Extracellular Matrix Rigidities Regulate the Tricarboxylic Acid Cycle and Antibiotic Resistance of Three‐Dimensionally Confined Bacterial Microcolonies

Abstract As a major cause of clinical chronic infection, microbial biofilms/microcolonies in host tissues essentially live in 3D‐constrained microenvironments, which potentially modulate their spatial self‐organization and morphodynamics. However, it still remains unclear whether and how mechanical...

Full description

Bibliographic Details
Main Authors: Yiming Han, Nan Jiang, Hongwei Xu, Zuoying Yuan, Jidong Xiu, Sheng Mao, Xiaozhi Liu, Jianyong Huang
Format: Article
Language:English
Published: Wiley 2023-03-01
Series:Advanced Science
Subjects:
Online Access:https://doi.org/10.1002/advs.202206153
_version_ 1797860808558903296
author Yiming Han
Nan Jiang
Hongwei Xu
Zuoying Yuan
Jidong Xiu
Sheng Mao
Xiaozhi Liu
Jianyong Huang
author_facet Yiming Han
Nan Jiang
Hongwei Xu
Zuoying Yuan
Jidong Xiu
Sheng Mao
Xiaozhi Liu
Jianyong Huang
author_sort Yiming Han
collection DOAJ
description Abstract As a major cause of clinical chronic infection, microbial biofilms/microcolonies in host tissues essentially live in 3D‐constrained microenvironments, which potentially modulate their spatial self‐organization and morphodynamics. However, it still remains unclear whether and how mechanical cues of 3D confined microenvironments, for example, extracellular matrix (ECM) stiffness, exert an impact on antibiotic resistance of bacterial biofilms/microcolonies. With a high‐throughput antibiotic sensitivity testing (AST) platform, it is revealed that 3D ECM rigidities greatly modulate their resistance to diverse antibiotics. The microcolonies in 3D ECM with human tissue‐specific rigidities varying from 0.5 to 20 kPa show a ≈2–10 000‐fold increase in minimum inhibitory concentration, depending on the types of antibiotics. The authors subsequently identified that the increase in 3D ECM rigidities leads to the downregulation of the tricarboxylic acid (TCA) cycle, which is responsible for enhanced antibiotic resistance. Further, it is shown that fumarate, as a potentiator of TCA cycle activity, can alleviate the elevated antibiotic resistance and thus remarkably improve the efficacy of antibiotics against bacterial microcolonies in 3D confined ECM, as confirmed in the chronic infection mice model. These findings suggest fumarate can be employed as an antibiotic adjuvant to effectively treat infections induced by bacterial biofilms/microcolonies in a 3D‐confined environment.
first_indexed 2024-04-09T21:53:00Z
format Article
id doaj.art-43b3e5469bef434da82cecaac9e9d401
institution Directory Open Access Journal
issn 2198-3844
language English
last_indexed 2024-04-09T21:53:00Z
publishDate 2023-03-01
publisher Wiley
record_format Article
series Advanced Science
spelling doaj.art-43b3e5469bef434da82cecaac9e9d4012023-03-24T12:30:04ZengWileyAdvanced Science2198-38442023-03-01109n/an/a10.1002/advs.202206153Extracellular Matrix Rigidities Regulate the Tricarboxylic Acid Cycle and Antibiotic Resistance of Three‐Dimensionally Confined Bacterial MicrocoloniesYiming Han0Nan Jiang1Hongwei Xu2Zuoying Yuan3Jidong Xiu4Sheng Mao5Xiaozhi Liu6Jianyong Huang7Department of Mechanics and Engineering Science, and Beijing Innovation Center for Engineering Science and Advanced Technology College of Engineering Peking University 100871 Beijing ChinaDepartment of Mechanics and Engineering Science, and Beijing Innovation Center for Engineering Science and Advanced Technology College of Engineering Peking University 100871 Beijing ChinaDepartment of Mechanics and Engineering Science, and Beijing Innovation Center for Engineering Science and Advanced Technology College of Engineering Peking University 100871 Beijing ChinaDepartment of Mechanics and Engineering Science, and Beijing Innovation Center for Engineering Science and Advanced Technology College of Engineering Peking University 100871 Beijing ChinaDepartment of Mechanics and Engineering Science, and Beijing Innovation Center for Engineering Science and Advanced Technology College of Engineering Peking University 100871 Beijing ChinaDepartment of Mechanics and Engineering Science, and Beijing Innovation Center for Engineering Science and Advanced Technology College of Engineering Peking University 100871 Beijing ChinaTianjin Key Laboratory of Epigenetics for Organ Development of Premature Infants Fifth Central Hospital of Tianjin Tianjin 300450 ChinaDepartment of Mechanics and Engineering Science, and Beijing Innovation Center for Engineering Science and Advanced Technology College of Engineering Peking University 100871 Beijing ChinaAbstract As a major cause of clinical chronic infection, microbial biofilms/microcolonies in host tissues essentially live in 3D‐constrained microenvironments, which potentially modulate their spatial self‐organization and morphodynamics. However, it still remains unclear whether and how mechanical cues of 3D confined microenvironments, for example, extracellular matrix (ECM) stiffness, exert an impact on antibiotic resistance of bacterial biofilms/microcolonies. With a high‐throughput antibiotic sensitivity testing (AST) platform, it is revealed that 3D ECM rigidities greatly modulate their resistance to diverse antibiotics. The microcolonies in 3D ECM with human tissue‐specific rigidities varying from 0.5 to 20 kPa show a ≈2–10 000‐fold increase in minimum inhibitory concentration, depending on the types of antibiotics. The authors subsequently identified that the increase in 3D ECM rigidities leads to the downregulation of the tricarboxylic acid (TCA) cycle, which is responsible for enhanced antibiotic resistance. Further, it is shown that fumarate, as a potentiator of TCA cycle activity, can alleviate the elevated antibiotic resistance and thus remarkably improve the efficacy of antibiotics against bacterial microcolonies in 3D confined ECM, as confirmed in the chronic infection mice model. These findings suggest fumarate can be employed as an antibiotic adjuvant to effectively treat infections induced by bacterial biofilms/microcolonies in a 3D‐confined environment.https://doi.org/10.1002/advs.202206153bacterial biofilmmatrix stiffnessmechanobiologymetabolismminimum biofilm elimination concentration
spellingShingle Yiming Han
Nan Jiang
Hongwei Xu
Zuoying Yuan
Jidong Xiu
Sheng Mao
Xiaozhi Liu
Jianyong Huang
Extracellular Matrix Rigidities Regulate the Tricarboxylic Acid Cycle and Antibiotic Resistance of Three‐Dimensionally Confined Bacterial Microcolonies
Advanced Science
bacterial biofilm
matrix stiffness
mechanobiology
metabolism
minimum biofilm elimination concentration
title Extracellular Matrix Rigidities Regulate the Tricarboxylic Acid Cycle and Antibiotic Resistance of Three‐Dimensionally Confined Bacterial Microcolonies
title_full Extracellular Matrix Rigidities Regulate the Tricarboxylic Acid Cycle and Antibiotic Resistance of Three‐Dimensionally Confined Bacterial Microcolonies
title_fullStr Extracellular Matrix Rigidities Regulate the Tricarboxylic Acid Cycle and Antibiotic Resistance of Three‐Dimensionally Confined Bacterial Microcolonies
title_full_unstemmed Extracellular Matrix Rigidities Regulate the Tricarboxylic Acid Cycle and Antibiotic Resistance of Three‐Dimensionally Confined Bacterial Microcolonies
title_short Extracellular Matrix Rigidities Regulate the Tricarboxylic Acid Cycle and Antibiotic Resistance of Three‐Dimensionally Confined Bacterial Microcolonies
title_sort extracellular matrix rigidities regulate the tricarboxylic acid cycle and antibiotic resistance of three dimensionally confined bacterial microcolonies
topic bacterial biofilm
matrix stiffness
mechanobiology
metabolism
minimum biofilm elimination concentration
url https://doi.org/10.1002/advs.202206153
work_keys_str_mv AT yiminghan extracellularmatrixrigiditiesregulatethetricarboxylicacidcycleandantibioticresistanceofthreedimensionallyconfinedbacterialmicrocolonies
AT nanjiang extracellularmatrixrigiditiesregulatethetricarboxylicacidcycleandantibioticresistanceofthreedimensionallyconfinedbacterialmicrocolonies
AT hongweixu extracellularmatrixrigiditiesregulatethetricarboxylicacidcycleandantibioticresistanceofthreedimensionallyconfinedbacterialmicrocolonies
AT zuoyingyuan extracellularmatrixrigiditiesregulatethetricarboxylicacidcycleandantibioticresistanceofthreedimensionallyconfinedbacterialmicrocolonies
AT jidongxiu extracellularmatrixrigiditiesregulatethetricarboxylicacidcycleandantibioticresistanceofthreedimensionallyconfinedbacterialmicrocolonies
AT shengmao extracellularmatrixrigiditiesregulatethetricarboxylicacidcycleandantibioticresistanceofthreedimensionallyconfinedbacterialmicrocolonies
AT xiaozhiliu extracellularmatrixrigiditiesregulatethetricarboxylicacidcycleandantibioticresistanceofthreedimensionallyconfinedbacterialmicrocolonies
AT jianyonghuang extracellularmatrixrigiditiesregulatethetricarboxylicacidcycleandantibioticresistanceofthreedimensionallyconfinedbacterialmicrocolonies