2019
DOI: 10.1186/s13567-019-0714-3
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Rev1 wbdR tagged vaccines against Brucella ovis

Abstract: Sheep brucellosis is a worldwide extended disease caused by B. melitensis and B. ovis, two species respectively carrying smooth or rough lipopolysaccharide. Vaccine B. melitensis Rev1 is used against B. melitensis and B. ovis but induces an anti-smooth-lipopolysaccharide response interfering with B. melitensis serodiagnosis, which precludes its use against B. ovis where B. melitensis is absent. In mice, Rev1 deleted in wbkC (Brucella lipopolysaccharide formyl-transferase) and carrying wbdR (E. coli acetyl-tran… Show more

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Cited by 10 publications
(7 citation statements)
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References 33 publications
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“…[14,15]. Vaccination and treatment of brucellosis in farm animals are not considered 100% safe for human health, hence are forbidden in many countries [7,[16][17][18][19].…”
Section: Introductionmentioning
confidence: 99%
“…[14,15]. Vaccination and treatment of brucellosis in farm animals are not considered 100% safe for human health, hence are forbidden in many countries [7,[16][17][18][19].…”
Section: Introductionmentioning
confidence: 99%
“…Isolation of the bacteria remains a gold standard but is hazardous for human health and requires advanced biosafety levels (i.e., level 3) and good training. Despite availability of newer and effective antimicrobials, the treatment of farm animals for brucellosis is generally forbidden as it poses significant public health risks [ 8 , 9 , 10 ].…”
Section: Introductionmentioning
confidence: 99%
“…Iannino et al designed the Bab-pgm strain (genetically engineered live B. abortus vaccine) as a heterologous carrier for the recombinant chimeric antigen to deliver Shiga toxin-producing E. coli (STEC) in a mouse model, which resulted in the induction of a protective immune response against two very different pathogens ( 162 ). Another approach to vaccine development is the use of a modified Brucella immunodominant antigen instead of deleting Brucella antigens or epitopes or introducing a foreign antigen, which could induce differential antibodies against B. ovis ( 163 ). Another approach to vaccine production is polysaccharide conjugate vaccines which are produced via the covalent glycan-protein conjugation of bacterial surface; they have been proven to be cost-effective tools to prevent dramatic infectious diseases.…”
Section: Other Vaccinesmentioning
confidence: 99%