Eradication of Multidrug- Resistant Bacteria using Biomolecule-encapsulated Two-dimensional Materials

abstract: The increasing pervasiveness of infections caused by multidrug-resistant bacteria (MDR) is a major global health issue that has been further exacerbated by the dearth of antibiotics developed over the past 40 years. Drug-resistant bacteria have led to significant morbidity and mortality, a...

Full description

Bibliographic Details
Other Authors: Debnath, Abhishek (Author)
Format: Doctoral Thesis
Language:English
Published: 2019
Subjects:
Online Access:http://hdl.handle.net/2286/R.I.54868
id ndltd-asu.edu-item-54868
record_format oai_dc
spelling ndltd-asu.edu-item-548682019-11-07T03:01:02Z Eradication of Multidrug- Resistant Bacteria using Biomolecule-encapsulated Two-dimensional Materials abstract: The increasing pervasiveness of infections caused by multidrug-resistant bacteria (MDR) is a major global health issue that has been further exacerbated by the dearth of antibiotics developed over the past 40 years. Drug-resistant bacteria have led to significant morbidity and mortality, and ever-increasing antibiotic resistance threatens to reverse many of the medical advances enabled by antibiotics over the last 40 years. The traditional strategy for combating these superbugs involves the development of new antibiotics. Yet, only two new classes of antibiotics have been introduced to the clinic over the past two decades, and both failed to combat broad spectrum gram-negative bacteria. This situation demands alternative strategies to combat drug-resistant superbugs. Herein, these dissertation reports the development of potent antibacterials based on biomolecule-encapsulated two-dimensional inorganic materials, which combat multidrug-resistant bacteria using alternative mechanisms of strong physical interactions with bacterial cell membrane. These systems successfully eliminate all members of the ‘Superbugs’ set of pathogenic bacteria, which are known for developing antibiotic resistance, providing an alternative to the limited ‘one bug-one drug’ approach that is conventionally used. Furthermore, these systems demonstrate a multimodal antibacterial killing mechanism that induces outer membrane destabilization, unregulated ion movement across the membranes, induction of oxidative stress, and finally apoptotic-like cell death. In addition, a peptide-encapsulation of the two-dimensional material successfully eliminated biofilms and persisters at micromolar concentrations. Overall, these novel systems have great potential as next-generation antimicrobial agents for eradication of broad spectrum multidrug-resistant bacteria. Dissertation/Thesis Debnath, Abhishek (Author) Green, Alexander A (Advisor) Liu, Yan (Committee member) Stephanopoulos, Nicholas (Committee member) Arizona State University (Publisher) Chemistry Antibacterial Biomolecule encapsulated Two dimensional material eng 131 pages Doctoral Dissertation Chemistry 2019 Doctoral Dissertation http://hdl.handle.net/2286/R.I.54868 http://rightsstatements.org/vocab/InC/1.0/ 2019
collection NDLTD
language English
format Doctoral Thesis
sources NDLTD
topic Chemistry
Antibacterial
Biomolecule encapsulated Two dimensional material
spellingShingle Chemistry
Antibacterial
Biomolecule encapsulated Two dimensional material
Eradication of Multidrug- Resistant Bacteria using Biomolecule-encapsulated Two-dimensional Materials
description abstract: The increasing pervasiveness of infections caused by multidrug-resistant bacteria (MDR) is a major global health issue that has been further exacerbated by the dearth of antibiotics developed over the past 40 years. Drug-resistant bacteria have led to significant morbidity and mortality, and ever-increasing antibiotic resistance threatens to reverse many of the medical advances enabled by antibiotics over the last 40 years. The traditional strategy for combating these superbugs involves the development of new antibiotics. Yet, only two new classes of antibiotics have been introduced to the clinic over the past two decades, and both failed to combat broad spectrum gram-negative bacteria. This situation demands alternative strategies to combat drug-resistant superbugs. Herein, these dissertation reports the development of potent antibacterials based on biomolecule-encapsulated two-dimensional inorganic materials, which combat multidrug-resistant bacteria using alternative mechanisms of strong physical interactions with bacterial cell membrane. These systems successfully eliminate all members of the ‘Superbugs’ set of pathogenic bacteria, which are known for developing antibiotic resistance, providing an alternative to the limited ‘one bug-one drug’ approach that is conventionally used. Furthermore, these systems demonstrate a multimodal antibacterial killing mechanism that induces outer membrane destabilization, unregulated ion movement across the membranes, induction of oxidative stress, and finally apoptotic-like cell death. In addition, a peptide-encapsulation of the two-dimensional material successfully eliminated biofilms and persisters at micromolar concentrations. Overall, these novel systems have great potential as next-generation antimicrobial agents for eradication of broad spectrum multidrug-resistant bacteria. === Dissertation/Thesis === Doctoral Dissertation Chemistry 2019
author2 Debnath, Abhishek (Author)
author_facet Debnath, Abhishek (Author)
title Eradication of Multidrug- Resistant Bacteria using Biomolecule-encapsulated Two-dimensional Materials
title_short Eradication of Multidrug- Resistant Bacteria using Biomolecule-encapsulated Two-dimensional Materials
title_full Eradication of Multidrug- Resistant Bacteria using Biomolecule-encapsulated Two-dimensional Materials
title_fullStr Eradication of Multidrug- Resistant Bacteria using Biomolecule-encapsulated Two-dimensional Materials
title_full_unstemmed Eradication of Multidrug- Resistant Bacteria using Biomolecule-encapsulated Two-dimensional Materials
title_sort eradication of multidrug- resistant bacteria using biomolecule-encapsulated two-dimensional materials
publishDate 2019
url http://hdl.handle.net/2286/R.I.54868
_version_ 1719287558028918784