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Ch. 10 - Controlling Microbial Growth in the Body: Antimicrobial Drugs
Bauman - Microbiology with Diseases by Taxonomy 6th Edition
Bauman6th EditionMicrobiology with Diseases by TaxonomyISBN: 9780134832302Non è quello che usi tu?Cambia libro di testo
Capitolo 10, Problema 4

Given that both human cells and pathogens synthesize proteins at ribosomal sites, how can antimicrobial agents that target this process be safe to use in humans?

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Understand that both human cells and many pathogens synthesize proteins using ribosomes, but the structure and composition of ribosomes differ between prokaryotic pathogens (like bacteria) and eukaryotic human cells.
Recognize that antimicrobial agents targeting protein synthesis are designed to specifically bind to bacterial ribosomes (70S ribosomes, composed of 50S and 30S subunits) without affecting human ribosomes (80S ribosomes, composed of 60S and 40S subunits).
Identify that this selective binding is possible because of differences in ribosomal RNA sequences and protein components between bacterial and human ribosomes, allowing drugs to inhibit bacterial protein synthesis selectively.
Consider that some antimicrobial agents may also target unique steps or factors involved in bacterial translation that are absent or significantly different in human cells, further increasing specificity and safety.
Conclude that the safety of these antimicrobial agents in humans arises from their ability to discriminate between pathogen and human ribosomes, thereby inhibiting protein synthesis in pathogens while sparing human cells.

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Differences Between Prokaryotic and Eukaryotic Ribosomes

Human cells have 80S ribosomes (60S and 40S subunits), while many pathogens, like bacteria, have 70S ribosomes (50S and 30S subunits). Antimicrobial agents target the structural and functional differences in bacterial ribosomes, allowing selective inhibition of protein synthesis in pathogens without affecting human ribosomes.
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Prokaryotic Ribosomes

Mechanism of Action of Ribosome-Targeting Antibiotics

Antibiotics such as tetracyclines, aminoglycosides, and macrolides bind specifically to bacterial ribosomal subunits, blocking critical steps in protein synthesis like initiation, elongation, or translocation. This selective binding disrupts bacterial growth while sparing human cells due to ribosomal differences.
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Structure of Prokaryotic Ribosomes

Selective Toxicity in Antimicrobial Therapy

Selective toxicity refers to the ability of a drug to target microbial cells without harming host cells. By exploiting unique features of microbial ribosomes, antimicrobial agents achieve this selectivity, making them safe for human use despite targeting a process also present in human cells.
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Selective Media
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