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1.
Clin Exp Immunol ; 196(3): 287-304, 2019 06.
Article in English | MEDLINE | ID: mdl-30985006

ABSTRACT

Plague caused by the Gram-negative bacterium, Yersinia pestis, is still endemic in parts of the world today. Protection against pneumonic plague is essential to prevent the development and spread of epidemics. Despite this, there are currently no licensed plague vaccines in the western world. Here we describe the means of delivering biologically active plague vaccine antigens directly to mucosal sites of plague infection using highly stable microvesicles (outer membrane vesicles; OMVs) that are naturally produced by the abundant and harmless human commensal gut bacterium Bacteroides thetaiotaomicron (Bt). Bt was engineered to express major plague protective antigens in its OMVs, specifically Fraction 1 (F1) in the outer membrane and LcrV (V antigen) in the lumen, for targeted delivery to the gastrointestinal (GI) and respiratory tracts in a non-human primate (NHP) host. Our key findings were that Bt OMVs stably expresses F1 and V plague antigens, particularly the V antigen, in the correct, immunogenic form. When delivered intranasally V-OMVs elicited substantive and specific immune and antibody responses, both in the serum [immunoglobulin (Ig)G] and in the upper and lower respiratory tract (IgA); this included the generation of serum antibodies able to kill plague bacteria. Our results also showed that Bt OMV-based vaccines had many desirable characteristics, including: biosafety and an absence of any adverse effects, pathology or gross alteration of resident microbial communities (microbiotas); high stability and thermo-tolerance; needle-free delivery; intrinsic adjuvanticity; the ability to stimulate both humoral and cell-mediated immune responses; and targeting of primary sites of plague infection.


Subject(s)
Antigens, Bacterial/metabolism , Bacterial Outer Membrane/metabolism , Bacteroides thetaiotaomicron/metabolism , Plague Vaccine/immunology , Plague/immunology , Pore Forming Cytotoxic Proteins/metabolism , Transport Vesicles/immunology , Yersinia pestis/physiology , Administration, Intranasal , Animals , Antibodies, Bacterial/blood , Antigens, Bacterial/genetics , Bacteroides thetaiotaomicron/genetics , Bioengineering , Cell Death , Cells, Cultured , Gastrointestinal Microbiome/genetics , Humans , Immunity, Cellular , Immunity, Humoral , Immunoglobulin A/metabolism , Immunoglobulin G/blood , Macaca , Plague/prevention & control , Plague Vaccine/metabolism , Pore Forming Cytotoxic Proteins/genetics , Transport Vesicles/metabolism
2.
Food Microbiol ; 57: 8-15, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27052696

ABSTRACT

Dairy products are perishable and have to be preserved from spoilage during the food chain to achieve the desired shelf-life. Ricotta is a typical Italian soft dairy food produced by heat coagulation of whey proteins and is considered to be a light and healthy product. The shelf-life of Ricotta could be extended, as required by the international food trade market; however, heat resistant microflora causes spoilage and poses issues regarding the safety of the product. Next-generation sequencing (NGS) applied to the Ricotta samples defined the composition of the microbial community in-depth during the shelf-life. The analysis demonstrated the predominance of spore-forming bacteria throughout the shelf-life, mostly belonging to Bacillus, Paenibacillus and Clostridium genera. A strain involved in spoilage and causing a pink discolouration of Ricotta was isolated and characterised as Bacillus mycoides/weihenstephanensis. This is the first report of a food discolouration caused by a toxigenic strain belonging to the Bacillus cereus group that resulted the predominant strain in the community of the defective ricotta. These results suggest that the processing of raw materials to eliminate spores and residual microflora could be essential for improving the quality and the safety of the product and to extend the shelf-life of industrial Ricotta.


Subject(s)
Bacillus/metabolism , Cheese/microbiology , Pigments, Biological/metabolism , Animals , Bacillus/classification , Bacillus/genetics , Bacillus/isolation & purification , Bacteria/classification , Bacteria/genetics , Bacteria/isolation & purification , Bacteria/metabolism , Cattle , Cheese/analysis , Food Storage , Milk/microbiology
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