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Enrichment of Native and Recombinant Extracellular Vesicles of Mycobacteria
Published on: December 8, 2023
Development of Different Methods for Preparing Acinetobacter baumannii Outer Membrane Vesicles Vaccine: Impact of
Sun Li1, Da-Qun Chen1, Lu Ji1
1Department of Microbiology and Biochemical Pharmacy, National Engineering Research Center of Immunological Products, College of Pharmacy, Third Military Medical University, Chongqing, China.
Abstract:
Acinetobacter baumannii (A. baumannii) is becoming a common global concern due to the emergence of multi-drug or pan-drug resistant strains. Confronting the issue of antimicrobial resistance by developing vaccines against the resistant pathogen is becoming a common strategy. In this study, different methods for preparing A. baumannii outer membrane vesicles (AbOMVs) vaccines were developed. sOMV (spontaneously released AbOMV) was extracted from the culture supernatant, while SuOMV (sucrose-extracted AbOMV) and nOMV (native AbOMV) were prepared from the bacterial cells. Three AbOMVs exhibited significant differences in yield, particle size, protein composition, and LPS/DNA content. To compare the protective efficacy of the three AbOMVs, groups of mice were immunized either intramuscularly or intranasally with each AbOMV. Vaccination via both routes conferred significant protection against lethal and sub-lethal A. baumannii challenge. Moreover, intranasal vaccination provided more robust protection, which may be attributed to the induction of significant sIgA response in mucosal sites. Among the three AbOMVs, SuOMV elicited the highest level of protective immunity against A. baumannii infection, whether intramuscular or intranasal immunization, which was characterized by the expression of the most profound specific serum IgG or mucosal sIgA. Taken together, the preparation method had a significant effect on the yield, morphology, and composition of AbOMVs, that further influenced the protective effect against A. baumannii infection.
Insights
Developing vaccines against drug-resistant Acinetobacter baumannii is crucial. Different preparation methods for outer membrane vesicles (AbOMVs) impact vaccine efficacy, with sucrose-extracted AbOMVs showing the most promise.
Area of Science:
- Microbiology
- Immunology
- Vaccine Development
Background:
- Acinetobacter baumannii is a growing global health threat due to multi-drug and pan-drug resistance.
- Antimicrobial resistance necessitates novel strategies, including vaccine development against resistant pathogens.
Purpose of the Study:
- To develop and compare different methods for preparing Acinetobacter baumannii outer membrane vesicles (AbOMVs) as vaccine candidates.
- To evaluate the protective efficacy of various AbOMV preparations against Acinetobacter baumannii infection in a mouse model.
Main Methods:
- Three distinct AbOMV preparation methods were employed: spontaneously released (sOMV), sucrose-extracted (SuOMV), and native (nOMV).
- AbOMVs were characterized based on yield, particle size, protein content, and LPS/DNA levels.
- Mice were immunized intramuscularly or intranasally with each AbOMV type and challenged with Acinetobacter baumannii.
Main Results:
- The three AbOMV types differed significantly in their yield, particle size, protein composition, and LPS/DNA content.
- Both intramuscular and intranasal vaccination routes provided significant protection against lethal and sub-lethal Acinetobacter baumannii challenge.
- Intranasal vaccination induced a more robust immune response, potentially due to increased mucosal sIgA.
- Sucrose-extracted AbOMVs (SuOMV) elicited the strongest protective immunity, indicated by high specific serum IgG and mucosal sIgA levels.
Conclusions:
- The method of AbOMV preparation significantly influences their characteristics and subsequent protective efficacy.
- Sucrose-extracted AbOMVs represent a promising candidate for developing effective vaccines against Acinetobacter baumannii infections.
- Vaccination strategies, particularly intranasal delivery, can enhance protection against this challenging pathogen.
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