Liposomal Antibiotic Booster Potentiates Carbapenems for Combating NDMs‐Producing Escherichia c oli

Abstract: Infections caused by Enterobacterales producing New Delhi Metallo‐β‐lactamases (NDMs), Zn (II)‐dependent enzymes hydrolyzing carbapenems, are difficult to treat. Depriving Zn (II) to inactivate NDMs is an effective solution to reverse carbapenems resistance in NDMs‐producing bacteria. However, specific Zn (II) deprivation and better bacterial outer membrane penetrability in vivo are challenges. Herein, authors present a pathogen‐primed liposomal antibiotic booster (M‐MFL@MB), facilitating drugs transportation into bacteria and removing Zn (II) from NDMs. M‐MFL@MB introduces bismuth nanoclusters (BiNCs) as a storage tank of Bi (III) for achieving ROS‐initiated Zn (II) removal. Inspired by bacteria‐specific maltodextrin transport pathway, meropenem‐loaded BiNCs are camouflaged by maltodextrin‐cloaked membrane fusion liposome to cross the bacterial envelope barrier via selectively targeting bacteria and directly outer membrane fusion. This fusion disturbs bacterial membrane homeostasis, then triggers intracellular ROS amplification, which activates Bi (III)‐mediated Zn (II) replacement and meropenem release, realizing more precise and efficient NDMs producer treatment. Benefiting from specific bacteria‐targeting, adequate drugs intracellular accumulation and self‐activation Zn (II) replacement, M‐MFL@MB rescues all mice infected by NDM producer without systemic side effects. Additionally, M‐MFL@MB decreases the bacterial outer membrane vesicles secretion, slowing down NDMs producer's transmission by over 35 times. Taken together, liposomal antibiotic booster as an efficient and safe tool provides new strategy for tackling NDMs producer‐induced infections.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
Liposomal Antibiotic Booster Potentiates Carbapenems for Combating NDMs‐Producing Escherichia c oli ; day:07 ; month:11 ; year:2023 ; extent:14
Advanced science ; (07.11.2023) (gesamt 14)

Urheber
Wu, Sixuan
Wei, Yongbin
Wang, Yang
Zhang, Zhenzhong
Liu, Dejun
Qin, Shangshang
Shi, Jinjin
Shen, Jianzhong

DOI
10.1002/advs.202304397
URN
urn:nbn:de:101:1-2023110814025539026721
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
14.08.2025, 10:54 MESZ

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Beteiligte

  • Wu, Sixuan
  • Wei, Yongbin
  • Wang, Yang
  • Zhang, Zhenzhong
  • Liu, Dejun
  • Qin, Shangshang
  • Shi, Jinjin
  • Shen, Jianzhong

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