生溶血性毒性或细胞毒性。最后,多西氟脲在体内能显著提高受 MRSA 感染的 G. mellonella 幼虫的存活率。简而言之,多西氟脲苷在体外和体内对 MRSA 都表现出了良好的抗菌活性,这表明它有潜力成为治疗慢性阻塞性肺病(COPD)患者耐药性细菌感染的再利用药物。多西呋啶作用迅速,能破坏生物膜,与其他抗生素有协同作用,而且安全性能良好,因此有可能成为一种再用途治疗药物。未来的临床试验对于证实这些发现并为其融入临床实践铺平道路至关重要。这项工作不仅为慢性阻塞性肺病细菌感染的治疗提供了候选药物,还体现了药物再利用在抗击抗生素耐药性感染方面的潜力。
Chronic obstructive pulmonary disease (COPD) is a leading cause of morbidity and mortality globally, often exacerbated by infections such as methicillin-resistant Staphylococcus aureus (MRSA). The rise in antibiotic-resistant strains complicates treatment and underscores the need for novel therapeutic drugs. In this paper, we further investigated the antimicrobial potential of a fluoropyrimidine anticancer drug doxifluridine against multidrug-resistant S. aureus. Determination of minimum inhibitory concentration (MIC) or minimum bactericidal concentration (MBC), monitoring of growth curve, time-kill assays, biofilm bactericidal assays, and chequerboard studies were conducted to evaluate the antibacterial efficacy of doxifluridine. Safety was assessed via hemolysis and cytotoxicity assays, and an in vivo Galleria mellonella larvae model was employed to test protective effects. Doxifluridine demonstrated significant antibacterial activity against clinical multidrug resistance (MDR) S. aureus isolates, with MIC and MBC values ranging from 0.5 to 2 µg/mL and 1 to 4 µg/mL, respectively. The results revealed doxifluridine's potent bactericidal effects within 8 hours. Moreover, doxifluridine-treated bacteria showed a substantial reduction in biofilm mass and viability. Furthermore, chequerboard assays indicated synergistic interactions between doxifluridine and other antibiotics, reducing MIC values by two- to eightfold. More importantly, safety evaluations confirmed that doxifluridine did not exhibit hemolytic toxicity or cytotoxicity. Finally, doxifluridine significantly increased the survival rate of MRSA-infected G. mellonella larvae in vivo. In brief, doxifluridine exhibited promising in vitro and in vivo antibacterial activity against MRSA, suggesting its potential as a repurposed drug for treating resistant bacterial infections in COPD patients.IMPORTANCEThe study provides robust evidence for the antibacterial efficacy of doxifluridine against Methicillin-resistant Staphylococcus aureus in chronic obstructive pulmonary disease (COPD) patients. Its rapid action, ability to disrupt biofilms, and synergistic effects with other antibiotics, combined with a favorable safety profile, highlight its potential as a repurposed therapeutic agent. Future clinical trials will be essential to confirm these findings and pave the way for its integration into clinical practice. This work not only provides candidate for tackling the management of bacterial infections in COPD but also exemplifies the potential of drug repurposing in combating antibiotic-resistant infections.
期刊介绍:
Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.