Bacterial modulins: a novel class of virulence factors which cause host tissue pathology by inducing cytokine synthesis

Author:

Henderson B1,Poole S1,Wilson M1

Affiliation:

1. Maxillofacial Surgery Research Unit, University College London, United Kingdom. B.Henderson@Eastman.ucl.ac.uk

Abstract

Cytokines are a diverse group of proteins and glycoproteins which have potent and wide-ranging effects on eukaryotic cell function and are now recognized as important mediators of tissue pathology in infectious diseases. It is increasingly recognized that for many bacterial species, cytokine induction is a major virulence mechanism. Until recent years, the only bacterial component known to stimulate cytokine synthesis was lipopolysaccharide (LPS). It is only within the past decade that it has been clearly shown that many components associated with the bacterial cell wall, including proteins, glycoproteins, lipoproteins, carbohydrates, and lipids, have the capacity to stimulate mammalian cells to produce a diverse array of cytokines. It has been established that many of these cytokine-inducing molecules act by mechanisms distinct from that of LPS, and thus their activities are not due to LPS contamination. Bacteria produce a wide range of virulence factors which cause host tissue pathology, and these diverse factors have been grouped into four families: adhesins, aggressins, impedins, and invasins. We suggest that the array of bacterial cytokine-inducing molecules represents a new class of bacterial virulence factor, and, by analogy with the known virulence families, we suggest the term "modulin" to describe these molecules, because the action of cytokines is to modulate eukaryotic cell behavior. This review summarizes our current understanding of cytokine biology in relation to tissue homeostasis and disease and concisely reviews the current literature on the cytokine-inducing molecules produced by gram-negative and gram-positive bacteria, with an emphasis on the cellular mechanisms responsible for cytokine induction. We propose that modulins, by controlling the host immune and inflammatory responses, maintain the large commensal flora that all multicellular organisms support.

Publisher

American Society for Microbiology

Subject

Applied Microbiology and Biotechnology

Reference269 articles.

1. Regulation of murine macrophage effector function by lipoarabinomannan from mycobacterial strains with different degrees of virulence;Adams L. B.;Infect. Immun.,1993

2. Modulation of endotoxin-induced monokine release in human monocytes by lipid A partial structures that inhibit binding of125I-lipopolysaccharide;Almer A. J.;Infect. Immun.,1992

3. Atkins E. 1989. Fever: historical aspects p. 3-15. In R. Bomford and B. Henderson (ed.) Interleukin-1 inflammation and disease. Elsevier/North-Holland Publishing Co. Amsterdam.

4. Defective ceramide response in C3H/HeJ (Lpsd) macrophages;Barber S. A.;J. Immunol.,1995

5. Cytokine production induced by Mycobacterium tuberculosis lipoarabinomannan: relationship to chemical structure;Barnes P. F.;J. Immunol.,1992

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3