2015, Number 2
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Vet Mex 2015; 2 (2)
Stability of the B. abortus S19 vaccine strain with a eukaryotic expression plasmid encoding the G glycoprotein from the rabies virus
Pazos SNG, Benítez SJC, Calderón CJL, Hernández-Castro R, Díaz AE, Aguilar SJA
Language: English/Spanish
References: 30
Page: 1-13
PDF size: 1065.57 Kb.
ABSTRACT
Brucella abortus S19 is an intracellular vaccine strain against bovine brucellosis.
Rabies is a lethal disease in cattle. Plasmids encoding the G glycoprotein
from the rabies virus induce a protective immune response in different animal
species. A vector called pBBR4-CMV-Ggp-SV40+, which encodes the G
gene, regulated by the cytomegalovirus eukaryotic expression promoter, and
which can be used to transform the
B. abortus S19 vaccine strain, was constructed.
The stability of the transformant strain was tested both
in vitro and
in vivo. In the
in vitro assays,
B. abortus S19 pBBR4-CMV-Ggp-SV40+ was
grown for 5 sequential passages, and for the
in vivo assays, female BALB/c
mice were infected. Colony-forming unit counting and plasmid identification
were performed in each passage and in the spleens at 7 days post-infection.
To test the plasmid stability in the strain, all parameters were determined
with and without antibiotic. The bacterial concentration was lower with antibiotic
than without it, but the bacterial growth was more homogeneous.
The plasmid was identified in antibiotic- and non-antibiotic-treated isolated
colonies under both
in vitro and
in vivo conditions. The plasmid construct was
also transfected into BHK-21 cells, which express the G glycoprotein. The
B.
abortus S19 pBBR4-CMV-Ggp-SV40+ strain showed stability, representing a
suitable candidate vector for developing a bivalent vaccine against brucellosis
and rabies. This is the first time that a
Brucella species has been transformed
with a eukaryotic expression plasmid.
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