Adenosine receptor Adora2b antagonism attenuates Brucella abortus 544 infection in professional phagocyte RAW 264.7 cells and BALB/c mice

2020 ◽  
Vol 242 ◽  
pp. 108586
Author(s):  
Alisha Wehdnesday Bernardo Reyes ◽  
Son Hai Vu ◽  
Tran Xuan Ngoc Huy ◽  
WonGi Min ◽  
Hu Jang Lee ◽  
...  
2018 ◽  
Vol 28 (10) ◽  
pp. 1723-1729 ◽  
Author(s):  
Tran Xuan Ngoc Huy ◽  
Alisha Wehdnesday Bernardo Reyes ◽  
Huynh Tan Hop ◽  
Lauren Togonon Arayan ◽  
Vu Hai Son ◽  
...  

2017 ◽  
Vol 27 (3) ◽  
pp. 616-623 ◽  
Author(s):  
Tran Xuan Ngoc Huy ◽  
Alisha Wehdnesday Bernardo Reyes ◽  
Huynh Tan Hop ◽  
Lauren Togonon Arayan ◽  
WonGi Min ◽  
...  

2012 ◽  
Vol 158 (3-4) ◽  
pp. 322-328 ◽  
Author(s):  
Dong Hyeok Kim ◽  
Jeong Ju Lim ◽  
Jin Ju Lee ◽  
Dae Geun Kim ◽  
Hu Jang Lee ◽  
...  

2021 ◽  
Vol 7 ◽  
Author(s):  
Tran Xuan Ngoc Huy ◽  
Trang Thi Nguyen ◽  
Alisha Wehdnesday Bernardo Reyes ◽  
Son Hai Vu ◽  
WonGi Min ◽  
...  

Protective efficiency of a combination of four recombinant Brucella abortus (B. abortus) proteins, namely outer membrane protein (Omp) 16, Omp19, Omp28, and 50S ribosomal protein L7/L12 was evaluated as a combined subunit vaccine (CSV) against B. abortus infection in RAW 264.7 cell line and murine model. The immunoreactivity of these four recombinant proteins as well as pCold-TF vector reacted with Brucella-positive serum individually, but not with Brucella-negative serum by immunoblotting assay. CSV-treated RAW 264.7 cells significantly induced production of IFN-γ and IL-12 while decreased IL-10 production at the late stage of infection compared to PBS-treated control cells. In addition, the enhancement of nitric oxide production together with cytokines secretion profile in CSV-treated cells proved that CSV notably activated bactericidal mechanisms in macrophages. Consistently, mice immunized with CSV strongly elicited production of pro-inflammatory cytokines TNF-α, IL-6 and MCP-1 compared to PBS control group. Moreover, the concentration of IFN-γ was >IL-10 and titers of IgG2a were also heightened compared to IgG1 in CSV-immunized mice which suggest that CSV induced predominantly T helper 1 T cell. These results suggest that the CSV used in the present study is a potential candidate as a preventive therapy against brucellosis.


2015 ◽  
Vol 362 (11) ◽  
Author(s):  
Lauren Togonon Arayan ◽  
Hannah Leah Simborio ◽  
Alisha Wehdnesday Bernardo Reyes ◽  
Huynh Tan Hop ◽  
WonGi Min ◽  
...  

2017 ◽  
Vol 103 ◽  
pp. 87-93 ◽  
Author(s):  
Alisha Wehdnesday Bernardo Reyes ◽  
Huynh Tan Hop ◽  
Lauren Togonon Arayan ◽  
Tran Xuan Ngoc Huy ◽  
Wongi Min ◽  
...  

2020 ◽  
Author(s):  
Zhiqiang Li ◽  
Shujuan Wei ◽  
Shuli Wang ◽  
Li Xi ◽  
Yanyan Cui ◽  
...  

Abstract Background: Brucellosis is an important zoonotic disease caused by the pathogen Brucella. Regulating apoptosis and autophagy is the prerequisite for the intracellular survival of Brucella. GntR is an important transcriptional regulator of Brucella that can regulate the expression of many target genes, and then play a regulatory role in many cell processes, including regulation apoptosis and autophagy. Therefore, understanding the relationship between GntR and apoptosis and autophagy is crucial to comprehending the pathogenic mechanism of Brucella. Methods: In the present study, we described the influence of GntR on apoptosis and autophagy after the infection of RAW 264.7 cells with Brucella. We constructed the GntR mutant strain (2308ΔGntR) of Brucella abortus 2308 (S2308). Following the infection of the RAW 264.7 cells with S2308 and 2308ΔGntR, apoptosis and autophagy were detected. Results: Western blot analysis and flow cytometry analysis indicated that the apoptosis rate of the 2308ΔGntR-infected group was remarkably higher than that of the S2308-infected group. Confocal laser microscopy experiments indicated the presence of the P62 protein as punctate aggregates in the 2308ΔGntR group. Conclusion: These results showed that 2308ΔGntR promoted apoptosis and inhibited autophagy in the RAW 264.7 cells during Brucella infection.


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