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Salmonella Persistence in Diverse Intracellular and Physiological Contexts
Salmonella Persistence in Diverse Intracellular and Physiological Contexts
Salmonella Persistence in Diverse Intracellular and Physiological Contexts

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20260202105136
ISBN  
9798265408471
DDC  
576
저자명  
Giorgio, Rachel Teresa.
서명/저자  
Salmonella Persistence in Diverse Intracellular and Physiological Contexts
발행사항  
[Sl] : Harvard University, 2025
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2025
형태사항  
153 p
주기사항  
Source: Dissertations Abstracts International, Volume: 87-05, Section: B.
주기사항  
Advisor: Helaine, Sophie.
학위논문주기  
Thesis (Ph.D.)--Harvard University, 2025.
초록/해제  
요약Antibiotic-recalcitrant infections, defined as the prolonged carriage of pathogenic bacteria even in the presence of antibiotics, are often caused by bacteria that are genetically susceptible to the drug. These recalcitrant bacteria fail to proliferate in the presence of antibiotics but remain viable such that they may recolonize their niche following antibiotic withdrawal. In the context of Salmonella infections, these antibiotic-recalcitrant infections are commonly caused by persisters, a non-growing, metabolically active bacterial subpopulation. Although much progress has been made in the study of persistent Salmonella, it remains unclear whether persister cells are the true source of relapsing disease, and whether other relevant intracellular persistence niches exist in addition to macrophages. In Chapter 1, I will provide a comprehensive overview of what is currently understood about antibiotic recalcitrance during Salmonella infection, including areas of active investigation. In Chapter 2, I will specifically explore the role of persister cells in infection relapse using the novel application of two methods to identify the source and nature of infection relapse. Then, in Chapter 3, I will discuss how we identified dendritic cells as an underappreciated niche for Salmonella persistence, and how the repeating O antigen moiety of lipopolysaccharide promotes persistence in both dendritic cells and macrophages by an as-yet unknown mechanism. Finally, Chapter 4 will summarize our broadened understanding of persistence and infection relapse and provide suggestions for future avenues of exploration. Through this dissertation and the work that will stem from it, we hope to gain a greater understanding of the mechanisms of infection relapse, allowing for more informed treatment decisions and a reduced incidence of recurrent disease.
일반주제명  
Microbiology
일반주제명  
Immunology
일반주제명  
Physiology
일반주제명  
Pathology
키워드  
Barcoding
키워드  
Dendritic cells
키워드  
Persistence
키워드  
Salmonella
키워드  
Antibiotics
기타저자  
Harvard University Biological and Biomedical Sciences
기본자료저록  
Dissertations Abstracts International. 87-05B.
전자적 위치 및 접속  
로그인 후 원문을 볼 수 있습니다.

MARC

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■1001  ▼aGiorgio,  Rachel  Teresa.
■24510▼aSalmonella  Persistence  in  Diverse  Intracellular  and  Physiological  Contexts
■260    ▼a[Sl]▼bHarvard  University▼c2025
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2025
■300    ▼a153  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  87-05,  Section:  B.
■500    ▼aAdvisor:  Helaine,  Sophie.
■5021  ▼aThesis  (Ph.D.)--Harvard  University,  2025.
■520    ▼aAntibiotic-recalcitrant  infections,  defined  as  the  prolonged  carriage  of  pathogenic  bacteria  even  in  the  presence  of  antibiotics,  are  often  caused  by  bacteria  that  are  genetically  susceptible  to  the  drug.  These  recalcitrant  bacteria  fail  to  proliferate  in  the  presence  of  antibiotics  but  remain  viable  such  that  they  may  recolonize  their  niche  following  antibiotic  withdrawal.  In  the  context  of  Salmonella  infections,  these  antibiotic-recalcitrant  infections  are  commonly  caused  by  persisters,  a  non-growing,  metabolically  active  bacterial  subpopulation.  Although  much  progress  has  been  made  in  the  study  of  persistent  Salmonella,  it  remains  unclear  whether  persister  cells  are  the  true  source  of  relapsing  disease,  and  whether  other  relevant  intracellular  persistence  niches  exist  in  addition  to  macrophages.  In  Chapter  1,  I  will  provide  a  comprehensive  overview  of  what  is  currently  understood  about  antibiotic  recalcitrance  during  Salmonella  infection,  including  areas  of  active  investigation.  In  Chapter  2,  I  will  specifically  explore  the  role  of  persister  cells  in  infection  relapse  using  the  novel  application  of  two  methods  to  identify  the  source  and  nature  of  infection  relapse.  Then,  in  Chapter  3,  I  will  discuss  how  we  identified  dendritic  cells  as  an  underappreciated  niche  for  Salmonella  persistence,  and  how  the  repeating  O  antigen  moiety  of  lipopolysaccharide  promotes  persistence  in  both  dendritic  cells  and  macrophages  by  an  as-yet  unknown  mechanism.  Finally,  Chapter  4  will  summarize  our  broadened  understanding  of  persistence  and  infection  relapse  and  provide  suggestions  for  future  avenues  of  exploration.  Through  this  dissertation  and  the  work  that  will  stem  from  it,  we  hope  to  gain  a  greater  understanding  of  the  mechanisms  of  infection  relapse,  allowing  for  more  informed  treatment  decisions  and  a  reduced  incidence  of  recurrent  disease.
■590    ▼aSchool  code:  0084.
■650  4▼aMicrobiology
■650  4▼aImmunology
■650  4▼aPhysiology
■650  4▼aPathology
■653    ▼aBarcoding
■653    ▼aDendritic  cells
■653    ▼aPersistence
■653    ▼aSalmonella
■653    ▼aAntibiotics
■690    ▼a0410
■690    ▼a0982
■690    ▼a0719
■690    ▼a0571
■71020▼aHarvard  University▼bBiological  and  Biomedical  Sciences.
■7730  ▼tDissertations  Abstracts  International▼g87-05B.
■790    ▼a0084
■791    ▼aPh.D.
■792    ▼a2025
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17359549▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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