| Literature DB >> 28852600 |
Sojib Bin Zaman1, Muhammed Awlad Hussain2, Rachel Nye3, Varshil Mehta4, Kazi Taib Mamun5, Naznin Hossain6.
Abstract
Antibiotics are the 'wonder drugs' to combat microbes. For decades, multiple varieties of antibiotics have not only been used for therapeutic purposes but practiced prophylactically across other industries such as agriculture and animal husbandry. Uncertainty has arisen, as microbes have become resistant to common antibiotics while the host remains unaware that antibiotic resistance has emerged. The aim of this review is to explore the origin, development, and the current state of antibiotic resistance, regulation, and challenges by examining available literature. We found that antibiotic resistance is increasing at an alarming rate. A growing list of infections i.e., pneumonia, tuberculosis, and gonorrhea are becoming harder and at times impossible to treat while antibiotics are becoming less effective. Antibiotic-resistant infections correlate with the level of antibiotic consumption. Non-judicial use of antibiotics is mostly responsible for making the microbes resistant. The antibiotic treatment repertoire for existing or emerging hard-to-treat multidrug-resistant bacterial infections is limited, resulting in high morbidity and mortality report. This review article reiterates the optimal use of antimicrobial medicines in human and animal health to reduce antibiotic resistance. Evidence from the literature suggests that the knowledge regarding antibiotic resistance in the population is still scarce. Therefore, the need of educating patients and the public is essential to fight against the antimicrobial resistance battle.Entities:
Keywords: antibiotic resistance; knowledge; rational use
Year: 2017 PMID: 28852600 PMCID: PMC5573035 DOI: 10.7759/cureus.1403
Source DB: PubMed Journal: Cureus ISSN: 2168-8184
Figure 1Graphical representation of onset of antibiotic resistance versus time to get antibiotic resistance
History of antibiotic discovery (green arrow) and time of first reported year of antibiotic resistance (right side). The red arrow (lower direction) indicates the discovery void and increased antibiotic resistance. The blue line indicates the time flow
Table representing the mechanism of drug resistance of common antibiotics
| Antibiotic class | Example(s) | Mode(s) of resistance |
| P-Lactams | Penicillins, Cephalosporins, Penems, Monobactams | Hydrolysis, efflux, altered target |
| Aminoglycosides | Gentamicin, Streptomycin, Spectinomycin | Phosphorylation, acetylation, nucleotidylation, efflux, altered target |
| Glycopeptides | Vancomycin, Teicoplanin | Reprogramming peptidoglycan biosynthesis |
| Tetracyclines | Minocycline, Tigecycline | Monooxygenation, efflux, altered target |
| Macrolides | Erythromycin, azithromycin | Hydrolysis, glycosylation, phosphorylation, efflux, altered target |
| Lincosamides | Clindamycin | Nucleotidylation, efflux, altered target |
| Streptogramins | Synercid | Carbon-Oxygen lyase, acetylation, efflux, altered target |
| Oxazolidinones | Linezolid | Efflux, altered target |
| Phenicols | Chloramphenicol | Acetylation, efflux, altered target |
| Quinolones | Ciprofloxacin | Acetylation, efflux, altered target |
| Pyrimidines | Trimethoprim | Efflux, altered target |
| Sulfonamides | Sulfamethoxazole | Efflux, altered target |
| Rifamycins | Rifampin | ADP-ribosylation, efflux, altered target |
| Lipopeptides | Daptomycin | Altered target |
| Cationic peptides | Colistin | Altered target, efflux |