Prescott's Microbiology
Prescott's Microbiology
10th Edition
ISBN: 9781259281594
Author: Joanne Willey, Linda Sherwood Adjunt Professor Lecturer, Christopher J. Woolverton Professor
Publisher: McGraw-Hill Education
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Chapter 33.3, Problem 1.5RIA
Summary Introduction

The complement system is made up of a huge number of serum proteins which plays a defensive immune response in mammals. Three pathways of complement activation are there, namely, the lectin, alternative, and classical pathways. The proteins that are involved in the complement activation is referred to as complement proteins. These proteins are involved in the lysis of cell membrane, augmenting phagocytosis, and promoting inflammation.

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Explain the mechanism underlying the molecular structure of C7, C8, and C9 complement protein that facilitates their insertion into the cell membrane of a pathogen?
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.
What are the roles of the following cytokines in defense against infections: 1) TNF 2) IL-12 3) Type I Interferon
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