Antimicrobials: An update on new strategies to diversify treatment for bacterial infections
Tegan Hibbert
1
,
Zeljka Krpetic
2
,
Joe Latimer
2
,
Hollie Leighton
1
,
Rebecca McHugh
3
,
Sian Pottenger
1
,
Charlotte Wragg
1
,
Chloë E. James
2
Publication type: Book Chapter
Publication date: 2024-03-16
SJR: —
CiteScore: 6.7
Impact factor: —
ISSN: 00652911, 21625468
PubMed ID:
38821632
Abstract
Ninety-five years after Fleming's discovery of penicillin, a bounty of antibiotic compounds have been discovered, modified, or synthesised. Diversification of target sites, improved stability and altered activity spectra have enabled continued antibiotic efficacy, but overwhelming reliance and misuse has fuelled the global spread of antimicrobial resistance (AMR). An estimated 1.27 million deaths were attributable to antibiotic resistant bacteria in 2019, representing a major threat to modern medicine. Although antibiotics remain at the heart of strategies for treatment and control of bacterial diseases, the threat of AMR has reached catastrophic proportions urgently calling for fresh innovation. The last decade has been peppered with ground-breaking developments in genome sequencing, high throughput screening technologies and machine learning. These advances have opened new doors for bioprospecting for novel antimicrobials. They have also enabled more thorough exploration of complex and polymicrobial infections and interactions with the healthy microbiome. Using models of infection that more closely resemble the infection state in vivo, we are now beginning to measure the impacts of antimicrobial therapy on host/microbiota/pathogen interactions. However new approaches are needed for developing and standardising appropriate methods to measure efficacy of novel antimicrobial combinations in these contexts. A battery of promising new antimicrobials is now in various stages of development including co-administered inhibitors, phages, nanoparticles, immunotherapy, anti-biofilm and anti-virulence agents. These novel therapeutics need multidisciplinary collaboration and new ways of thinking to bring them into large scale clinical use.
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Metrics
7
Total citations:
7
Citations from 2024:
7
(100%)
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GOST
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Hibbert T. et al. Antimicrobials: An update on new strategies to diversify treatment for bacterial infections // Advances in Microbial Physiology. 2024. Vol. 84. pp. 135-241.
GOST all authors (up to 50)
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Hibbert T., Krpetic Z., Latimer J., Leighton H., McHugh R., Pottenger S., Wragg C., James C. E. Antimicrobials: An update on new strategies to diversify treatment for bacterial infections // Advances in Microbial Physiology. 2024. Vol. 84. pp. 135-241.
Cite this
RIS
Copy
TY - GENERIC
DO - 10.1016/bs.ampbs.2023.12.002
UR - https://linkinghub.elsevier.com/retrieve/pii/S0065291123000309
TI - Antimicrobials: An update on new strategies to diversify treatment for bacterial infections
T2 - Advances in Microbial Physiology
AU - Hibbert, Tegan
AU - Krpetic, Zeljka
AU - Latimer, Joe
AU - Leighton, Hollie
AU - McHugh, Rebecca
AU - Pottenger, Sian
AU - Wragg, Charlotte
AU - James, Chloë E.
PY - 2024
DA - 2024/03/16
PB - Elsevier
SP - 135-241
VL - 84
PMID - 38821632
SN - 0065-2911
SN - 2162-5468
ER -
Cite this
BibTex (up to 50 authors)
Copy
@incollection{2024_Hibbert,
author = {Tegan Hibbert and Zeljka Krpetic and Joe Latimer and Hollie Leighton and Rebecca McHugh and Sian Pottenger and Charlotte Wragg and Chloë E. James},
title = {Antimicrobials: An update on new strategies to diversify treatment for bacterial infections},
publisher = {Elsevier},
year = {2024},
volume = {84},
pages = {135--241},
month = {mar}
}