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   <dim:field mdschema="dc" element="contributor" qualifier="advisor">Collins, James J.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author">Andrews, Ian Wayne</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Biological Engineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2024-02-08T15:11:14Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2024-02-08T15:11:14Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued">2022-05</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="submitted">2024-02-02T20:55:40.718Z</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://hdl.handle.net/1721.1/153464</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract">While it is widely understood that antibiotic resistance is challenging the efficacy of our antibiotic therapies, there is a growing appreciation for the clinical importance of other ways that bacteria can survive antibiotic treatment. In particular, antibiotic tolerance describes a set of phenotypes where genetically susceptible bacteria can survive antibiotic treatment. Thus, there is a need for methods to improve our understanding of currently used antibiotics, as well as the discovery and development of new antibiotic therapeutic strategies, particularly focused on addressing antibiotic tolerance.&#xd;
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In this thesis, I present advancements to our understanding of antibiotic efficacy and our methods for discovering treatment strategies against antibiotic tolerant bacterial populations. First, I present an investigation into the metabolic processes that drive beta-lactam lethality, where we showed that drug-induced disruption of anabolic- catabolic homeostasis is an important factor for beta-lactam activity. Next, I describe an approach towards the discovery of antibiotic adjuvants for treating antibiotic tolerance. Finally, I present work towards the development of a method for discovering new antibiotics with activity against antibiotic tolerant bacteria. I describe characterization of compounds that were identified in primary screening efforts, as well as the results of a deep learning approach to this challenge in antibiotic discovery. Together, these projects demonstrate a set of advancements in our understanding of antibiotic activity and towards the challenge of antibiotic discovery.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree">Ph.D.</dim:field>
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   <dim:field mdschema="dc" element="rights">Copyright MIT</dim:field>
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   <dim:field mdschema="dc" element="title">Approaches to investigating antibiotic efficacy and discovery of treatment strategies against antibiotic tolerance</dim:field>
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   	&lt;Title>Approaches to investigating antibiotic efficacy and discovery of treatment strategies against antibiotic tolerance&lt;/Title>
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   	&lt;PublicationDate>2022-05&lt;/PublicationDate>
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        	&lt;DisplayName>Andrews, Ian Wayne&lt;/DisplayName>
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   	&lt;Abstract>While it is widely understood that antibiotic resistance is challenging the efficacy of our antibiotic therapies, there is a growing appreciation for the clinical importance of other ways that bacteria can survive antibiotic treatment. In particular, antibiotic tolerance describes a set of phenotypes where genetically susceptible bacteria can survive antibiotic treatment. Thus, there is a need for methods to improve our understanding of currently used antibiotics, as well as the discovery and development of new antibiotic therapeutic strategies, particularly focused on addressing antibiotic tolerance.&#xd;
&#xd;
In this thesis, I present advancements to our understanding of antibiotic efficacy and our methods for discovering treatment strategies against antibiotic tolerant bacterial populations. First, I present an investigation into the metabolic processes that drive beta-lactam lethality, where we showed that drug-induced disruption of anabolic- catabolic homeostasis is an important factor for beta-lactam activity. Next, I describe an approach towards the discovery of antibiotic adjuvants for treating antibiotic tolerance. Finally, I present work towards the development of a method for discovering new antibiotics with activity against antibiotic tolerant bacteria. I describe characterization of compounds that were identified in primary screening efforts, as well as the results of a deep learning approach to this challenge in antibiotic discovery. Together, these projects demonstrate a set of advancements in our understanding of antibiotic activity and towards the challenge of antibiotic discovery.&lt;/Abstract>
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