TY - CHAP
T1 - Novel targets of antimicrobial therapies
AU - Maddocks, Sarah E.
N1 - Publisher Copyright:
© 2016 American Society for Microbiology.
PY - 2016/4/9
Y1 - 2016/4/9
N2 - During the golden age of antibiotic discovery, from the 1930s through the 1960s, methods of antibiotic identification relied solely on scientific observation, and while chemical analogues such as amoxicillin, derived from penicillin, continued to be developed, they retained the same mechanisms of action and hence the same bacterial targets. Moreover, there are finite modifications that can ultimately be made to "old" classes of antibiotics. Consequently, only two new classes of antibiotics have been discovered in the past 40 years, and both entered the market early in the new millennium. The advent of the genomics revolution offered a new hope for the discovery of novel antimicrobial targets. Genomic strategies were utilized to identify potential antibacterial targets, namely those that, if inhibited, resulted in the death of the bacterium. Such targets were to be present in pathogenic strains of bacteria and absent from the human host; they could include metabolic pathways, receptor ligands, and virulence traits, to name a few. Despite the abundance of targets identified using this strategy, no new antibiotics have reached the marketplace as a result of the genomics approach. However, new antimicrobials with novel targets continue to be identified and contribute to the ongoing struggle against antimicrobial resistance that threatens to return humankind to a situation comparable to the preantibiotic era.
AB - During the golden age of antibiotic discovery, from the 1930s through the 1960s, methods of antibiotic identification relied solely on scientific observation, and while chemical analogues such as amoxicillin, derived from penicillin, continued to be developed, they retained the same mechanisms of action and hence the same bacterial targets. Moreover, there are finite modifications that can ultimately be made to "old" classes of antibiotics. Consequently, only two new classes of antibiotics have been discovered in the past 40 years, and both entered the market early in the new millennium. The advent of the genomics revolution offered a new hope for the discovery of novel antimicrobial targets. Genomic strategies were utilized to identify potential antibacterial targets, namely those that, if inhibited, resulted in the death of the bacterium. Such targets were to be present in pathogenic strains of bacteria and absent from the human host; they could include metabolic pathways, receptor ligands, and virulence traits, to name a few. Despite the abundance of targets identified using this strategy, no new antibiotics have reached the marketplace as a result of the genomics approach. However, new antimicrobials with novel targets continue to be identified and contribute to the ongoing struggle against antimicrobial resistance that threatens to return humankind to a situation comparable to the preantibiotic era.
KW - Anti-quorum sensing
KW - Antibiofilm antimicrobial peptide
KW - Antimicrobial resistance
KW - Antimicrobial therapies
KW - Combination therapies
KW - Microbial communication
KW - Multidrug-resistant bacteria
KW - Nano-formulated antibiotics
KW - Receptor-mediated pathogenicity
KW - Toxicogenomics
UR - http://www.scopus.com/inward/record.url?scp=85029617528&partnerID=8YFLogxK
U2 - 10.1128/9781555819286.ch26
DO - 10.1128/9781555819286.ch26
M3 - Chapter
AN - SCOPUS:85029617528
SN - 9781555819279
SP - 739
EP - 752
BT - Virulence Mechanisms of Bacterial Pathogens
PB - wiley
ER -