scholarly journals Evaluation of the Antibacterial Effects and Mechanism of Plantaricin 149 from Lactobacillus Plantarum NRIC 149 on the Peri-Implantitis Pathogens

Author(s):  
Xiaolong Lin ◽  
Jiajia Xu ◽  
Yuedan Xu ◽  
Zhiwei Shi ◽  
Tao Fu ◽  
...  

Abstract Peri-implantitis is a common reversible disease after tooth implantation, caused by a variety of pathogenic microorganisms. Based on non-surgical or surgical treatment principles, supplementation by local or systemic drugs might enhance treatment efficacy. Porphyromonas gingivalis (Pg) (ATCC 33277) and Prevotella intermedius (Pi) (ATCC 25611) were used as test strains. The effects of Pln 149 on the biofilm formation and growth of four periodontal pathogens were evaluated by RT-PCR, fluorescence microscopy, and scanning electron microscopy. The antibacterial mechanism was tested by the patch-clamp technique. The cytotoxicity of Pln 149 (125 µg/ml) to bone marrow stromal cell (BMSC) was assessed using an MTT assay. Pln 149 exhibited significant inhibitory effects on Pg and Pi (P<0.05), with significant differences in the biofilm images of fluorescence microscope and scanning electron microscope (P<0.05). Pln 149 could change the sodium channel currents and exerted no cytotoxicity on bone marrow stromal cell. Pln 149 could inhibit the biofilm formation and growth of periodontal pathogens. Considering the absence of antimicrobial resistance and cytotoxicity, we suggest that the Pln 149 from Lactobacillus plantarum 149 might be a promising option for managing peri-implantitis.

2012 ◽  
Vol 41 (4) ◽  
pp. 437-442 ◽  
Author(s):  
Hidetaka Nishida ◽  
Masanari Nakayama ◽  
Hiroshi Tanaka ◽  
Masahiko Kitamura ◽  
Shingo Hatoya ◽  
...  

Biomaterials ◽  
2013 ◽  
Vol 34 (10) ◽  
pp. 2389-2398 ◽  
Author(s):  
Wojtek Tutak ◽  
Sumona Sarkar ◽  
Sheng Lin-Gibson ◽  
Tanya M. Farooque ◽  
Giri Jyotsnendu ◽  
...  

PLoS ONE ◽  
2010 ◽  
Vol 5 (3) ◽  
pp. e9690 ◽  
Author(s):  
Fariba Rezaee ◽  
Stephanie L. Rellick ◽  
Giovanni Piedimonte ◽  
Stephen M. Akers ◽  
Heather A. O'Leary ◽  
...  

2015 ◽  
Vol 34 (1) ◽  
pp. 154-160 ◽  
Author(s):  
Chunfeng Zhao ◽  
Yasuhiro Ozasa ◽  
Haruhiko Shimura ◽  
Ramona L. Reisdorf ◽  
Andrew R. Thoreson ◽  
...  

Cell ◽  
1987 ◽  
Vol 48 (6) ◽  
pp. 1009-1021 ◽  
Author(s):  
Cheryl A. Whitlock ◽  
George F. Tidmarsh ◽  
Christa Muller-Sieburg ◽  
Irving L. Weissman

1992 ◽  
Vol 51 (S1) ◽  
pp. S16-S20 ◽  
Author(s):  
Kohei Notoya ◽  
Ryoichi Tsukuda ◽  
Keiji Yoshida ◽  
Shigehisa Taketomi

2010 ◽  
Vol 16 (6) ◽  
pp. 1913-1923 ◽  
Author(s):  
John T. Connelly ◽  
Eric J. Vanderploeg ◽  
Janna K. Mouw ◽  
Christopher G. Wilson ◽  
Marc E. Levenston

2018 ◽  
Vol 82 ◽  
pp. 1-11 ◽  
Author(s):  
Melanie J. Gupte ◽  
W. Benton Swanson ◽  
Jiang Hu ◽  
Xiaobing Jin ◽  
Haiyun Ma ◽  
...  

Blood ◽  
1989 ◽  
Vol 74 (3) ◽  
pp. 1144-1151
Author(s):  
P Anklesaria ◽  
TJ FitzGerald ◽  
K Kase ◽  
A Ohara ◽  
JS Greenberger

The ability of a clonal hematopoiesis-supportive bone-marrow stromal cell line GBlneor to engraft and alter the microenvironment-induced anemia of Sl/Sld mice was studied. Prior to stromal cell transplantation, Sl/Sld mice received 1 Gy total body irradiation (TBI) and 13 Gy to the right hind limb. Two months after intravenous (IV) injection of 5 x 10(5) GBlneor cells, 54.4% +/- 17.0% donor origin (G418r) colony-forming cells were recovered from the right hind limb of Sl/Sld mice. Long-term bone marrow cultures (LTBMCs) established from GBlneor-transplanted mice produced 189.5 CFU-GEMM-forming progenitors/flask over 10 weeks compared with 52.7 +/- 6.2 CFU-GEMM forming progenitors/flask from irradiated nontransplanted Sl/Sld mice. A partial correction of macrocytic anemia was detected 2 months after GBlneor transplantation in splenectomized, irradiated Sl/Sld mice (HgB 7.2 +/- 0.4 g/dL; MCV 68.3 +/- 7.0 fL) compared to splenectomized, irradiated, nontransplanted Sl/Sld mice (HgB 5.5 +/- 1.1 g/dL; MCV 76 +/- 8.5 fL) or control Sl/Sld mice (HgB 5.4 +/- 0.5 g/dL; MCV 82.4 +/- 1.3 fL). Mean RBC volume distribution analysis showed a 2.5-fold increase in percentage of peripheral blood RBCs with MCV less than or equal to 45 fL and confirmed reduction of the MCV in splenectomized- GBlneor-transplanted mice compared to control Sl/Sld mice. A hematopoiesis-suppressive clonal stromal cell line derived from LTBMCs of Sl/Sld mice (Sldneor) engrafted as effectively (43.5% +/- 1.2% G418r CFU-F/limb) as did GBlneor cells (38.3% +/- 0.16% G418r CFU-F/limb) to the irradiated right hind limbs of C57Bl/6 mice. LTBMCs established after 2 or 6 months from Sldneor-transplanted mice showed decreased hematopoiesis (182 +/- 12 [2 months] and 3494.3 +/- 408.1 [6 months] CFU-GEMM forming progenitors/flask over 10 weeks) compared to those established from GBlneor-transplanted mice (5980 +/- 530 [2 months] and 7728 +/- 607, [6 months] CFU-GEMM progenitors forming/flask). Thus, transplantation of clonal bone-marrow stromal cell lines in vivo can stably transfer their physiologic properties to normal or mutant mice.


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