KAIST 생명과학과동창회
  • News & Events
  • News

News

Antibiotic tolerance study paves way for new treatments

Posted on Mar 02, 2021, 3 p.m.


A new study identifies a mechanism that makes bacteria tolerant to penicillin and related antibiotics, findings that could lead to new therapies that boost the effectiveness of these treatments.


Antibiotic tolerance is the ability of bacteria to survive exposure to antibiotics, in contrast to antibiotic resistance, when bacteria actually grow in the presence of antibiotics. Tolerant bacteria can lead to infections that persist after treatment and may develop into resistance over time.


The study in mice, “A Multifaceted Cellular Damage Repair and Prevention Pathway Promotes High Level Tolerance to Beta-lactam Antibiotics,” published Feb. 3 in the journal EMBO Reports, reveals how tolerance occurs, thanks to a system that mitigates iron toxicity in bacteria that have been exposed to penicillin.


“We’re hoping we can design a drug or develop antibiotic adjuvants that would then basically kill off these tolerant cells,” said senior author Tobias Dörr, assistant professor of microbiology in the Weill Institute for Cell and Molecular Biology in the College of Agriculture and Life Sciences.


Co-authors included Ilana Brito, the Mong Family Sesquicentennial Faculty Scholar and assistant professor in the Meinig School of Biomedical Engineering in the College of Engineering, and Lars Westblade, associate professor of pathology and laboratory medicine at Weill Cornell Medicine.


Some bacteria, including the model bacterium used in the study, Vibrio cholerae, which causes cholera in humans, are remarkably tolerant to penicillin and related antibiotics, known as beta-lactam antibiotics. It has been known for a long time that beta-lactam antibiotics break down bacterial cell walls, but how bacteria survive loss of their cell walls was poorly understood.


In the study, the researchers developed a V. cholerae mutant that lacked a two-component damage repair response system that controls a gene network encoding diverse functions. Without the system, known as VxrAB, when the cell wall is damaged by antibiotics, the transfer of electrons across the cell membrane goes awry, leading to electrons ending up on the wrong molecules. This misdirection causes hydrogen peroxide to accumulate in the cell, which changes the oxidation state of cellular iron and disrupts signals for the cell to tell how much iron it has.  


In the presence of hydrogen peroxide, the mutant bacteria cannot sense how much iron has been acquired, and it behaves as if it is iron-starved and seeks to acquire more iron. Left unchecked, these circumstances cause iron toxicity, which will kill the cell, according to the experiments the researchers conducted. In further tests with mutant V. cholerae bacteria, both in test tubes and in mice, the researchers showed that reducing the influx of iron increased the bacteria’s tolerance to beta-lactams.


Fortunately for normal V. cholerae, exposure to antibiotics and the breakdown of the cell’s walls activate the VxrAB system, which works to repair cell walls and downregulates iron uptake systems, and thereby creates antibiotic tolerance. More study is needed to understand what triggers the VxrAB system in the presence of beta-lactam antibiotics.


The research opens the door for developing new drugs that could be combined with antibiotics to exploit oxidative damage and iron influx in tolerant bacteria. In future work, the researchers will search for parallel mechanisms of tolerance in other bacterial pathogens.


Jung-Ho Shin, a postdoctoral researcher in Dörr’s lab, is the paper’s first author. Co-authors include researchers from the Korea Advanced Institute of Science and Technology, the Korea Advanced Institute of Science and Technology, and the Intelligent Synthetic Biology Center in Korea.

The study was funded by the National Research Foundation of Korea and the National Institutes of Health.


https://www.worldhealth.net/news/antibiotic-tolerance-study-paves-way-new-treatments/


List of Articles
번호 제목 글쓴이 날짜 조회 수
412 [강석조 교수님] 이행 호염구, 알레르기 매개 세포에 대한 새로운 이해 생명과학과 2023.11.08 301
411 [정인경 교수님] 기저 질환이 없는 코로나19 환자의 중증 신규 유전적 위험 인자 규명 생명과학과 2022.09.29 336
410 [강창원, 서연수 교수님, 팔린다 박사님] 논문 Nucleic Acids Research 게재 생명과학과 2023.02.17 342
409 [정인경 교수님] 암, 노화 등에 미치는 게놈 3차 구조의 신규 원리 발견​ 생명과학과 2023.04.10 348
408 [메디포럼 정재언 대표] 메디포럼, 정재언 연구소장 신임 대표이사 선임…“임상 R&D 중심 경영 집중” 생명과학과 2022.03.14 371
407 [김진우 교수님] 새로운 세포핵 단백질의 이동 루트 발견​ 생명과학과 2023.02.28 381
406 [김학성 교수님, 김홍식 박사님] 암세포에만 약물 전달 가능한 클라트린 조립체 개발​ 생명과학과 2023.03.15 382
405 [김은준 교수님] 자폐 진단․ 치료 골든타임, 동물실험으로 확인 생명과학과 2022.09.27 386
404 [김찬혁 교수님] 말기 고형암 표적 2세대 면역치료제 개발​ 생명과학과 2023.04.20 397
403 [이승희 교수님] 신경전달물질 소마토스타틴의 알츠하이머 독성 개선효과 발견​ 생명과학과 2022.07.25 404
402 [김은준 교수님] 대규모 한국인 자폐증 가족 유전체 연구를 통한 새로운 자폐 유전변이 최초 발견​ 생명과학과 2022.07.19 407
401 [김보람 박사님(서성배 교수님 연구실)] 한국뇌연구원 제2회 다한우수논문상 선정 생명과학과 2022.12.07 411
400 [전상용, 조병관 교수님] 나노입자로 염증부터 면역치료까지 가능 생명과학과 2023.06.21 416
399 [루닛 서범석 대표] 바이오업계 유니콘 기대 루닛, 서범석 '치료 예측 AI' 고도화 박차 생명과학과 2022.04.27 422
398 [송지준 교수님] 헌팅턴병 발병원인 제거를 위한 치료제 개발 방법 제시​ 생명과학과 2022.09.02 423
397 충북도, 글로벌 바이오 캠퍼스 유치에 KAIST와 '맞손' 생명과학과 2022.03.15 434
396 [정인경 교수님] 파킨슨병 발병 3차원 게놈 지도 최초 제시​ 생명과학과 2023.05.08 439
395 [오병하 교수님] 오미크론에도 듣는 범용 항체, 국내에서 개발 생명과학과 2022.02.04 441
394 [이승재 교수님] 건강한 장수를 유도하는 돌연변이 유전자 발굴 생명과학과 2021.11.24 446
393 [김대수 교수님] 네이버 열린연단 '자유와 이성' 주제로 시즌9 강연 시작 생명과학과 2022.04.22 446
Board Pagination Prev 1 2 3 4 5 6 7 8 9 10 ... 22 Next
/ 22