Impact of Live <i>Ligilactobacillus salivarius</i> CCFM1332 and Its Postbiotics on <i>Porphyromonas gingivalis</i> Colonization, Alveolar Bone Resorption and Inflammation in a Rat Model of Periodontitis

Periodontitis is a chronic inflammatory disease caused by periodontopathic bacteria such as <i>Porphyromonas gingivalis</i> (<i>P. gingivalis</i>), which leads to alveolar bone destruction and systemic inflammation. Emerging evidence suggests that probiotics may mitigate peri...

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Main Authors: Qing Hong, Yu Ren, Xin Tang, Bingyong Mao, Qiuxiang Zhang, Jianxin Zhao, Shumao Cui, Zhenmin Liu
Format: Article
Language:English
Published: MDPI AG 2025-07-01
Series:Microorganisms
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Online Access:https://www.mdpi.com/2076-2607/13/7/1701
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author Qing Hong
Yu Ren
Xin Tang
Bingyong Mao
Qiuxiang Zhang
Jianxin Zhao
Shumao Cui
Zhenmin Liu
author_facet Qing Hong
Yu Ren
Xin Tang
Bingyong Mao
Qiuxiang Zhang
Jianxin Zhao
Shumao Cui
Zhenmin Liu
author_sort Qing Hong
collection DOAJ
description Periodontitis is a chronic inflammatory disease caused by periodontopathic bacteria such as <i>Porphyromonas gingivalis</i> (<i>P. gingivalis</i>), which leads to alveolar bone destruction and systemic inflammation. Emerging evidence suggests that probiotics may mitigate periodontal pathology. To systematically evaluate the alleviative effects and mechanisms of different forms of probiotics, including live bacteria and postbiotics, on periodontitis, we first screened and identified <i>Ligilactobacillus salivarius</i> CCFM1332 (<i>L. salivarius</i> CCFM1332) through in vitro antibacterial and anti-biofilm activity assays. Subsequently, we investigated its therapeutic potential in a rat model of experimental periodontitis. The results demonstrated that both live <i>L. salivarius</i> CCFM1332 (PL) and its postbiotics (PP) significantly reduced the gingival index (GI) and probing depth (PD) in rats, while suppressing oral colonization of <i>P. gingivalis</i>. Serum pro-inflammatory cytokine levels were differentially modulated: the PL group exhibited reductions in interleukin-17A (IL-17A), interleukin-6 (IL-6), and interleukin-1β (IL-1β) by 39.31% (<i>p</i> < 0.01), 17.26% (<i>p</i> < 0.05), and 14.74% (<i>p</i> < 0.05), respectively, whereas the PP group showed decreases of 34.79% (<i>p</i> < 0.05), 29.85% (<i>p</i> < 0.01), and 19.74% (<i>p</i> < 0.05). Micro-computed tomography (Micro-CT) analysis demonstrated that compared to the periodontitis model group (PM), the PL group significantly reduced alveolar bone loss (ABL) by 30.1% (<i>p</i> < 0.05) and increased bone volume fraction (BV/TV) by 49.5% (<i>p</i> < 0.01). In contrast, while the PP group similarly decreased ABL by 32.7% (<i>p</i> < 0.05), it resulted in a 40.4% improvement in BV/TV (<i>p</i> > 0.05). Histological assessments via hematoxylin and eosin (H&E) and tartrate-resistant acid phosphatase (TRAP) staining confirmed that both the PL group and the PP group alleviated structural damage to alveolar bone-supporting tissues and reduced osteoclast-positive cell counts. This study suggests that live <i>L. salivarius</i> CCFM1332 and its postbiotics reduce alveolar bone resorption and attachment loss in rats through antibacterial and anti-inflammatory pathways, thereby alleviating periodontal inflammation in rats.
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spelling doaj-art-a3b78c1999ff46caa16f40547f6bbb422025-08-20T03:08:13ZengMDPI AGMicroorganisms2076-26072025-07-01137170110.3390/microorganisms13071701Impact of Live <i>Ligilactobacillus salivarius</i> CCFM1332 and Its Postbiotics on <i>Porphyromonas gingivalis</i> Colonization, Alveolar Bone Resorption and Inflammation in a Rat Model of PeriodontitisQing Hong0Yu Ren1Xin Tang2Bingyong Mao3Qiuxiang Zhang4Jianxin Zhao5Shumao Cui6Zhenmin Liu7State Key Laboratory of Dairy Biotechnology, Shanghai Engineering Research Center of Dairy Biotechnology, Dairy Research Institute, Bright Dairy & Food Co., Ltd., Shanghai 200436, ChinaState Key Laboratory of Food Science and resources, Jiangnan University, Wuxi 214122, ChinaState Key Laboratory of Food Science and resources, Jiangnan University, Wuxi 214122, ChinaState Key Laboratory of Food Science and resources, Jiangnan University, Wuxi 214122, ChinaState Key Laboratory of Food Science and resources, Jiangnan University, Wuxi 214122, ChinaState Key Laboratory of Food Science and resources, Jiangnan University, Wuxi 214122, ChinaState Key Laboratory of Dairy Biotechnology, Shanghai Engineering Research Center of Dairy Biotechnology, Dairy Research Institute, Bright Dairy & Food Co., Ltd., Shanghai 200436, ChinaState Key Laboratory of Dairy Biotechnology, Shanghai Engineering Research Center of Dairy Biotechnology, Dairy Research Institute, Bright Dairy & Food Co., Ltd., Shanghai 200436, ChinaPeriodontitis is a chronic inflammatory disease caused by periodontopathic bacteria such as <i>Porphyromonas gingivalis</i> (<i>P. gingivalis</i>), which leads to alveolar bone destruction and systemic inflammation. Emerging evidence suggests that probiotics may mitigate periodontal pathology. To systematically evaluate the alleviative effects and mechanisms of different forms of probiotics, including live bacteria and postbiotics, on periodontitis, we first screened and identified <i>Ligilactobacillus salivarius</i> CCFM1332 (<i>L. salivarius</i> CCFM1332) through in vitro antibacterial and anti-biofilm activity assays. Subsequently, we investigated its therapeutic potential in a rat model of experimental periodontitis. The results demonstrated that both live <i>L. salivarius</i> CCFM1332 (PL) and its postbiotics (PP) significantly reduced the gingival index (GI) and probing depth (PD) in rats, while suppressing oral colonization of <i>P. gingivalis</i>. Serum pro-inflammatory cytokine levels were differentially modulated: the PL group exhibited reductions in interleukin-17A (IL-17A), interleukin-6 (IL-6), and interleukin-1β (IL-1β) by 39.31% (<i>p</i> < 0.01), 17.26% (<i>p</i> < 0.05), and 14.74% (<i>p</i> < 0.05), respectively, whereas the PP group showed decreases of 34.79% (<i>p</i> < 0.05), 29.85% (<i>p</i> < 0.01), and 19.74% (<i>p</i> < 0.05). Micro-computed tomography (Micro-CT) analysis demonstrated that compared to the periodontitis model group (PM), the PL group significantly reduced alveolar bone loss (ABL) by 30.1% (<i>p</i> < 0.05) and increased bone volume fraction (BV/TV) by 49.5% (<i>p</i> < 0.01). In contrast, while the PP group similarly decreased ABL by 32.7% (<i>p</i> < 0.05), it resulted in a 40.4% improvement in BV/TV (<i>p</i> > 0.05). Histological assessments via hematoxylin and eosin (H&E) and tartrate-resistant acid phosphatase (TRAP) staining confirmed that both the PL group and the PP group alleviated structural damage to alveolar bone-supporting tissues and reduced osteoclast-positive cell counts. This study suggests that live <i>L. salivarius</i> CCFM1332 and its postbiotics reduce alveolar bone resorption and attachment loss in rats through antibacterial and anti-inflammatory pathways, thereby alleviating periodontal inflammation in rats.https://www.mdpi.com/2076-2607/13/7/1701periodontitis<i>Ligilactobacillus salivarius</i>postbioticsinflammationalveolar bone resorption
spellingShingle Qing Hong
Yu Ren
Xin Tang
Bingyong Mao
Qiuxiang Zhang
Jianxin Zhao
Shumao Cui
Zhenmin Liu
Impact of Live <i>Ligilactobacillus salivarius</i> CCFM1332 and Its Postbiotics on <i>Porphyromonas gingivalis</i> Colonization, Alveolar Bone Resorption and Inflammation in a Rat Model of Periodontitis
Microorganisms
periodontitis
<i>Ligilactobacillus salivarius</i>
postbiotics
inflammation
alveolar bone resorption
title Impact of Live <i>Ligilactobacillus salivarius</i> CCFM1332 and Its Postbiotics on <i>Porphyromonas gingivalis</i> Colonization, Alveolar Bone Resorption and Inflammation in a Rat Model of Periodontitis
title_full Impact of Live <i>Ligilactobacillus salivarius</i> CCFM1332 and Its Postbiotics on <i>Porphyromonas gingivalis</i> Colonization, Alveolar Bone Resorption and Inflammation in a Rat Model of Periodontitis
title_fullStr Impact of Live <i>Ligilactobacillus salivarius</i> CCFM1332 and Its Postbiotics on <i>Porphyromonas gingivalis</i> Colonization, Alveolar Bone Resorption and Inflammation in a Rat Model of Periodontitis
title_full_unstemmed Impact of Live <i>Ligilactobacillus salivarius</i> CCFM1332 and Its Postbiotics on <i>Porphyromonas gingivalis</i> Colonization, Alveolar Bone Resorption and Inflammation in a Rat Model of Periodontitis
title_short Impact of Live <i>Ligilactobacillus salivarius</i> CCFM1332 and Its Postbiotics on <i>Porphyromonas gingivalis</i> Colonization, Alveolar Bone Resorption and Inflammation in a Rat Model of Periodontitis
title_sort impact of live i ligilactobacillus salivarius i ccfm1332 and its postbiotics on i porphyromonas gingivalis i colonization alveolar bone resorption and inflammation in a rat model of periodontitis
topic periodontitis
<i>Ligilactobacillus salivarius</i>
postbiotics
inflammation
alveolar bone resorption
url https://www.mdpi.com/2076-2607/13/7/1701
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