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 mebooksfree.com  mebooksfree.com           mebooksfree.com          •  Exotoxins have different mechanisms of action and different        mebooksfree.com
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                      PART I  Basic Bacteriology
                 50
                    hyaluronic acid in the subcutaneous tissue, allowing the organ-
                    ism to spread rapidly.
                                                                       targets within the cell and therefore cause a variety of diseases
                                                                       with characteristic symptoms (see Tables 7–9 and 7–10). Sev-
                   •  IgA protease degrades secretory IgA, allowing bacteria to
                                                                       eral exotoxins are enzymes that attach ADP-ribose to a cell
                    attach to mucous membranes.
                                                                       component (ADP-ribosylation). Some exotoxins act by pro-
                   •  The  capsule surrounding bacteria is  antiphagocytic (i.e., it
                                                                       teolytic cleavage of a cell component, whereas others act as
                    retards the phagocyte from ingesting the organism). Mutant
                                                                       superantigens, causing the overproduction of cytokines.
                    strains of many pathogens that do not produce capsules are
                    nonpathogenic.                                   Endotoxins
 mebooksfree.com  mebooksfree.com           mebooksfree.com          •  Lipid A is the toxic component of LPS. It induces the overpro-     mebooksfree.com
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                   •  Inflammation is an important host defense induced by the
                                                                     •  Endotoxins are  lipopolysaccharides (LPS) located in the
                    presence of bacteria in the body. There are two types of inflam-
                                                                       outer membrane only of gram-negative bacteria. They are not
                    mation, pyogenic and granulomatous, and bacteria typically
                                                                       secreted by bacteria.
                    elicit one type or the other. Pyogenic inflammation, the host
                    defense against pyogenic (pus-producing) bacteria such as S.
                                                                       duction of cytokines, such as tumor necrosis factor, interleu-
                    pyogenes, consists of neutrophils (and antibody and comple-
                                                                       kin-1, and nitric oxide, from macrophages, which causes the
                    ment).  Granulomatous  inflammation, the host defense
                                                                       symptoms of septic shock, such as fever and hypotension. In
                    against intracellular, granuloma-producing bacteria, such as M.
                                                                       addition, LPS activates the  complement cascade (alternate
                    tuberculosis, consists of macrophages and CD4-positive T cells.
                                                                       pathway), resulting in increased vascular permeability, and the
                    The type of inflammatory lesion is an important diagnostic
                                                                       coagulation cascade, resulting in increased vascular permea-
                    criterion.
                                                                       bility and disseminated intravascular coagulation.
                   •  Bacteria can evade our host defenses by a process called intra-
                    cellular survival  (i.e.,  bacteria  that  can  live within  cells  are   •  Endotoxins are poorly antigenic, do not induce antitoxins, and
                                                                       do not form toxoids.
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 mebooksfree.com  mebooksfree.com           mebooksfree.com          •  There are often four discrete stages. The incubation period is     mebooksfree.com
                    protected from attack by macrophages and neutrophils). Note
                    that many of these bacteria (e.g., M. tuberculosis) are not obli-
                                                                     Typical Stages of an Infectious Disease
                    gate intracellular parasites (which can grow only within cells),
                    but rather have the ability to enter and survive inside cells.
                                                                       the time between the moment the person is exposed to the
                   Exotoxins
                                                                       microbe (or toxin) and the appearance of symptoms. The pro-
                   •  Exotoxins are polypeptides secreted by certain bacteria that
                                                                       drome period is the time during which nonspecific symptoms
                    alter specific cell functions resulting in the symptoms of dis-
                                                                       occur. The specific-illness period is the time during which the
                    ease.  They  are  produced  by  both  gram-positive  and  gram-
                                                                       characteristic features of the disease occur.  The  recovery
                    negative bacteria, whereas endotoxin is found only in
                                                                       period is the time during which symptoms resolve and health
                    gram-negative bacteria.
                                                                       is restored.
                   •  Exotoxins are antigenic and induce antibodies called antitox-
                    ins. Exotoxins can be modified to form  toxoids, which are   •  After the recovery period, some people become chronic carri-
                                                                       ers of the organism and in others latent infections develop.
                    antigenic but not toxic. Toxoids, such as tetanus toxoid, are
 mebooksfree.com  mebooksfree.com           mebooksfree.com           2.  Vertical transmission is the transmission of organisms from      mebooksfree.com
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                                                                     •  Some people have  subclinical infections during which they
                    used to immunize against disease.
                                                                       remain asymptomatic. The presence of antibodies reveals that
                   •  Many exotoxins have an A–B subunit structure in which the A
                                                                       a prior infection has occurred.
                    subunit is the active (toxic) one and the B subunit is the one
                    that binds to the cell membrane and mediates the entry of the
                    A subunit into the cell.
                 SELF-ASSESSMENT QUESTIONS
                 1.  Handwashing is an important means of interrupting the chain
                                                                        following bacteria is most likely to be transmitted vertically?
                    of transmission from one person to another. Infection by which
                                                                        (A)  Chlamydia trachomatis
                    one of the following bacteria is most likely to be interrupted by   mother to fetus or newborn child. Infection by which one of the
                                                                        (B)  Clostridium tetani
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                    handwashing?
                                                                        (C)  Haemophilus influenzae
                    (A)  Borrelia burgdorferi
                                                                        (D)  Shigella dysenteriae
                    (B)  Legionella pneumophila
                                                                        (E)  Streptococcus pneumoniae
                    (C)  Staphylococcus aureus
                    (D)  Streptococcus agalactiae (group B streptococcus)
                    (E)  Treponema pallidum
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