Lowering Mortality Risk in CR-HvKP Infection in Intestinal Immunohistological and Microbiota Restoration
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review
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Detail(s)
Original language | English |
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Article number | 107254 |
Journal / Publication | Pharmacological Research |
Volume | 206 |
Online published | 9 Jun 2024 |
Publication status | Published - Aug 2024 |
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DOI | DOI |
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Link to Scopus | https://www.scopus.com/record/display.uri?eid=2-s2.0-85196296073&origin=recordpage |
Permanent Link | https://scholars.cityu.edu.hk/en/publications/publication(4fa46ba1-78e0-476f-aa57-b0d09aae8b7c).html |
Abstract
Gut damage during carbapenem-resistant and hypervirulent Klebsiella pneumoniae (CR-HvKP) infection is associated with a death risk. Understanding the mechanisms by which CR-HvKP causes intestinal damage and gut
microbiota alteration, and the impact on immunity, is crucial for developing therapeutic strategies. This study
investigated if gastrointestinal tract damage and disruption of gut microbiota induced by CR-HvKP infection
undermined host immunity and facilitated multi-organ invasion of CR-HvKP; whether the therapeutic value of
the rifampicin (RIF) and zidovudine (ZDV) combination was attributed to their ability to repair damages and
restore host immunity was determined. A sepsis model was utilized to assess the intestinal pathological changes.
Metagenomic analysis was performed to characterize the alteration of gut microbiota. The effects of the RIF and
ZDV on suppressing inflammatory responses and improving immune functions and gut microbiota were evaluated by immunopathological and transcriptomic analyses. Rapid colonic damage occurred upon activation of the
inflammation signaling pathways during lethal infections. Gut inflammation compromised host innate immunity
and led to a significant decrease in probiotics abundance, including Bifidobacterium and Lactobacillus. Treatment
with combination drugs significantly attenuated the inflammatory response, up-regulated immune cell differentiation signaling pathways, and promoted the abundance of Bifidobacterium (33.40 %). Consistently, supplementation of Bifidobacterium alone delayed the death in sepsis model. Gut inflammation and disrupted
microbiota are key disease features of CR-HvKP infection but can be reversed by the RIF and ZDV drug combination. The finding that these drugs can restore host immunity through multiple mechanisms is novel and
deserves further investigation of their clinical application potential.
© 2024 The Authors. Published by Elsevier Ltd.
© 2024 The Authors. Published by Elsevier Ltd.
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Citation Format(s)
Lowering Mortality Risk in CR-HvKP Infection in Intestinal Immunohistological and Microbiota Restoration. / Ni, Hongyuhang; Chan, Bill Kwan-Wai; Ye, Lianwei et al.
In: Pharmacological Research, Vol. 206, 107254, 08.2024.
In: Pharmacological Research, Vol. 206, 107254, 08.2024.
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review
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