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Community-Acquired Respiratory Distress Syndrome Toxin: Unique Exotoxin for M. pneumoniae

Mycoplasma pneumoniae infection often causes respiratory diseases in humans, particularly in children and adults with atypical pneumonia and community-acquired pneumonia (CAP), and is often exacerbated by co-infection with other lung diseases, such as asthma, bronchitis, and chronic obstructive pulm...

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Autores principales: Su, Xiaoling, You, Xiaoxing, Luo, Haodang, Liang, Keying, Chen, Li, Tian, Wei, Ye, Zufeng, He, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8640204/
https://www.ncbi.nlm.nih.gov/pubmed/34867898
http://dx.doi.org/10.3389/fmicb.2021.766591
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author Su, Xiaoling
You, Xiaoxing
Luo, Haodang
Liang, Keying
Chen, Li
Tian, Wei
Ye, Zufeng
He, Jun
author_facet Su, Xiaoling
You, Xiaoxing
Luo, Haodang
Liang, Keying
Chen, Li
Tian, Wei
Ye, Zufeng
He, Jun
author_sort Su, Xiaoling
collection PubMed
description Mycoplasma pneumoniae infection often causes respiratory diseases in humans, particularly in children and adults with atypical pneumonia and community-acquired pneumonia (CAP), and is often exacerbated by co-infection with other lung diseases, such as asthma, bronchitis, and chronic obstructive pulmonary disorder. Community-acquired respiratory distress syndrome toxin (CARDS TX) is the only exotoxin produced by M. pneumoniae and has been extensively studied for its ADP-ribosyltransferase (ADPRT) activity and cellular vacuolization properties. Additionally, CARDS TX induces inflammatory responses, resulting in cell swelling, nuclear lysis, mucus proliferation, and cell vacuolization. CARDS TX enters host cells by binding to the host receptor and is then reverse transported to the endoplasmic reticulum to exert its pathogenic effects. In this review, we focus on the structural characteristics, functional activity, distribution and receptors, mechanism of cell entry, and inflammatory response of CARDS TX was examined. Overall, the findings of this review provide a theoretical basis for further investigation of the mechanism of M. pneumoniae infection and the development of clinical diagnosis and vaccines.
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spelling pubmed-86402042021-12-04 Community-Acquired Respiratory Distress Syndrome Toxin: Unique Exotoxin for M. pneumoniae Su, Xiaoling You, Xiaoxing Luo, Haodang Liang, Keying Chen, Li Tian, Wei Ye, Zufeng He, Jun Front Microbiol Microbiology Mycoplasma pneumoniae infection often causes respiratory diseases in humans, particularly in children and adults with atypical pneumonia and community-acquired pneumonia (CAP), and is often exacerbated by co-infection with other lung diseases, such as asthma, bronchitis, and chronic obstructive pulmonary disorder. Community-acquired respiratory distress syndrome toxin (CARDS TX) is the only exotoxin produced by M. pneumoniae and has been extensively studied for its ADP-ribosyltransferase (ADPRT) activity and cellular vacuolization properties. Additionally, CARDS TX induces inflammatory responses, resulting in cell swelling, nuclear lysis, mucus proliferation, and cell vacuolization. CARDS TX enters host cells by binding to the host receptor and is then reverse transported to the endoplasmic reticulum to exert its pathogenic effects. In this review, we focus on the structural characteristics, functional activity, distribution and receptors, mechanism of cell entry, and inflammatory response of CARDS TX was examined. Overall, the findings of this review provide a theoretical basis for further investigation of the mechanism of M. pneumoniae infection and the development of clinical diagnosis and vaccines. Frontiers Media S.A. 2021-11-19 /pmc/articles/PMC8640204/ /pubmed/34867898 http://dx.doi.org/10.3389/fmicb.2021.766591 Text en Copyright © 2021 Su, You, Luo, Liang, Chen, Tian, Ye and He. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Su, Xiaoling
You, Xiaoxing
Luo, Haodang
Liang, Keying
Chen, Li
Tian, Wei
Ye, Zufeng
He, Jun
Community-Acquired Respiratory Distress Syndrome Toxin: Unique Exotoxin for M. pneumoniae
title Community-Acquired Respiratory Distress Syndrome Toxin: Unique Exotoxin for M. pneumoniae
title_full Community-Acquired Respiratory Distress Syndrome Toxin: Unique Exotoxin for M. pneumoniae
title_fullStr Community-Acquired Respiratory Distress Syndrome Toxin: Unique Exotoxin for M. pneumoniae
title_full_unstemmed Community-Acquired Respiratory Distress Syndrome Toxin: Unique Exotoxin for M. pneumoniae
title_short Community-Acquired Respiratory Distress Syndrome Toxin: Unique Exotoxin for M. pneumoniae
title_sort community-acquired respiratory distress syndrome toxin: unique exotoxin for m. pneumoniae
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8640204/
https://www.ncbi.nlm.nih.gov/pubmed/34867898
http://dx.doi.org/10.3389/fmicb.2021.766591
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