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The Crisis in Antibiotic Resistance
Abstract
The synthesis of large numbers of antibiotics over the past three decades has caused complacency about the threat of bacterial resistance. Bacteria have become resistant to antimicrobial agents as a result of chromosomal changes or the exchange of the exchange of genetic material via plasmids and transposons. Streptococcus pneumoniae, Streptococcus pyogenes, and staphylococci, organisms that cause respiratory and cutaneous infections, and members of the Enterobacteriaceae and Pseudomonas families, organisms that cause diarrhea, urinary infection, and sepsis, are now resistant to virtually all of the older antibiotics. The extensive use of antibiotics in the community and hospitals has fueled this crisis. Mechanisms such as antibiotic control programs, better hygiene, and synthesis of agents with improved antimicrobial activity need to be adopted in order to limit bacterial resistance.
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“Overuse and antibiotic resistance have proliferated[422]”
From Enterosalivary nitrate metabolism and the microbiome: Intersection of microbial metabolism, nitric oxide and diet in cardiac and pulmonary vascular health (2017) · cites this paper as [422]
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“They show resistance to many commercially available antibiotics that target general metabolic pathways, including synthesis of proteins, RNA, DNA, and the cell wall (2, 3).”
BackgroundThe use of nanomaterials for the mitigation of pathogenic biofilm formation
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“Since the EU banned most of the antibiotic growth promoters in broiler nutrition (ANONYMOUS, 2003) due to cross and multiple resistance (NEU, 1992), much research has been conducted to explore the use of plants, plant extracts and EO as effective substitutes.”
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“The emerging resistance of bacteria to penicillin is a frightening problem with a number of common pathogenic bacterial species (12, 35, 44, 45).”
BackgroundDerivatives of a Vancomycin-ResistantStaphylococcus aureusStrain Isolated at Hershey Medical Center
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“As shown in Scheme 1, commercially available vancomycin ( 1 ) reacted with 3-picolylamine, 4-picolylamine, 3-(2-aminoethyl)pyridine, or 1-(3-aminopropyl)imidazole to give the vancomycin carboxamide derivatives (Van-CONH-L) 2a-d in good yields (>65%), respectively.”
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“2001; Livermore 2004) or the improvement of efficacy of established antibiotics by the development of new agents capable of enhancing antibiotic activity (Neu 1992).”
Background
Metadata
- Authors
- Neu, H. C.
- Affiliations
- Columbia University (US)
- Corresponding author
- Neu, Harold C.
- Venue
- Science
- Published
- 1992-08-21
- Volume
- 257
- Issue
- 5073
- Pages
- 1064-1073
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W1980595924
- Cited by
- 2,834
- References
- 109
- Citations by year
- 2026: 23 · 2025: 48 · 2024: 57 · 2023: 71 · 2022: 91 · 2021: 93 · 2020: 123 · 2019: 100 · 2018: 122 · 2017: 123 · 2016: 105 · 2015: 87 · 2014: 95 · 2013: 109 · 2012: 99
- FWCI
- 46.70
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Microbiology (medical) › Antibiotic Resistance in Bacteria
- Health Sciences › Medicine › Infectious Diseases › Antibiotic Use and Resistance
- Health Sciences › Medicine › Infectious Diseases › Antimicrobial Resistance in Staphylococcus
- Keywords
- antibiotic resistance, bacterial resistance, plasmids, transposable elements, horizontal gene transfer, Streptococcus pneumoniae, Streptococcus pyogenes, Staphylococcus, Enterobacteriaceae, Pseudomonas, antibiotic overuse, hygiene, novel antimicrobial agents
- MeSH terms
- Anti-Bacterial Agents, Bacterial Infections, Cross Infection, Drug Resistance, Microbial, Enterobacteriaceae, Haemophilus influenzae, Humans, Staphylococcus, Streptococcus pneumoniae, Streptococcus pyogenes, Enterococcus
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