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The in vitro effects of synthetic complement peptide C3a during Brucella abortus 544 infection in a murine professional phagocyte RAW264.7 cell lineThe in vitro effects of synthetic complement peptide C3a during Brucella abortus 544 infection in a murine professional phagocyte RAW264.7 cell line

Other Titles
The in vitro effects of synthetic complement peptide C3a during Brucella abortus 544 infection in a murine professional phagocyte RAW264.7 cell line
Authors
Alisha Wehdnesday Bernardo Reyes김희진TRAN XUAN NGOC HUYTrang Thi Nguyen민원기김현진이후장김석
Issue Date
2021
Publisher
한국예방수의학회
Keywords
Brucella abortus; C3a; internalization; nitrite; RAW264.7
Citation
예방수의학회지, v.45, no.4, pp 188 - 193
Pages
6
Indexed
KCI
Journal Title
예방수의학회지
Volume
45
Number
4
Start Page
188
End Page
193
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/4769
ISSN
2287-7991
2287-8009
Abstract
We investigated the effect of a synthetic complement peptide C3a on the outcome of Brucella abortus 544 infection in a murine macrophage cell line RAW264.7 cell. First, we determined the highest non-cytotoxic concentration of the peptide in the cell line. We also found that the peptide significantly increased the growth of the bacteria at 8 and 24 h. Although the number of bacterial CFU was also elevated at 48 and 72 h, the increases were not significant as compared to controls. We further investigated the effect of C3a peptide on the growth of Brucella by pre-incubating the peptide at various temperatures and found that the effect was reversed at 24 h post-incubation suggesting that incubation of peptide at high temperatures including 65°C or 95°C could inactivate its action. This also could indicate the beneficial effect of high temperature during infection. Although several studies reported the inhibitory effect of different antimicrobial peptides including C3a, the present study preliminarily revealed that it had no positive contribution on the control of B. abortus 544 infection in vitro and indirectly to its receptor, CD88, which belongs to GPCR. Moreover, the encouraged further exploration of the effect of other similar peptides would be performed for the purpose of finding Brucella-host cell interaction for the control of disease progression.
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