The Center for Microbial Pathogenesis, The Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, Ohio, USA.
The Department of Pediatrics, The Ohio State University College of Medicine, Columbus, Ohio, USA.
mSphere. 2022 Oct 26;7(5):e0036222. doi: 10.1128/msphere.00362-22. Epub 2022 Sep 12.
Gonorrhea remains a major global public health problem because of the high incidence of infection (estimated 82 million cases in 2020) and the emergence and spread of Neisseria gonorrhoeae strains resistant to previous and current antibiotics used to treat infections. Given the dearth of new antibiotics that are likely to enter clinical practice in the near future, there is concern that cases of untreatable gonorrhea might emerge. In response to this crisis, the World Health Organization (WHO), in partnership with the Global Antibiotic Research and Development Partnership (GARDP), has made the search for and development of new antibiotics against N. gonorrhoeae a priority. Ideally, these antibiotics should also be active against other sexually transmitted organisms, such as Chlamydia trachomatis and/or Mycoplasma genitalium, which are often found with N. gonorrhoeae as co-infections. Corallopyronin A is a potent antimicrobial that exhibits activity against Chlamydia spp. and inhibits transcription by binding to the RpoB switch region. Accordingly, we tested the effectiveness of corallopyronin A against N. gonorrhoeae. We also examined the mutation frequency and modes of potential resistance against corallopyronin A. We report that corallopyronin A has potent antimicrobial action against antibiotic-susceptible and antibiotic-resistant N. gonorrhoeae strains and could eradicate gonococcal infection of cultured, primary human cervical epithelial cells. Critically, we found that spontaneous corallopyronin A-resistant mutants of N. gonorrhoeae are exceedingly rare (≤10) when selected at 4× the MIC. Our results support pre-clinical studies aimed at developing corallopyronin A for gonorrheal treatment regimens. The high global incidence of gonorrhea, the lack of a protective vaccine, and the emergence of N. gonorrhoeae strains expressing resistance to currently used antibiotics demand that new treatment options be developed. Accordingly, we investigated whether corallopyronin A, an antibiotic which is effective against other pathogens, including C. trachomatis, which together with gonococci frequently cause co-infections in humans, could exert anti-gonococcal action and , and potential resistance emergence. We propose that corallopyronin A be considered a potential future treatment option for gonorrhea because of its potent activity, low resistance development, and recent advances in scalable production.
淋病仍然是一个主要的全球公共卫生问题,因为感染率高(据估计,2020 年有 8200 万例),而且淋病奈瑟菌菌株对以前和目前用于治疗感染的抗生素产生了耐药性,并出现了耐药性菌株的传播。鉴于近期不太可能有新的抗生素进入临床实践,人们担心可能会出现无法治愈的淋病病例。针对这一危机,世界卫生组织(WHO)与全球抗生素研究与开发伙伴关系(GARDP)合作,将寻找和开发针对淋病奈瑟菌的新抗生素作为优先事项。理想情况下,这些抗生素也应该对其他性传播病原体(如沙眼衣原体和/或生殖支原体)有效,因为这些病原体通常与淋病奈瑟菌一起作为合并感染存在。珊瑚素 A 是一种有效的抗菌药物,对沙眼衣原体具有活性,并通过与 RpoB 开关区域结合来抑制转录。因此,我们测试了珊瑚素 A 对淋病奈瑟菌的有效性。我们还研究了珊瑚素 A 的潜在耐药突变频率和模式。我们报告称,珊瑚素 A 对敏感和耐药的淋病奈瑟菌菌株具有强大的抗菌作用,并能清除培养的原代人宫颈上皮细胞中的淋病奈瑟菌感染。至关重要的是,我们发现,当选择在 4 倍 MIC 时,淋病奈瑟菌自发产生珊瑚素 A 耐药突变体的频率极低(≤10)。我们的结果支持旨在开发珊瑚素 A 用于淋病治疗方案的临床前研究。淋病的全球发病率很高,没有保护性疫苗,而且淋病奈瑟菌菌株对目前使用的抗生素产生耐药性的情况也在出现,这都要求开发新的治疗选择。因此,我们研究了珊瑚素 A 是否能发挥抗淋病作用,珊瑚素 A 是一种对其他病原体有效的抗生素,包括沙眼衣原体,沙眼衣原体与淋病奈瑟菌一起经常导致人类的合并感染。并且,潜在的耐药性出现。我们提出,由于珊瑚素 A 的强大活性、低耐药性发展和最近在可扩展生产方面的进展,应将其视为淋病的潜在未来治疗选择。