Tetracycline antibiotics: Difference between revisions

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{{Short description|A class of broad-spectrum antibiotics derived from Streptomyces bacteria}}
{{short description|Class of antibiotics}}
{{Use dmy dates|date=October 2023}}


'''Tetracycline antibiotics''' are a group of broad-spectrum antibiotics that are effective against a wide range of microorganisms, including gram-positive and gram-negative bacteria, chlamydiae, mycoplasmas, rickettsiae, and protozoan parasites. These antibiotics are derived from the bacterium ''[[Streptomyces]]'' and are characterized by their four-ring molecular structure.
'''Tetracycline antibiotics''' are a class of [[antibiotics]] that are used to treat a wide variety of infections. They are derived from the bacterium ''[[Streptomyces]]'' and are characterized by their four-ring molecular structure.
 
==Structure==
[[File:Tetracycline_numbering.svg|thumb|right|250px|Numbering of the tetracycline structure.]]
Tetracyclines are defined by their four hydrocarbon rings, which are fused together. The basic structure of tetracyclines allows for various modifications, leading to different derivatives with varying properties and spectrum of activity.


==Mechanism of Action==
==Mechanism of Action==
Tetracyclines work by inhibiting protein synthesis in bacteria. They achieve this by binding to the 30S ribosomal subunit, preventing the attachment of aminoacyl-tRNA to the ribosomal acceptor (A) site. This action effectively halts the addition of new amino acids to the nascent peptide chain, thereby inhibiting bacterial growth and reproduction.
Tetracyclines work by inhibiting [[protein synthesis]] in bacteria. They bind to the 30S ribosomal subunit, preventing the attachment of [[aminoacyl-tRNA]] to the [[ribosome]] and thus inhibiting the addition of new amino acids to the growing peptide chain. This action is generally bacteriostatic, meaning it inhibits the growth and reproduction of bacteria rather than killing them outright.
 
==Spectrum of Activity==
Tetracyclines are broad-spectrum antibiotics, effective against a wide range of [[Gram-positive]] and [[Gram-negative]] bacteria. They are also active against certain intracellular pathogens such as ''[[Chlamydia]]'', ''[[Mycoplasma]]'', and ''[[Rickettsia]]''.


==Clinical Uses==
==Clinical Uses==
Tetracyclines are used to treat a variety of infections, including:
Tetracyclines are used to treat various infections, including:
* [[Respiratory tract infections]]
* [[Urinary tract infections]]
* [[Acne vulgaris]]
* [[Acne vulgaris]]
* [[Cholera]]
* [[Cholera]]
* [[Brucellosis]]
* [[Lyme disease]]
* [[Plague]]
* [[Rocky Mountain spotted fever]]
* [[Rickettsial infections]] such as [[Rocky Mountain spotted fever]]
* [[Chlamydia trachomatis]] infections
* [[Mycoplasma pneumoniae]] infections


==Side Effects==
==Side Effects==
Common side effects of tetracycline antibiotics include gastrointestinal disturbances such as nausea, vomiting, and diarrhea. They can also cause photosensitivity, leading to an increased risk of sunburn. Long-term use can result in discoloration of teeth and affect bone growth in children.
Common side effects of tetracyclines include gastrointestinal disturbances, such as nausea and diarrhea. They can also cause photosensitivity, leading to an increased risk of sunburn. Tetracyclines can affect bone and tooth development, so they are generally avoided in children under the age of 8 and in pregnant women.


==Resistance==
==Resistance==
Bacterial resistance to tetracyclines can occur through several mechanisms, including:
[[Bacterial resistance]] to tetracyclines can occur through several mechanisms, including efflux pumps that expel the drug from the cell, ribosomal protection proteins that prevent tetracycline binding, and enzymatic inactivation of the drug.
* Efflux pumps that expel the antibiotic from the bacterial cell
* Ribosomal protection proteins that prevent tetracycline binding
* Enzymatic inactivation of the antibiotic
 
==Examples of Tetracyclines==
Some commonly used tetracycline antibiotics include:
* [[Tetracycline]]
* [[Doxycycline]]
* [[Minocycline]]
* [[Tigecycline]]
 
==History==
The first tetracycline, chlortetracycline, was discovered in the late 1940s. It was isolated from ''[[Streptomyces aureofaciens]]''. Since then, several derivatives have been developed to improve efficacy and reduce side effects.


==Images==
==Derivatives==
[[File:Tetracycline.svg|thumb|right|Chemical structure of tetracycline]]
[[File:6deoxy6demethyltetracycline.jpg|thumb|left|250px|6-Deoxy-6-demethyltetracycline, a derivative of tetracycline.]]
[[File:Doxycycline.png|thumb|left|Chemical structure of doxycycline]]
Several derivatives of tetracycline have been developed to overcome resistance and improve pharmacokinetic properties. These include doxycycline and minocycline, which have improved absorption and longer half-lives compared to the original tetracycline.


==Related Pages==
==Related pages==
* [[Antibiotic resistance]]
* [[Antibiotic resistance]]
* [[Protein synthesis inhibitors]]
* [[Protein synthesis inhibitors]]
* [[Broad-spectrum antibiotics]]
* [[Streptomyces]]


[[Category:Antibiotics]]
[[Category:Antibiotics]]
[[Category:Tetracyclines]]
[[Category:Tetracyclines]]

Revision as of 14:17, 21 February 2025

Class of antibiotics



Tetracycline antibiotics are a class of antibiotics that are used to treat a wide variety of infections. They are derived from the bacterium Streptomyces and are characterized by their four-ring molecular structure.

Structure

Numbering of the tetracycline structure.

Tetracyclines are defined by their four hydrocarbon rings, which are fused together. The basic structure of tetracyclines allows for various modifications, leading to different derivatives with varying properties and spectrum of activity.

Mechanism of Action

Tetracyclines work by inhibiting protein synthesis in bacteria. They bind to the 30S ribosomal subunit, preventing the attachment of aminoacyl-tRNA to the ribosome and thus inhibiting the addition of new amino acids to the growing peptide chain. This action is generally bacteriostatic, meaning it inhibits the growth and reproduction of bacteria rather than killing them outright.

Spectrum of Activity

Tetracyclines are broad-spectrum antibiotics, effective against a wide range of Gram-positive and Gram-negative bacteria. They are also active against certain intracellular pathogens such as Chlamydia, Mycoplasma, and Rickettsia.

Clinical Uses

Tetracyclines are used to treat various infections, including:

Side Effects

Common side effects of tetracyclines include gastrointestinal disturbances, such as nausea and diarrhea. They can also cause photosensitivity, leading to an increased risk of sunburn. Tetracyclines can affect bone and tooth development, so they are generally avoided in children under the age of 8 and in pregnant women.

Resistance

Bacterial resistance to tetracyclines can occur through several mechanisms, including efflux pumps that expel the drug from the cell, ribosomal protection proteins that prevent tetracycline binding, and enzymatic inactivation of the drug.

Derivatives

File:6deoxy6demethyltetracycline.jpg
6-Deoxy-6-demethyltetracycline, a derivative of tetracycline.

Several derivatives of tetracycline have been developed to overcome resistance and improve pharmacokinetic properties. These include doxycycline and minocycline, which have improved absorption and longer half-lives compared to the original tetracycline.

Related pages