Differential Immune Response Following Intranasal and Intradermal Infection with <i>Francisella tularensis:</i> Implications for Vaccine Development

<i>Francisella tularensis</i> (<i>Ft)</i> is a Gram-negative, facultative intracellular coccobacillus that is the etiological agent of tularemia. Interestingly, the disease tularemia has variable clinical presentations that are dependent upon the route of infection with <i...

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Main Authors: McKayla J. Nicol, David R. Williamson, David E. Place, Girish S. Kirimanjeswara
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:Microorganisms
Subjects:
Online Access:https://www.mdpi.com/2076-2607/9/5/973
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author McKayla J. Nicol
David R. Williamson
David E. Place
Girish S. Kirimanjeswara
author_facet McKayla J. Nicol
David R. Williamson
David E. Place
Girish S. Kirimanjeswara
author_sort McKayla J. Nicol
collection DOAJ
description <i>Francisella tularensis</i> (<i>Ft)</i> is a Gram-negative, facultative intracellular coccobacillus that is the etiological agent of tularemia. Interestingly, the disease tularemia has variable clinical presentations that are dependent upon the route of infection with <i>Ft</i>. Two of the most likely routes of <i>Ft</i> infection include intranasal and intradermal, which result in pneumonic and ulceroglandular tularemia, respectively. While there are several differences between these two forms of tularemia, the most notable disparity is between mortality rates: the mortality rate following pneumonic tularemia is over ten times that of the ulceroglandular disease. Understanding the differences between intradermal and intranasal <i>Ft</i> infections is important not only for clinical diagnoses and treatment but also for the development of a safe and effective vaccine. However, the immune correlates of protection against <i>Ft</i>, especially within the context of infection by disparate routes, are not yet fully understood. Recent advances in different animal models have revealed new insights in the complex interplay of innate and adaptive immune responses, indicating dissimilar patterns in both responses following infection with <i>Ft</i> via different routes. Further investigation of these differences will be crucial to predicting disease outcomes and inducing protective immunity via vaccination or natural infection.
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spelling doaj.art-fabaf6de62a14343873545fb11de18362023-11-21T17:55:27ZengMDPI AGMicroorganisms2076-26072021-04-019597310.3390/microorganisms9050973Differential Immune Response Following Intranasal and Intradermal Infection with <i>Francisella tularensis:</i> Implications for Vaccine DevelopmentMcKayla J. Nicol0David R. Williamson1David E. Place2Girish S. Kirimanjeswara3Department of Veterinary and Biomedical Sciences, The Pennsylvania State University, University Park, PA 16802, USADepartment of Veterinary and Biomedical Sciences, The Pennsylvania State University, University Park, PA 16802, USADepartment of Veterinary and Biomedical Sciences, The Pennsylvania State University, University Park, PA 16802, USADepartment of Veterinary and Biomedical Sciences, The Pennsylvania State University, University Park, PA 16802, USA<i>Francisella tularensis</i> (<i>Ft)</i> is a Gram-negative, facultative intracellular coccobacillus that is the etiological agent of tularemia. Interestingly, the disease tularemia has variable clinical presentations that are dependent upon the route of infection with <i>Ft</i>. Two of the most likely routes of <i>Ft</i> infection include intranasal and intradermal, which result in pneumonic and ulceroglandular tularemia, respectively. While there are several differences between these two forms of tularemia, the most notable disparity is between mortality rates: the mortality rate following pneumonic tularemia is over ten times that of the ulceroglandular disease. Understanding the differences between intradermal and intranasal <i>Ft</i> infections is important not only for clinical diagnoses and treatment but also for the development of a safe and effective vaccine. However, the immune correlates of protection against <i>Ft</i>, especially within the context of infection by disparate routes, are not yet fully understood. Recent advances in different animal models have revealed new insights in the complex interplay of innate and adaptive immune responses, indicating dissimilar patterns in both responses following infection with <i>Ft</i> via different routes. Further investigation of these differences will be crucial to predicting disease outcomes and inducing protective immunity via vaccination or natural infection.https://www.mdpi.com/2076-2607/9/5/973<i>Francisella tularensis</i>disparate routes of infectionvaccine developmentimmune response
spellingShingle McKayla J. Nicol
David R. Williamson
David E. Place
Girish S. Kirimanjeswara
Differential Immune Response Following Intranasal and Intradermal Infection with <i>Francisella tularensis:</i> Implications for Vaccine Development
Microorganisms
<i>Francisella tularensis</i>
disparate routes of infection
vaccine development
immune response
title Differential Immune Response Following Intranasal and Intradermal Infection with <i>Francisella tularensis:</i> Implications for Vaccine Development
title_full Differential Immune Response Following Intranasal and Intradermal Infection with <i>Francisella tularensis:</i> Implications for Vaccine Development
title_fullStr Differential Immune Response Following Intranasal and Intradermal Infection with <i>Francisella tularensis:</i> Implications for Vaccine Development
title_full_unstemmed Differential Immune Response Following Intranasal and Intradermal Infection with <i>Francisella tularensis:</i> Implications for Vaccine Development
title_short Differential Immune Response Following Intranasal and Intradermal Infection with <i>Francisella tularensis:</i> Implications for Vaccine Development
title_sort differential immune response following intranasal and intradermal infection with i francisella tularensis i implications for vaccine development
topic <i>Francisella tularensis</i>
disparate routes of infection
vaccine development
immune response
url https://www.mdpi.com/2076-2607/9/5/973
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