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Inactivated Vibrio cholerae Strains That Express TcpA via the toxT-139F Allele Induce Antibody Responses against TcpA

Cholera remains a major global public health problem, for which oral cholera vaccines (OCVs) being a valuable strategy. Patients, who have recovered from cholera, develop antibody responses against LPS, cholera toxin (CT), toxin-coregulated pilus (TCP) major subunit A (TcpA) and other antigens; thus...

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Autores principales: Kim, Eun Jin, Bae, Jonghyun, Ju, Young-Jun, Ju, Do-Bin, Lee, Donghyun, Son, Seonghyeon, Choi, Hunseok, Ramamurthy, Thandavarayan, Yun, Cheol-Heui, Kim, Dong Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Microbiology and Biotechnology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720071/
https://www.ncbi.nlm.nih.gov/pubmed/36317425
http://dx.doi.org/10.4014/jmb.2209.09001
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author Kim, Eun Jin
Bae, Jonghyun
Ju, Young-Jun
Ju, Do-Bin
Lee, Donghyun
Son, Seonghyeon
Choi, Hunseok
Ramamurthy, Thandavarayan
Yun, Cheol-Heui
Kim, Dong Wook
author_facet Kim, Eun Jin
Bae, Jonghyun
Ju, Young-Jun
Ju, Do-Bin
Lee, Donghyun
Son, Seonghyeon
Choi, Hunseok
Ramamurthy, Thandavarayan
Yun, Cheol-Heui
Kim, Dong Wook
author_sort Kim, Eun Jin
collection PubMed
description Cholera remains a major global public health problem, for which oral cholera vaccines (OCVs) being a valuable strategy. Patients, who have recovered from cholera, develop antibody responses against LPS, cholera toxin (CT), toxin-coregulated pilus (TCP) major subunit A (TcpA) and other antigens; thus, these responses are potentially important contributors to immunity against Vibrio cholerae infection. However, assessments of the efficacy of current OCVs, especially inactivated OCVs, have focused primarily on O-antigen-specific antibody responses, suggesting that more sophisticated strategies are required for inactivated OCVs to induce immune responses against TCP, CT, and other antigens. Previously, we have shown that the toxT-139F allele enables V. cholerae strains to produce CT and TCP under simple laboratory culture conditions. Thus, we hypothesized that V. cholerae strains that express TCP via the toxT-139F allele induce TCP-specific antibody responses. As anticipated, V. cholerae strains that expressed TCP through the toxT-139F allele elicited antibody responses against TCP when the inactivated bacteria were delivered via a mouse model. We have further developed TCP-expressing V. cholerae strains that have been used in inactivated OCVs and shown that they effect an antibody response against TcpA in vivo, suggesting that V. cholerae strains with the toxT-139F allele are excellent candidates for cholera vaccines.
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spelling pubmed-97200712022-12-13 Inactivated Vibrio cholerae Strains That Express TcpA via the toxT-139F Allele Induce Antibody Responses against TcpA Kim, Eun Jin Bae, Jonghyun Ju, Young-Jun Ju, Do-Bin Lee, Donghyun Son, Seonghyeon Choi, Hunseok Ramamurthy, Thandavarayan Yun, Cheol-Heui Kim, Dong Wook J Microbiol Biotechnol Research article Cholera remains a major global public health problem, for which oral cholera vaccines (OCVs) being a valuable strategy. Patients, who have recovered from cholera, develop antibody responses against LPS, cholera toxin (CT), toxin-coregulated pilus (TCP) major subunit A (TcpA) and other antigens; thus, these responses are potentially important contributors to immunity against Vibrio cholerae infection. However, assessments of the efficacy of current OCVs, especially inactivated OCVs, have focused primarily on O-antigen-specific antibody responses, suggesting that more sophisticated strategies are required for inactivated OCVs to induce immune responses against TCP, CT, and other antigens. Previously, we have shown that the toxT-139F allele enables V. cholerae strains to produce CT and TCP under simple laboratory culture conditions. Thus, we hypothesized that V. cholerae strains that express TCP via the toxT-139F allele induce TCP-specific antibody responses. As anticipated, V. cholerae strains that expressed TCP through the toxT-139F allele elicited antibody responses against TCP when the inactivated bacteria were delivered via a mouse model. We have further developed TCP-expressing V. cholerae strains that have been used in inactivated OCVs and shown that they effect an antibody response against TcpA in vivo, suggesting that V. cholerae strains with the toxT-139F allele are excellent candidates for cholera vaccines. The Korean Society for Microbiology and Biotechnology 2022-11-28 2022-10-12 /pmc/articles/PMC9720071/ /pubmed/36317425 http://dx.doi.org/10.4014/jmb.2209.09001 Text en Copyright © 2022 by the authors. Licensee KMB. https://creativecommons.org/licenses/by/4.0/This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research article
Kim, Eun Jin
Bae, Jonghyun
Ju, Young-Jun
Ju, Do-Bin
Lee, Donghyun
Son, Seonghyeon
Choi, Hunseok
Ramamurthy, Thandavarayan
Yun, Cheol-Heui
Kim, Dong Wook
Inactivated Vibrio cholerae Strains That Express TcpA via the toxT-139F Allele Induce Antibody Responses against TcpA
title Inactivated Vibrio cholerae Strains That Express TcpA via the toxT-139F Allele Induce Antibody Responses against TcpA
title_full Inactivated Vibrio cholerae Strains That Express TcpA via the toxT-139F Allele Induce Antibody Responses against TcpA
title_fullStr Inactivated Vibrio cholerae Strains That Express TcpA via the toxT-139F Allele Induce Antibody Responses against TcpA
title_full_unstemmed Inactivated Vibrio cholerae Strains That Express TcpA via the toxT-139F Allele Induce Antibody Responses against TcpA
title_short Inactivated Vibrio cholerae Strains That Express TcpA via the toxT-139F Allele Induce Antibody Responses against TcpA
title_sort inactivated vibrio cholerae strains that express tcpa via the toxt-139f allele induce antibody responses against tcpa
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720071/
https://www.ncbi.nlm.nih.gov/pubmed/36317425
http://dx.doi.org/10.4014/jmb.2209.09001
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