TY - JOUR
T1 - The role of ST2 receptor in the regulation of Brucella abortus oral infection
AU - Santos, Raiany
AU - Campos, Priscila C.
AU - Rungue, Marcella
AU - Rocha, Victor
AU - Santos, David
AU - Mendes, Viviani
AU - Marinho, Fabio V.
AU - Martins, Flaviano
AU - Ricci, Mayra F.
AU - Dos Reis, Diego C.
AU - Cassali, Geovanni D.
AU - Alves-Filho, José Carlos
AU - Vieira, Angelica T.
AU - Oliveira, Sergio C.
N1 - Funding Information:
financial support of CNPq (grants# 302660/2015-1 and and APQ-01945-17) and National Institute of HealthR01
Funding Information:
This study was carried out with the financial support of CNPq (grants# 302660/2015-1 and 406883/2018-1), FAPEMIG (grants# APQ-00837-15 and APQ-01945-17) and National Institute of Health R01 AI116453.
Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/5
Y1 - 2020/5
N2 - The ST2 receptor plays an important role in the gut such as permeability regulation, epithelium regeneration, and promoting intestinal immune modulation. Here, we studied the role of ST2 receptor in a murine model of oral infection with Brucella abortus, its influence on gut homeostasis and control of bacterial replication. Balb/c (wild-type, WT) and ST2 deficient mice (ST2-/-) were infected by oral gavage and the results were obtained at 3 and 14 days post infection (dpi). Our results suggest that ST2-/- are more resistant to B. abortus infection, as a lower bacterial colony-forming unit (CFU) was detected in the livers and spleens of knockout mice, when compared to WT. Additionally, we observed an increase in intestinal permeability in WT-infected mice, compared to ST2-/- animals. Breakage of the intestinal epithelial barrier and bacterial dissemination might be associated with the presence of the ST2 receptor; since, in the knockout mice no change in intestinal permeability was observed after infection. Together with enhanced resistance to infection, ST2-/-produced greater levels of IFN-γ and TNF-α in the small intestine, compared to WT mice. Nevertheless, in the systemic model of infection ST2 plays no role in controlling Brucella replication in vivo. Our results suggest that the ST2 receptor is involved in the invasion process of B. abortus by the mucosa in the oral infection model.
AB - The ST2 receptor plays an important role in the gut such as permeability regulation, epithelium regeneration, and promoting intestinal immune modulation. Here, we studied the role of ST2 receptor in a murine model of oral infection with Brucella abortus, its influence on gut homeostasis and control of bacterial replication. Balb/c (wild-type, WT) and ST2 deficient mice (ST2-/-) were infected by oral gavage and the results were obtained at 3 and 14 days post infection (dpi). Our results suggest that ST2-/- are more resistant to B. abortus infection, as a lower bacterial colony-forming unit (CFU) was detected in the livers and spleens of knockout mice, when compared to WT. Additionally, we observed an increase in intestinal permeability in WT-infected mice, compared to ST2-/- animals. Breakage of the intestinal epithelial barrier and bacterial dissemination might be associated with the presence of the ST2 receptor; since, in the knockout mice no change in intestinal permeability was observed after infection. Together with enhanced resistance to infection, ST2-/-produced greater levels of IFN-γ and TNF-α in the small intestine, compared to WT mice. Nevertheless, in the systemic model of infection ST2 plays no role in controlling Brucella replication in vivo. Our results suggest that the ST2 receptor is involved in the invasion process of B. abortus by the mucosa in the oral infection model.
KW - Brucella abortus
KW - Oral infection
KW - ST2 receptor
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U2 - 10.3390/pathogens9050328
DO - 10.3390/pathogens9050328
M3 - Article
C2 - 32353980
AN - SCOPUS:85084203325
SN - 2076-0817
VL - 9
JO - Pathogens
JF - Pathogens
IS - 5
M1 - 328
ER -