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Mapping Epitopes of a Novel Peptidoglycan Cross-Linking Enzyme Cwp22 Recognized by Human Sera Obtained from Patients with Clostridioides difficile Infection and Cord Blood

Clostridioides difficile (CD) cause a severe diarrhea which can lead to pseudomembranous colitis and even patient death. CD infection (CDI) is connected mainly with changes in intestinal microbiota as a consequence of antibiotic treatment. The growing resistance to antibiotics, justifies the search...

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Autores principales: Razim, Agnieszka, Pacyga, Katarzyna, Martirosian, Gajane, Szuba, Andrzej, Gamian, Andrzej, Myc, Andrzej, Górska, Sabina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6920951/
https://www.ncbi.nlm.nih.gov/pubmed/31739602
http://dx.doi.org/10.3390/microorganisms7110565
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author Razim, Agnieszka
Pacyga, Katarzyna
Martirosian, Gajane
Szuba, Andrzej
Gamian, Andrzej
Myc, Andrzej
Górska, Sabina
author_facet Razim, Agnieszka
Pacyga, Katarzyna
Martirosian, Gajane
Szuba, Andrzej
Gamian, Andrzej
Myc, Andrzej
Górska, Sabina
author_sort Razim, Agnieszka
collection PubMed
description Clostridioides difficile (CD) cause a severe diarrhea which can lead to pseudomembranous colitis and even patient death. CD infection (CDI) is connected mainly with changes in intestinal microbiota as a consequence of antibiotic treatment. The growing resistance to antibiotics, justifies the search for new methods of combating CD. Despite of ongoing research on the immunity against the pathogen, there is still lack of any reliable vaccine. Most recently, Cwp22, that is a cross-linking enzyme involved in the production of CD peptidoglycan, seems to be a promising target to prevent CDI in high-risk patients. In this paper, the Cwp22 protein polypeptide-specific epitopes were mapped in silico and using PEPSCAN procedure. They were recognized not only by antibodies from CDI patients’ but also by umbilical cord blood sera. We identified three epitopes (54)EFRVAT(59), (201)KVNGKM(206) and (268)WQEKNGKKYY(277) of Cwp22 protein. Since Cwp22 protein has key functionality and the described above epitopes are also recognized by umbilical cord blood serum, we postulate that they could have important protective properties. In this paper, we propose Cwp22 protein as a good antigen candidate for CDI preventive vaccine. Our results open the possibility to use (54)EFRVAT(59), (201)KVNGKM(206) and (268)WQEKNGKKYY(277), epitopes as suitable anti-CD vaccine antigens.
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spelling pubmed-69209512019-12-24 Mapping Epitopes of a Novel Peptidoglycan Cross-Linking Enzyme Cwp22 Recognized by Human Sera Obtained from Patients with Clostridioides difficile Infection and Cord Blood Razim, Agnieszka Pacyga, Katarzyna Martirosian, Gajane Szuba, Andrzej Gamian, Andrzej Myc, Andrzej Górska, Sabina Microorganisms Article Clostridioides difficile (CD) cause a severe diarrhea which can lead to pseudomembranous colitis and even patient death. CD infection (CDI) is connected mainly with changes in intestinal microbiota as a consequence of antibiotic treatment. The growing resistance to antibiotics, justifies the search for new methods of combating CD. Despite of ongoing research on the immunity against the pathogen, there is still lack of any reliable vaccine. Most recently, Cwp22, that is a cross-linking enzyme involved in the production of CD peptidoglycan, seems to be a promising target to prevent CDI in high-risk patients. In this paper, the Cwp22 protein polypeptide-specific epitopes were mapped in silico and using PEPSCAN procedure. They were recognized not only by antibodies from CDI patients’ but also by umbilical cord blood sera. We identified three epitopes (54)EFRVAT(59), (201)KVNGKM(206) and (268)WQEKNGKKYY(277) of Cwp22 protein. Since Cwp22 protein has key functionality and the described above epitopes are also recognized by umbilical cord blood serum, we postulate that they could have important protective properties. In this paper, we propose Cwp22 protein as a good antigen candidate for CDI preventive vaccine. Our results open the possibility to use (54)EFRVAT(59), (201)KVNGKM(206) and (268)WQEKNGKKYY(277), epitopes as suitable anti-CD vaccine antigens. MDPI 2019-11-14 /pmc/articles/PMC6920951/ /pubmed/31739602 http://dx.doi.org/10.3390/microorganisms7110565 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Razim, Agnieszka
Pacyga, Katarzyna
Martirosian, Gajane
Szuba, Andrzej
Gamian, Andrzej
Myc, Andrzej
Górska, Sabina
Mapping Epitopes of a Novel Peptidoglycan Cross-Linking Enzyme Cwp22 Recognized by Human Sera Obtained from Patients with Clostridioides difficile Infection and Cord Blood
title Mapping Epitopes of a Novel Peptidoglycan Cross-Linking Enzyme Cwp22 Recognized by Human Sera Obtained from Patients with Clostridioides difficile Infection and Cord Blood
title_full Mapping Epitopes of a Novel Peptidoglycan Cross-Linking Enzyme Cwp22 Recognized by Human Sera Obtained from Patients with Clostridioides difficile Infection and Cord Blood
title_fullStr Mapping Epitopes of a Novel Peptidoglycan Cross-Linking Enzyme Cwp22 Recognized by Human Sera Obtained from Patients with Clostridioides difficile Infection and Cord Blood
title_full_unstemmed Mapping Epitopes of a Novel Peptidoglycan Cross-Linking Enzyme Cwp22 Recognized by Human Sera Obtained from Patients with Clostridioides difficile Infection and Cord Blood
title_short Mapping Epitopes of a Novel Peptidoglycan Cross-Linking Enzyme Cwp22 Recognized by Human Sera Obtained from Patients with Clostridioides difficile Infection and Cord Blood
title_sort mapping epitopes of a novel peptidoglycan cross-linking enzyme cwp22 recognized by human sera obtained from patients with clostridioides difficile infection and cord blood
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6920951/
https://www.ncbi.nlm.nih.gov/pubmed/31739602
http://dx.doi.org/10.3390/microorganisms7110565
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