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Title: Structure of CARDS toxin, a unique ADP-ribosylating and vacuolating cytotoxin from Mycoplasma pneumoniae

Journal Article · · Proceedings of the National Academy of Sciences of the United States of America
 [1];  [2];  [3]; ORCiD logo [4];  [1];  [2];  [5];  [1];  [2];  [6]
  1. Univ. of Texas Health Science Center, San Antonio, TX (United States). Dept. of Biochemistry
  2. Univ. of Texas Health Science Center, San Antonio, TX (United States). Dept. of Microbiology and Immunology. Center for Airway Inflammation Research
  3. Univ. of Texas Health Science Center, San Antonio, TX (United States). Dept. of Biochemistry. X-Ray Crystallography Core Lab.
  4. Univ. of Texas Health Science Center, San Antonio, TX (United States). Dept. of Biochemistry; Old Dominion Univ., Norfolk, VA (United States). Frank Reidy Center for Bioelectrics
  5. Univ. of Texas Health Science Center, San Antonio, TX (United States). Dept. of Biochemistry; St. Mary's Univ., San Antonio, TX (United States). Dept. of Biological Sciences
  6. Univ. of Texas Health Science Center, San Antonio, TX (United States). Dept. of Biochemistry. X-Ray Crystallography Core Lab.; US Dept. of Veterans Affairs, San Antonio, TX (United States). South Texas Veterans Health Care System

Mycoplasma pneumoniae (Mp) infections cause tracheobronchitis and “walking” pneumonia, and are linked to asthma and other reactive airway diseases. As part of the infectious process, the bacterium expresses a 591-aa virulence factor with both mono-ADP ribosyltransferase (mART) and vacuolating activities known as Community-Acquired Respiratory Distress Syndrome Toxin (CARDS TX). CARDS TX binds to human surfactant protein A and annexin A2 on airway epithelial cells and is internalized, leading to a range of pathogenetic events. In this paper, we present the structure of CARDS TX, a triangular molecule in which N-terminal mART and C-terminal tandem β-trefoil domains associate to form an overall architecture distinct from other well-recognized ADP-ribosylating bacterial toxins. We demonstrate that CARDS TX binds phosphatidylcholine and sphingomyelin specifically over other membrane lipids, and that cell surface binding and internalization activities are housed within the C-terminal β-trefoil domain. Finally, the results enhance our understanding of Mp pathogenicity and suggest a novel avenue for the development of therapies to treat Mp-associated asthma and other acute and chronic airway diseases.

Research Organization:
Univ. of Texas Health Science Center, San Antonio, TX (United States)
Sponsoring Organization:
USDOE; National Inst. of Health (NIH) (United States); Kleberg Foundation (United States); R. A. Welch Foundation (United States)
Contributing Organization:
Old Dominion Univ., Norfolk, VA (United States); St. Mary's Univ., San Antonio, TX (United States); US Dept. of Veterans Affairs, San Antonio, TX (United States)
Grant/Contract Number:
AC02-06CH11357; U19 AI070412; AQ-1399; P41 GM103403; P30 CA054174
OSTI ID:
1178475
Journal Information:
Proceedings of the National Academy of Sciences of the United States of America, Vol. 112, Issue 16; ISSN 0027-8424
Publisher:
National Academy of Sciences, Washington, DC (United States)Copyright Statement
Country of Publication:
United States
Language:
ENGLISH
Citation Metrics:
Cited by: 42 works
Citation information provided by
Web of Science

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Cited By (22)

High expression of miR-222-3p in children with Mycoplasma pneumoniae pneumonia journal December 2019
A novel Ffu fusion system for secretory expression of heterologous proteins in Escherichia coli journal December 2017
A Compendium for Mycoplasma pneumoniae journal April 2016
Mycoplasma pneumoniae Community-Acquired Respiratory Distress Syndrome Toxin Uses a Novel KELED Sequence for Retrograde Transport and Subsequent Cytotoxicity journal March 2018
Infection with and carriage of Mycoplasma pneumoniae in children text January 2016
Benefits and risks of therapeutic alternatives for macrolide resistant Mycoplasma pneumoniae pneumonia in children journal June 2019
NLRP3 Is a Critical Regulator of Inflammation and Innate Immune Cell Response during Mycoplasma pneumoniae Infection journal October 2017
The Mycoplasma pneumoniae HapE alters the cytokine profile and growth of human bronchial epithelial cells journal January 2019
Mycoplasma pneumoniae from the Respiratory Tract and Beyond journal May 2017
Comparative “-omics” in Mycoplasma pneumoniae Clinical Isolates Reveals Key Virulence Factors journal September 2015
Potential Molecular Targets for Narrow-Spectrum Agents to Combat Mycoplasma pneumoniae Infection and Disease journal February 2016
Structure of tRNA splicing enzyme Tpt1 illuminates the mechanism of RNA 2′-PO4 recognition and ADP-ribosylation journal January 2019
Pneumonia, Acute Respiratory Distress Syndrome, and Early Immune-Modulator Therapy journal February 2017
Infection with and Carriage of Mycoplasma pneumoniae in Children journal March 2016
Pneumonia, Acute Respiratory Distress Syndrome and Early Immune-Modulator Therapy preprint November 2016
Mycoplasma pneumoniae: A Potentially Severe Infection journal January 2018
CReasPy-Cloning: A Method for Simultaneous Cloning and Engineering of Megabase-Sized Genomes in Yeast Using the CRISPR-Cas9 System journal October 2019
Mycoplasma pneumoniae infection: Basics journal April 2017
Mycoplasma pneumoniae CARDS toxin elicits a functional IgE response in Balb/c mice journal February 2017
MIB–MIP is a mycoplasma system that captures and cleaves immunoglobulin G journal April 2016
Disulfide bond of Mycoplasma pneumoniae community‐acquired respiratory distress syndrome toxin is essential to maintain the ADP‐ribosylating and vacuolating activities journal May 2019
MIB-MIP is a mycoplasma system that captures and cleaves immunoglobulin G. text January 2016

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