| Literature DB >> 31592430 |
Fataneh Hashempour-Baltork1, Hedayat Hosseini2,3, Saeedeh Shojaee-Aliabadi2, Mohammadali Torbati4, Adel Mirza Alizadeh1, Matin Alizadeh5.
Abstract
Antibiotic therapy is among the most important treatments against infectious diseases and has tremendously improved effects on public health. Nowadays, development in using this treatment has led us to the emergence and enhancement of drug-resistant pathogens which can result in some problems including treatment failure, increased mortality as well as treatment costs, reduced infection control efficiency, and spread of resistant pathogens from hospital to community. Therefore, many researches have tried to find new alternative approaches to control and prevent this problem. This study, has been revealed some possible and effective approaches such as using farming practice, natural antibiotics, nano-antibiotics, lactic acid bacteria, bacteriocin, cyclopeptid, bacteriophage, synthetic biology and predatory bacteria as alternatives for traditional antibiotics to prevent or reduce the emergence of drug resistant bacteria.Entities:
Keywords: Drug resistance; Food borne pathogens; Food safety; Health; Prevention strategies
Year: 2019 PMID: 31592430 PMCID: PMC6773942 DOI: 10.15171/apb.2019.041
Source DB: PubMed Journal: Adv Pharm Bull ISSN: 2228-5881
A few food borne pathogens, related disease, antimicrobials and resistance mechanism
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| Tuberculosis | Fluoroquinolones | Modifying enzymes, target mimicry |
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| Pneumococcal meningitis | Penicillin | Genetic alteration of penicillin-binding protein |
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| Severe watery diarrhea | Sulfonamides | Chromosomal alterations in encoding dihydropteroate synthase |
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| Tetracycline | Preventing binding of the antibiotic |
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| Severe diarrhea | Chloramphenicol, tetracycline | Decreased permeability, efflux |
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| Typhoid | Chloramphenicol | Alteration in target site, production of chloramphenicol acetyltransferase, active efflux |
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| Gastrointestinal illnesses | Tetracycline | Target protection, Change in ribosomal conformation and preventing binding of the antibiotic |
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| Yeast infections, oral Thrush | Azoles |
Alteration in ergosterol sites, incorporation of different |
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| Sore throat, scarlet fever | Tetracycline | Target protection, Change in ribosomal conformation and preventing binding of the antibiotic |
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| - | B-lactam antibiotics | Decrease permeability cell membrane |
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| Quinolone | Alteration in DNA gyrase, antibiotic efflux systems |
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| Aminoglycoside | Cell-wall impermeability, enzymatic modification. |
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| Blood infection, necrotizing enterocolitis | Carbapenem | Mutational loss of porin channel, acquired zinc b-lactamase |
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| Soft tissue infections | Vancomycin | Bypass of antibiotic target |
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| Vomiting, diarrhea, dehydration | Methicillin, |
Related to |
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| Streptogramin antibiotics, macrolide, lincosamide | Inactivating enzymes, modification of target sites, active efflux |
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| Quinolone | Active efflux, changing in DNA topoisomerases |
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| Pyogenic, meningitis and septicemia | Chloramphenicol | Production of chloramphenicol acetyltransferase |
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| Rifampin | Alteration in RNA polymerase, membrane permeability |
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| Sulfonamides | Chromosomal alterations in encoding dihydropteroate synthase |
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| Penicillin | Alterations in penicillin-binding proteins |
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Figure 1Fractional inhibitory concentration (FIC) indices of classical and natural antimicrobial pairs against antibiotic resistant bacteria
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| Meropenem–peppermint | - | 0.26 |
| Synergistic |
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| Meropenem (µg/mL) | 0.13 | ||||
| Peppermint (%, v/v) | 0.13 | ||||
| Cefoperazone-coriander | - | 0.750 |
| No interaction |
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| Cefoperazone (µg/mL) | 0.500 | ||||
| Coriander oil(%, v/v) | 0.250 | ||||
| Erythromycin-eugenol | - | < 0.50 |
| Synergistic |
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| Ampicillin-eugenol | - | 1 |
| No interaction |
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| Gentamicin-tea tree | - | 0.5 |
| Synergistic |
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| Meropenem-cinnamon | - | 1.5 |
| No interaction |
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| Chloramphenicol-coriander | - | 0.312 |
| Synergistic |
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| Chloramphenicol (µg/mL) | 0.062 | ||||
| Coriander(%, v/v) | 0.250 | ||||
| Tetracycline- Lemon thyme | - | 0.95–1.08 |
| No interaction |
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| Meropenem–tea tree | - | 1 |
| No interaction |
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| Meropenem (µg/mL) | 0.50 | ||||
| Tea tree (%, v/v) | 0.50 | ||||
| Tetracycline-cinnamaldehyde | - | 0.37 |
| Synergistic |
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| Chloramphenicol-coriander | - | 0.047 |
| Synergistic |
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| Chloramphenicol (µg/ml) | 0.016 | ||||
| Coriander(%, v/v) | 0.031 | ||||
| Gentamicin-rosewood | - | 0.11 |
| Synergistic |
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Piperacillin- Coriander | - | 0.625 |
| No interaction |
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| 0.125 | |||||
| 0.500 | |||||
| Penicillin-carvacrol | - | 0.32 | Salmonella Typhimurium SGI 1 | Synergistic |
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| Ampicillin-eugenol | - | <0.50 |
| Synergistic |
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| Penicillin-Allyl isothiocyanate | - | 0.66 |
| No interaction |
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| Meropenem-lemon | - | 2 |
| No interaction |
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| Tetracycline-coriander | - | 0.185 |
| Synergistic |
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| Tetracycline (µg/mL) | 0.125 | - | |||
| Coriander oil (%, v/v) | 0.062 | - | |||
| Cefixime-thyme | - | 1.25 |
| No interaction |
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| Cefixime-thyme | - | 1 |
| No interaction |
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| Ampicillin-thymol | - | 0.12 |
| Synergistic |
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| Amoxicillin-sandarac | - | 1 |
| No interaction |
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| Chloramphenicol-geraniol | - | 0.32–0.87 |
| Synergistic |
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| Ceftazidime–cinnamon bark | - | 2 |
| No interaction |
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| Ceftazidime (µg/mL) | 1 | - | |||
| Cinnamon bark (%, v/v) | 1 | - |
FIC of oil = MIC of oil in mixing by antibiotic/MIC of oil alone.
FIC of antibiotic = MIC of antibiotic in mixing by oil/MIC of antibiotic alone.
FIC index = FIC of oil + FIC of antibiotic.