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抗感染替代抗生素的前沿。

Frontiers in antibiotic alternatives for infection.

机构信息

Department of Molecular Tropical Medicine and Genetics, Faculty of Tropical Medicine, Mahidol University, Bangkok 10400, Thailand.

Department of Biology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.

出版信息

World J Gastroenterol. 2021 Nov 14;27(42):7210-7232. doi: 10.3748/wjg.v27.i42.7210.

DOI:10.3748/wjg.v27.i42.7210
PMID:34876784
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8611198/
Abstract

() is a gram-positive, anaerobic spore-forming bacterium and a major cause of antibiotic-associated diarrhea. Humans are naturally resistant to infection (CDI) owing to the protection provided by healthy gut microbiota. When the gut microbiota is disturbed, can colonize, produce toxins, and manifest clinical symptoms, ranging from asymptomatic diarrhea and colitis to death. Despite the steady-if not rising-prevalence of CDI, it will certainly become more problematic in a world of antibiotic overuse and the post-antibiotic era. is naturally resistant to most of the currently used antibiotics as it uses multiple resistance mechanisms. Therefore, current CDI treatment regimens are extremely limited to only a few antibiotics, which include vancomycin, fidaxomicin, and metronidazole. Therefore, one of the main challenges experienced by the scientific community is the development of alternative approaches to control and treat CDI. In this Frontier article, we collectively summarize recent advances in alternative treatment approaches for CDI. Over the past few years, several studies have reported on natural product-derived compounds, drug repurposing, high-throughput library screening, phage therapy, and fecal microbiota transplantation. We also include an update on vaccine development, pre- and pro-biotics for CDI, and toxin antidote approaches. These measures tackle CDI at every stage of disease pathology multiple mechanisms. We also discuss the gaps and concerns in these developments. The next epidemic of CDI is not a matter of if but a matter of when. Therefore, being well-equipped with a collection of alternative therapeutics is necessary and should be prioritized.

摘要

艰难梭菌是一种革兰氏阳性、厌氧的产芽孢细菌,也是抗生素相关性腹泻的主要病因。由于健康的肠道微生物群提供的保护,人类天生对艰难梭菌感染(CDI)具有抵抗力。当肠道微生物群受到干扰时,艰难梭菌能够定植、产生毒素并表现出临床症状,从无症状腹泻和结肠炎到死亡不等。尽管 CDI 的患病率稳定(如果不是上升的话),但在抗生素过度使用和后抗生素时代,它肯定会成为一个更具挑战性的问题。艰难梭菌对目前使用的大多数抗生素天然耐药,因为它使用多种耐药机制。因此,目前 CDI 的治疗方案极其有限,仅包括万古霉素、非达霉素和甲硝唑。因此,科学界面临的主要挑战之一是开发替代方法来控制和治疗 CDI。在这篇前沿文章中,我们共同总结了 CDI 替代治疗方法的最新进展。在过去的几年中,有几项研究报告了天然产物衍生化合物、药物再利用、高通量文库筛选、噬菌体治疗和粪便微生物群移植。我们还包括 CDI 疫苗开发、预防和治疗性益生菌以及毒素解毒剂方法的最新进展。这些措施针对疾病病理的各个阶段采取了多种机制来解决 CDI 问题。我们还讨论了这些发展中的差距和关注点。下一次 CDI 疫情不是会不会发生的问题,而是何时发生的问题。因此,拥有一系列替代疗法是必要的,应该优先考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91fb/8611198/fb3ef6502d50/WJG-27-7210-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91fb/8611198/fb3ef6502d50/WJG-27-7210-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91fb/8611198/fb3ef6502d50/WJG-27-7210-g001.jpg

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6
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