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Whole-cell vaccine candidates induce a protective response against virulent Acinetobacter baumannii

Acinetobacter baumannii causes multi-system diseases in both nosocomial settings and a pre-disposed general population. The bacterium is not only desiccation-resistant but also notoriously resistant to multiple antibiotics and drugs of last resort including carbapenem, colistin, and sulbactam. The W...

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Detalles Bibliográficos
Autores principales: Dollery, Stephen J., Zurawski, Daniel V., Bushnell, Ruth V., Tobin, John K., Wiggins, Taralyn J., MacLeod, David A., Tasker, Naomi J. P. E. R., Alamneh, Yonas A., Abu-Taleb, Rania, Czintos, Christine M., Su, Wanwen, Escatte, Mariel G., Meeks, Heather N., Daly, Michael J., Tobin, Gregory J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9553005/
https://www.ncbi.nlm.nih.gov/pubmed/36238282
http://dx.doi.org/10.3389/fimmu.2022.941010
Descripción
Sumario:Acinetobacter baumannii causes multi-system diseases in both nosocomial settings and a pre-disposed general population. The bacterium is not only desiccation-resistant but also notoriously resistant to multiple antibiotics and drugs of last resort including carbapenem, colistin, and sulbactam. The World Health Organization has categorized carbapenem-resistant A. baumannii at the top of its critical pathogen list in a bid to direct urgent countermeasure development. Several early-stage vaccines have shown a range of efficacies in healthy mice, but no vaccine candidates have advanced into clinical trials. Herein, we report our findings that both an ionizing γ-radiation-inactivated and a non-ionizing ultraviolet C-inactivated whole-cell vaccine candidate protects neutropenic mice from pulmonary challenge with virulent AB5075, a particularly pathogenic isolate. In addition, we demonstrate that a humoral response is sufficient for this protection via the passive immunization of neutropenic mice.