Department of Comparative Pathobiology, College of Veterinary Medicine, Purdue University, West Lafayette, Indiana, United States of America.
Department of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United States of America.
PLoS One. 2022 Aug 8;17(8):e0267859. doi: 10.1371/journal.pone.0267859. eCollection 2022.
Clostridioides difficile infection is a global health threat and remains the primary cause of hospital-acquired infections worldwide. The burgeoning incidence and severity of infections coupled with high rates of recurrence have created an urgent need for novel therapeutics. Here, we report a novel natural product scaffold as a potential anticlostridial lead with antivirulence properties and potent activity both in vitro and in vivo. A whole cell phenotypic screening of 1,000 purified natural products identified 6 compounds with potent activity against C. difficile (minimum inhibitory concentration (MIC) range from 0.03 to 2 μg/ml). All these 6 compounds were non-toxic to human colorectal cells. The natural product compounds also inhibited the production of key toxins, TcdA and TcdB, the key virulence determinants of C. difficile infection pathology. Additionally, the compounds exhibited rapid bactericidal activity and were superior to the standard-of-care antibiotic vancomycin, in reducing a high inoculum of C. difficile in vitro. Furthermore, a murine model of C. difficile infection revealed that compound NP-003875 conferred 100% protection to the infected mice from clinical manifestations of the disease. Collectively, the current study lays the foundation for further investigation of the natural product NP-003875 as a potential therapeutic choice for C. difficile infection.
艰难梭菌感染是一个全球性的健康威胁,仍然是全球医院获得性感染的主要原因。感染的发病率和严重程度不断上升,加上高复发率,这就迫切需要新的治疗方法。在这里,我们报告了一种新型天然产物支架作为一种具有抗病毒特性的潜在抗梭状芽胞杆菌先导化合物,具有体外和体内的强大活性。对 1000 种纯化天然产物进行全细胞表型筛选,发现有 6 种化合物对艰难梭菌具有很强的活性(最小抑菌浓度(MIC)范围为 0.03 至 2 μg/ml)。所有这 6 种化合物对人结直肠细胞均无毒性。天然产物化合物还抑制了关键毒素 TcdA 和 TcdB 的产生,这是艰难梭菌感染病理学的关键毒力决定因素。此外,这些化合物具有快速杀菌活性,在体外减少高浓度艰难梭菌方面优于标准治疗抗生素万古霉素。此外,艰难梭菌感染的小鼠模型表明,化合物 NP-003875 能使感染的小鼠 100%免受疾病的临床症状的影响。总的来说,目前的研究为进一步研究天然产物 NP-003875 作为治疗艰难梭菌感染的潜在治疗选择奠定了基础。