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Title:Ribotype classification of Clostridioides difficile isolates Is not predictive of the amino acid sequence diversity of the toxin virulence factors TcdA and TcdB
Authors:ID Li, Zhenghui (Author)
ID Lee, Kwok (Author)
ID Rajyaguru, Urvi (Author)
ID Jones, C. Hal (Author)
ID Janežič, Sandra (Author)
ID Rupnik, Maja (Author)
ID Anderson, Annaliesa S. (Author)
ID Liberator, Paul (Author)
Files:.pdf Li-2020-Ribotype_Classification_of_i_Clostridi.pdf (1,21 MB)
MD5: 77647C50953C17B59D9B1DCDAE47CC1C
 
URL https://doi.org/10.3389/fmicb.2020.01310
 
Language:English
Work type:Scientific work
Typology:1.01 - Original Scientific Article
Organization:MF - Faculty of Medicine
Abstract:Clostridioides (Clostridium) difficile is the most commonly recognized cause of infectious diarrhea in healthcare settings. Currently there is no vaccine to prevent initial or recurrent C. difficile infection (CDI). Two large clostridial toxins, TcdA and TcdB, are the primary virulence factors for CDI. Immunological approaches to prevent CDI include antibody-mediated neutralization of the cytotoxicity of these toxins. An understanding of the sequence diversity of the two toxins expressed by disease causing isolates is critical for the interpretation of the immune response to the toxins. In this study, we determined the whole genome sequence (WGS) of 478 C. difficile isolates collected in 12 countries between 2004 and 2018 to probe toxin variant diversity. A total of 44 unique TcdA variants and 37 unique TcdB variants were identified. The amino acid sequence conservation among the TcdA variants (>98%) is considerably greater than among the TcdB variants (as low as 86.1%), suggesting that different selection pressures may have contributed to the evolution of the two toxins. Phylogenomic analysis of the WGS data demonstrate that isolates grouped together based on ribotype or MLST code for multiple different toxin variants. These findings illustrate the importance of determining not only the ribotype but also the toxin sequence when evaluating strain coverage using vaccine strategies that target these virulence factors. We recommend that toxin variant type and sequence type (ST), be used together with ribotype data to provide a more comprehensive strain classification scheme for C. difficile surveillance during vaccine development objectives.
Keywords:Clostridioides difficile, Clostridium difficile, TCDB, TcdA, vaccines, whole genome sequencing
Publication status:Published
Publication version:Version of Record
Submitted for review:11.12.2019
Article acceptance date:25.05.2020
Publication date:19.06.2020
Publisher:Frontiers Research Foundation
Year of publishing:2020
Number of pages:Str. 1-13
Numbering:Letn. 11, št. članka 1310
PID:20.500.12556/DKUM-91689 New window
UDC:579.852.13
ISSN on article:1664-302X
COBISS.SI-ID:26304259 New window
DOI:10.3389/fmicb.2020.01310 New window
Publication date in DKUM:28.01.2025
Views:238
Downloads:14
Metadata:XML DC-XML DC-RDF
Categories:Misc.
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Record is a part of a journal

Title:Frontiers in microbiology
Shortened title:Front. microbiol.
Publisher:Frontiers Research Foundation
ISSN:1664-302X
COBISS.SI-ID:4146296 New window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:19.06.2020

Secondary language

Language:Slovenian
Keywords:Clostridioides difficile, Clostridium difficile, cepiva, sekvenciranje genoma


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