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P22-Based Nanovaccines Against Enterohemorrhagic Escherichia Coli

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Specialty Microbiology
Date 2023 Mar 21
PMID 36943089
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Abstract

Enterohemorrhagic Escherichia coli (EHEC) is an important causative agent of diarrhea in humans that causes outbreaks worldwide. Efforts have been made to mitigate the morbidity and mortality caused by these microorganisms; however, the global incidence is still high, causing hundreds of deaths per year. Several vaccine candidates have been evaluated that demonstrate some stability and therapeutic potential but have limited overarching effect. Virus-like particles have been used successfully as nanocontainers for the targeted delivery of drugs, proteins, or nucleic acids. In this study, phage P22 nanocontainers were used as a carrier for the highly antigenic T3SS structural protein EscC that is conserved between EHEC and other enteropathogenic bacteria. We were able to stably incorporate the EscC protein into P22 nanocontainers. The EscC-P22 particles were used to intranasally inoculate mice, which generated specific antibodies against EscC. These antibodies increased the phagocytic activity of murine macrophages infected with EHEC and reduced bacterial adherence to Caco-2 epithelial cells , illustrating their functionality. The EscC-P22-based particles are a potential nanovaccine candidate for immunization against EHEC O157:H7 infections. This study describes the initial attempt to use P22 viral-like particles as nanocontainers expressing enterohemorrhagic Escherichia coli (EHEC) proteins that are immunogenic and could be used as effective vaccines against EHEC infections.

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References
1.
Villanueva-Flores F, Zarate-Romero A, Torres A, Huerta-Saquero A . Encapsulation of Asparaginase as a Promising Strategy to Improve In Vivo Drug Performance. Pharmaceutics. 2021; 13(11). PMC: 8625962. DOI: 10.3390/pharmaceutics13111965. View

2.
Perez O, Lastre M, Cabrera O, Del Campo J, Bracho G, Cuello M . New vaccines require potent adjuvants like AFPL1 and AFCo1. Scand J Immunol. 2007; 66(2-3):271-7. DOI: 10.1111/j.1365-3083.2007.01981.x. View

3.
Cai K, Gao X, Li T, Wang Q, Hou X, Tu W . Enhanced immunogenicity of a novel Stx2Am-Stx1B fusion protein in a mice model of enterohemorrhagic Escherichia coli O157:H7 infection. Vaccine. 2010; 29(5):946-52. DOI: 10.1016/j.vaccine.2010.11.035. View

4.
Patterson D, Rynda-Apple A, Harmsen A, Harmsen A, Douglas T . Biomimetic antigenic nanoparticles elicit controlled protective immune response to influenza. ACS Nano. 2013; 7(4):3036-44. PMC: 3773536. DOI: 10.1021/nn4006544. View

5.
Nguyen Y, Sperandio V . Enterohemorrhagic E. coli (EHEC) pathogenesis. Front Cell Infect Microbiol. 2012; 2:90. PMC: 3417627. DOI: 10.3389/fcimb.2012.00090. View