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1.
Microbiol Immunol ; 62(11): 711-719, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30357922

ABSTRACT

Protein subunit vaccines are often preferred because of their protective efficacy and safety. Lactic acid bacteria expressing heterologous antigens constitute a promising approach to vaccine development. However, their safety in terms of toxicity and bacterial clearance must be evaluated. Anti-Streptococcus pyogenes (S. pyogenes) vaccines face additional safety concerns because they may elicit autoimmune responses. The assessment of toxicity, clearance and autoimmunity of an anti-streptococcal vaccine based on Lactococcus lactis (L. lactis) expressing 10 different M protein fragments from S. pyogenes (L. lactis-Mx10) is here reported. Clearance of L. lactis from the oropharynges of immunocompetent mice and mice devoid of T/B lymphocytes mice was achieved without using antibiotics. The absence of autoimmune responses against human tissues was demonstrated with human brain, heart and kidney. Assessment of toxicity showed that leucocyte counts and selected serum biochemical factors were not affected in L. lactis-Mx10-immunized mice. In contrast, mice immunized with L. lactis wild type vector (L. lactis-WT) showed increased neutrophil and monocyte counts and altered histopathology of lymph nodes, lungs and nasal epithelium. Two days after immunization, L. lactis-Mx10-immunized and L. lactis-WT-immunized mice weighed significantly less than unimmunized mice. However, both groups of immunized mice recovered their body weights by Day 6. Our results demonstrate that L. lactis-WT, but not the vaccine L. lactis-Mx10, induces alterations in certain hematologic and histopathological variables. We consider these data a major contribution to data on L. lactis as a bacterial vector for vaccine delivery.


Subject(s)
Administration, Intranasal/methods , Antigens, Bacterial/immunology , Lactococcus lactis/immunology , Streptococcal Infections/prevention & control , Streptococcal Vaccines/immunology , Streptococcus pyogenes/immunology , Vaccination/methods , Vaccines, Attenuated/immunology , Animals , Antibodies, Bacterial/blood , Antigens, Bacterial/genetics , Autoimmunity/immunology , Bacterial Outer Membrane Proteins/genetics , Bacterial Outer Membrane Proteins/immunology , Brain/immunology , Carrier Proteins/genetics , Carrier Proteins/immunology , Disease Models, Animal , Female , Humans , Immunization , Kidney/immunology , Lactococcus lactis/genetics , Lung/microbiology , Lung/pathology , Lymph Nodes/pathology , Mice , Mice, Inbred BALB C , Myocardium/immunology , Nasal Mucosa/pathology , Streptococcal Infections/immunology , Streptococcal Vaccines/administration & dosage , Streptococcal Vaccines/genetics , Streptococcal Vaccines/toxicity , Streptococcus pyogenes/genetics , Vaccines, Attenuated/administration & dosage , Vaccines, Attenuated/genetics
2.
Microbiology (Reading) ; 158(Pt 5): 1279-1283, 2012 May.
Article in English | MEDLINE | ID: mdl-22343353

ABSTRACT

Reactive oxygen species (ROSs) affect several macromolecules and cellular components in eukaryotic and prokaryotic cells. In this work, the effect of various ROS-generating compounds on the Escherichia coli membrane was studied. Membrane fatty acid profiles, oxidative damage levels and bacterial resistance to these toxicants were determined. Studies included wild-type cells as well as a strain exhibiting a modified monounsaturated fatty acid (MUFA) profile (accomplished by overexpressing the ß-hydroxyacyl acyl carrier protein dehydratase-encoding gene, fabA). Levels of membrane MUFAs and oxidative damage markers decreased slightly upon toxicant exposure with a concomitant increase in cell resistance to these ROS-generating compounds. A direct relationship between MUFAs and lipid peroxidation was observed. The lower the MUFA the lower the peroxide levels, suggesting that MUFAs are targets for membrane lipid oxidation.


Subject(s)
Escherichia coli/metabolism , Fatty Acids, Monounsaturated/metabolism , Oxidative Stress , Reactive Oxygen Species/metabolism , Escherichia coli Proteins/metabolism , Fatty Acid Synthase, Type II/metabolism , Hydro-Lyases/metabolism , Lipid Peroxidation , Protein Carbonylation
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