ACS Central Science · 2021 · 47 citations · 22 references
<i>Acinetobacter baumannii</i> exhibits resistance to most first-line antibiotics; thus, development of new antibacterial agents is urgently required. Pseudaminic acid exists as the surface glycan of <i>A. baumannii</i>. In this study, we chemically synthesized pseudaminic acid, conjugated it to carrier protein CRM197 using the OPA (<i>ortho</i>-phthalaldehyde) chemistry, and obtained three Pse-CRM197 conjugates with different Pse loadings. These Pse-CRM197 conjugates were found to stimulate high immune responses in mice, which protected the vaccinated mice from infections caused by Pse-producing <i>A. baumannii</i>. Our data indicate that chemically synthesized Pse-CRM197 conjugates can be developed into vaccines against Pse-bearing pathogens, thus offering a feasible alternative for the control of clinical infections caused by multidrug-resistant (MDR) <i>A. baumannii</i>, for which current treatment options are extremely limited.
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Sara Tomczyk, Nancy M. Bennett, Charles Stoecker et al. · PubMed · 2014 · 664 citations · Full text
Colistin-Resistant Acinetobacter baumannii: Beyond Carbapenem Resistance
Zubair Qureshi, Lauren Hittle, Jessica A. O’Hara et al. · Clinical Infectious Diseases · 2015 · 394 citations · Full text
Celina Jin, Malick M. Gibani, Maria Moore et al. · The Lancet · 2017 · 308 citations · Full text