TY - JOUR
T1 - Exogenous metabolite feeding on altering antibiotic susceptibility in Gram-negative bacteria through metabolic modulation
T2 - a review
AU - Chung, Wan Yean
AU - Zhu, Yan
AU - Mahamad Maifiah, Mohd Hafidz
AU - Hawala Shivashekaregowda, Naveen Kumar
AU - Wong, Eng Hwa
AU - Abdul Rahim, Nusaibah
N1 - Funding Information:
This work was supported by the Fundamental Research Grant Scheme, Ministry of Higher Education, Malaysia [FRGS/1/2019/SKK11/TAYLOR/03/1].
Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2022/7
Y1 - 2022/7
N2 - Background: The rise of antimicrobial resistance at an alarming rate is outpacing the development of new antibiotics. The worrisome trends of multidrug-resistant Gram-negative bacteria have enormously diminished existing antibiotic activity. Antibiotic treatments may inhibit bacterial growth or lead to induce bacterial cell death through disruption of bacterial metabolism directly or indirectly. In light of this, it is imperative to have a thorough understanding of the relationship of bacterial metabolism with antimicrobial activity and leverage the underlying principle towards development of novel and effective antimicrobial therapies. Objective: Herein, we explore studies on metabolic analyses of Gram-negative pathogens upon antibiotic treatment. Metabolomic studies revealed that antibiotic therapy caused changes of metabolites abundance and perturbed the bacterial metabolism. Following this line of thought, addition of exogenous metabolite has been employed in in vitro, in vivo and in silico studies to activate the bacterial metabolism and thus potentiate the antibiotic activity. Key scientific concepts of review: Exogenous metabolites were discovered to cause metabolic modulation through activation of central carbon metabolism and cellular respiration, stimulation of proton motive force, increase of membrane potential, improvement of host immune protection, alteration of gut microbiome, and eventually facilitating antibiotic killing. The use of metabolites as antimicrobial adjuvants may be a promising approach in the fight against multidrug-resistant pathogens.
AB - Background: The rise of antimicrobial resistance at an alarming rate is outpacing the development of new antibiotics. The worrisome trends of multidrug-resistant Gram-negative bacteria have enormously diminished existing antibiotic activity. Antibiotic treatments may inhibit bacterial growth or lead to induce bacterial cell death through disruption of bacterial metabolism directly or indirectly. In light of this, it is imperative to have a thorough understanding of the relationship of bacterial metabolism with antimicrobial activity and leverage the underlying principle towards development of novel and effective antimicrobial therapies. Objective: Herein, we explore studies on metabolic analyses of Gram-negative pathogens upon antibiotic treatment. Metabolomic studies revealed that antibiotic therapy caused changes of metabolites abundance and perturbed the bacterial metabolism. Following this line of thought, addition of exogenous metabolite has been employed in in vitro, in vivo and in silico studies to activate the bacterial metabolism and thus potentiate the antibiotic activity. Key scientific concepts of review: Exogenous metabolites were discovered to cause metabolic modulation through activation of central carbon metabolism and cellular respiration, stimulation of proton motive force, increase of membrane potential, improvement of host immune protection, alteration of gut microbiome, and eventually facilitating antibiotic killing. The use of metabolites as antimicrobial adjuvants may be a promising approach in the fight against multidrug-resistant pathogens.
KW - Antibiotic susceptibility
KW - Antimicrobial resistance
KW - Gram-negative bacteria
KW - Metabolic modulation
KW - Metabolism
UR - http://www.scopus.com/inward/record.url?scp=85133286623&partnerID=8YFLogxK
U2 - 10.1007/s11306-022-01903-w
DO - 10.1007/s11306-022-01903-w
M3 - Review Article
C2 - 35781167
AN - SCOPUS:85133286623
SN - 1573-3882
VL - 18
JO - Metabolomics
JF - Metabolomics
IS - 7
M1 - 47
ER -