Microbiology: An Evolving Science (Fourth Edition)
Microbiology: An Evolving Science (Fourth Edition)
4th Edition
ISBN: 9780393615098
Author: John W. Foster, Joan L. Slonczewski
Publisher: W. W. Norton & Company
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Chapter 23.6, Problem 1TQ
Summary Introduction

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The advantage of the H factor in bacteria.

Introduction:

The series of 20 proteins naturally found in serum form the complement. The complement pathway is the cascade process that attacks foreign invaders by enhancing the effect of antibodies. The complement system induces pores in the bacterial membrane leading to cytoplasmic leakage. Sometimes the pathogen can take advantage of these controls to avoid being destroyed by the immune system of the human body.

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Mannose binding lectins (MBL) and ficolins are the two classes of proteins that can initiate the lectin pathway of complement activation. These proteins are selective for activating complement on the surfaces of microbial pathogens rather than host cells because: Their higher-order oligomeric structure can be assembled only after the monomers first bind to pathogen membranes. They only recruit MASP (MBL-associated serine proteases) proteins when bound to pathogen surfaces and not when bound to host cells. They only undergo the conformational change needed to activate MASP proteins when bound to a pathogen and not when bound to a host cell. They only bind to carbohydrate side chains and oligosaccharide modifications found on pathogen surfaces but not on host cell membranes. The activated MASP proteins are rapidly inactivated by hydrolysis when present on the surface of a host cell.
4)  A patient has their spleen removed due to an accident.  How will this affect the immune response? 5)  You come in contact with staphylococci through a cut.  What cellular features will the immune cells recognize? 6)  Name two opsonins and how do these molecules help the immune response? 7)  Fever is part of the inflammatory process.   What is the role of fever during an immune response? 8)  This chemical is used to induce anti-viral responses in cells to protect the cells from viral infections. 9)  This complement activation pathway is activated when complement binds to an antibody bound to antigens.
The formation of the C3 convertase is a key step in complement activation that occurs in all three complement pathways. This enzyme cleaves C3 in blood plasma, leading to a conformational change in the C3b fragment that exposes its reactive thioester group. The activated C3b is potentially harmful to the host, if it becomes covalently attached to a host cell, rather than to the surface of a pathogen. This deleterious outcome is largely avoided by:  The inability of active C3b to diffuse away in the blood plasma. The inability of active C3b to covalently attach to the membranes of eukaryotic cells. The rapid hydrolysis of active C3b in solution, rendering it inactive. The tight binding of active C3b to the C3 convertase. The ability of active C3b to recruit phagocytic cells.
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