Biology: Life on Earth with Physiology (11th Edition)
Biology: Life on Earth with Physiology (11th Edition)
11th Edition
ISBN: 9780133923001
Author: Gerald Audesirk, Teresa Audesirk, Bruce E. Byers
Publisher: PEARSON
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Chapter 37.2, Problem 1CSC

If phagocytes kill most species of bacteria that enter mucous membranes or a wound, how did infection kill Jim Henson and destroy Aimee Copeland’s tissues? Both S pyogenes and deadly strains of A. hydrophila are surrounded by polysaccharide capsules that phagocytic cells often do not recognize as foreign. Consequently, the phagocytes do not attack these bacteria. If such nonspecific defenses fail, can the adaptive immune response step in?

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What is a cytokine? A ) a. a chemical mediator (stimulus) of inflammation that is released by cells in response to tissue or cell damage O b. an antimicrobial substance made by neutrophils O c. a repair stimulator produced by Eosinophils during an allergic reaction O d. cellular (cyto-) substance that mediates noisy arguments between macrophages and lymphocytes And that I put A Cardiac disease is considered a(n) O a. acute, 3 O b. acute, 10 1 c. chronic, 3 O d. chronic, 10 Oe, acutely chronic, 114 And that I put Chronic 3 Are the 3 questions correct?
The classical complement pathway is initiated by C1q binding to the surface of a pathogen. In some cases, C1q can directly bind the pathogen, for instance by recognizing proteins of bacterial cell walls, but in most cases C1q binds to IgM antibodies that are bound to the pathogen surface. How does this IgM-binding feature of C1q contribute to rapid, innate immune responses rather than to slow, adaptive responses? C1q induces B lymphocytes to begin secreting antibody within hours of pathogen exposure. Natural antibody that binds to many microbial pathogens is produced prior to pathogen exposure. C1q binds to C-reactive protein which then binds to IgM on the pathogen surface. C1q directly induces inflammation, recruiting phagocytes and antibodies from the blood into the infected tissue. C1q binds to dendritic cells in the infected tissue, inducing them to secrete inflammatory cytokines.
Mycobacteria are intracellular pathogens that have adapted to life inside phagocytic cells, such as macrophages. These intracellular bacteria are taken up by phagocytosis, similar to other pathogens, but the bacteria are not killed. One possible mechanism that could account for this immune evasion by mycobacteria is their ability to: Prevent induction of nitric oxide production in the phagosome Prevent the acidification of phagosomes Prevent the expression of antimicrobial peptides in the phagosome Prevent fusion of phagosomes with lysosomes Kill the macrophage before it kills them

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Biology: Life on Earth with Physiology (11th Edition)

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