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Section 19.5: Chemical Defenses - Antimicrobial Peptides (AMP)

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    Antimicrobial Peptides

    The antimicrobial peptides (AMPs) are a special class of nonspecific cell-derived mediators with broad-spectrum antimicrobial properties. Some AMPs are produced routinely by the body, whereas others are primarily produced (or produced in greater quantities) in response to the presence of an invading pathogen. Research has begun exploring how AMPs can be used in the diagnosis and treatment of disease.

    AMPs may induce cell damage in microorganisms in a variety of ways, including by inflicting damage to membranes, destroying DNA and RNA, or interfering with cell-wall synthesis. Depending on the specific antimicrobial mechanism, a particular AMP may inhibit only certain groups of microbes (e.g., gram-positive or gram-negative bacteria) or it may be more broadly effective against bacteria, fungi, protozoa, and viruses. Many AMPs are found on the skin, but they can also be found in other regions of the body.

    A family of AMPs called defensins can be produced by epithelial cells throughout the body as well as by cellular defenses such as macrophages and neutrophils (see Cellular Defenses). Defensins may be secreted or act inside host cells; they combat microorganisms by damaging their plasma membranes. AMPs called bacteriocins are produced exogenously by certain members of the resident microbiota within the gastrointestinal tract. The genes coding for these types of AMPs are often carried on plasmids and can be passed between different species within the resident microbiota through lateral or horizontal gene transfer.

    There are numerous other AMPs throughout the body. The characteristics of a few of the more significant AMPs are summarized in Table \(\PageIndex{1}\).

    Table \(\PageIndex{1}\): Characteristics of Selected Antimicrobial Peptides (AMPs)
    AMP Secreted by Body site Pathogens inhibited Mode of action
    Bacteriocins Resident microbiota Gastrointestinal tract Bacteria Disrupt membrane
    Cathelicidin Epithelial cells, macrophages, and other cell types Skin Bacteria and fungi Disrupts membrane
    Defensins Epithelial cells, macrophages, neutrophils Throughout the body Fungi, bacteria, and many viruses Disrupt membrane
    Dermicidin Sweat glands Skin Bacteria and fungi Disrupts membrane integrity and ion channels
    Histatins Salivary glands Oral cavity Fungi Disrupt intracellular function
    Exercise \(\PageIndex{2}\)

    Why are antimicrobial peptides (AMPs) considered nonspecific defenses?

    Key Concepts and Summary

    • Numerous chemical mediators produced endogenously and exogenously exhibit nonspecific antimicrobial functions.
    • Many chemical mediators are found in body fluids such as sebum, saliva, mucus, gastric and intestinal fluids, urine, tears, cerumen, and vaginal secretions.
    • Antimicrobial peptides (AMPs) found on the skin and in other areas of the body are largely produced in response to the presence of pathogens. These include dermcidin, cathelicidin, defensins, histatins, and bacteriocins.
    • Plasma contains various proteins that serve as chemical mediators, including acute-phase proteins, complement proteins, and cytokines.
    • The complement system involves numerous precursor proteins that circulate in plasma. These proteins become activated in a cascading sequence in the presence of microbes, resulting in the opsonization of pathogens, chemoattraction of leukocytes, induction of inflammation, and cytolysis through the formation of a membrane attack complex (MAC).
    • Cytokines are proteins that facilitate various nonspecific responses by innate immune cells, including production of other chemical mediators, cell proliferation, cell death, and differentiation.
    • Cytokines play a key role in the inflammatory response, triggering production of inflammation-eliciting mediators such as acute-phase proteins, histamine, leukotrienes, prostaglandins, and bradykinin.

    This page titled Section 19.5: Chemical Defenses - Antimicrobial Peptides (AMP) is shared under a CC BY 4.0 license and was authored, remixed, and/or curated by Ying Liu via source content that was edited to the style and standards of the LibreTexts platform.