共 144 条
Engineered Remolding and Application of Bacterial Membrane Vesicles
被引:18
作者:

Qiao, Li
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机构:
Army Med Univ, Xinqiao Hosp, Dept Emergency, Chongqing, Peoples R China Army Med Univ, Xinqiao Hosp, Dept Emergency, Chongqing, Peoples R China

Rao, Yifan
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机构:
Army Med Univ, Xinqiao Hosp, Dept Emergency, Chongqing, Peoples R China Army Med Univ, Xinqiao Hosp, Dept Emergency, Chongqing, Peoples R China

Zhu, Keting
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h-index: 0
机构:
Army Med Univ, Xinqiao Hosp, Dept Emergency, Chongqing, Peoples R China Army Med Univ, Xinqiao Hosp, Dept Emergency, Chongqing, Peoples R China

Rao, Xiancai
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机构:
Army Med Univ, Key Lab Microbial Engn Educ Comm Chongqing, Coll Basic Med Sci, Dept Microbiol, Chongqing, Peoples R China Army Med Univ, Xinqiao Hosp, Dept Emergency, Chongqing, Peoples R China

Zhou, Renjie
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h-index: 0
机构:
Army Med Univ, Xinqiao Hosp, Dept Emergency, Chongqing, Peoples R China Army Med Univ, Xinqiao Hosp, Dept Emergency, Chongqing, Peoples R China
机构:
[1] Army Med Univ, Xinqiao Hosp, Dept Emergency, Chongqing, Peoples R China
[2] Army Med Univ, Key Lab Microbial Engn Educ Comm Chongqing, Coll Basic Med Sci, Dept Microbiol, Chongqing, Peoples R China
基金:
中国国家自然科学基金;
关键词:
extracellular vesicles;
vesicle production;
vesicle immunogenicity;
vaccine;
delivery system;
genetic modification;
B MENINGOCOCCAL DISEASE;
GRAM-POSITIVE BACTERIA;
OUTER-MEMBRANE;
EXTRACELLULAR VESICLES;
HELICOBACTER-PYLORI;
PROTEOMIC ANALYSIS;
ESCHERICHIA-COLI;
FUNCTIONAL-CHARACTERIZATION;
PERIPLASMIC PROTEINS;
CORE OLIGOSACCHARIDE;
D O I:
10.3389/fmicb.2021.729369
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Bacterial membrane vesicles (MVs) are produced by both Gram-positive and Gram-negative bacteria during growth in vitro and in vivo. MVs are nanoscale vesicular structures with diameters ranging from 20 to 400 nm. MVs incorporate bacterial lipids, proteins, and often nucleic acids, and can effectively stimulate host immune response against bacterial infections. As vaccine candidates and drug delivery systems, MVs possess high biosafety owing to the lack of self-replication ability. However, wild-type bacterial strains have poor MV yield, and MVs from the wild-type strains may be harmful due to the carriage of toxic components, such as lipopolysaccharides, hemolysins, enzymes, etc. In this review, we summarize the genetic modification of vesicle-producing bacteria to reduce MV toxicity, enhance vesicle immunogenicity, and increase vesicle production. The engineered MVs exhibit broad applications in vaccine designs, vaccine delivery vesicles, and drug delivery systems.</p>
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页数:14
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