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工程化噬菌体穿膜肽用于胞内细菌感染。

Engineered phage with cell-penetrating peptides for intracellular bacterial infections.

机构信息

Department of Neonatology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, Chongqing Key Laboratory of Pediatrics , Chongqing, China.

CAS Key Laboratory of Quantitative Engineering Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences , Shenzhen, China.

出版信息

mSystems. 2023 Oct 26;8(5):e0064623. doi: 10.1128/msystems.00646-23. Epub 2023 Aug 18.

Abstract

infection is a significant threat to global public health, and the increasing prevalence of antibiotic resistance exacerbates the situation. Therefore, finding new and effective ways to combat this pathogen is essential. Phages are natural predators of bacteria and can be used as an alternative to antibiotics to kill specific bacteria, including drug-resistant strains. One significant limitation of using phages as antimicrobial agents is their low cellular uptake, which limits their effectiveness against intracellular bacterial infections. Therefore, finding ways to enhance phage uptake is crucial. Our study provides a straightforward strategy for displaying cell-penetrating peptides on non-model phages, offering a promising novel and effective therapeutic approach for treating intracellular and drug-resistant bacteria. This approach has the potential to address the global challenge of antibiotic resistance and improve public health outcomes.

摘要

感染是对全球公共卫生的重大威胁,而抗生素耐药性的日益普遍使情况更加恶化。因此,寻找新的有效方法来对抗这种病原体至关重要。噬菌体是细菌的天然捕食者,可以作为抗生素的替代品来杀死特定的细菌,包括耐药菌株。使用噬菌体作为抗菌剂的一个显著限制是其细胞摄取率低,这限制了它们对细胞内细菌感染的有效性。因此,寻找增强噬菌体摄取的方法至关重要。我们的研究为非模型噬菌体展示穿膜肽提供了一种简单直接的策略,为治疗细胞内和耐药细菌提供了一种有前途的新型有效治疗方法。这种方法有可能解决抗生素耐药性的全球挑战,改善公共卫生成果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d756/10654057/07a762437e6b/msystems.00646-23.f001.jpg

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