The opportunistic pathogen Enterococcus faecalis resists phagosome acidification and autophagy to promote intracellular survival in macrophages

被引:57
作者
Zou, Jun [1 ]
Shankar, Nathan [1 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Pharmaceut Sci, Oklahoma City, OK USA
关键词
NITRIC-OXIDE SYNTHASE; PERITONEAL-MACROPHAGES; AGGREGATION SUBSTANCE; IN-VITRO; PHAGOCYTOSIS; ACTIVATION; INFECTION; IMMUNITY; DEFENSE; IDENTIFICATION;
D O I
10.1111/cmi.12556
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
While many strains of Enterococcus faecalis have been reported to be capable of surviving within macrophages for extended periods, the exact mechanisms involved are largely unknown. In this study, we found that after phagocytosis by macrophages, enterococci-containing vacuoles resist acidification, and E. faecalis is resistant to low pH. Ultrastructural examination of the enterococci-containing vacuole by transmission electron microscopy revealed a single membrane envelope, with no evidence of the classical double-membraned autophagosomes. Western blot analysis further confirmed that E. faecalis could trigger inhibition of the production of LC3-II during infection. By employing cells transfected with RFP-LC3 plasmid and infected with GFP-labelled E. faecalis, we also observed that E. faecalis was not delivered into autophagosomes during macrophage infection. While these observations indicated no role for autophagy in elimination of intracellular E. faecalis, enhanced production of reactive oxygen species and nitric oxide were keys to this process. Stimulation of autophagy suppressed the intracellular survival of E. faecalis in macrophages in vitro and decreased the burden of E. faecalis in vivo. In summary, the results from this study offer new insights into the interaction of E. faecalis with host cells and may provide a new approach to treatment of enterococcal infections.
引用
收藏
页码:831 / 843
页数:13
相关论文
共 41 条
[1]   Secretory phospholipase A2-potentiated inducible nitric oxide synthase expression by macrophages requires NF-κB activation [J].
Baek, SH ;
Kwon, TK ;
Lim, JH ;
Lee, YJ ;
Chang, HW ;
Lee, SJ ;
Kim, JH ;
Kwun, KB .
JOURNAL OF IMMUNOLOGY, 2000, 164 (12) :6359-6365
[2]   Glycosaminoglycans mediate invasion and survival of Enterococcus faecalis into macrophages [J].
Baldassarri, L ;
Bertuccini, L ;
Creti, R ;
Filippini, P ;
Ammendolia, MG ;
Koch, S ;
Huebner, J ;
Orefici, G .
JOURNAL OF INFECTIOUS DISEASES, 2005, 191 (08) :1253-1262
[3]   Intestinal Epithelial Autophagy Is Essential for Host Defense against Invasive Bacteria [J].
Benjamin, Jamaal L. ;
Sumpter, Rhea, Jr. ;
Levine, Beth ;
Hooper, Lora V. .
CELL HOST & MICROBE, 2013, 13 (06) :723-734
[4]   Autophagy controls Salmonella infection in response to damage to the Salmonella-containing vacuole [J].
Birmingham, CL ;
Smith, AC ;
Bakowski, MA ;
Yoshimori, T ;
Brumell, JH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (16) :11374-11383
[5]  
Brass AL, 2008, SCIENCE, V319, P921, DOI 10.1126/science.1152725
[6]   Autophagy induction by vitamin D inhibits both Mycobacterium tuberculosis and human immunodeficiency virus type 1 [J].
Campbell, Grant R. ;
Spector, Stephen A. .
AUTOPHAGY, 2012, 8 (10) :1523-1525
[7]   EVIDENCE FOR A GAMMA-INTERFERON RECEPTOR THAT REGULATES MACROPHAGE TUMORICIDAL ACTIVITY [J].
CELADA, A ;
GRAY, PW ;
RINDERKNECHT, E ;
SCHREIBER, RD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 160 (01) :55-74
[8]   Autophagy and bacterial infection: an evolving arms race [J].
Choy, Augustine ;
Roy, Craig R. .
TRENDS IN MICROBIOLOGY, 2013, 21 (09) :451-456
[9]   An AraC-Type Transcriptional Regulator Encoded on the Enterococcus faecalis Pathogenicity Island Contributes to Pathogenesis and Intracellular Macrophage Survival [J].
Coburn, Phillip S. ;
Baghdayan, Arto S. ;
Dolan, G. T. ;
Shankar, Nathan .
INFECTION AND IMMUNITY, 2008, 76 (12) :5668-5676
[10]   Vancomycin resistance in gram-positive cocci [J].
Courvalin, P .
CLINICAL INFECTIOUS DISEASES, 2006, 42 :S25-S34