In silico designing of vaccine candidate against Clostridium difficile
Abstract Clostridium difficile is a spore-forming gram-positive bacterium, recognized as the primary cause of antibiotic-associated nosocomial diarrhoea. Clostridium difficile infection (CDI) has emerged as a major health-associated infection with increased incidence and hospitalization over the yea...
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doaj-9924c74dfa4f4691ac2c591253e818fb2021-07-11T11:30:21ZengNature Publishing GroupScientific Reports2045-23222021-07-0111112210.1038/s41598-021-93305-6In silico designing of vaccine candidate against Clostridium difficileSrijita Basak0Debashrito Deb1Utkarsh Narsaria2Tamalika Kar3Filippo Castiglione4Indraneel Sanyal5Pratap D. Bade6Anurag P. Srivastava7Biopharmaceutical Development Department, Syngene International LimitedBiopharmaceutical Development Department, Syngene International LimitedBiopharmaceutical Development Department, Syngene International LimitedBiopharmaceutical Development Department, Syngene International LimitedInstitute for Applied Computing (IAC), National Research Council of ItalyBiopharmaceutical Development Department, Syngene International LimitedBiopharmaceutical Development Department, Syngene International LimitedBiopharmaceutical Development Department, Syngene International LimitedAbstract Clostridium difficile is a spore-forming gram-positive bacterium, recognized as the primary cause of antibiotic-associated nosocomial diarrhoea. Clostridium difficile infection (CDI) has emerged as a major health-associated infection with increased incidence and hospitalization over the years with high mortality rates. Contamination and infection occur after ingestion of vegetative spores, which germinate in the gastro-intestinal tract. The surface layer protein and flagellar proteins are responsible for the bacterial colonization while the spore coat protein, is associated with spore colonization. Both these factors are the main concern of the recurrence of CDI in hospitalized patients. In this study, the CotE, SlpA and FliC proteins are chosen to form a multivalent, multi-epitopic, chimeric vaccine candidate using the immunoinformatics approach. The overall reliability of the candidate vaccine was validated in silico and the molecular dynamics simulation verified the stability of the vaccine designed. Docking studies showed stable vaccine interactions with Toll‐Like Receptors of innate immune cells and MHC receptors. In silico codon optimization of the vaccine and its insertion in the cloning vector indicates a competent expression of the modelled vaccine in E. coli expression system. An in silico immune simulation system evaluated the effectiveness of the candidate vaccine to trigger a protective immune response.https://doi.org/10.1038/s41598-021-93305-6 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Srijita Basak Debashrito Deb Utkarsh Narsaria Tamalika Kar Filippo Castiglione Indraneel Sanyal Pratap D. Bade Anurag P. Srivastava |
spellingShingle |
Srijita Basak Debashrito Deb Utkarsh Narsaria Tamalika Kar Filippo Castiglione Indraneel Sanyal Pratap D. Bade Anurag P. Srivastava In silico designing of vaccine candidate against Clostridium difficile Scientific Reports |
author_facet |
Srijita Basak Debashrito Deb Utkarsh Narsaria Tamalika Kar Filippo Castiglione Indraneel Sanyal Pratap D. Bade Anurag P. Srivastava |
author_sort |
Srijita Basak |
title |
In silico designing of vaccine candidate against Clostridium difficile |
title_short |
In silico designing of vaccine candidate against Clostridium difficile |
title_full |
In silico designing of vaccine candidate against Clostridium difficile |
title_fullStr |
In silico designing of vaccine candidate against Clostridium difficile |
title_full_unstemmed |
In silico designing of vaccine candidate against Clostridium difficile |
title_sort |
in silico designing of vaccine candidate against clostridium difficile |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-07-01 |
description |
Abstract Clostridium difficile is a spore-forming gram-positive bacterium, recognized as the primary cause of antibiotic-associated nosocomial diarrhoea. Clostridium difficile infection (CDI) has emerged as a major health-associated infection with increased incidence and hospitalization over the years with high mortality rates. Contamination and infection occur after ingestion of vegetative spores, which germinate in the gastro-intestinal tract. The surface layer protein and flagellar proteins are responsible for the bacterial colonization while the spore coat protein, is associated with spore colonization. Both these factors are the main concern of the recurrence of CDI in hospitalized patients. In this study, the CotE, SlpA and FliC proteins are chosen to form a multivalent, multi-epitopic, chimeric vaccine candidate using the immunoinformatics approach. The overall reliability of the candidate vaccine was validated in silico and the molecular dynamics simulation verified the stability of the vaccine designed. Docking studies showed stable vaccine interactions with Toll‐Like Receptors of innate immune cells and MHC receptors. In silico codon optimization of the vaccine and its insertion in the cloning vector indicates a competent expression of the modelled vaccine in E. coli expression system. An in silico immune simulation system evaluated the effectiveness of the candidate vaccine to trigger a protective immune response. |
url |
https://doi.org/10.1038/s41598-021-93305-6 |
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