{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,28]],"date-time":"2026-09-28T01:23:32Z","timestamp":1790558612412,"version":"4.1.0"},"reference-count":66,"publisher":"Microbiology Society","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2022,5,30]]},"abstract":"<jats:p>\n                  <jats:bold>Introduction.<\/jats:bold> Cholera is an acute enteric infection caused by <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.2947\" xlink:type=\"simple\">Vibrio cholerae<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic>, particularly in areas lacking access to clean water. Despite the global effort to improve water quality in these regions, the burden of cholera in recent years has not yet declined. Interest has therefore extended in the use of bicistronic DNA vaccine encoding <jats:italic>ctxB<\/jats:italic> and <jats:italic>tcpA<\/jats:italic> genes of <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.2947\" xlink:type=\"simple\">V. cholerae<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic> as a potential vaccine.<\/jats:p>\n               <jats:p>\n                  <jats:bold>Hypothesis\/Gap Statement.<\/jats:bold> The potential of a bicistronic DNA vaccine, pVAX-<jats:italic>ctxB-tcpA<\/jats:italic> has not been determined <jats:italic>in vitro<\/jats:italic> and <jats:italic>in vivo<\/jats:italic>.<\/jats:p>\n               <jats:p>\n                  <jats:bold>Aim.<\/jats:bold> The goal of present study was to evaluate <jats:italic>in vitro<\/jats:italic> expression and <jats:italic>in vivo<\/jats:italic> potential of pVAX-<jats:italic>ctxB-tcpA<\/jats:italic> vaccine against <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.2947\" xlink:type=\"simple\">V. cholerae<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic>.<\/jats:p>\n               <jats:p>\n                  <jats:bold>Methodology.<\/jats:bold> The pVAX-<jats:italic>ctxB-tcpA<\/jats:italic> was transiently transfected into mammalian COS-7 cells, and the <jats:italic>in vitro<\/jats:italic> expression was assessed using fluorescence and Western blot analyses. Next, the vaccine was encapsulated into sodium alginate using water-in-oil emulsification and evaluated for its efficiency in different pH conditions. Subsequently, oral vaccination using en(pVAX-<jats:italic>ctxB-tcpA<\/jats:italic>) was performed <jats:italic>in vivo<\/jats:italic>. The animals were challenged with <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.2947\" xlink:type=\"simple\">V. cholerae<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic> O1 El Tor after 2\u2009weeks of vaccination using the Removable Intestinal Tie-Adult Rabbit Diarrhoea (RITARD) model. Following the infection challenge, the rabbits were monitored for evidence of symptoms, and analysed for systemic cytokine expression level (TNF-\u03b1, IFN-\u03b3, IL-6 and IL-10) using quantitative real-time polymerase chain reaction.<\/jats:p>\n               <jats:p>\n                  <jats:bold>Results.<\/jats:bold> The <jats:italic>in vitro<\/jats:italic> expression of pVAX-<jats:italic>ctxB-tcpA<\/jats:italic> was successfully verified via fluorescence and Western blot analyses. Meanwhile, <jats:italic>in vivo<\/jats:italic> analysis demonstrated that the en(pVAX-<jats:italic>ctxB-tcpA<\/jats:italic>) was able to protect the RITARD model against <jats:italic>\n                     <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.2947\" xlink:type=\"simple\">V. cholerae<\/jats:ext-link>\n                     <\/jats:named-content>\n                  <\/jats:italic> infection due to a lack of evidence on the clinical manifestations of cholera following bacterial challenge. Furthermore, the bicistronic group showed an upregulation of systemic IFN-\u03b3 and IL-10 following 12\u2009days of vaccination, though not significant, suggesting the possible activation of both T-helper 1 and 2 types of response. However, upon bacterial challenge, the gene expression of all cytokines did not change.<\/jats:p>\n               <jats:p>\n                  <jats:bold>Conclusion.<\/jats:bold> Our findings suggest that the bicistronic plasmid DNA vaccine, pVAX-<jats:italic>ctxB-tcpA<\/jats:italic>, showed a potential role in inducing immune response against cholera through upregulation of <jats:italic>in vitro<\/jats:italic> gene and protein expression as well as <jats:italic>in vivo<\/jats:italic> cytokine gene expression, particularly IFN-\u03b3 and IL-10.<\/jats:p>","DOI":"10.1099\/jmm.0.001536","type":"journal-article","created":{"date-parts":[[2022,5,30]],"date-time":"2022-05-30T17:16:21Z","timestamp":1653930981000},"source":"Crossref","is-referenced-by-count":3,"title":["Immunization with a bicistronic DNA vaccine modulates systemic IFN-\u03b3 and IL-10 expression against Vibrio cholerae 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