Filifactor alocis modulates human neutrophil antimicrobial functional responses.

Filifactor alocis modulates human neutrophil antimicrobial functional responses.
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DOI:
10.1111/cmi.12829
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发表时间:
2018-06
影响因子:
3.4
通讯作者:
Uriarte SM
Uriarte SM
中科院分区:
生物学2区
文献类型:
--
作者:
Edmisson JS;Tian S;Armstrong CL;Vashishta A;Klaes CK;Miralda I;Jimenez-Flores E;Le J;Wang Q;Lamont RJ;Uriarte SM

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Filifactor alocis is a newly appreciated pathogen in periodontal diseases. Neutrophils are the predominant innate immune cell in the gingival crevice. In this study we examined modulation of human neutrophil antimicrobial functions by F. alocis. Both non-opsonized and serum opsonized F. alocis were engulfed by neutrophils, but were not efficiently eliminated. Challenge of neutrophils with either non-opsonized or serum opsonized F. alocis induced a minimal intracellular as well as extracellular respiratory burst response compared to opsonized Staphylococcus aureus and fMLF, respectively. However, pre-treatment or simultaneous challenge of neutrophils with F. alocis did not affect the subsequent oxidative response to a particulate stimulus, suggesting that the inability to trigger the respiratory response was only localized to F. alocis phagosomes. In addition, while neutrophils engulfed live or heat-killed F. alocis with the same efficiency, heat-killed F. alocis elicited a higher intracellular respiratory burst response compared to viable organisms, along with decreased surface expression of CD35, a marker of secretory vesicles. F. alocis phagosomes remained immature by delayed and reduced recruitment of specific and azurophil granules, respectively. These results suggest that F. alocis withstands neutrophil antimicrobial responses by preventing intracellular ROS production, along with specific and azurophil granule recruitment to the bacterial phagosome.
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