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ESX-5-targeted export of ESAT-6 in BCG combines enhanced immunogenicity & efficacy against murine tuberculosis with low virulence and reduced persistence.

Authors :
Heijmenberg I
Husain A
Sathkumara HD
Muruganandah V
Seifert J
Miranda-Hernandez S
Kashyap RS
Field MA
Krishnamoorthy G
Kupz A
Source :
Vaccine [Vaccine] 2021 Dec 08; Vol. 39 (50), pp. 7265-7276. Date of Electronic Publication: 2021 Aug 19.
Publication Year :
2021

Abstract

Tuberculosis (TB) is the leading infectious cause of death globally. The only licensed TB vaccine, Bacille Calmette-Guérin (BCG), has low efficacy against TB in adults and is not recommended in people with impaired immunity. The incorporation of the Mycobacterium tuberculosis (Mtb) secretion system ESX-1 into BCG improves immunogenicity and protection against TB in animal models, which is associated with the secretion of the ESX-1-dependent protein ESAT-6. However, the resulting strain, BCG::ESX1 <superscript>Mtb</superscript> , has been deemed unsafe as a human vaccine, due to prolonged persistence and increased virulence in immunocompromised mice. In this study, we describe a new recombinant BCG strain that uncouples the beneficial aspects of ESAT-6 secretion from the detrimental ESX-1effects on virulence and persistence. The strain was constructed by fusing the ESAT-6-encoding gene esxA to the general secretion signal for the mycobacterial type VII secretion pathway protein PE25. This new strain, BCG::ESAT6-PE25SS, secretes full-length ESAT-6 via the ESX-5 secretion system, which in contrast to ESX-1 is also present in BCG. In vivo testing revealed that ESX-5-targeted ESAT-6 export, induces cytosolic contact, generates ESAT-6-specific T cells and enhances the protective efficacy against TB disease, but is associated with low virulence and reduced persistence in immunocompetent and immunocompromised mice. Additionally, compared to BCG::ESX1 <superscript>Mtb</superscript> and parental BCG, mucosal administration of BCG::ESAT6-PE25SS is associated with more rapid clearance from the lung. These results warrant further studies to evaluate BCG::ESAT6-PE25SS as a potential live attenuated vaccine candidate for TB.<br />Competing Interests: Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Andreas Kupz reports financial support was provided by Australian National Health and Medical Research Council. Aliabbas Husain reports financial support was provided by Indian Government. Andreas Kupz reports a relationship with Collaboration for Tuberculosis Vaccine Discovery (Bill and Melinda Gates Foundation) that includes: board membership and travel reimbursement. Andreas Kupz has patent filing # number 2021900320 pending to James Cook University.<br /> (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1873-2518
Volume :
39
Issue :
50
Database :
MEDLINE
Journal :
Vaccine
Publication Type :
Academic Journal
Accession number :
34420788
Full Text :
https://doi.org/10.1016/j.vaccine.2021.08.030